A
ABO Group and Rh Type
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Test Name:
ABO Group and Rh Type
-
Test Code:
R7788
-
Alias:
Type and Group, Blood Type
-
CPT Code(s):
86900, 86901
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Preferred Specimen:
5 mL whole blood collected in an EDTA (pink-top) tube
-
Min. Volume:
5 mL
-
Transport Container:
EDTA (pink-top) tube
-
Collection Instruction:
If submitting with a CBC, HbA1c, or any other test requiring an EDTA (lavender-top) tube, please submit a separate tube for this test
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
ABO Group and Rh Type - ABO type and Rh are needed to identify candidates for Rh immune globulin and to assess the risk of hemolytic disease of the newborn.
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Performing Lab:
Quest Diagnostics - Great Lakes Region
ACTIQ (MEDICATION)
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Test Name:
ACTIQ (MEDICATION)
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Test Code:
501680
ADDERALL (MEDICATION)
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Test Name:
ADDERALL (MEDICATION)
-
Test Code:
500730
ADDERALL XR (MEDICATION)
-
Test Name:
ADDERALL XR (MEDICATION)
-
Test Code:
500740
AIRACOF (MEDICATION)
-
Test Name:
AIRACOF (MEDICATION)
-
Test Code:
501370
ALA-HIST AC (MEDICATION)
-
Test Name:
ALA-HIST AC (MEDICATION)
-
Test Code:
501480
ALANINE AMINOTRANSFERASE (ALT, SGPT)
-
Test Name:
ALANINE AMINOTRANSFERASE (ALT, SGPT)
-
Test Code:
SGPT
-
Alias:
ALT, SGPT
-
CPT Code(s):
84460
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
.3 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 3 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Alanine aminotransferase (ALT) measurements are useful in the diagnostics and treatment of certain liver diseases (e.g. viral hepatitis and cirrhosis) and heart disease.
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Performing Lab:
Simple Laboratories
ALKALINE PHOSPHATASE, TOTAL
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Test Name:
ALKALINE PHOSPHATASE, TOTAL
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Test Code:
ALK
-
Alias:
ALK PHOS. ALP
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CPT Code(s):
84075
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Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow serum specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 4 days Frozen: 2 Months
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Mesurements of serum alkaline phosphatase (ALP) are used in the diagnosis of hepatobiliary disorders and bone disease associated with increased osteoblastic activity. Certain conditions such as Hodgkin's Disease, congestive heart failure and ulcerative colitis will produce moderate elevation in alkaline phosphatase levels. Non-pathologic elevations can be observed in the thrid trimester of pregnancy.
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Performing Lab:
Simple Laboratories
ALMAZINE (MEDICATION)
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Test Name:
ALMAZINE (MEDICATION)
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Test Code:
501780
ALZAPAM (MEDICATION)
-
Test Name:
ALZAPAM (MEDICATION)
-
Test Code:
501790
AMIDONE (MEDICATION)
-
Test Name:
AMIDONE (MEDICATION)
-
Test Code:
501640
AMITRIPTYLINE HCL (MEDICATION)
-
Test Name:
AMITRIPTYLINE HCL (MEDICATION)
-
Test Code:
500420
AMOBARBITAL (MEDICATION)
-
Test Name:
AMOBARBITAL (MEDICATION)
-
Test Code:
500510
AMP ASPARTATE (MEDICATION)
-
Test Name:
AMP ASPARTATE (MEDICATION)
-
Test Code:
500760
AMP SULFATE (MEDICATION)
-
Test Name:
AMP SULFATE (MEDICATION)
-
Test Code:
500780
AMPHETAMINE SULFATE (MEDICATION)
-
Test Name:
AMPHETAMINE SULFATE (MEDICATION)
-
Test Code:
500800
AMYLASE, SERUM
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Test Name:
AMYLASE, SERUM
-
Test Code:
AMYL
-
CPT Code(s):
82150
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Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-hep tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 7 days Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Amylase is found primarily in the pancreas and salivary glands. Elevated serum levels are associated with acute pancreatitis and other pancreatic disorders as well as mumps and bacterial parotitis.
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Performing Lab:
Simple Laboratories
ANA Multiplex, Panel 1 with Reflexes
-
Test Name:
ANA Multiplex, Panel 1 with Reflexes
-
Test Code:
R37521
-
CPT Code(s):
86038, 86235 (x5), 86255, 86431
-
Test Includes:
ANA Screen, Immunoassay with Reflex to Titer and Pattern Rheumatoid Factor DNA (ds) Antibody, Crithidia IFA with Reflex to Titer Sm Antibody Sm/RNP Antibody Scleroderma Antibody (Scl-70) Sjogren's Antibodies (SS-A, SS-B)
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Preferred Specimen:
3 mL serum
-
Min. Volume:
1.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
ANA Multiplex, Panel 1 with Reflexes - This panel can be helpful in the diagnosis of autoimmune rheumatic diseases, including systemic lupus erythematosus, systemic sclerosis, Sjogren syndrome, mixed connective tissue disease, and rheumatoid arthritis. All specimens are screened for antinuclear antibodies (ANAs) with multiplex immunoassay. This approach simultaneously detects antibodies to dsDNA, chromatin, ribosomal protein, SSA, SSB, Smith (Sm), Sm/RNP, RNP, Scl-70, Jo-1, and centromere B. A positive result indicates the presence of at least 1 of these antibodies; a negative result indicates that none of the component antibodies were detected. Regardless of the result, this panel also detects antibodies to dsDNA, Sm, Sm/RNP, Scl-70, SSA and SSB as well as rheumatoid factor. ANA immunofluorescence assay (IFA) on HEp-2 cells is considered by the American College of Rheumatology as the current gold standard for ANA screening because of its overall high sensitivity for several autoimmune diseases [1]. However, because patients with other diseases and healthy individuals may be positive for ANA IFA, using immunoassays for screening may be more specific for a systemic rheumatic disorder [2]. On the other hand, multiplex immunoassay screening cannot rule out autoimmune diseases characterized by other antibodies, such as autoimmune hepatitis and primary biliary cholangitis, which may be positive for ANA IFA. The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.
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Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
ANA SCREEN ONLY
-
Test Name:
ANA SCREEN ONLY
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Test Code:
ANA
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CPT Code(s):
86038
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
The antinuclear antibody (ANA) test is an indirect immunofluorescent test to detect antinuclear antibody activity in sera of patients with autoimmune rheumatic disease and connective tissue disease.
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Performing Lab:
Simple Laboratories
ANCA Screen with MPO and PR3, with Reflex to ANCA Titer
-
Test Name:
ANCA Screen with MPO and PR3, with Reflex to ANCA Titer
-
Test Code:
R70159
-
CPT Code(s):
86021 (x2), 86036
-
Test Includes:
ANCA Screen with Reflex to ANCA Titer Myeloperoxidase Antibody (MPO) Proteinase-3 Antibody If ANCA Screen is positive, then C-ANCA Titer and/or P-ANCA Titer and/or atypical P-ANCA Titer will be performed at an additional charge (CPT code(s): 86037 for each titer performed).
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
0.8 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
ANCA Screen with MPO and PR3, with Reflex to ANCA Titer - Testing for anti-neutrophil cytoplasmic antibodies (P-ANCA and/or C-ANCA) has been found to be useful in establishing the diagnosis of suspected vascular diseases, inflammatory bowel disease, as well as other autoimmune diseases.
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Performing Lab:
Quest Diagnostics - Great Lakes Region
Angiotensin Converting Enzyme
-
Test Name:
Angiotensin Converting Enzyme
-
Test Code:
R683
-
Alias:
ACE,Angiotensin-1-Converting Enzyme,Sarcoidosis
-
CPT Code(s):
82164
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 60 days
-
Clinical Significance:
Angiotensin Converting Enzyme - This test is useful in evaluating patients presenting with sarcoidosis, Gaucher's disease and lymphangiomyomatosis in that the enzyme is increased in these clinical settings.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Anti-Mullerian Hormone (AMH), Female
-
Test Name:
Anti-Mullerian Hormone (AMH), Female
-
Test Code:
R37227
-
Alias:
Mullerian Inhibiting Substance,AMH/MIS
-
CPT Code(s):
82166
-
Preferred Specimen:
0.5 mL serum
-
Min. Volume:
0.3 mL
-
Transport Container:
Plastic transport tube
-
Collection Instruction:
Separate serum/plasma from the cells within 2 hours of collection, ship in a plastic leak-proof container refrigerated or frozen.
Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. For patients receiving STRENSIQ, consideration should be given to using alternate methods.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 24 hours Refrigerated: 6 days Frozen: 28 days
-
Clinical Significance:
Anti-Mullerian Hormone (AMH), Female - AMH-MIS may be used in the investigation of ovarian reserve since AMH concentrations in adult women reflect the number of small antral and preantral follicles entering the growth phase of their life cycle. These follicles are proportional to the number of primordial follicles that still remain in the ovary, or the ovarian reserve. AMH decreases throughout a woman's reproductive life, which reflects the continuous decline of the oocyte/follicle pool with age and, accordingly, ovarian aging
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Performing Lab:
Quest Diagnostics - Great Lakes Region
Anti-Mullerian Hormone (AMH), Male
-
Test Name:
Anti-Mullerian Hormone (AMH), Male
-
Test Code:
R37226
-
Alias:
Mullerian Inhibiting Substance,AMH/MIS
-
CPT Code(s):
82166
-
Preferred Specimen:
0.5 mL serum
-
Min. Volume:
0.3 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Separate serum/plasma from the cells within 2 hours of collection, ship in a plastic leak-proof container refrigerated or frozen.
Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. For patients receiving STRENSIQ, consideration should be given to using alternate methods
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 24 hours Refrigerated: 6 days Frozen: 28 days
-
Clinical Significance:
Anti-Mullerian Hormone (AMH), Male - AMH/MIS may be used in the detection of the onset of puberty in males, in the differential diagnosis of intersex disorders, cryptorchidism, or anorchidism and in the evaluation of male gonadal function in all ages.
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Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
ANXIEDIN (MEDICATION)
-
Test Name:
ANXIEDIN (MEDICATION)
-
Test Code:
501800
APLACASSEE (MEDICATION)
-
Test Name:
APLACASSEE (MEDICATION)
-
Test Code:
501810
Apolipoprotein B
-
Test Name:
Apolipoprotein B
-
Test Code:
R5224
-
Alias:
Apo B
-
CPT Code(s):
82172
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Apolipoprotein B - Apolipoprotein B (APO B) has been reported to be a powerful indicator of CAD. In some patients with CAD, APO B is elevated even in the presence of normal LDL cholesterol.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
ASO (ANTISTREPTOLYSIN O TITER)
-
Test Name:
ASO (ANTISTREPTOLYSIN O TITER)
-
Test Code:
ASO
-
Alias:
ASO
-
CPT Code(s):
86060
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted. If the specimen is collected in a Plain Red (no additive/gel) tube, transfer the separated serum to a properly labeled plastic transfer tube. Specify specimen type (serum) on the transfer tube.
-
Transport Temperature:
Refrigerated
-
Schedule:
1-2 Days
-
Clinical Significance:
An elevated level of ASO is an indication of recent infection, and can be an aid in the diagnosis of acute rheumatic fever and post-streptococcal glomerulonephritis.
-
Performing Lab:
Simple Laboratories
ASPARTATE AMINOTRANSFERASE (AST,SGOT)
-
Test Name:
ASPARTATE AMINOTRANSFERASE (AST,SGOT)
-
Test Code:
SGOT
-
Alias:
AST, SGOT
-
CPT Code(s):
84450
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 24 hours Refrigerated: 4 weeks days
-
Schedule:
1-2 Days
-
Clinical Significance:
Serum AST is one of a group of enzymes which catalyzes the interconversion of amino acids and keto acids by transfer of amino groups. Transaminases are widely distributed in body tissues with significant amounts found in the heart and liver. Lesser amounts are also found in skeletal muscles, kidneys, pancreas, spleen, lungs, and brain. Injury to these tissues result in the release of the AST enzyme to general circulation
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Performing Lab:
Simple Laboratories
ATIVAN (MEDICATION)
-
Test Name:
ATIVAN (MEDICATION)
-
Test Code:
501820
AVINZA (MEDICATION)
-
Test Name:
AVINZA (MEDICATION)
-
Test Code:
500640
B
B12 + FOLIC ACID
-
Test Name:
B12 + FOLIC ACID
-
Test Code:
043
-
Alias:
B12 / Folic AcidCobalamin, True / Folic Acid
-
CPT Code(s):
82746, 82607
-
Test Includes:
Vitamin B12Folate, Serum
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 mL serumThis volume does not allow for repeat testing.
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
A fasting specimen is preferred. Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection into a properly labeled transfer tube.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hoursRefrigerated: 3 days
-
Schedule:
1-2 Days
-
Clinical Significance:
See individual test
-
Performing Lab:
Simple Laboratories
BACTERIAL VAGINOSIS PANEL
-
Test Name:
BACTERIAL VAGINOSIS PANEL
-
Test Code:
LS5002
-
CPT Code(s):
81513
-
Test Includes:
ATOPOBIUM; BVAB2; MEGASPHAERA 1
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected
-
Transport Container:
APTIMA MULTI-TEST SWAB (ORANGE)
-
Collection Instruction:
1. Open Aptima Multitest swab package (orange) and remove the swab. Do not touch the soft tip.
2. Hold the swab in the middle of the shaft at the score line.
3. Inser t the swab into the vagina about 2 inches and gently rotate the swab clockwise for 10-30 seconds.
4. While holding the swab, remove the cap from the tube. Do not spill the contents. If the contents of the tube are spilled, use a new Aptima Multitest kit.
5. Place the swab n the transport tube and break the swab shaft at the score line.
6. Tightly screw the cap onto the tube.
-
Transport Temperature:
Room Temperature or Refrigerated
-
Stability:
After collection, swab specimens in transport tubes can be stored at 2ºC to 30ºC for up to 30 days.
-
Schedule:
1-3 Days
-
Clinical Significance:
The Aptima BV assay is an in vitro nucleic acid amplification test that utilizes real time transcription-mediated amplification (TMA) for detection and quantitation of ribosomal RNA from bacteria associated with bacterial vaginosis (BV), including Lactobacillus (L. gasseri, L. crispatus, and L. jensenii), Gardnerella vaginalis, and Atopobium vaginae.
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Performing Lab:
Simple Laboratories
Bartonella Species Antibodies (IgG, IgM) with Reflex to Titers
-
Test Name:
Bartonella Species Antibodies (IgG, IgM) with Reflex to Titers
-
Test Code:
R34251
-
Alias:
Cat Scratch Disease
-
CPT Code(s):
86611 (x4)
-
Test Includes:
Bartonella henselae Antibodies (IgG, IgM) with Reflex to Titers Bartonella quintana Antibodies (IgG, IgM) with Reflex to Titers If B. henselae (IgG) Screen is positive, then B. henselae (IgG) titer will be performed at an additional charge (CPT code(s): 86317). If B. henselae (IgM) Screen is positive, then B. henselae (IgM) titer will be performed at an additional charge (CPT code(s): 86317). If B. quintana (IgG) Screen is positive, then B. quintana (IgG) titer will be performed at an additional charge (CPT code(s): 86317). If B. quintana (IgM) Screen is positive, then B. quintana (IgM) titer will be performed at an additional charge (CPT code(s): 86317).
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Bartonella Species Antibodies (IgG, IgM) with Reflex to Titers - This antibody panel helps diagnose infections with Bartonella henselae and Bartonella quintana. This panel includes IgM and IgG antibodies with reflexes to titers for positive results.B henselae causes cat scratch disease, a self-limiting bacterial infection transmitted via exposure to cats or cat fleas. B quintana causes trench fever, a febrile bacteremic illness transmitted via body lice. B henselae and B quintana are the 2 Bartonella species that most frequently cause blood culture-negative endocarditis. In immunocompromised individuals, infections with B henselae and B quintana may present as bacillary angiomatosis, a vasculoproliferative disease of the skin [1-4].Because of the fastidious nature of B henselae and B quintana, recovery of these bacteria is rarely successful, especially from blood. Serology is commonly used for diagnosing Bartonella infections [1,3]. Confirmation of recent or current infection with either B henselae or B quintana may require testing of serial specimens to demonstrate a 4-fold increase of IgG titers or the presence of IgM. A B henselae or B quintana IgG titer of 1:800 has been proposed as a major criterion for diagnosing Bartonella endocarditis [4].IgG cross-reactivity between B henselae and B quintana often occurs [1,3]. Qualitative real-time polymerase chain reaction is a highly specific and sensitive method to detect the presence of Bartonella species DNA in clinical specimens and can differentiate between B henselae and B quintana.The results of this test should be interpreted in the context of pertinent clinical history and physical examination findings.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
BENZEDRINE (MEDICATION)
-
Test Name:
BENZEDRINE (MEDICATION)
-
Test Code:
500810
BETA HUMAN CHORIONIC GONADOTROPIN (BHCG), QUANTITATIVE
-
Test Name:
BETA HUMAN CHORIONIC GONADOTROPIN (BHCG), QUANTITATIVE
-
Test Code:
HCGQNT
-
Alias:
Beta HCG,Quantitative hCG,Quantitative Pregnancy Test, Quantitative βHCG, Tumor Marker βHCG,Quantitative
-
CPT Code(s):
84702
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted. If the specimen is collected in a Plain Red (no additive/gel) or an anticoagulant tube, centrifuge and transfer the serum/plasma into a properly labeled transfer tube. Specify specimen type (serum or plasma) on transfer tube
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 48 hours Frozen: 6 months
-
Schedule:
1-2 Days
-
Clinical Significance:
Human chorionic gonadotropin (hCG) is a glycoprotein hormone produced by the placenta. The hormone is an excellent marker for pregnancy. Healthy, non-pregnant females have low to undetectable hCG levels. During pregnancy, hCG concentrations increase then show a gradual decrease after the first trimester. Unusually low or rapidly declining levels may indicate an abnormal condition such as ectopic pregnancy or impending spontaneous abortion. A quantitative hCG test may also be ordered to help diagnose gestational trophoblastic disease or germ cell tumors of the testes or ovary.
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Performing Lab:
Simple Laboratories
Beta-2-Glycoprotein I Antibody (IgG)
-
Test Name:
Beta-2-Glycoprotein I Antibody (IgG)
-
Test Code:
R36554
-
CPT Code(s):
86146
-
Preferred Specimen:
1 mL plasma collected in a 3.2% sodium citrate (light blue-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Plasma: Centrifuge light blue-top tube for 15 minutes at approximately 1500 g within 60 minutes of collection. Using a plastic pipette, remove plasma, taking care to avoid the WBC/platelet buffy layer and place into a plastic vial. Centrifuge a second time and transfer platelet-poor plasma into a new plastic vial. Plasma must be free of platelets (<10,000/mcL).
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Beta-2-Glycoprotein I Antibody (IgG) - Beta-2-Glycoprotein 1, apolipoprotein H, is a cofactor in antiphospholipid antibody binding and is the critical antigen in the antiphospholipid antibody syndrome. Beta-2- Glycoprotein 1 antibody is more specific than cardiolipin antibody that may express reactivity in patients with syphilis and other infectious diseases.
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Performing Lab:
Quest Diagnostics - Great Lakes Region
Beta-2-Glycoprotein I Antibody (IgM)
-
Test Name:
Beta-2-Glycoprotein I Antibody (IgM)
-
Test Code:
R36553
-
CPT Code(s):
86146
-
Preferred Specimen:
1 mL plasma collected in a 3.2% sodium citrate (light blue-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Plasma: Centrifuge light blue-top tube for 15 minutes at approximately 1500 g within 60 minutes of collection. Using a plastic pipette, remove plasma, taking care to avoid the WBC/platelet buffy layer and place into a plastic vial. Centrifuge a second time and transfer platelet-poor plasma into a new plastic vial. Plasma must be free of platelets (<10,000/mcL).
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Beta-2-Glycoprotein I Antibody (IgM) - Beta-2-Glycoprotein 1, apolipoprotein H, is a cofactor in antiphospholipid antibody binding and is the critical antigen in the antiphospholipid antibody syndrome. Beta-2- Glycoprotein 1 antibody is more specific than cardiolipin antibody that may express reactivity in patients with syphilis and other infectious diseases.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Beta-2-Microglobulin, Serum
-
Test Name:
Beta-2-Microglobulin, Serum
-
Test Code:
R852
-
Alias:
B2MG,Beta 2 Microglobulin, Serum,B2-MIC,Low Molecular Weight B2 Globulin,B2M
-
CPT Code(s):
82232
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Beta-2-Microglobulin, Serum - Beta-2-microglobulin normally passes through the glomerulus into the proximal tubule where much of it is reabsorbed. Serum levels are therefore an index of glomerular function. When impaired, serum levels rise in inverse ratio to glomerular filtration rate. Increased amounts of beta-2-microglobulin are excreted in several renal disorders, e.g., Balkan nephropathy, heavy metal poisoning and renal tubular disease due to therapeutic agents. Serial levels of beta-2-microglobulin in serum and urine are used to evaluate transplant viability and anticipate rejection. Following a successful graft, serum levels decline toward normal. Increasing serum levels provide an early sign of rejection. Elevated levels are also noted in lymphproliferative disorders, neoplasms (malignant and benign), inflammatory disease, and autoimmune diseases such as systemic lupus erythematosus (SLE) and Sjögren's disease.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
BILIRUBIN DIRECT
-
Test Name:
BILIRUBIN DIRECT
-
Test Code:
DB
-
Alias:
Bilirubin, conjugated
-
CPT Code(s):
82248
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-hep tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 3 DAYS *Specimen should be protected from light as much as possible prior to testing
-
Schedule:
1-2 Days
-
Clinical Significance:
The assessment of direct bilirubin is helpful in the determination of hepatic disorders. The increase in the total bilirubin associated with obstructive jaundice is primarily due to the direct fraction. Both direct and indirect bilirubin are increased in the serum with hepatitis. In the newborn patient with hemolytic jaundice and neonatal jaundice, the increase in the total bilirubin is primarily due to the indirect bilirubin fraction. This jaundice may be caused by Rh, ABO, or other blood group incompatibilities, by hepatic immaturity, or by hereditary defects in bilirubin conjugation.
-
Performing Lab:
Simple Laboratories
BILIRUBIN TOTAL
-
Test Name:
BILIRUBIN TOTAL
-
Test Code:
BT
-
CPT Code(s):
82247
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-hep tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 3 days Frozen: 3 Months
-
Schedule:
1-2 Days
-
Clinical Significance:
Used in the diagnosis and treatment of liver, hemolytic, hematological, and metabolic disorders, including hepatitis and gall bladder blockage.
-
Performing Lab:
Simple Laboratories
BILIRUBIN, TOTAL AND DIRECT WITH INDIRECT CALC.
-
Test Name:
BILIRUBIN, TOTAL AND DIRECT WITH INDIRECT CALC.
-
Test Code:
TB
-
CPT Code(s):
82248; 82247
-
Test Includes:
Total Bilirubin Direct Bilirubin Indirect Bilirubin (calculated)
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-Heparin tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 3 days Frozen: 3 Months
-
Schedule:
1-2 Days
-
Clinical Significance:
Bilirubin measurements are used in the diagnosis and treatment of liver, hemolytic, hematological, and metabolic disorders, including hepatitis and gall bladder blockage.
-
Performing Lab:
Simple Laboratories
BIPHETAMINE (MEDICATION)
-
Test Name:
BIPHETAMINE (MEDICATION)
-
Test Code:
500790
BMP (BASIC METABOLIC PANEL)
-
Test Name:
BMP (BASIC METABOLIC PANEL)
-
Test Code:
BMP
-
CPT Code(s):
80048
-
Test Includes:
Glucose, Urea Nitrogen (BUN), Creatinine, Sodium (Na), Potassium (K), Chloride (CL), Carbon Dioxide (CO2), Anion Gap, Calcium, GFR (African American), GFR (Others)
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-hep tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 3 DAYS
-
Schedule:
1-2 Days
-
Clinical Significance:
BMP can evaluate kidney, electrolyte, acid-base balance, blood sugar, and calcium levels. Significant changes in these test results can indicate acute problems such as kidney failure, insulin shock or diabetic coma, respiratory distress, or heart rhythm changes.
-
Performing Lab:
Simple Laboratories
BONATRANQUAN (MEDICATION)
-
Test Name:
BONATRANQUAN (MEDICATION)
-
Test Code:
501830
BUTALBITAL (MEDICATION)
-
Test Name:
BUTALBITAL (MEDICATION)
-
Test Code:
500520
C
C-Peptide
-
Test Name:
C-Peptide
-
Test Code:
R372
-
Alias:
C-Terminal Insulin
-
CPT Code(s):
84681
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 7 days
-
Clinical Significance:
C-Peptide - C-Peptide is useful in the evaluation of pancreatic beta cell function (e.g., helping distinguish type 1 from type 2 diabetes mellitus, or monitoring patients who have received islet cell or pancreatic transplants) and for determining the source of insulin in patients with hyperinsulinemic hypoglycemia (e.g., distinguishing insulin-secreting tumors from exogenous insulin administration). It is also sometimes measured as an additional means (more resistant to hemolysis than is insulin itself) for evaluating glucose tolerance tests.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
C-REACTIVE PROTEIN
-
Test Name:
C-REACTIVE PROTEIN
-
Test Code:
CRP
-
Alias:
CRP
-
CPT Code(s):
86140
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 11 days Refrigerated: 2 months
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Measurement of CRP is useful for the detection and evaluation of infection, tissue injury, inflammatory disorders and associated diseases. Measurements may also be useful as an aid in the identification of individuals at risk for future cardiovascular disease. High sensitivity CRP (hsCRP) measurements, when used in conjunction with traditional clinical laboratory evaluation of acute coronary syndromes, may be useful as an independent marker of prognosis for recurrent events, in patients with stable coronary disease or acute coronary syndromes.
-
Performing Lab:
Simple Laboratories
C-REACTIVE PROTEIN, HIGH SENITIVITY
-
Test Name:
C-REACTIVE PROTEIN, HIGH SENITIVITY
-
Test Code:
HSCRP
-
Alias:
Cardiac C-Reactive Protein Cardiac CRP CRP High Sensitivity CRP Hs HsCRP
-
CPT Code(s):
86141
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 ML SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 11 days Refrigerated: 2 months
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Measurement of C-reactive protein aids in the evaluation of stress, trauma, infection, inflammation, surgery, and associated diseases as part of the body’s non-specific inflammatory response to infection or injury. Cardiac CRP assays are indicated for use as an aid in the identification and stratification of individuals at risk for future cardiovascular disease. When used in conjunction with traditional clinical laboratory evaluation of acute coronary syndromes, CRP may be useful as an independent marker of prognosis for recurrent events in patients with stable coronary disease or acute coronary syndrome. A prognostic value for measuring CRP has been suggested from studies with cardiac patients where elevated levels of CRP were associated with a higher risk of having a future cardiac event. Elevated levels of CRP have been associated with poor prognosis in cases of stable angina, unstable angina, and myocardial infarction.
-
Performing Lab:
Simple Laboratories
CA 19-9
-
Test Name:
CA 19-9
-
Test Code:
R4698
-
Alias:
Carbohydrate Antigen 19-9,Cancer Antigen 19-9
-
CPT Code(s):
86301
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
CA 19-9 - A large percentage of patients with gastrointestinal tumors (such as pancreatic, liver, gastric, colorectal tumors) and some other malignancies have been shown to have elevated serum CA 19-9 levels. Serum CA 19-9 levels may be useful for monitoring disease activity or predicting relapse following treatment. CA 19-9 should not be used as a screening test.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Calcitonin
-
Test Name:
Calcitonin
-
Test Code:
R30742
-
Alias:
Thyrocalcitonin
-
CPT Code(s):
82308
-
Preferred Specimen:
1 mL frozen serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Spin to separate serum and transfer to transport tube vial. Freeze immediately and submit to laboratory frozen.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: Unacceptable Refrigerated: Unacceptable Frozen: 28 days
-
Clinical Significance:
Calcitonin - Calcitonin concentration is increased in patients with medullary thyroid carcinoma. Calcitonin concentrations may be used to monitor disease.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
Calcium, Ionized
-
Test Name:
Calcium, Ionized
-
Test Code:
R306
-
Alias:
CA++,CA, Ionized,Calcium Free,Calcium, Free,Free CA,Free Calcium,Ionized CA,Ionized Calcium
-
CPT Code(s):
82330
-
Preferred Specimen:
2 mL serum collected in a gel barrier tube
-
Min. Volume:
0.6 mL
-
Transport Container:
Unopened gel barrier tube
-
Collection Instruction:
Let clot and spin immediately with the cap on. Do not open tube. Ship the unopened gel barrier tube at room temperature.
If submitting with any other assay, please submit a separate tube for this test. -
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Calcium, Ionized - Ionized calcium represents the true "bioavailable" calcium in the circulation. In situations where the total calcium is normal but does not fit the clinical picture, e.g. , hyperparathyroidism, a determination of the ionized calcium will, many times, show an elevation in the "bioavailable" calcium component. This may be due to alterations in protein concentrations, especially albumin, that binds most of the calcium in the circulation.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
CALCIUM, SERUM
-
Test Name:
CALCIUM, SERUM
-
Test Code:
CA
-
CPT Code(s):
82310
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-hep tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 7 days Refrigerated: 3 weeks Frozen: 8 months
-
Schedule:
1-2 Days
-
Clinical Significance:
Measurement of calcium is used in the diagnosis and treatment of parathyroid disease, a variety of bone diseases, chronic renal disease and tetany (intermittent muscular contractions or spasms). Although more than 99% of body calcium exists in bones and teeth, it is the calcium in blood which is of most concern clinically. The bones serve as a reservoir to maintain relative constancy of serum calcium by releasing calcium when required to prevent hypocalcemia and trapping calcium to prevent excessively high levels of serum calcium. The uptake and release of calcium from bone is under the control of parathyroid hormone.
-
Performing Lab:
Simple Laboratories
CANDIDA VAGINITIS (CV)/ TRICHOMONAS VAGINALIS (TV)
-
Test Name:
CANDIDA VAGINITIS (CV)/ TRICHOMONAS VAGINALIS (TV)
-
Test Code:
LS5010
-
CPT Code(s):
87481(X2); 87661
-
Test Includes:
CV, TV
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected
-
Transport Container:
APTIMA MULTI-TEST SWAB (ORANGE)
-
Collection Instruction:
1. Open Aptima Multitest swab package (orange) and remove the swab. Do not touch the soft tip.
2. Hold the swab in the middle of the shaft at the score line.
3. Inser t the swab into the vagina about 2 inches and gently rotate the swab clockwise for 10-30 seconds.
4. While holding the swab, remove the cap from the tube. Do not spill the contents. If the contents of the tube are spilled, use a new Aptima Multitest kit.
5. Place the swab n the transport tube and break the swab shaft at the score line.
6. Tightly screw the cap onto the tube.
-
Transport Temperature:
Room Temperature or Refrigerated
-
Stability:
After collection, swab specimens in transport tubes can be stored at 2ºC to 30ºC for up to 30 days.
-
Schedule:
1-3 Days
-
Clinical Significance:
The Aptima CV/TV assay is an in vitro nucleic acid amplification test for the detection of RNA from microorganisms associated with vulvovaginal candidiasis and trichomoniasis. The assay utilizes real time transcription-mediated amplification (TMA) to detect and qualitatively report results for the following organisms: • Candida species group (C. albicans, C. tropicalis, C. parapsilosis, C. dubliniensis) • Candida glabrata • Trichomonas vaginalis
-
Performing Lab:
Simple Laboratories
CAPCOF (MEDICATION)
-
Test Name:
CAPCOF (MEDICATION)
-
Test Code:
501310
Cardiolipin Antibodies (IgA, IgG, IgM)
-
Test Name:
Cardiolipin Antibodies (IgA, IgG, IgM)
-
Test Code:
R7352
-
CPT Code(s):
86147 (x3)
-
Preferred Specimen:
1 mL citrated plasma collected in a 3.2% sodium citrate (light blue-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Cardiolipin Antibodies (IgA, IgG, IgM) - Cardiolipin antibodies (CA) are seen in a subgroup of patients with autoimmune disorders, particularly systemic lupus erythematosus (SLE), who are at risk for vascular thrombosis, thrombocytopenia, cerebral infarct and/or recurrent spontaneous abortion. Elevations of CA associated with increased risk have also been seen in idiopathic thrombocytopenic purpura, rheumatoid and psoriatic arthritis, and primary Sjögren's syndrome.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
CEA (CARCINOEMBRYONIC ANTIGEN)
-
Test Name:
CEA (CARCINOEMBRYONIC ANTIGEN)
-
Test Code:
CEA
-
CPT Code(s):
82378
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted. If the specimen is collected in a Plain Red (no additive/gel) or an anticoagulant tube, centrifuge and transfer the serum/plasma into a properly labeled transfer tube. Specify specimen type (serum or plasma) on transfer tube.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 48 hours
-
Schedule:
1-2 Days
-
Clinical Significance:
The measurement of serum CEA has shown substantial bene t in the prognosis and management of patients with malignant diseases, especially colorectal cancer. Serial measurements can be used to monitor patients for progression, regression or recurrence of cancer following treatment. A persistent elevation of CEA following therapeutic or surgical intervention signals residual disease or recurrence, whereas decreasing levels to within the normal range is indicative of successful intervention.
-
Performing Lab:
Simple Laboratories
Cell Count and Differential, Synovial Fluid
-
Test Name:
Cell Count and Differential, Synovial Fluid
-
Test Code:
R4562
-
CPT Code(s):
89051
-
Test Includes:
Color, Appearance, Total Nucleated Cell Count, Neutrophils %, Lymphocytes %, Monocyte/Macrophage %, Eosinophils %, Synoviocytes %
-
Preferred Specimen:
3 mL synovial fluid in an EDTA (lavender-top) tube or sodium heparin (green-top) tube
-
Min. Volume:
1 mL
-
Transport Container:
EDTA (lavender-top) tube or sodium heparin (green-top) tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 48 hours Refrigerated: 48 hours Frozen: Unacceptable
-
Clinical Significance:
Cell Count and Differential, Synovial Fluid - Immunologic, mechanical, chemical or bacteriologic damage may alter the permeability of the membrane and capillaries to produce varying degrees of inflammatory response. Various disorders produce changes in the chemical constituents of the joint fluid and in the type of cell population present.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Ceruloplasmin
-
Test Name:
Ceruloplasmin
-
Test Code:
R326
-
Alias:
Ferroxidase,Copper Binding Globulin
-
CPT Code(s):
82390
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 8 days Refrigerated: 14 days Frozen: 90 days
-
Clinical Significance:
Ceruloplasmin - Decreased levels of ceruloplasmin are found in Wilson's Disease, fulminant liver failure, intestinal malabsorption, renal failure resulting in proteinuria, chronic active hepatitis and malnutrition. Elevated levels are found in primary biliary cirrhosis, pregnancy (first trimester), oral contraceptive use and in acute inflammatory conditions since ceruloplasmin is an acute phase reactant.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
CHERATUSSIN AC (MEDICATION)
-
Test Name:
CHERATUSSIN AC (MEDICATION)
-
Test Code:
501380
CHERATUSSIN DAC (MEDICATION)
-
Test Name:
CHERATUSSIN DAC (MEDICATION)
-
Test Code:
501460
CHLAMYDIA TRACHOMATIS, GENITAL, PCR
-
Test Name:
CHLAMYDIA TRACHOMATIS, GENITAL, PCR
-
Test Code:
LS5006
-
Alias:
C. trachomatis Chlamydia CT
-
CPT Code(s):
87491
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA MULTI-TEST SWAB (ORANGE)
-
Collection Instruction:
For endocervical swab, vaginal swab or male urethral swab: Collect specimen according to printed instructions on APTIMA unisex swab collection kit packaging
-
Transport Temperature:
Refrigerated
-
Stability:
60 days - after testing, specimens are stored in the lab for 7 days
-
Schedule:
1-3 Days
-
Clinical Significance:
This assay may be used to test specimens from symptomatic and asymptomatic individuals to aid in the diagnosis of chlamydial urogenital disease.
-
Performing Lab:
Simple Laboratories
CHLAMYDIA TRACHOMATIS, URINE, PCR
-
Test Name:
CHLAMYDIA TRACHOMATIS, URINE, PCR
-
Test Code:
LS5008
-
Alias:
C. trachomatis Chlamydia CT
-
CPT Code(s):
87491
-
Preferred Specimen:
MALE OR FEMALE URINE
-
Transport Container:
APTIMA URINE TRANSPORT TUBE (YELLOW)
-
Collection Instruction:
For male or female urine specimen: Patient should not have urinated for at least one hour prior to sampling. Patient should provide first-catch urine sample (approximately 20-30mL of initial urine stream) into a sterile urine collection cup. Specimen may be sent to lab in primary collection sterile urine cup, transferred to yellow cap vacutainer tube or transferred to Aptima urine transport tube according to printed instructions on APTIMA urine specimen collection kit packaging.
-
Transport Temperature:
Refrigerated
-
Stability:
Urine, sterile container: Room temperature or refrigerated 24 hour APTIMA urine specimen tube: Room temperature or refrigerated 30 days (Note: after testing, specimens are saved in the lab for 7 days.)
-
Schedule:
1-3 Days
-
Clinical Significance:
This assay may be used to test specimens from symptomatic and asymptomatic individuals to aid in the diagnosis of chlamydial urogenital disease.
-
Performing Lab:
Simple Laboratories
CHLAMYDIA/GONORRHOEAE, GENITAL, PCR
-
Test Name:
CHLAMYDIA/GONORRHOEAE, GENITAL, PCR
-
Test Code:
LS5066
-
Alias:
C. trachmoatis CT GC N. gonorrhoeae
-
CPT Code(s):
87661
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA SWAB (UNI-SEX OR VAGINAL SWAB)
-
Collection Instruction:
For endocervical swab, vaginal swab or male urethral swab: Collect specimen according to printed instructions on APTIMA unisex swab collection kit packaging
-
Transport Temperature:
Refrigerated
-
Stability:
60 days - after testing, specimens are stored in the lab for 7 days
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
CHLAMYDIA/GONORRHOEAE, ORAL, PCR
-
Test Name:
CHLAMYDIA/GONORRHOEAE, ORAL, PCR
-
Test Code:
LS5003
-
Alias:
C. trachmoatis CT GC N. gonorrhoeae
-
CPT Code(s):
87491; 87591
-
Test Includes:
CHLAMYDIA; GONORRHOEAE
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA SWAB (UNI-SEX)
-
Transport Temperature:
Refrigerated
-
Stability:
60 days - after testing, specimens are stored in the lab for 7 days
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
CHLAMYDIA/GONORRHOEAE, URINE, PCR
-
Test Name:
CHLAMYDIA/GONORRHOEAE, URINE, PCR
-
Test Code:
LS5063
-
Alias:
C. trachmoatis CT GC N. gonorrhoeae
-
CPT Code(s):
87491;87591
-
Test Includes:
Chlamydia trachomatis & Neisseria gonorrhoeae detection
-
Preferred Specimen:
MALE OR FEMALE URINE
-
Transport Container:
APTIMA URINE TRANSPORT TUBE (YELLOW)
-
Collection Instruction:
For male or female urine specimen: Patient should not have urinated for at least one hour prior to sampling. Patient should provide first-catch urine sample (approximately 20-30mL of initial urine stream) into a sterile urine collection cup. Specimen may be sent to lab in primary collection sterile urine cup, transferred to yellow cap vacutainer tube or transferred to Aptima urine transport tube according to printed instructions on APTIMA urine specimen collection kit packaging. (Note: sterile cup and/or yellow cap vacutainer tube cannot be shared with other tests that require a midstream specimen.)
-
Transport Temperature:
Refrigerated
-
Stability:
Urine, sterile container: Room temperature or refrigerated 24 hours APTIMA urine specimen tube: Room temperature or refrigerated 30 days (Note: after testing, specimens are saved in the lab for 7 days.)
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
CHLORIDE
-
Test Name:
CHLORIDE
-
Test Code:
CL
-
CPT Code(s):
82435
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-hep tube, centrifuge for 15 minutes
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temp: 7 Days Refrigerated: 7 Days
-
Schedule:
1-2 Days
-
Clinical Significance:
Electrolytes affect most metabolic processes. They serve to maintain osmotic pressure and hydration of various body fluids, proper body pH and regulation of appropriate heart and muscle functions. Electrolytes are also involved in oxidation-reduction reactions and participate as essential parts or, cofactors, in enzyme reactions.
-
Performing Lab:
Simple Laboratories
CHOLESTEROL, TOTAL
-
Test Name:
CHOLESTEROL, TOTAL
-
Test Code:
CHOL
-
CPT Code(s):
82465
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Patient should fast for 12 hours prior to collection, unless instructed differently by physician. Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 Days
-
Schedule:
1-2 Days
-
Clinical Significance:
Cholesterol measurements are used in the diagnosis and treatment of atherosclerotic coronary artery disease. Cholesterol measurements are also used in the diagnosis of metabolic disorders involving lipids and lipoproteins. Total serum cholesterol concentrations depend on many factors including age, gender, diet, physical activity, liver disease, and other metabolic disorders
-
Performing Lab:
Simple Laboratories
Chromogranin A, LC/MS/MS
-
Test Name:
Chromogranin A, LC/MS/MS
-
Test Code:
R31911
-
Alias:
CgA
-
CPT Code(s):
86316
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Collect blood in a standard red-top serum vacutainer tube. Allow blood to clot at room temperature. Centrifuge and separate the serum from the cells immediately. Do not store refrigerated.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: 7 days Refrigerated: Unacceptable frozen: 31 days
-
Clinical Significance:
Chromogranin A, LC/MS/MS - Chromogranin-A (CgA) is an acidic glycoprotein expressed in the secretory granules of most normal and neoplastic neuroendocrine (NE) cell types, where it is released together with peptide hormones and biogenic amines. Neuroendocrine tumors (NETs) are a form of cancer that differ from other neoplasia in that they synthesize, store, and secrete peptides, e.g., CgA and amines. CgA is secreted from neuroendocrine-derived tumors including foregut, midgut and hindgut gastrointestinal NETs, pheochromocytomas, neuroblastomas, medullary thyroid carcinomas, some pituitary tumors, functioning and non-functioning pancreatic NETs. Significantly elevated CgA levels have been found in patients with other diseases, such as impaired renal function, untreated benign essential hypertension, gastritis, prostatic carcinoma, and hyperparathyroidism. The best-characterized circulating biomarker that identifies NETs in general is CgA. Monitoring blood CgA levels may effectively provide information that is helpful in delineating tumor burden and rate of tumor growth, predicting tumor response to therapy and providing some indication as to prognosis.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
CLOMIPRAMINE HCL (MEDICATION)
-
Test Name:
CLOMIPRAMINE HCL (MEDICATION)
-
Test Code:
500490
CMP (COMPREHENSIVE METABOLIC PANEL)
-
Test Name:
CMP (COMPREHENSIVE METABOLIC PANEL)
-
Test Code:
CMP
-
Alias:
cmp, comp
-
CPT Code(s):
80053
-
Test Includes:
Glucose, Urea Nitrogen (BUN), Creatinine, Sodium (Na), Potassium (K), Chloride (CL), Carbon Dioxide (CO2), Anion Gap, Calcium, Total Protein, Albumin, AST (SGOT), ALT (SGPT), Alkaline Phosphatase, Total Bilirubin, GFR (African American), GFR (Others)
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Patient should fast 8 hours prior to collection unless instructed differently by a physician. Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temp: 24 Hours Refrigerated: 3 Days
-
Schedule:
1-2 Days
-
Clinical Significance:
The tests in a Comprehensive Metabolic Panel (CMP) are used as a broad screening tool to evaluate kidney and liver function, electrolyte and acid-base balance, as well as blood sugar and protein levels.
-
Performing Lab:
Simple Laboratories
CO2 (CARBON DIOXIDE)
-
Test Name:
CO2 (CARBON DIOXIDE)
-
Test Code:
CO2
-
CPT Code(s):
82374
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 DAYS
-
Schedule:
1-2 Days
-
Clinical Significance:
CO2 measurements are used in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance.
-
Performing Lab:
Simple Laboratories
CODIMAL PH (MEDICATION)
-
Test Name:
CODIMAL PH (MEDICATION)
-
Test Code:
501520
Complement Component C3c
-
Test Name:
Complement Component C3c
-
Test Code:
R351
-
CPT Code(s):
86160
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: Unacceptable Refrigerated: 8 days Frozen: 8 days
-
Clinical Significance:
Complement Component C3c - Decreased C3 may be associated with acute glomerulonephritis, membranoproliferative glomerulonephritis, immune complex disease, active systemic lupus erythematosis, and generalized autoimmune processes.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Complement Component C4c
-
Test Name:
Complement Component C4c
-
Test Code:
R353
-
CPT Code(s):
86160
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: Unacceptable Refrigerated: 8 days Frozen: 21 days
-
Clinical Significance:
Complement Component C4c - Decreased C4 level is associated with acute systemic lupus erythematosis, glomerulonephritis, immune complex disease, cryoglobulinemia, congenital C4 deficiency and generalized autoimmune disease.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Complement, Total (CH50)
-
Test Name:
Complement, Total (CH50)
-
Test Code:
R618
-
Alias:
Hemolytic Complement
-
CPT Code(s):
86162
-
Preferred Specimen:
1 mL frozen serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: Unacceptable Refrigerated: Unacceptable Frozen: 7 days
-
Clinical Significance:
Complement, Total (CH50) - CH50 is a screening test for total complement activity. Levels of complement may be depressed in genetic deficiency, liver disease, chronic glomerulonephritis, rheumatoid arthritis, hemolytic anemias, graft rejection, systemic lupus erythematosis, acute glomerulonephritis, subacute bacterial endocarditis and cryoglobulinemia. Elevated complement may be found in acute inflammatory conditions, leukemia, Hodgkin's Disease, sarcoma, and Behcet's Disease.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
COMPLETE BLOOD COUNT (CBC) WITH DIFFERENTIAL
-
Test Name:
COMPLETE BLOOD COUNT (CBC) WITH DIFFERENTIAL
-
Test Code:
LS5067
-
Alias:
CBC W/DIFF
-
CPT Code(s):
85025
-
Test Includes:
WBC, RBC, Hemoglobin, Hematocrit, MCV, MCH, MCHC, Platelet Count, RDW-CV and Differential (Absolute and Percent - Neutrophils, Lymphocytes, Monocytes, Eosinophils, Basophils and Immature Granulocytes).
-
Preferred Specimen:
4.0 mL WHOLE BLOOD
-
Min. Volume:
1.0 mL WHOLE BLOOD
-
Transport Container:
EDTA (LAVENDER)
-
Collection Instruction:
Invert tube 5 to 10 times immediately after filling.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 24 hoursRefrigerated: 48 hours
-
Schedule:
1-2 DAYS
-
Clinical Significance:
This test is used to evaluate overall health and detect a wide range of hematologic disorders, including anemia, leukemia and inflammatory processes. It is also used to assist in managing medications and chemotherapeutic decisions.
-
Performing Lab:
Simple Laboratories
COMPLETE BLOOD COUNT (CBC) WITHOUT DIFFERENTIAL
-
Test Name:
COMPLETE BLOOD COUNT (CBC) WITHOUT DIFFERENTIAL
-
Test Code:
LS5077
-
CPT Code(s):
85027
-
Test Includes:
White Blood Cells (WBC), Red Blood Cells (RBC), Hemoglobin, Hematocrit, Mean Corpuscular Volume (MCV), Mean Corpuscular Hemoglobin (MCH), Mean Corpuscular Hemoglobin Concentration (MCHC), Platelet Count, RBC Distribution Width-Coefficient of Variation (RDW-CV)
-
Preferred Specimen:
3.0 mL WHOLE BLOOD
-
Min. Volume:
1.0 mL WHOLE BLOOD These volumes do not allow for repeat testing.
-
Transport Container:
EDTA (LAVENDER)
-
Collection Instruction:
Invert tube 5 to 10 times immediately after filling
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 24 hoursRefrigerated: 48 hours
-
Clinical Significance:
1-2 Days
-
Performing Lab:
Simple Laboratories
Copper, Blood
-
Test Name:
Copper, Blood
-
Test Code:
R35378
-
CPT Code(s):
82525
-
Preferred Specimen:
1 mL blood collected in an EDTA trace metal-free (royal blue-top) plastic tube
-
Min. Volume:
0.3 mL
-
Transport Container:
EDTA trace metal-free (royal blue-top) tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 30 days Refrigerated: 30 days Frozen: 30 days
-
Clinical Significance:
Copper, Blood - Exposure monitoring/investigation.
-
Performing Lab:
NMS Labs 200 Welsh Road Horsham, PA 19044
CORTISOL, SERUM
-
Test Name:
CORTISOL, SERUM
-
Test Code:
CORT
-
Alias:
COMPUND F; HYDROCORTISONE
-
CPT Code(s):
82533
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temp: 8 hours Refrigerated: 48 Hours
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Abnormal changes in cortisol levels occur due to hypothalamic, pituitary, or adrenal malfunction. If undiagnosed and untreated, these disorders can lead to severe metabolic imbalance which may be life-threatening. The measurement of serum or plasma cortisol - utilizing morning and evening levels and/or stress tests such as ACTH stimulation or dexamethasone suppression - aids in the diagnosis of adrenal related disease. Excess cortisol levels are found in Cushing’s syndrome (adrenal cortical hyperfunction) while decreased levels are found in Addison’s Disease (adrenal cortical insufficiency).
-
Performing Lab:
Simple Laboratories
COTAB A (MEDICATION)
-
Test Name:
COTAB A (MEDICATION)
-
Test Code:
501300
COTABFLU (MEDICATION)
-
Test Name:
COTABFLU (MEDICATION)
-
Test Code:
501020
COVID-19/FLU/RSV, PCR
-
Test Name:
COVID-19/FLU/RSV, PCR
-
Test Code:
LS5021
-
Alias:
4PLEX
-
Test Includes:
Influenza A, Influenza B, Respiratory Syncytial virus (RSV), and SARS-CoV-2
-
Preferred Specimen:
Nasopharyngeal or nasal swab
-
Transport Container:
RED CAP VIRAL PBS SWAB
-
Collection Instruction:
Nasopharyngeal: Insert the swab into either nostril, passing it into the posterior nasopharynx. Rotate swab by firmly brushing against the nasopharynx several times. Remove and place the swab into a viral transport tube (3 mL). Break swab at the indicated break line and cap the specimen collection tube tightly.
Nasal: Carefully insert the swab into the nostril. Using gentle rotation, push the swab until resistance is met at the level of the first turbinate (approximately 1 inch into the nostril). Rotate the swab several times against the nasal wall. Slowly remove from the nostril. Repeat this process in the other nares with the same swab (using both nares will increase chances of detection).
-
Schedule:
1 Days
-
Clinical Significance:
This test is for use in individuals suspected of a respiratory viral infection.
-
Performing Lab:
Simple Laboratories
CREATININE
-
Test Name:
CREATININE
-
Test Code:
CREAT
-
CPT Code(s):
82565
-
Test Includes:
CREATININE, GFR(AFRICAN AMERICAN, GRF(OTHERS)
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 3 Months
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Measurements of creatinine are used in the diagnosis and treatment of renal disease. Serum creatinine measurements prove useful in evaluation of kidney glomerular function and in monitoring renal dialysis. However, the serum level is not sensitive to early renal damage and responds more slowly than blood urea nitrogen (BUN) to hemodialysis during treatment of renal failure. Both serum creatinine and BUN are used to differentiate prerenal and postrenal (obstructive) azotemia. An increase in serum BUN without concomitant increase of serum creatinine is key to identifying prerenal azotemia. With postrenal azotemia, both serum BUN and creatinine rise, but the rise is disproportionately greater for BUN.
-
Performing Lab:
Simple Laboratories
CREATININE KINASE (CK)
-
Test Name:
CREATININE KINASE (CK)
-
Test Code:
CPK
-
Alias:
CPK, Creatine Phosphokinase
-
CPT Code(s):
82550
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 8-12 hours Frozen: 1 month *Freeze if testing will be delayed* If freezing is required, spin and separate serum prior to freezing
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Measurements of Creatine Kinase are used in the diagnosis and treatment of myocardial infarction and muscle disease, such as progressive Duchenne-type muscular dystrophy.
-
Performing Lab:
Simple Laboratories
Creatinine, 24-Hour Urine
-
Test Name:
Creatinine, 24-Hour Urine
-
Test Code:
R381
-
CPT Code(s):
82570
-
Test Includes:
CPT code 81050 may be added at an additional charge for volume measurement
-
Preferred Specimen:
10 mL urine aliquot from a well-mixed, 24-hour collection - no preservative
-
Min. Volume:
2 mL
-
Transport Container:
Plastic screw-cap container
-
Collection Instruction:
Record total volume and collection time on specimen container and test requisition
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Creatinine, 24-Hour Urine - Creatinine is the endproduct of creatine metabolism. Creatine is present primarily in muscle and the amount of creatinine produced is related to total skeletal muscle mass. Daily creatinine production is fairly constant except when there is massive injury to muscle. The kidneys excrete creatinine very efficiently and blood levels and daily urinary excretion of creatinine fluctuates very little in healthy normal people. Since blood and daily urine excretion of creatinine shows minimal fluctuation, creatinine excretion is useful in determining whether 24-hour urine specimens for other analytes (e.g., protein) have been completely and accurately collected.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
CREATININE, RANDOM URINE
-
Test Name:
CREATININE, RANDOM URINE
-
Test Code:
CREAU
-
CPT Code(s):
82570
-
Preferred Specimen:
RANDOM URINE
-
Min. Volume:
1.0 mL RANDOM URINE
-
Transport Container:
STERILE CUP
-
Collection Instruction:
Collect random urine in a sterile urine cup. Transfer to a BD Non-Additive container. Label it with patient’s name and the date and time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 2 days Refrigerated: 6 days *BD UA Preservative tube: 24 hours refrigerated
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Creatinine is a waste product derived from creatine, excreted by the kidneys and is a measure of renal function. Creatinine measurements are used in the diagnosis and treatment of renal diseases, in monitoring renal dialysis, and as a calculation basis for measuring other urine analytes.
-
Performing Lab:
Simple Laboratories
Crystals, Synovial Fluid
-
Test Name:
Crystals, Synovial Fluid
-
Test Code:
R4563
-
Alias:
Uric Acid Crystals
-
CPT Code(s):
89060
-
Preferred Specimen:
3 mL synovial fluid in an EDTA (lavender-top) tube or sodium heparin (green-top) tube
-
Min. Volume:
1 mL
-
Transport Container:
EDTA (lavender-top) tube or sodium heparin (green-top) tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 48 hours Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Crystals, Synovial Fluid - To rule out pathologic crystals.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
CT/GC/TV, GENITAL, PCR
-
Test Name:
CT/GC/TV, GENITAL, PCR
-
Test Code:
LS9011
-
CPT Code(s):
87491; 87591; 87661
-
Test Includes:
CT, GC, TV
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA SWAB (UNI-SEX OR VAGINAL SWAB)
-
Collection Instruction:
For endocervical swab, vaginal swab or male urethral swab: Collect specimen according to printed instructions on APTIMA unisex swab collection kit packaging
-
Transport Temperature:
Refrigerated
-
Stability:
60 days - after testing, specimens are stored in the lab for 7 days
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
CT/GC/TV, URINE, PCR
-
Test Name:
CT/GC/TV, URINE, PCR
-
Test Code:
LS9010
-
CPT Code(s):
87491; 87591; 87661
-
Test Includes:
CT, GC, TV
-
Preferred Specimen:
MALE OR FEMALE URINE
-
Transport Container:
APTIMA URINE TRANSPORT TUBE (YELLOW)
-
Collection Instruction:
For male or female urine specimen: Patient should not have urinated for at least one hour prior to sampling. Patient should provide first-catch urine sample (approximately 20-30mL of initial urine stream) into a sterile urine collection cup. Specimen may be sent to lab in primary collection sterile urine cup, transferred to yellow cap vacutainer tube or transferred to Aptima urine transport tube according to printed instructions on APTIMA urine specimen collection kit packaging.
-
Transport Temperature:
Refrigerated
-
Stability:
Urine, sterile container: Room temperature or refrigerated 24 hour APTIMA urine specimen tube: Room temperature or refrigerated 30 days (Note: after testing, specimens are saved in the lab for 7 days.)
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
CT/GC/TV/MGEN, GENITAL, PCR
-
Test Name:
CT/GC/TV/MGEN, GENITAL, PCR
-
Test Code:
LS9013
-
CPT Code(s):
87491; 87591; 87661; 87581
-
Test Includes:
CT, GC, TV, MGEN
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA SWAB (UNI-SEX OR VAGINAL SWAB)
-
Collection Instruction:
For endocervical swab, vaginal swab or male urethral swab: Collect specimen according to printed instructions on APTIMA unisex swab collection kit packaging
-
Transport Temperature:
Refrigerated
-
Stability:
60 days - after testing, specimens are stored in the lab for 7 days
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
CT/GC/TV/MGEN, URINE, PCR
-
Test Name:
CT/GC/TV/MGEN, URINE, PCR
-
Test Code:
LS9012
-
CPT Code(s):
87491; 87591; 87661; 87581
-
Test Includes:
CT, GC, TV, MGEN
-
Preferred Specimen:
MALE OR FEMALE URINE
-
Transport Container:
APTIMA URINE TRANSPORT TUBE (YELLOW)
-
Collection Instruction:
For male or female urine specimen: Patient should not have urinated for at least one hour prior to sampling. Patient should provide first-catch urine sample (approximately 20-30mL of initial urine stream) into a sterile urine collection cup. Specimen may be sent to lab in primary collection sterile urine cup, transferred to yellow cap vacutainer tube or transferred to Aptima urine transport tube according to printed instructions on APTIMA urine specimen collection kit packaging.
-
Transport Temperature:
Refrigerated
-
Stability:
Urine, sterile container: Room temperature or refrigerated 24 hour APTIMA urine specimen tube: Room temperature or refrigerated 30 days (Note: after testing, specimens are saved in the lab for 7 days.)
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
CULTURE: ANAEROBIC/AEROBIC
-
Test Name:
CULTURE: ANAEROBIC/AEROBIC
-
Test Code:
LS5047
-
CPT Code(s):
87070;87075
-
Test Includes:
Aerobic culture Anaerobic culture Gram stain Organism ID and Susceptibility testing (when appropriate)
-
Preferred Specimen:
TISSUE BIOPSY OR ASPIRATED MATERIAL
-
Transport Container:
STERILE CUP OR ESWAB
-
Collection Instruction:
Collect specimen (aspirate or exudate) after disinfecting skin surface.
-
Transport Temperature:
ROOM TEMPERATURE
-
Stability:
24 HOURS
-
Schedule:
Gram stains are reported within 24 hours of specimen receipt. Aerobic culture plates are examined daily for at least 3 days. Anaerobic culture plates are examined daily for at least 4 days.
-
Clinical Significance:
The demonstration of anaerobes from normally sterile sites (i.e. blood, joint fluid, tissue) is generally clinically significant. The quality and usefulness of an anaerobic culture is directly related to the appropriateness of the specimen, the collection method, and the timely transport and processing of the specimen.
-
Performing Lab:
Simple Laboratories
CULTURE: BLOOD
-
Test Name:
CULTURE: BLOOD
-
Test Code:
LS5048
-
CPT Code(s):
87040
-
Test Includes:
Culture Organism ID and susceptibility testing (when appropriate)
-
Preferred Specimen:
20.0 mL WHOLE BLOOD
-
Min. Volume:
1.0 mL whole blood
-
Transport Container:
Blood culture bottles, (1 set = one aerobic bottle and one anaerobic bottle)
-
Collection Instruction:
Check expiration date on blood culture bottles. Do not use if expired.
Cleanse rubber stoppers on blood culture bottles with an alcohol swab; let air dry. After locating appropriate vein, remove tourniquet, scrub site vigorously back and forth for 2 minutes using Chlorascrub Swabstick. Allow the site to completely air dry for 90 seconds. Do not retouch site.
If inoculating blood culture bottles using a butterfly blood collection set and direct draw adapter cap, inoculate first the aerobic bottle and then the anaerobic bottle, so that any oxygen trapped in the tubing will not be transferred into the anaerobic bottle.
If using a syringe draw, inoculate first the anaerobic bottle and then the aerobic bottle so any oxygen trapped in the syringe will not be transferred to the anaerobic bottle.
-
Transport Temperature:
ROOM TEMPERATURE
-
Stability:
24 HOURS
-
Schedule:
Blood culture bottles are placed on continuously monitoring instrument, they are removed when flagged "positive" or after 5 days if negative.
-
Clinical Significance:
Bacterial sepsis constitutes one of the most serious infectious diseases. The detection of microorganisms in a patient's blood has importance in the diagnosis and prognosis of endocarditis, septicemia, or chronic bacteremia.
-
Performing Lab:
Simple Laboratories
CULTURE: BODY FLUID
-
Test Name:
CULTURE: BODY FLUID
-
Test Code:
LS5062
CULTURE: EYE
-
Test Name:
CULTURE: EYE
-
Test Code:
LS5049
-
Performing Lab:
Simple Laboratories
CULTURE: NASAL, R/O MRSA
-
Test Name:
CULTURE: NASAL, R/O MRSA
-
Test Code:
LS5039
-
Performing Lab:
Simple Laboratories
CULTURE: SPUTUM
-
Test Name:
CULTURE: SPUTUM
-
Test Code:
LS5050
-
Performing Lab:
Simple Laboratories
CULTURE: STOOL
-
Test Name:
CULTURE: STOOL
-
Test Code:
LS5043
-
CPT Code(s):
87045, 87046
-
Test Includes:
Bacterial culture
-
Preferred Specimen:
Stool (feces)
-
Min. Volume:
Add specimen up to the red line as indicated on stool collection vial
-
Transport Container:
Para-pak C & S (orange cap) vial
-
Collection Instruction:
Specimen should be submitted in stool culture preservative vial. Mix sample well.
Fresh stool specimens in a sterile leak-proof container can be submitted and should reach the lab within 1 hour after collection or refrigerated up to 24 hours.
Refer to separate patient instructions for detailed stool culture collection.
-
Transport Temperature:
ROOM TEMPERATURE OR REFRIGERATED
-
Stability:
Preservative Vial: Room temperature or refrigerated: 4 days Non-preserved Stool: Room temperature: 1 hour Refrigerated: 24 hours
-
Schedule:
Culture plates are examined daily for at least 2 days.
-
Clinical Significance:
This test includes bacterial culture for intestinal pathogens. The final report will list presence or absence of Salmonella, Shigella, E.coli: 0157 and Campylobacter.
-
Performing Lab:
Simple Laboratories
CULTURE: THROAT (INCL STREP A)
-
Test Name:
CULTURE: THROAT (INCL STREP A)
-
Test Code:
LS5044
-
CPT Code(s):
87070
-
Test Includes:
Throat culture to detect Group A strep, Group C strep, Group G strep and Arcanobacterium haemolyticum.
-
Preferred Specimen:
Throat swab
-
Transport Container:
E-SWAB
-
Collection Instruction:
Using a sterile culture swab, rub the tonsils and pharynx touching any areas of exudate or ulceration present. Avoid touching the cheek, tongue, or uvula tissues with the swab.
-
Transport Temperature:
ROOM TEMPERATURE
-
Stability:
Room temperature or refrigerated: 48 hours
-
Schedule:
Culture plates are examined daily for at least 2 days.
-
Clinical Significance:
This test may be useful in the detection of yeast (Candida species) or bacterial agents of pharyngitis (such as Group A strep, Group C strep, Group G strep or Arcanobacterium hemolyticum). Other bacterial agents, such as Neisseria gonorrhoeae or Bordetella pertussis require specialized testing. (Order GC screen culture or Bordetella pertussis PCR).
-
Performing Lab:
Simple Laboratories
CULTURE: UROGENITAL
-
Test Name:
CULTURE: UROGENITAL
-
Test Code:
LS5051
-
Performing Lab:
Simple Laboratories
CULTURE: VAGINAL GROUP B
-
Test Name:
CULTURE: VAGINAL GROUP B
-
Test Code:
LS5060
-
CPT Code(s):
87081
-
Preferred Specimen:
Swab (vaginal and rectal site during pregnancy)
-
Transport Container:
E-SWAB
-
Collection Instruction:
Specimen should be submitted on a culture swab. Swab vagina first, then anus.
-
Transport Temperature:
ROOM TEMPERATURE
-
Stability:
Room Temperature: 24 hours Refrigerated: 4 days
-
Schedule:
Cultures are examined daily for up to 3 days.
-
Clinical Significance:
This test includes a bacterial culture for the detection of Group B beta hemolytic strep. Most cases of early onset neonatal group B streptococcal (GBS) disease have intrapartum pathogenesis. Attack rates increase 20 fold for infants born to group B streptococcal colonized mothers. Intrapartum prophylaxis in women with positive perinatal screens and certain perinatal risk factors can prevent early onset neonatal group B streptococcal disease.
-
Performing Lab:
Simple Laboratories
CULTURE: WOUND
-
Test Name:
CULTURE: WOUND
-
Test Code:
LS5057
-
Alias:
Anaerobic Culture, Wound
-
CPT Code(s):
87070, 87075, 87205
-
Test Includes:
Gram stain, isolation, and identification of potential anaerobic and aerobic pathogens (additional charges/CPT code[s] may apply); susceptibility testing if culture results warrant (at an additional charge). CPT coding for microbiology and virology procedures often cannot be determined before the culture is performed.
-
Preferred Specimen:
SWAB
-
Transport Container:
BLUE CAP GEL SWAB
-
Collection Instruction:
Some anaerobes will be killed by contact with molecular oxygen for only a few seconds. Overlying and adjacent areas must be carefully disinfected to eliminate contamination with indigenous flora. Ideally, pus or other fluid obtained by needle aspiration through intact skin or mucosal surface that has been cleaned with antiseptic should be collected. Sampling of open lesions is enhanced by deep aspiration using a sterile plastic catheter. Curettings of the base of an open lesion are optimal. If irrigation is necessary, nonbacteriostatic sterile normal saline may be used. Lower respiratory samples must be obtained by transtracheal percutaneous needle aspiration, transbronchial biopsy, transthoracic needle biopsy, or open lung biopsy by physicians trained in these procedures. If swabs must be used, collect two, use one for Gram stain and one for culture. Anaerobic transports must be used for swabs and for aspirates. Specimens are to be collected from a prepared site using sterile technique. Contamination with normal flora from skin, rectum, vaginal tract, or other body surfaces must be avoided.
-
Transport Temperature:
Room Temperature
-
Schedule:
1-4 Days
-
Performing Lab:
Simple Laboratories
CULTURE:URINE
-
Test Name:
CULTURE:URINE
-
Test Code:
LS5056
-
CPT Code(s):
87086
-
Test Includes:
Bacterial culture Organism ID and Susceptibility testing (when appropriate)
-
Preferred Specimen:
5.0 mL URINE
-
Min. Volume:
3.0 mL urine in urine culture tube (gray) or 0.5 mL urine in sterile urine cup (if cup is sent for UA and culture, pour off a portion of the sample for UA so culture portion is not contaminated)
-
Transport Container:
Urine culture tube (gray cap) or sterile cup
-
Collection Instruction:
Collect random urine in a sterile urine cup and label it with the patient’s name and the date and time of collection.
A “clean-catch” urine sample is necessary to assure accurate results. By following the directions carefully, it is possible to collect a sample that is free from possible contamination that may negatively affect the results of the test. Please read directions completely before beginning. The specimen must be collected in a sterile container obtained from a hospital, clinical laboratory or your physician.
Refer to separate patient instructions for detailed urine and/or culture collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Urine culture tube (gray) Room temperature: 48 hours Refrigerated: 48 hours Sterile urine cup Room temperature: 2 hours Refrigerated: 24 hours
-
Schedule:
2-4 Days
-
Clinical Significance:
If culture is positive, identification and susceptibility will be performed when appropriate at an additional charges/CPT codes. Cultures are useful and important in the isolation and identification of potentially pathogenic organisms that can cause a variety of human infections. With the aid of the susceptibility studies, results of cultures can assist the clinicians with the diagnosis and treatment of patients with bacterial infections.
-
Performing Lab:
Simple Laboratories
Cystatin C with Glomerular Filtration Rate, Estimated (eGFR)
-
Test Name:
Cystatin C with Glomerular Filtration Rate, Estimated (eGFR)
-
Test Code:
R94588
-
Alias:
CysX,CysC
-
CPT Code(s):
82610
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 14 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
ystatin C with Glomerular Filtration Rate, Estimated (eGFR) - Cystatin C is a non-glycosylated, low molecular weight (13,250 kD) cysteine proteinase inhibitor that is produced by all nucleated cells and found in body fluids, including serum. Since it is formed at a constant rate and freely filtered by the kidneys, its serum concentration is inversely correlated with the glomerular filtration rate (GFR); that is,high values indicate low GFRs while lower values indicate higher GFRs, similar to creatinine. The renal handling of cystatin C differs from creatinine. While both are freely filtered by glomeruli, once it is filtered, cystatin C, unlike creatinine, is reabsorbed and metabolized by the proximal renal tubules. Thus, under normal conditions, cystatin C does not enter the final excreted urine to any significant degree. The serum concentration of cystatin C remains unchanged with infections, inflammatory or neoplastic states, and is not affected by body mass, diet, or drugs. Thus, cystatin C may be a more reliable marker of renal function (GFR) than creatinine.GFR can be estimated (eGFR) from serum cystatin C utilizing an equation which includes the age and gender of the patient. The CKD-EPI cystatin C equation was developed by Inker et al, and demonstrated good correlation with measured iothalamate clearance in patients with all common causes of kidney disease, including kidney transplant recipients. Cystatin C eGFR may have advantages over creatinine eGFR in certain patient groups in whom muscle mass is abnormally high or low (for example quadriplegics, very elderly, or malnourished individuals). Blood levels of cystatin C also equilibrate more quickly than creatinine, and therefore, serum cystatin C may be more accurate than serum creatinine when kidney function is rapidly changing (for example amongst hospitalized individuals).
-
Performing Lab:
Quest Diagnostics-Lenexa 10101 Renner Blvd Lenexa, KS 66219-9752
Cytomegalovirus Antibody (IgG)
-
Test Name:
Cytomegalovirus Antibody (IgG)
-
Test Code:
R403
-
Alias:
Cytomegalic Inclusion Virus,CMV IgG Ab,Cytomegalovirus IgG Antibody,CMV Antibody IgG
-
CPT Code(s):
86644
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Cytomegalovirus Antibody (IgG) - CMV infections are common and usually asymptomatic. In patients who are immunocompromised, CMV may cause severe disseminated disease. CMV may cause birth defects in a minority of infected newborns. CMV IgG antibodies may represent prior exposure or recent infection.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Cytomegalovirus Antibody (IgM)
-
Test Name:
Cytomegalovirus Antibody (IgM)
-
Test Code:
R8503
-
Alias:
CMV Antibody IgM,Cytomegalovirus IgM Antibody,CMV IgM Ab
-
CPT Code(s):
86645
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Cytomegalovirus Antibody (IgM) - CMV infections are common and usually asymptomatic. In patients who are immunocompromised, CMV may cause disseminated, severe disease. CMV may cause birth defects in a minority of infected newborns.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
D
11-Deoxycortisol
-
Test Name:
11-Deoxycortisol
-
Test Code:
R30543
-
Alias:
Compound S,Metyrapone Response
-
CPT Code(s):
82634
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Separate serum after clotting. An early morning specimen is preferred.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 72 hours Refrigerated: 14 days Frozen: 1 year
-
Clinical Significance:
11-Deoxycortisol - 11-Deoxycortisol (Compound S) is useful in diagnosing patients with 11-beta-hydroxylase deficiency (second leading cause of congenital adrenal hyperplasia) and primary (adrenal failure) or secondary (hypothalamic-pituitary ACTH deficiency) adrenal insufficiency.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
D-Dimer, Quantitative
-
Test Name:
D-Dimer, Quantitative
-
Test Code:
R86594
-
CPT Code(s):
85379
-
Preferred Specimen:
One full unopened 3.2% sodium citrate (light blue-top) tube
-
Min. Volume:
0.5 mL plasma - ratio of blood to citrate is critical. Submit difficult draws in pediatric (light blue-top) tube
-
Transport Container:
3.2% sodium citrate (light blue-top) tube
-
Collection Instruction:
A completely filled tube is necessary because the correct ratio of blood to citrate is critical (9:1). Mix by gentle inversion 3-4 times. Do not uncap.
-
Transport Temperature:
Room temperature
-
Stability:
Unopened light blue-top tube Room temperature: 72 hours Refrigerated: 24 hours Frozen: Unacceptable Separated platelet-poor plasma Room temperature: Unacceptable Refrigerated: Unacceptable Frozen: 30 days
-
Clinical Significance:
D-Dimer, Quantitative - D-Dimer is one of the measurable by-products of activation of the fibrinolytic system. Quantitation of D-Dimer assesses fibrinolytic activation and intravascular thrombosis. D-Dimer is of particular value in excluding the diagnosis of venous thromboembolism among patients at high risk.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
DELORMETAZEPAM (MEDICATION)
-
Test Name:
DELORMETAZEPAM (MEDICATION)
-
Test Code:
501840
DESIPRAMINE HCL (MEDICATION)
-
Test Name:
DESIPRAMINE HCL (MEDICATION)
-
Test Code:
500430
DEXTROAMP SACCHARATE (MEDICATION)
-
Test Name:
DEXTROAMP SACCHARATE (MEDICATION)
-
Test Code:
500750
DEXTROAMP SULFATE (MEDICATION)
-
Test Name:
DEXTROAMP SULFATE (MEDICATION)
-
Test Code:
500770
DHEA SULFATE
-
Test Name:
DHEA SULFATE
-
Test Code:
DHEAS
-
Alias:
DEHYDROEPIANDROSTERONE SULFATE DHEA SO4 DHEAS DHEA-S
-
CPT Code(s):
82627
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temp: 8 hours Refrigerated: 48 hours Freeze at <-20 C for longer stability
-
Schedule:
1-2 Days
-
Clinical Significance:
DHEA-S may be used in the differential diagnosis of Cushing’s syndrome. DHEA-S may also be used to evaluate adrenocortical diseases, such as congenital adrenal hyperplasia and adrenal tumors. In hirsute female patients, increased DHEA-S levels have been associated with virilizing adrenal tumors. Patients with polycystic ovary syndrome have often demonstrated elevated levels of DHEA-S, suggesting an adrenal androgen contribution to the defect in this disorder.
-
Performing Lab:
Simple Laboratories
Digoxin
-
Test Name:
Digoxin
-
Test Code:
R418
-
Alias:
Lanoxin
-
CPT Code(s):
80162
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 10 days Frozen: 30 days
-
Clinical Significance:
Digoxin - Digoxin is a cardiac glycoside derived from the digitalis plant. It is used to treat congestive heart failure and atrial dysrhythmias. Digoxin levels are monitored to assure adequate therapeutic levels are achieved and to avoid toxicity.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
DIHISTINE DH (MEDICATION)
-
Test Name:
DIHISTINE DH (MEDICATION)
-
Test Code:
501330
Dihydrotestosterone
-
Test Name:
Dihydrotestosterone
-
Test Code:
R90567
-
Alias:
DHT
-
CPT Code(s):
82642
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.6 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 6 months
-
Clinical Significance:
Dihydrotestosterone - DHT is a potent androgen derived from testosterone via 5-Alpha-Reductase activity. 5-Alpha-Reductase deficiency results in incompletely virilized males (phenotypic females). This diagnosis is supported by an elevated ratio of testosterone to DHT.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
DOLOPHINE (MEDICATION)
-
Test Name:
DOLOPHINE (MEDICATION)
-
Test Code:
501630
DOXEPIN HCL (CIS/TRANS) (MEDICATION)
-
Test Name:
DOXEPIN HCL (CIS/TRANS) (MEDICATION)
-
Test Code:
500440
DURAGESIC (MEDICATION)
-
Test Name:
DURAGESIC (MEDICATION)
-
Test Code:
501690
E
ECSTASY (MEDICATION)
-
Test Name:
ECSTASY (MEDICATION)
-
Test Code:
501880
ELECTROLYTE PANEL
-
Test Name:
ELECTROLYTE PANEL
-
Test Code:
LYTES
-
CPT Code(s):
80051
-
Test Includes:
Sodium (Na), Potassium (K+), Chloride (Cl), Carbon Dioxide (CO2), Anion Gap
-
Preferred Specimen:
2.0 mL SERUM OR PLASMA
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes.
-
Transport Temperature:
REFRIGERATED
-
Stability:
Room temperature: 12 hours Refrigerated: 7 days
-
Schedule:
Set up: Daily; Results in 24-48 hours
-
Clinical Significance:
Electrolytes are electrically charged minerals that are found in body tissues and blood in the form of dissolved salts. They help move nutrients and wastes out of the body's cells, maintain a healthy water balance, and help stabilize the body's pH level. The electrolyte panel is used to screen for an electrolyte or acid-base imbalance and to monitor the effect of treatment on a known imbalance that is affecting bodily organ function.
-
Performing Lab:
Simple Laboratories
EMOTIVAL (MEDICATION)
-
Test Name:
EMOTIVAL (MEDICATION)
-
Test Code:
501850
ENCEPHALITIS ANTIBODY EVALUATION W/REFL TO TITER AND LINE BLOT, SERUM
-
Test Name:
ENCEPHALITIS ANTIBODY EVALUATION W/REFL TO TITER AND LINE BLOT, SERUM
-
Test Code:
R94955
-
CPT Code(s):
86255 (x19), 86052, 86341, 83519 (x2), 86596 (x2)
-
Test Includes:
Encephalitis Ab Screen Tissue IFA, AMPAR1, AMPAR2, Aquaporin 4, DPPX, GABAbR, NMDAR1, CASPAR2, LGI1, Ganglionic AChR, VGCC N-Type, VGCC P/Q-Type, and VGKC
-
Preferred Specimen:
8 mL frozen serum
-
Min. Volume:
4 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 24 hours Refrigerated: 14 days Frozen: 21 days
-
Clinical Significance:
Encephalitis Antibody Evaluation with Reflex to Titer and Line Blot, Serum - The Encephalitis Antibody Panel provides an evaluation of possible autoantibodies in patients with suspected autoimmune encephalitis, and optimizes the likelihood of detecting neuronal specific autoantibodies, whether present singly or occurring as multiple autoantibodies.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
ENDACOF-C (MEDICATION)
-
Test Name:
ENDACOF-C (MEDICATION)
-
Test Code:
501270
ENDAL CD (MEDICATION)
-
Test Name:
ENDAL CD (MEDICATION)
-
Test Code:
501320
Epstein-Barr Virus Viral Capsid Antigen (VCA) Antibody (IgG)
-
Test Name:
Epstein-Barr Virus Viral Capsid Antigen (VCA) Antibody (IgG)
-
Test Code:
R8474
-
Alias:
VCA EBV IgG,EBV VCA IgG,EBV Capsid Antibody IgG,Viral Capsid Antigen EBV IgG
-
CPT Code(s):
86665
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Epstein-Barr Virus Viral Capsid Antigen (VCA) Antibody (IgG) - Primary infection by EBV causes infectious mononucleosis, usually a self-limiting disease in children and young adults. Infection with EBV can cause lymphoproliferative disorders including tumors. VCA-IgG is typically detectable at clinical presentation, and persists for life. Absence of VCA-IgG usually indicates the patient is susceptible to EBV infection.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Epstein-Barr Virus Viral Capsid Antigen (VCA) Antibody (IgM)
-
Test Name:
Epstein-Barr Virus Viral Capsid Antigen (VCA) Antibody (IgM)
-
Test Code:
R8426
-
Alias:
EBV Current Infection,VCA IgM,EBV Capsid Antibody IgM,EBV VCA IgM
-
CPT Code(s):
86665
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Epstein-Barr Virus Viral Capsid Antigen (VCA) Antibody (IgM) - Primary infection by EBV causes infectious mononucleosis, usually a self-limiting disease in children and young adults. Infection with EBV can cause lymphoproliferative disorders including tumors. VCA-IgM is typically detectable at clinical presentation, then declines to undetectable levels within a month in young children and within 3 months in other individuals.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
ESTRADIOL
-
Test Name:
ESTRADIOL
-
Test Code:
ESTRA
-
Alias:
E2 Estradiol 17 Estradiol 946
-
CPT Code(s):
82670
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 48 hours Frozen: 1 week
-
Schedule:
1-2 Days
-
Clinical Significance:
Levels of estradiol are used to monitor ovulatory status. Because estradiol levels reflect follicular maturation, the measurement of estradiol as citied in the scientific literature has been used as a valuable tool in the assessment of sexual development, etiology of amenorrhea, causes of infertility and menopause. Abnormally high levles in males are indicative of feminizing syndromes such as gynecomastia.
-
Performing Lab:
Simple Laboratories
Estriol, Serum
-
Test Name:
Estriol, Serum
-
Test Code:
R34883
-
CPT Code(s):
82677
-
Preferred Specimen:
0.5 mL serum collected in a red-top tube (no-gel)
-
Min. Volume:
0.3 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 5 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Estriol, Serum
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
Estrogens, Total, Immunoassay
-
Test Name:
Estrogens, Total, Immunoassay
-
Test Code:
R439
-
CPT Code(s):
82672
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.6 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Note: The stability study demonstrated a sharp decrease after 4 days at room temperature, which increases the risk of rejection if not shipped refrigerated.
The total estrogens assay is not recommended for use in pre-pubertal children.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 4 days Refrigerated: 14 days Frozen: 60 days
-
Clinical Significance:
Estrogens, Total, Immunoassay - Estrogens are secreted by the gonads, adrenal glands, and placenta. Total estrogens provide an overall picture of estrogen status for men and women.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-204
ETHYL BETA-D-GLUCURONIDE (MEDICATION)
-
Test Name:
ETHYL BETA-D-GLUCURONIDE (MEDICATION)
-
Test Code:
500400
ETHYL SULFATE (MEDICATION)
-
Test Name:
ETHYL SULFATE (MEDICATION)
-
Test Code:
500410
F
Drug Monitoring, Fentanyl, with Confirmation, Urine
-
Test Name:
Drug Monitoring, Fentanyl, with Confirmation, Urine
-
Test Code:
R39375
-
Alias:
Prescription Drug Monitoring,Pain Management
-
CPT Code(s):
80307
-
Test Includes:
If you require medMATCH for this order code, you must also order code 39158 - Prescribed Drugs, medMATCH®. If 39158 is ordered, all Drug Monitoring order codes will be treated as medMATCH. If this test code is not ordered with 39158, all medMATCH result codes will be DNR’d. . If the presumptive (screen) is positive, a confirmation will be performed at an additional charge (CPT code(s): 80354). Confirmation includes the following analytes: Fentanyl, Norfentanyl
-
Preferred Specimen:
30 mL urine
-
Min. Volume:
7 mL
-
Transport Container:
Clinical drug test transport vial
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Drug Monitoring, Fentanyl, with Confirmation, Urine - Fentanyl is an opioid analgesic with a potency approximately 80 times that of morphine. The test is a screening assay using a homogeneous enzyme immunoassay method of analysis. Presumptive positive screen results are reflexed to a more specific and sensitive liquid chromatography mass spectroscopy (LC/MS/MS) methodology. Therapeutic urine drug monitoring of fentanyl is important for ensuring compliance to treatment strategies, as well as ensuring non-diversion for illicit purposes. Urine or oral fluid are the specimens of choice for routine monitoring of patients taking prescription drugs. Use of serum/plasma should be limited to anuretic patients, or where a patient's clinical appearance does not coincide with their prescribed medications. No single monitoring approach provides adequate information about the pattern or dose of patient drug use. Safest prescribing habits should include a combination of tools and laboratory test results to correctly detect drug use patterns. Urine drug test results equal to or greater than cutoff are reported as positive and results less than cutoff are reported as negative. Quantitative values cannot be used to assess the drug dose, because the drug is extensively metabolized and excreted in the urine.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
FECAL IMMUNOCHEMICAL TEST (FIT)
-
Test Name:
FECAL IMMUNOCHEMICAL TEST (FIT)
-
Test Code:
LS5042
-
Alias:
FIT iFOBT
-
CPT Code(s):
82274
-
Preferred Specimen:
STOOL
-
Transport Container:
STERILE CUP
-
Collection Instruction:
Place collection paper inside toilet bowl on top of water. Deposit fecal sample on top of collection paper. Do not allow fecal sample to contact toilet water until after specimen has been collected. Open the green cap on the sampling bottle by twisting and pulling upwards. Scrape the surface of the fecal sample with the sampling probe. Cover the grooved portion of the sampling probe completely with the fecal sample. Close the sampling bottle by inserting the sampling probe and snap the green cap on tight. Do not reopen. Flush remaining stool and used collection paper. Return the sampling bottle to the physician or laboratory. Only one stool specimen collected from one bowel movement is required.
-
Transport Temperature:
Room Temperature
-
Stability:
Room Temperature: 15 days
-
Schedule:
1-3 Days
-
Clinical Significance:
Qualitative detection of fecal occult blood
-
Performing Lab:
Simple Laboratories
FENTORA (MEDICATION)
-
Test Name:
FENTORA (MEDICATION)
-
Test Code:
501700
FERRITIN
-
Test Name:
FERRITIN
-
Test Code:
FERR
-
CPT Code(s):
82728
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection. If the specimen is collected in an anticoagulant tube without a gel barrier, centrifuge and transfer plasma into a properly labeled transfer tube within two hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 5 days* Frozen: 1 month
-
Schedule:
1-2 Days
-
Clinical Significance:
Useful as indicator of body iron stores. Used in the diagnosis of hypochromic, microcytic anemias.
-
Performing Lab:
Simple Laboratories
FERRITIN/IRON/TRANSFERRIN/TIBC
-
Test Name:
FERRITIN/IRON/TRANSFERRIN/TIBC
-
Test Code:
TIBCF
FOLATE, SERUM
-
Test Name:
FOLATE, SERUM
-
Test Code:
FOL
-
Alias:
FOLIC ACID
-
CPT Code(s):
82746
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
A fasting specimen is preferred. Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 48 hours Frozen: 6 months
-
Schedule:
1-2 Days
-
Clinical Significance:
Folate deficiency can be caused by insufficient dietary intake, malabsorption or excessive folate utilization. Excessive utilization occurs very commonly during pregnancy. Alcoholism, hepatitis, or other liver-damaging diseases can also cause excessive folate utilization. Folate levels in both serum and red blood cells are used to assess folate status. The serum folate level is an indicator of recent folate intake. Red blood cell (RBC) folate is the best indicator of long term folate stores. A low RBC folate value can indicate a prolonged folate deciency.
-
Performing Lab:
Simple Laboratories
Food Allergy Profile with Reflexes
-
Test Name:
Food Allergy Profile with Reflexes
-
Test Code:
R91682
-
CPT Code(s):
86003
-
Test Includes:
IgE allergy testing for: Almond (f20) Cashew Nut (f202) Codfish (f3) Cow's Milk (f2) IgE with Reflex to Milk Component Panel Egg White (f1) IgE with Reflex to Egg Component Panel Hazelnut (f17) Peanut, Total with Reflex to Peanut Component Panel Salmon (f41) Scallop (f338) Sesame Seed (f10) Shrimp (f24) Soybean (f14) Tuna (f40) Walnut (f256) Wheat (f4)
-
Preferred Specimen:
2.5 mL serum
-
Min. Volume:
1.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 14 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Food Allergy Profile with Reflexes - This in vitro allergen-specific IgE panel is used to quantitatively measure an individual's IgE response to 15 different foods that are commonly associated with allergies. These foods include almond, cashew nut, codfish, cow's milk, egg white, hazelnut, peanut, salmon, scallop, sesame seed, shrimp, soybean, tuna, walnut, and wheat. If the IgE result for egg white, cow's milk, or peanut is abnormal, the corresponding allergen component panel will be performed. This IgE panel is intended to be used in conjunction with other clinical information to aid in the diagnosis of food allergies [1]. While allergen-specific serum IgE testing is considered comparable to skin testing in many instances, both the American Academy of Allergy, Asthma, and Immunology and the American College of Allergy, Asthma, and Immunology recognize that allergen-specific serum IgE testing may be preferred in some clinical situations. These include (1) the presence of widespread skin disease, (2) the recent use of antihistamines or other medications that can affect the results of allergy skin tests, (3) uncooperative patients, and (4) medical history suggesting that allergen skin testing would pose a significant risk for a serious allergic reaction [1]. Food-specific IgE tests are extremely sensitive. However, a positive test result only indicates that a patient is IgE-sensitized to the food of concern. Many IgE-sensitized individuals do not develop any symptoms when the food is ingested. A diagnosis of food allergy should only be made by a trained medical provider after conducting a thorough clinical evaluation [2,3]. While food-specific IgE test results may contribute to that evaluation, they cannot replace it. Moreover, several forms of food hypersensitivity are not associated with the presence of food-specific IgE in serum. The results of this panel should be interpreted in the context of pertinent clinical and family history and physical examination findings. More specific information about each allergen included in this panel may be found on the Quest Diagnostics Test Directory.
-
Performing Lab:
Quest Diagnostics-Lenexa 10101 Renner Blvd Lenexa, KS 66219-9752
FSH (FOLLICLE STIMULATING HORMONE)
-
Test Name:
FSH (FOLLICLE STIMULATING HORMONE)
-
Test Code:
FSH
-
Alias:
hFSH, Pituitary Gonadotropin
-
CPT Code(s):
83001
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 48 hours* Refrigerated: 48 hours (tubes containg gel) Refrigerated: 7 days (all other tubes) Frozen: 6 months
-
Schedule:
1-2 Days
-
Clinical Significance:
Human LH and FSH levels are commonly determined in investigations of menstrual, fertility, and pubertal developmental disorders such as premature ovarian failure, menopause, ovulatory disorders and pituitary failure. The ratio of hLH/hFSH has been used to assist in the diagnosis of polycystic ovary disease. Low levels of hLH and hFSH may indicate pituitary failure while elevated hLH and hFSH levels along with decreased levels of gonadal steroids may indicate gonadal failure (menopause, ovariectomy, premature ovarian syndrome, Turner’s Syndrome). Low gonadotropin levels are usually observed in females taking oral steroid-based contraceptives. In the male, elevated hFSH and hLH with low levels of gonadal steroids may indicate testicular failure or anorchia. In Klinefelter’s syndrome hFSH may be elevated due to Sertoli cell failure.
-
Performing Lab:
Simple Laboratories
G
GAMMA GLUTAMYL TRANSFERASE (GGT)
-
Test Name:
GAMMA GLUTAMYL TRANSFERASE (GGT)
-
Test Code:
GGTP
-
CPT Code(s):
82977
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL serum (Note: This volume does not allow for repeat testing.)
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: ASAP Refrigerated: 1 month
-
Schedule:
1-2 Days
-
Clinical Significance:
GGT measurements are used in the diagnosis and treatment of liver diseases such as alcoholic cirrhosis and primary and secondary liver tumors.
-
Performing Lab:
Simple Laboratories
GASTROINTESTINAL PATHOGEN PANEL (PCR)
-
Test Name:
GASTROINTESTINAL PATHOGEN PANEL (PCR)
-
Test Code:
LS5011
-
Alias:
MOLECULAR
-
Test Includes:
Campylobacter Enteroaggregative E.coli (EAEC) Enteropathogenic E.coli (EPEC) Enterotoxigenic E.coli (ETEC) Salmonella Shiga-like toxin producing E.coli (STEC), including E.coli O157 Shigella / Enteroinvasive E.coli (EIEC) Plesiomonas shigelloides Vibrio, including Vibrio cholera Yersinia enterocolitica Cryptosporidium Cyclospora cayetanensis Entamoeba histolytica Giardia lamblia Adenovirus F 40/41 Astrovirus Norovirus GI/GII Rotavirus A Sapovirus (genogroups I, II, IV and V)
-
Preferred Specimen:
STOOL
-
Min. Volume:
0.5 mL
-
Transport Container:
STERILE CUP
-
Collection Instruction:
NULL
-
Transport Temperature:
ROOM TEMPERATURE
-
Performing Lab:
Simple Laboratories
Gentamicin
-
Test Name:
Gentamicin
-
Test Code:
R481
-
Alias:
Garamycin
-
CPT Code(s):
80170
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Gentamicin - Gentamicin is an aminoglycoside antibiotic used in the treatment of gram-positive and gram-negative bacterial infections, especially Pseudomonas, Proteus, Klebsiella and Staphylococcus. Gentamicin is potentially nephrotoxic and ototoxic. Serial monitoring of peak and trough serum levels may provide the clinician with information to maintain safe and therapeutic levels.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
GILTUSS PED-C (MEDICATION)
-
Test Name:
GILTUSS PED-C (MEDICATION)
-
Test Code:
501450
GLUCOSE
-
Test Name:
GLUCOSE
-
Test Code:
GLU
-
Alias:
BLOOD SUGAR
-
CPT Code(s):
82947
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Plasma or serum samples without preservative (NaF) should be separated from the cells or clot a half hour after being drawn. Allow specimen to completely clot and centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier (red top), centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 3 days Room Temperature (Sodium Fluoride only): 3 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders, including diabetes mellitus, neonatal hypoglycemia and idiopathic hypoglycemia, and pancreatic islet cell carcinoma.
-
Performing Lab:
Simple Laboratories
Glucose-6-Phosphate Dehydrogenase, Quantitative
-
Test Name:
Glucose-6-Phosphate Dehydrogenase, Quantitative
-
Test Code:
R500
-
Alias:
G6PD,G6PDH
-
CPT Code(s):
82955
-
Preferred Specimen:
1 mL whole blood collected in an EDTA (lavender-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
EDTA (lavender-top) tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 48 hours Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Glucose-6-Phosphate Dehydrogenase, Quantitative - Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency in the world, affecting an estimated 400 million people worldwide [1]. It is more common in people of African, Mediterranean, and Asian descent. G6PD deficiency is an X-linked genetic disorder and, in general, affects males more than females. Severity ranges from mild to severe subtypes. Newborns with G6PD deficiency may have prolonged and more pronounced neonatal jaundice than other newborns. Adults with G6PD deficiency may have episodes of acute hemolytic anemia, and symptoms may include jaundice, fatigue, splenomegaly, and dark urine. Episodes may be induced by illness (infections), certain foods (fava beans), and particular medications (for example some sulfonamides and antimalarial drugs)[2]; therefore, some precautions may be recommended to avoid offending triggers. Quantitative Glucose-6-Phosphate Dehydrogenase is an assay that measures the G6PD enzyme level. A low value may indicate G6PD deficiency (as opposed to values either within or above the reference range). [Perkins[3]] has found that some females with G-6-PD deficiency have difficulty in carrying a pregnancy to term. Erythrocytic G-6-PD appears to be sensitive to the endocrine changes associated with pregnancy. [Vergnes and Clerc [4]] found that 65% of their patients showed a significant fall in the G-6-PD activity in the later months of pregnancy with return to normal after delivery. Of note, as reticulocytes have higher G6PD activity than mature erythrocytes, if the blood sample is collected just after an acute hemolytic episode, G6PD activity levels can be falsely normal [5]. Therefore, if G6PD deficiency is suspected, consider repeating the test. Molecular genetic testing may also be indicated in cases where the disorder is suspected, or where there is a family history of G6PD deficiency, as enzyme activity may be normal in heterozygous females.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
GLUCOSE, FASTING
-
Test Name:
GLUCOSE, FASTING
-
Test Code:
FBS
-
Alias:
Blood Sugar
-
CPT Code(s):
82947
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL serum or plasma This volume does not allow for repeat testing.
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Plasma or serum samples without preservative (NaF) should be separated from the cells or clot a half hour after being drawn. Allow specimen to completely clot and centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier (red top), centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 3 days Room Temperature (Sodium Fluoride only): 3 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders, including diabetes mellitus, neonatal hypoglycemia and idiopathic hypoglycemia, and pancreatic islet cell carcinoma.
-
Performing Lab:
Simple Laboratories
Glutamic Acid Decarboxylase-65 Antibody
-
Test Name:
Glutamic Acid Decarboxylase-65 Antibody
-
Test Code:
R34878
-
CPT Code(s):
86341
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 60 days
-
Clinical Significance:
Glutamic Acid Decarboxylase-65 Antibody - Key clinical use and differentiators Measurement of Glutamic acid decarboxylase (GAD65) is used to: 1. Screen for presymptomatic type 1 diabetes (T1D) in individuals with a family history of T1D or those known to have a high-risk HLA genotype, 2. Distinguish between T1D, type 2 diabetes mellitus (T2D), and atypical forms of diabetes such as latent autoimmune diabetes in adults (LADA). [1] Glutamic acid decarboxylase (GAD65) is a key protein that the immune system mistakenly attacks in people with T1D, and positivity to GAD65 antibodies represents a key marker of the disease. [1] GAD65 is the most common autoantibody found in adult-onset autoimmune diabetes. In addition to its importance in guiding the diagnosis of T1D, glutamic acid decarboxylase (GAD65) is also helpful to confirm the diagnosis of stiff-man syndrome, autoimmune encephalitis, autoimmune ataxia, brain stem encephalitis, autoimmune epilepsy, autoimmune myelopathy or pernicious anemia. Intended Clinical Use This test is crucial for differentiating between T1D and T2D. It is important to note that classifying diabetes type can be challenging at the time of presentation, and misdiagnosis can occur in approximately 40% of adults with new T1D. [1] Identifying individuals affected by stage 1 T1D is important for applying eligibility criteria to drugs, such as Teplizumab, which have demonstrated the ability to delay the transition of stage 1 to stage 3 T1D in clinical trials. [2,3] GAD65 has some distinctive features. It is commonly the first detected autoantibody in childhood, up until age 15 years. [4] Adult-onset T1D cases most often present with GADA. [5] It is associated with slower progression to T1D and is often found as a single positive islet autoantibody, especially in adults. Limitations T1D is classified into three stages, with stages 1 and 2 considered presymptomatic. Since the presence of stage 1 and 2 T1D requires at least two islet autoantibodies, relying solely on GAD65 as a screening test limits the ability to make an accurate diagnosis. Professional organizations, including the American Diabetes Association (ADA), recommend using tests for all four islet cell autoantibodies: IAA, glutamic acid decarboxylase (GAD65) Zinc Transporter 8 (ZnT8), and islet cell antigen 2 antibody (IA-2). [1]
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
GRAM STAIN
-
Test Name:
GRAM STAIN
-
Test Code:
LS5053
-
CPT Code(s):
87205
-
Preferred Specimen:
Any site (swab, body fluid, respiratory samples)
-
Transport Container:
culture swab or sterile cup
-
Transport Temperature:
ROOM TEMPERATURE OR REFRIGERATED
-
Stability:
Room temperature: 24 hours Refrigerated: 48 hours
-
Schedule:
Set up: Daily; Results in 24-48 hours
-
Clinical Significance:
The gram stain is used to differentiate intact morphologically similar bacteria into two groups based on cell color after staining. In addition, cell form, size and structural details are evident. Such preliminary information provides important clues to the types of organisms present, the further techniques required to characterize them, and the therapy to initiate while awaiting test results.
-
Performing Lab:
Simple Laboratories
Growth Hormone (GH)
-
Test Name:
Growth Hormone (GH)
-
Test Code:
R521
-
Alias:
GH,HGH,Human Growth Hormone (hGH)
-
CPT Code(s):
83003
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. For patients receiving STRENSIQ, consideration should be given to using alternate methods.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 28 days
-
Clinical Significance:
Growth Hormone (GH) - Measurement of GH is primarily of interest in the diagnosis and treatment of various forms of inappropriate growth hormone secretion. Growth hormone measurements in children are used in the evaluation of short stature and help differentiate low GH production from other sources of growth failure. Stimulation and suppression tests are often more meaningful than random measurements.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
GUIATUSS AC (MEDICATION)
-
Test Name:
GUIATUSS AC (MEDICATION)
-
Test Code:
501410
H
17-Hydroxypregnenolone
-
Test Name:
17-Hydroxypregnenolone
-
Test Code:
R8352
-
CPT Code(s):
84143
-
Preferred Specimen:
2 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.4 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 24 hours Refrigerated: 5 days Frozen: 28 days
-
Clinical Significance:
17-Hydroxypregnenolone - 17-Hydroxypregnenolone is useful in the diagnosis of 3-Beta-Hydroxylase enzyme deficiency, a rare cause of congenital adrenal hyperplasia, and 17-Hydroxylase (P450c17) enzyme deficiency.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
5-Hydroxyindoleacetic Acid (5-HIAA), 24-Hour Urine without Creatinine
-
Test Name:
5-Hydroxyindoleacetic Acid (5-HIAA), 24-Hour Urine without Creatinine
-
Test Code:
R523
-
Alias:
Carcinoid Screen,Serotonin 5-HIAA,5-HIAA
-
CPT Code(s):
83497
-
Test Includes:
CPT code 81050 may be added at an additional charge for volume measurement
-
Preferred Specimen:
10 mL aliquot from a 24-hour urine that has been preserved with 25 mL 6N HCl, collected in a plastic 24-hour urine container
-
Min. Volume:
5 mL
-
Transport Container:
Plastic urine container
-
Collection Instruction:
Collect 24-hour urine with 25 mL 6N HCl to maintain a pH ≤3. If no preservative is used, specimen must be stored refrigerated during collection but shipped frozen and pH must be ≤6.
Record 24-hour urine volume and patient’s age on test request form and urine container. -
Transport Temperature:
Preserved urine: Room temperature Unpreserved urine: Frozen
-
Stability:
Preserved urine Room temperature: 7 days Refrigerated: 30 days Frozen: 30 days Unpreserved urine Room temperature: Unacceptable Refrigerated: Unacceptable Frozen: 30 days
-
Clinical Significance:
5-Hydroxyindoleacetic Acid (5-HIAA), 24-Hour Urine without Creatinine - Values above 10 mg/24-hours occur in carcinoid syndrome. Slight elevations also occur in nontropical sprue and after reserpine administration. Drugs which can interfere with testing due to physiologic response: Acetaminophen, alpha and beta blockers, atenolol, bromocriptine, broncholdilators, clonidine, digoxin, isoniazid, L-dopa, labetalol, methyldopa, monoamine oxidase inhibitors, nitroglycerin, sympathomimetic amines, phenobarbital, phenothiazines, phentolamine, reserpine, salicylates, tricyclic antidepressants.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
Haptoglobin
-
Test Name:
Haptoglobin
-
Test Code:
R502
-
CPT Code(s):
83010
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 14 days
-
Clinical Significance:
Quest Diagnostics - Great Lakes Region
HCG (BETA) QUALITATIVE, URINE
-
Test Name:
HCG (BETA) QUALITATIVE, URINE
-
Test Code:
UCG
-
Alias:
hCG hCG-U Pregnancy test
-
CPT Code(s):
81025
-
Preferred Specimen:
RANDOM URINE
-
Min. Volume:
1.0 mL URINE
-
Transport Container:
URINE CUP
-
Collection Instruction:
For early determination of pregnancy, the first morning urine specimen is recommended since it generally contains the highest concentration of hCG; however a urine specimen collected at any time during the day may be used.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: not recommended Refrigerated: 48 hours
-
Schedule:
1-2 Days
-
Clinical Significance:
Human chorionic gonadotropin (hCG) is a glycoprotein hormone secreted by the developing placenta shortly after fertilization. In normal pregnancy, hCG can be detected in both urine and serum as early as 7 to 10 days after conception. The appearance of hCG in both urine and serum soon after conception, and its subsequent rapid rise in concentration during early gestational growth, make it an excellent marker for the early detection of pregnancy.
-
Performing Lab:
Simple Laboratories
HCG (HUMAN CHORIONIC GONADOTROPIN), QUALITATIVE SERUM
-
Test Name:
HCG (HUMAN CHORIONIC GONADOTROPIN), QUALITATIVE SERUM
-
Test Code:
HCG
-
Alias:
HCG, Qualitative Serum Pregnancy Test, Qualitative Serum βHCG,Qualitative Serum
-
CPT Code(s):
84703
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 ML SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: not recommended Refrigerated: 48 hours
-
Schedule:
1-2 Days
-
Clinical Significance:
Human chorionic gonadotropin (hCG) is a glycoprotein hormone secreted by the developing placenta shortly after fertilization. In normal pregnancy, hCG can be detected in both urine and serum as early as 7 to 10 days after conception. The appearance of hCG in both urine and serum soon after conception, and its subsequent rapid rise in concentration during early gestational growth, make it an excellent marker for the early detection of pregnancy.
-
Performing Lab:
Simple Laboratories
hCG, Total, Quantitative
-
Test Name:
hCG, Total, Quantitative
-
Test Code:
R8396
-
Alias:
B-hCG, Pregnancy,hCG Tumor Marker,Human Chorionic Gonadotropin (hCG),Beta hCG, Quantitative,BhCG Serum Quant,Chorionic Gonadotropin
-
CPT Code(s):
84702
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.3 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
hCG, Total, Quantitative - hCG may reach detectable limits within 7-10 days of conception. hCG is produced by the placenta and reaches a peak between the 7th and 10th week of gestation. hCG is a glycoprotein hormone produced by the syncytiotrophoblast of the placenta and secreted during normal pregnancy and with pathologic conditions such as hydatidiform mole, choriocarcinoma and testicular neoplasm. Order hCG, Total, Qualitative, Urine, if hCG serum result is inconsistent with clinical presentation.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
HDL (HIGH-DENSITY LIPOPROTEIN)
-
Test Name:
HDL (HIGH-DENSITY LIPOPROTEIN)
-
Test Code:
HDL
-
Alias:
Alpha-Lipoprotein HDL Cholesterol HDLC
-
CPT Code(s):
83718
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 ML SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 14 hours Refrigerated: 7 days Frozen: 3 months
-
Schedule:
1-2 Days
-
Clinical Significance:
HDL cholesterol is inversely related to the risk of developing coronary artery disease. A low HDL/LDL cholesterol ratio is directly related to the risk of developing coronary artery disease. A high HDL cholesterol is associated with the “longevity” syndrome.
-
Performing Lab:
Simple Laboratories
HEMATOCRIT
-
Test Name:
HEMATOCRIT
-
Test Code:
LS0874
-
Alias:
HCT; PACKED CELL VOLUME, PCV
-
CPT Code(s):
85014
-
Preferred Specimen:
4.0 mL WHOLE BLOOD
-
Min. Volume:
1.0 mL WHOLE BLOOD
-
Transport Container:
EDTA (LAVENDER)
-
Collection Instruction:
Invert tube 5 to 10 times immediately after filling.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 24 hoursRefrigerated: 48 hours
-
Schedule:
1-2 Days
-
Clinical Significance:
Hematocrit is used to evaluate anemia, polycythemia, blood loss, and state of hydration and response to treatment.
-
Performing Lab:
Simple Laboratories
HEMOGLOBIN A1C
-
Test Name:
HEMOGLOBIN A1C
-
Test Code:
LS5064
-
Alias:
HGB A1C
-
CPT Code(s):
83036
-
Preferred Specimen:
2.0 mL WHOLE BLOOD
-
Min. Volume:
1.0 mL WHOLE BLOOD
-
Transport Container:
EDTA (LAVENDER)
-
Collection Instruction:
For accurate results, the specimen should be from a dedicated draw, or sampled before the capped tube has been opened. Cap sample with white cap if tube is opened.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 3 daysRefrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Hemoglobin A1C measurements are used in the clinical management of diabetes to assess the long-term efficacy of diabetic control. Diabetes causes elevated levels of glucose to circulate in the blood. Maintaining normal levels of blood glucose is part of the routine management of diabetics. Continuous and careful management of blood glucose levels prevents development of serious long term complications resulting from vascular impairment such as retinopathy, nephropathy, and neuropathy. Although a fasting blood glucose measurement gives the clinician information about the patient’s status over the last twelve hours, the stable HbA1C offers a more accurate indication of the patient’s long-term diabetic control over the last two to three months.
-
Performing Lab:
Simple Laboratories
HEMOGLOBIN and HEMATOCRIT
-
Test Name:
HEMOGLOBIN and HEMATOCRIT
-
Test Code:
LS5083
-
Alias:
HGB, HCT
-
CPT Code(s):
85018; 85014
-
Test Includes:
HemoglobinHematocrit
-
Preferred Specimen:
4.0 mL WHOLE BLOOD
-
Min. Volume:
1.0 mL WHOLE BLOOD
-
Transport Container:
EDTA (LAVENDER)
-
Collection Instruction:
Invert tube 5 to 10 times immediately after filling.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 24 hoursRefrigerated: 48 hours
-
Schedule:
1-2 Days
-
Clinical Significance:
Used to evaluate anemia, polycythemia, blood loss, state of hydration, and response to treatment.
-
Performing Lab:
Simple Laboratories
Hemoglobinopathy Evaluation
-
Test Name:
Hemoglobinopathy Evaluation
-
Test Code:
R35489
-
Alias:
HGB Evaluation,Hemoglobin A2,Hemoglobin Variants,HGB Variants,Hemoglobin Electrophoresis,HGB Electrophoresis,Hemoglobin S,Thalassemia Screen,HB A2,HB F,HB S,Hemoglobin F
-
CPT Code(s):
83020, 85014, 85018, 85041
-
Test Includes:
Hemoglobin A, Hemoglobin F, Hemoglobin A2 (Quant), Hemoglobin S, Hemoglobin C, Hemoglobin E, and any hemoglobin variants Red Blood Cell Count, Hemoglobin, Hematocrit, MCV, MCH, RDW
-
Preferred Specimen:
1 full (5 mL) EDTA (lavender-top) tube
-
Min. Volume:
1 mL
-
Transport Container:
EDTA (lavender-top) tube
-
Collection Instruction:
Patient age and ethnicity are necessary for proper interpretation.
Blood transfusions within the last 4 months may affect results.Note: If tube drawn is shared with lead testing, trace metal-free EDTA (i.e. royal blue-top or tan-top) tube is required.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Hemoglobinopathy Evaluation - The detection and proper identification of hemoglobinopathies and thalassemias is an important aspect of the evaluation of patients with anemia, microcytosis and erythrocytosis.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Heparin-Induced Platelet Antibody
-
Test Name:
Heparin-Induced Platelet Antibody
-
Test Code:
R414
-
Alias:
Heparin Associated Platelet Antibody
-
CPT Code(s):
86022
-
Preferred Specimen:
1 mL frozen serum collected in a red-top tube (no gel)
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Serum (preferred): Centrifuge red top tube 15 minutes at approximately 1500 g as soon as possible after clotting.
Plasma (acceptable): Centrifuge blue top tube 20 minutes at approximately 2500 g. Remove plasma from the cells as soon as possible. -
Transport Temperature:
Frozen
-
Stability:
Room temperature: Unacceptable Rrefrigerated: Unacceptable Frozen: 6 months
-
Clinical Significance:
Heparin-Induced Platelet Antibody - Heparin can induce thrombocytopenia, a decreased platelet count, due to antibody stimulation. False positive results may be due to immune complexes. False negative results may be due to low titer, low avidity antibodies.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
HEPATIC FUNCTION PANEL
-
Test Name:
HEPATIC FUNCTION PANEL
-
Test Code:
HF
-
Alias:
LFT, Liver Function Tests, Liver Panel
-
CPT Code(s):
80076
-
Test Includes:
ALBUMIN, ALKALINE PHOSPHATASE, ALT(SGPT), AST (SGOT), DIRECT BILIRUBIN, TOTAL PROTEIN
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-hep tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 12 hours Refrigerated: 2 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Used to evaluate the liver for injury, infection, or inflammation.
-
Performing Lab:
Simple Laboratories
Hepatitis A Antibody, Total
-
Test Name:
Hepatitis A Antibody, Total
-
Test Code:
R508
-
Alias:
HAV Antibody,HAV Total
-
CPT Code(s):
86708
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
Dietary supplements containing biotin may interfere in assays and may skew analyte results to be either falsely high or falsely low. For patients receiving the recommended daily doses of biotin, draw samples at least 8 hours following the last biotin supplementation. For patients on mega-doses of biotin supplements, draw samples at least 72 hours following the last biotin supplementation.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 14 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Hepatitis A Antibody, Total - HAV antibody indicates prior or acute infection with, or immunization to, Hepatitis A virus.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
HEPATITIS A IGM
-
Test Name:
HEPATITIS A IGM
-
Test Code:
HAIGM
-
Alias:
Anti-HAV, IgM HAV Antibody, IgM HAV, IgM
-
CPT Code(s):
86709
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 48 hours Freeze for longer stability.
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Appearance of anti-hepatitis A IgM antibodies in the circulation demonstrates a recent exposure to HAV. Anti-HAV IgM antibodies appear a few days after infection and persist at elevated levels in the bloodstream for a few months. Detection of anti-HAV IgM does not necessarily imply an acute HAV infection due to the longevity of anti-HAV IgM. The detection of anti-HAV IgM can be useful for the differential diagnosis of hepatitis A from other forms of viral hepatitis. Any diagnosis should take into consideration the patient’s clinical history and symptoms, as well as other laboratory data.Patients with specimens exhibiting borderline results should be re-tested at approximately two week intervals. These patients may be at the beginning or the end of the acute infection. Testing for anti-HAV IgM at two week intervals will distinguish between early acute or a recovering individual. Rapid rise is associated with an early acute infection. Gradual decrease or a steady level of antibody is normally associated with late acute stage of infection.
-
Performing Lab:
Simple Laboratories
HEPATITIS B CORE ANTIBODY, IgM
-
Test Name:
HEPATITIS B CORE ANTIBODY, IgM
-
Test Code:
HBCIGM
-
Alias:
Anti-HBc, IgM HBc Antibody, IgM
-
CPT Code(s):
86705
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 48 hours
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Hepatitis B Core IgM is intended for use in the qualitative detection of IgM antibodies to hepatitis B core antigen (anti-HBc IgM) in human serum or plasma.
-
Performing Lab:
Simple Laboratories
Hepatitis B Core Antibody, Total
-
Test Name:
Hepatitis B Core Antibody, Total
-
Test Code:
R501
-
CPT Code(s):
86704
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
Dietary supplements containing biotin may interfere in assays and may skew analyte results to be either falsely high or falsely low. For patients receiving the recommended daily doses of biotin, draw samples at least 8 hours following the last biotin supplementation. For patients on mega-doses of biotin supplements, draw samples at least 72 hours following the last biotin supplementation. -
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Hepatitis B Core Antibody, Total - This assay does not distinguish between Total B Core Antibody IgG and IgM detected before or at the onset of symptoms; however, such reactivity can persist for years after illness, and may even outlast anti-HBS. Occasionally Hepatitis B Core Antibody may be the only marker of either current or past Hepatitis B infection. HBV vaccination leads to development of HBsAb but not to HBcAb.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
HEPATITIS B SURFACE ANTIBODY, QUALITATIVE
-
Test Name:
HEPATITIS B SURFACE ANTIBODY, QUALITATIVE
-
Test Code:
HAB
-
Alias:
Anti-HBs HBsAb Hep B
-
CPT Code(s):
86706
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.2 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
Specify specimen type (serum or plasma) on transfer tube. -
Transport Temperature:
Refrigerated
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Anti-HBs is used for the detection of antibody to hepatitis B surface antigen in human serum or and EDTA, heprin or citrated plasma. Results may be used as an aid in the determination of susceptibility to hepatitis B virus (HBV) infection in individuals prior to or following HBV vaccination or where vaccination status is unknown.
-
Performing Lab:
Simple Laboratories
HEPATITIS B SURFACE ANTIGEN
-
Test Name:
HEPATITIS B SURFACE ANTIGEN
-
Test Code:
HEP
-
Alias:
HBSAg Hep B Hepatitis
-
CPT Code(s):
87340
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.2 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted. If the specimen is collected in a Plain Red (no additive/gel) or an anticoagulant tube, centrifuge and transfer the serum/plasma into a properly labeled transfer tube. Specify specimen type (serum or plasma) on transfer tube.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 6 days Refrigerated: 14 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Assays for Hepatitis B Surface Antigen (HBsAg) are routinely used to aid in the diagnosis of suspected hepatitis B virus (HBV) infections and to monitor the status of infected individuals, i.e. whether the patient's infection has resolved or the patient has become a chronic carrier of the virus. For the diagnosis of acute or chronic hepatitis, HBsAg reactivity should be correlated with patient history and the presence of other hepatitis B serological markers. Prenatal testing has been recommended by the Centers for Disease Control and Prevention (CDC) to identify newborns from HBV carrier mothers that may benefit from prophylactic treatment.
-
Performing Lab:
Simple Laboratories
Hepatitis B Virus DNA, Quantitative, Real-Time PCR
-
Test Name:
Hepatitis B Virus DNA, Quantitative, Real-Time PCR
-
Test Code:
R8369
-
CPT Code(s):
87517
-
Preferred Specimen:
3 mL plasma collected and separated from an EDTA (lavender-top) tube
-
Min. Volume:
1 mL
-
Transport Container:
Transport tubeÂ
-
Collection Instruction:
Do not freeze whole blood or any samples stored in primary tube. Freshly drawn specimens (whole blood) may be stored at 2-25°C for up to 24 hours prior to centrifugation. Separate plasma or serum from cells within 24 hours of collection by centrifugation. Follow manufacturer’s instructions for collection tube handling.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: Unacceptable Refrigerated: 6 days Frozen: 84 days
-
Clinical Significance:
Hepatitis B Virus DNA, Quantitative, Real-Time PCR - This test is intended for use in conjunction with clinical presentation and other laboratory markers for the clinical management of patients with chronic HBV infection undergoing antiviral therapy. The test can be used to measure HBV DNA levels at baseline and during treatment to aid in assessing response to treatment. The cobas® HBV Test is not intended for use as a screening test for the presence of HBV in blood or blood products or as a diagnostic test to confirm the presence of HBV infection. Reportable range is 10 to 1,000,000,000 IU/mL (1.00 to 9.00 Log IU/mL).
-
Performing Lab:
Quest Diagnostics-Schaumburg 506 E State Pkwy Schaumburg, IL 60173-4538
Hepatitis Be Antibody
-
Test Name:
Hepatitis Be Antibody
-
Test Code:
R556
-
Alias:
HBe Antibody,Anti-Hepatitis Be
-
CPT Code(s):
86707
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
Dietary supplements containing biotin may interfere in assays and may skew analyte results to be either falsely high or falsely low. For patients receiving the recommended daily doses of biotin, draw samples at least 8 hours following the last biotin supplementation. For patients on mega-doses of biotin supplements, draw samples at least 72 hours following the last biotin supplementation.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Hepatitis Be Antibody - HBeAb appears in the early convalescence of HBV infection. With carrier state and chronic hepatitis, HBeAb may not develop.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Hepatitis Be Antigen
-
Test Name:
Hepatitis Be Antigen
-
Test Code:
R555
-
Alias:
HBe Antigen
-
CPT Code(s):
87350
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
Dietary supplements containing biotin may interfere in assays and may skew analyte results to be either falsely high or falsely low. For patients receiving the recommended daily doses of biotin, draw samples at least 8 hours following the last biotin supplementation. For patients on mega-doses of biotin supplements, draw samples at least 72 hours following the last biotin supplementation.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Hepatitis Be Antigen - HBeAg indicates active HBV replication. Infectivity is evaluated based on HBeAg and HBsAg. When HBeAg persists much longer than 10 weeks, the patient is likely to develop chronic hepatitis and be a carrier.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
HEPATITIS C ANTIBODY, REFLEX CONFIRMATION
-
Test Name:
HEPATITIS C ANTIBODY, REFLEX CONFIRMATION
-
Test Code:
HEPC
-
Alias:
Anti-HCV HCV Hep C
-
CPT Code(s):
86803
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM
-
Transport Container:
2-SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted. If the specimen is collected in an anticoagulant tube, centrifuge and transfer the plasma into a properly labeled transfer tube. Specify specimen type (serum or plasma) on transfer tube.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
The presence of anti-HCV indicates that an individual may have been infected with HCV, may harbor infectious HCV, and/or may be capable of transmitting HCV infection. Although the majority of infected individuals may be asymptomatic, HCV infection may develop into chronic hepatitis, cirrhosis, and/or increased risk of hepatocellular carcinoma.
-
Performing Lab:
Simple Laboratories
Hepatitis C Viral RNA, Quantitative, Real-Time PCR
-
Test Name:
Hepatitis C Viral RNA, Quantitative, Real-Time PCR
-
Test Code:
R35645
-
CPT Code(s):
87522
-
Preferred Specimen:
3 mL plasma collected and separated from an EDTA (lavender-top) tube
-
Min. Volume:
1 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Do not freeze whole blood or any samples stored in primary tube. Freshly drawn specimens (whole blood) may be stored at 2-25°C for up to 24 hours prior to centrifugation. Separate plasma or serum from cells within 24 hours of collection by centrifugation. Follow manufacturer’s instructions for collection tube handling.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 72 hours Refrigerated: 14 days Frozen: 84 days
-
Clinical Significance:
Hepatitis C Viral RNA, Quantitative, Real-Time PCR - Useful in monitoring therapy and/or disease progression. Reportable range is 15 to 100,000,000 IU/mL (1.18-8.00 log IU/mL)
-
Performing Lab:
Quest Diagnostics-Schaumburg 506 E State Pkwy Schaumburg, IL 60173-4538
Hepatitis C Virus RNA Genotype
-
Test Name:
Hepatitis C Virus RNA Genotype
-
Test Code:
R37811
-
Alias:
HCV RNA Genotype,Hep C Genotype,HEP C Virus Genotype,HCV Viral RNA Genotype,Hep C RNA Genotype,Hepatitis C RNA Genotype,Hepatitis C Genotype
-
CPT Code(s):
87902
-
Preferred Specimen:
2 mL plasma collected in an EDTA (lavender-top) tube
-
Min. Volume:
0.6 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Separate plasma from whole blood within 24 hours of collection by centrifugation. Transfer to a transport tube and refrigerate or freeze.
Serum is collected in a serum separator tube or red-top tube (no gel). Transfer to a transport tube and refrigerate or freeze.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 72 hours Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Hepatitis C Virus RNA Genotype - Determination of hepatitis C genotype is often required to select the most appropriate direct acting agent(s) (DAA) for the treatment of hepatitis C. Some DAA's are only effective for the treatment of hepatitis C genotype 1, whereas others may be used for additional genotypes. A concurrent patient HCV viral load of ≥2000 IU/mL is required for this test.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
Hepatitis D Virus (HDV) Antibody, Total
-
Test Name:
Hepatitis D Virus (HDV) Antibody, Total
-
Test Code:
R4990
-
CPT Code(s):
86692
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Hepatitis D Virus (HDV) Antibody, Total - Hepatitis D Virus (HDV) infection occurs only in association with Hepatitis B Virus (HBV) infection. A positive result for HDV total antibody may indicate acute infection, chronic infection, or past infection with recovery.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
HEPATITIS PANEL, ACUTE
-
Test Name:
HEPATITIS PANEL, ACUTE
-
Test Code:
033
-
CPT Code(s):
80074
-
Preferred Specimen:
8.0 mL SERUM
-
Min. Volume:
Hepatitis A, IgM Hepatitis B Core Antibody, IgM Hepatitis B Surface AntigenHepatitis C Antibody with Confirmation
-
Transport Container:
4 - SST(GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes as soon as the specimen is clotted.
-
Transport Temperature:
Refrigerated
-
Stability:
REFER TO INDIVIDUAL TESTS
-
Schedule:
1-3 Days
-
Clinical Significance:
REFER TO INDIVIDUAL TESTS
-
Performing Lab:
Simple Laboratories
HEPTADON (MEDICATION)
-
Test Name:
HEPTADON (MEDICATION)
-
Test Code:
501670
HERPES SIMPLEX VIRUS (HSV) TYPE SPECIFIC 1
-
Test Name:
HERPES SIMPLEX VIRUS (HSV) TYPE SPECIFIC 1
-
Test Code:
86695
-
CPT Code(s):
86695
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum or plasma should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days Frozen: 1 month
-
Schedule:
1-3 Days
-
Clinical Significance:
Herpes simplex virus (HSV) infects neonates, children and adults. Transmission can result from direct contact with infected secretions from either a symptomatic or asymptomatic host. HSV has been characterized into 2 distinct serotypes: HSV-1 and HSV-2. HSV-1 is generally associated with infection in the tongue, mouth, lips, pharynx and eyes, whereas HSV-2 is primarily associated with genital and neonate infection. As with other serological tests, negative results do not rule out the diagnosis of herpes simplex disease. The time required to seroconvert following primary infection varies with the individual, the specimen many have been drawn prior to the appearance of detectable antibodies. There are reports of sero-reversion. When appropriate, e.g., in suspected early herpes simplex disease, the test should be repeated or tested with a different assay. If on re-testing, the result remains negative, then a second sample should be drawn 4-12 weeks later and testing repeated. A single positive result only indicates previous immunologic exposure; level of antibody response or class of antibody response may not be used to determine active infection or disease stage.
-
Performing Lab:
Simple Laboratories
HERPES SIMPLEX VIRUS (HSV) TYPE SPECIFIC 2
-
Test Name:
HERPES SIMPLEX VIRUS (HSV) TYPE SPECIFIC 2
-
Test Code:
86696
-
CPT Code(s):
86696
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum or plasma should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days Frozen: 1 month
-
Schedule:
1-3 Days
-
Clinical Significance:
Herpes simplex virus (HSV) infects neonates, children and adults. Transmission can result from direct contact with infected secretions from either a symptomatic or asymptomatic host. HSV has been characterized into 2 distinct serotypes: HSV-1 and HSV-2. HSV-1 is generally associated with infection in the tongue, mouth, lips, pharynx and eyes, whereas HSV-2 is primarily associated with genital and neonate infection. As with other serological tests, negative results do not rule out the diagnosis of herpes simplex disease. The time required to seroconvert following primary infection varies with the individual, the specimen many have been drawn prior to the appearance of detectable antibodies. There are reports of sero-reversion. When appropriate, e.g., in suspected early herpes simplex disease, the test should be repeated or tested with a different assay. If on re-testing, the result remains negative, then a second sample should be drawn 4-12 weeks later and testing repeated. A single positive result only indicates previous immunologic exposure; level of antibody response or class of antibody response may not be used to determine active infection or disease stage.
-
Performing Lab:
Simple Laboratories
HERPES SIMPLEX VIRUS TYPE 1/2 IGG
-
Test Name:
HERPES SIMPLEX VIRUS TYPE 1/2 IGG
-
Test Code:
86694
-
Alias:
Herpes Simplex Virus (HSV), Type Specific 1/2 IgG
-
CPT Code(s):
86695; 86696
-
Test Includes:
HSV-1 IgG Antibody; HSV-2 IgG Antibody
-
Preferred Specimen:
2.0 mL serum
-
Min. Volume:
1.0 mL serum *This volume does not allow for repeat testing.
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum or plasma should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days Frozen: 1 month
-
Schedule:
1-3 Days
-
Clinical Significance:
Herpes simplex virus (HSV) infects neonates, children and adults. Transmission can result from direct contact with infected secretions from either a symptomatic or asymptomatic host. HSV has been characterized into 2 distinct serotypes: HSV-1 and HSV-2. HSV-1 is generally associated with infection in the tongue, mouth, lips, pharynx and eyes, whereas HSV-2 is primarily associated with genital and neonate infection. As with other serological tests, negative results do not rule out the diagnosis of herpes simplex disease. The time required to seroconvert following primary infection varies with the individual, the specimen many have been drawn prior to the appearance of detectable antibodies. There are reports of sero-reversion. When appropriate, e.g., in suspected early herpes simplex disease, the test should be repeated or tested with a different assay. If on re-testing, the result remains negative, then a second sample should be drawn 4-12 weeks later and testing repeated. A single positive result only indicates previous immunologic exposure; level of antibody response or class of antibody response may not be used to determine active infection or disease stage.
-
Performing Lab:
Simple Laboratories
HERPES SIMPLEX VIRUS TYPE 1/2 PCR
-
Test Name:
HERPES SIMPLEX VIRUS TYPE 1/2 PCR
-
Test Code:
LS5025
-
CPT Code(s):
87529x2
-
Test Includes:
Detection of HSV 1 & 2 subtypes by RT-PCR
-
Preferred Specimen:
APTIMA ORANGE SWAB
-
Transport Container:
APTIMA ORANGE SWAB
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days
-
Clinical Significance:
HSV-1 and HSV-2 are members of the alpha-herpesviridae subfamily. HSV is an enveloped virus with a capsid containing viral DNA. Although HSV-1 and HSV-2 are closely related, the two viruses are serologically and genetically distinct. Encephalitis is inflammation of the brain associated with clinical evidence of neurologic dysfunction. Of the pathogens reported to cause encephalitis, the majority are viruses. In general, the most commonly identified etiologies in the United States are herpes simplex virus, West Nile virus, and the enteroviruses, followed by other herpes viruses. HSV causes about 5–10% of all encephalitis cases, and is one of the most common causes of identified sporadic encephalitis globally. HSV encephalitis occurs in all ages, and during all seasons. HSV-1 encephalitis is more common in adults; and HSV-2 encephalitis is more common in neonates. One study reported a neonatal herpes rate of 1 case per 3,200 live births in the U.S. Clinical features involved with HSV encephalitis include fever, hemicranial headache, language and behavioral abnormalities, memory impairment, and seizures.
-
Performing Lab:
Simple Laboratories
Heterophile, Mono Screen
-
Test Name:
Heterophile, Mono Screen
-
Test Code:
R654
-
Alias:
Mono Screen,Infectious Mononucleosis
-
CPT Code(s):
86308
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Heterophile, Mono Screen - Heterophile antibodies, in patients with infectious mononucleosis, may be present as early as the fourth day of illness, and by the twenty-first day of illness, 90% of patients will exhibit a positive test. The Epstein-Barr virus causes infectious mononucleosis.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
HIV-1 RNA, Quantitative, Real-Time PCR
-
Test Name:
HIV-1 RNA, Quantitative, Real-Time PCR
-
Test Code:
R40085
-
Alias:
Viral Load, HIV,HIV Viral Load
-
CPT Code(s):
87536
-
Preferred Specimen:
3 mL plasma collected in an EDTA (lavender-top) or PPT (white-top) tube
-
Min. Volume:
1 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Do not freeze whole blood or any samples stored in primary tube. Freshly drawn specimens (whole blood) may be stored at 2-25° C for up to 24 hours prior to centrifugation. Separate plasma from cells within 24 hours of collection by centrifugation. If shipping frozen, transfer plasma to a leak-proof transport tube, then freeze prior to shipment. Follow manufacturer’s instructions for collection tube handling.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: Unacceptable Refrigerated: 6 days Frozen: 84 days
-
Clinical Significance:
HIV-1 RNA, Quantitative, Real-Time PCR - This test is intended for use in conjunction with clinical presentation and other laboratory markers of disease progress for the clinical management of HIV-1 infected patients. The test can be used to assess patient prognosis by measuring the baseline HIV-1 RNA level or to monitor the effects of antiretroviral therapy by measuring changes in EDTA plasma HIV-1 RNA levels during the course of antiretroviral treatment.
-
Performing Lab:
Quest Diagnostics-Schaumburg 506 E State Pkwy Schaumburg, IL 60173-4538
HIV-1/2 AG/AB WITH REFLEX
-
Test Name:
HIV-1/2 AG/AB WITH REFLEX
-
Test Code:
013001
-
Alias:
HIV
-
CPT Code(s):
87389
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum or plasma should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
This qualitative assay is intended to be used as an aid in the diagnosis of HIV-1/HIV-2 infection, including acute or primary HIV-1 infection. The assay may also be used as an aid in the diagnosis of HIV-1/HIV-2 infection in pediatric subjects (children as young as two years) and in pregnant women. A test result that is non-reactive does not exclude the possibility of exposure to HIV-1 and/or HIV-2 may be due to antigen and antibody levels that are below the limit of detection of this assay.
-
Performing Lab:
Simple Laboratories
HIV-1/2 Antigen and Antibodies, Fourth Generation, with Reflexes
-
Test Name:
HIV-1/2 Antigen and Antibodies, Fourth Generation, with Reflexes
-
Test Code:
R91431
-
Alias:
Fourth Generation HIV,4th Generation HIV
-
CPT Code(s):
87389
-
Test Includes:
If HIV Antigen and Antibody, 4th Generation Screen is Reactive, then HIV-1/2 Antibody Differentiation will be performed at an additional charge (CPT code(s): 86701, 86702). If HIV-1/2 Antibody Differentiation is Indeterminate or Negative, then HIV-1 and HIV-2 RNA, Qualitative Real-Time PCR will be performed at an additional charge (CPT code(s): 87535, 87538).
-
Preferred Specimen:
3 mL serum
-
Min. Volume:
2 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
Serum: Collect in a serum separator tube or red-top tube (no gel). The tube should be centrifuged after clotting. Spun serum separator tubes may be submitted at room temperature or refrigerated unopened without transfer to a plastic screw-cap vial. Red-top tube (no gel) serum should be transferred to a plastic screw-cap vial and submitted for testing.
Plasma: Collect in an EDTA (lavender-top) tube and centrifuge tube within 24 hours of collection. Transfer plasma to a plastic screw-cap vial, label as plasma, and submit for testing.
Submitted tubes must be labeled with patient identifier and submitted only for HIV testing.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: 5 days Frozen: 30 days
-
Clinical Significance:
HIV-1/2 Antigen and Antibodies, Fourth Generation, with Reflexes - This algorithm is used to help diagnose HIV-1 and HIV-2 infection, including acute infection, and to differentiate HIV-1 from HIV-2. It is consistent with the HIV diagnostic algorithm recommended by the Centers for Disease Control and Prevention [2]. It can be used in adults, including pregnant women, and in children 2 years or older. This panel begins with an antigen/antibody assay that allows for detection of acute HIV-1 infection based on the presence of p24 antigen before seroconversion occurs, and HIV-1 and HIV-2 antibodies post-seroconversion. If the HIV-1/HIV-2 antigen/antibody test is positive, an antibody-differentiation test is done (at additional charge) to confirm infection and identify the presence of HIV-1 or HIV-2 specific antibodies. However, the HIV-1/HIV-2 differentiation test can be negative during acute infection (prior to development of specific antibodies). If the antibody-based HIV-1/HIV-2 supplemental test is negative, the specimen will be reflexed to the HIV-1 and HIV-2 RNA, Qualitative, Real-Time PCR test (at additional charge), which can detect the presence of HIV-1 and 2 RNA and identify patients with acute HIV-1 or 2 infection [1]. The United States Preventive Services Task Force (USPSTF) recommends HIV screening for all pregnant women, and for individuals between 15 and 65 years of age who live in regions with an HIV prevalence of >0.1% [2]. In addition, antigen/antibody-based HIV testing is recommended for high-risk individuals who want to begin pre-exposure prophylaxis (PrEP) therapy, because HIV-positive patients who start PrEP without knowing their HIV status face an elevated risk of antiretroviral resistance [3,4]. Because 40% of new HIV infections are transmitted unknowingly by people unaware of their HIV status, early diagnosis is important to reduce HIV transmission [5]. Antigen/antibody-based HIV screening assays have >99.7% sensitivity and >99.3% specificity for HIV infection and can identify most (>80%) acute infections that would otherwise require nucleic acid testing for detection [6,7].
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Homocysteine
-
Test Name:
Homocysteine
-
Test Code:
R31789
-
CPT Code(s):
83090
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Red-top tubes (no gel): Place the specimen in the refrigerator or ice bath for 30 minutes after collection. Centrifuge the specimen as soon as possible after complete clot formation. Transfer the serum to a plastic specimen transport tube. Mark the specimen type as serum on the transport tube.
Barrier gel separator tubes: Place the specimen in a refrigerator for 30 minutes after collection. Do not place barrier tubes in an ice bath as freezing may prevent the barrier gel from adequately separating from cells. Centrifuge specimen as soon as possible after complete clot formation, ensuring that the barrier gel completely separates serum from cells.
EDTA or heparin tubes: Place the specimen in the refrigerator or ice bath after collection. Centrifuge the specimen as soon as possible. Transfer the plasma to a plastic specimen transport container. Mark the specimen type as plasma on the transport tube. Do not submit whole blood.
Note: It is very important to centrifuge and separate serum or plasma from red blood cells as soon as possible to avoid falsely elevated results.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 14 days Frozen: 6 months
-
Clinical Significance:
Homocysteine - An elevated concentration of homocysteine is an independent risk factor for cardiovascular disease. When used in conjunction with methylmalonic acid (MMA), these tests are useful to diagnose and monitor vitamin B12 (cobalamin) and folic acid deficiency and are often useful in evaluating macrocytosis (an elevated MCV, an erythrocytic index).
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
HUMAN SEX HORMONE BINDING GLOBULIN
-
Test Name:
HUMAN SEX HORMONE BINDING GLOBULIN
-
Test Code:
SEXHOR
-
Alias:
SHBG
-
CPT Code(s):
84270
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days Frozen: 2 months
-
Schedule:
1-2 Days
-
Clinical Significance:
Testosterone, dihydrotestosterone, and estrogens circulate in serum bound to Sex Hormone Binding Globulin (SHBG). SHBG concentrations are increased in pregnancy, hyperthyroidism, cirrhosis, oral estrogen administration, and by certain drugs. Concentrations are decreased by testosterone, hypothyroidism, Cushing's syndrome, acromegaly, and obesity.
-
Performing Lab:
Simple Laboratories
I
IA-2 Antibody
-
Test Name:
IA-2 Antibody
-
Test Code:
R37933
-
Alias:
Tyrosine Phosphatase,ICA 512 Antibody,Insulinoma-associated Protein 2,Islet Cell Antigen 512 Antibodies
-
CPT Code(s):
86341
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
IA-2 Antibody - Key clinical use and differentiators Measurement of Islet cell antigen 2 antibodies (IA-2) is used to: 1. Screen for presymptomatic T1D in individuals with a family history of type 1 diabetes (T1D) or those known to have a high-risk HLA genotype, 2. Distinguish between T1D, type 2 diabetes mellitus (T2D), and atypical forms of diabetes such as latent autoimmune diabetes in adults (LADA). [1] Positivity to IA-2 represents a key marker of T1D. [1] Intended Clinical Use This test is crucial for differentiating between T1D and T2D. It is important to note that classifying diabetes type can be challenging at the time of presentation, and misdiagnosis can occur in approximately 40% of adults with new T1D. [1] Identifying individuals affected by stage 1 T1D is important for applying eligibility criteria to drugs, such as Teplizumab, which have demonstrated the ability to delay the transition of stage 1 to stage 3 T1D in clinical trials. [2,3] IA-2 has some distinctive features. Its presence is associated with more-advanced islet autoimmunity and faster progression to stage 3 T1D. [4] Limitations T1D is classified into three stages, with stages 1 and 2 considered presymptomatic. Since the presence of stage 1 and 2 T1D requires at least two islet autoantibodies, relying solely on IA-2 as a screening test limits the ability to make an accurate diagnosis. Professional organizations, including the American Diabetes Association (ADA), recommend using tests for all four islet cell autoantibodies: IAA, glutamic acid decarboxylase (GAD65), Zinc Transporter 8 (ZnT8), and islet cell antigen 2 antibody (IA-2). [1]
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
IDALPREM (MEDICATION)
-
Test Name:
IDALPREM (MEDICATION)
-
Test Code:
501860
IgA
-
Test Name:
IgA
-
Test Code:
R539
-
Alias:
Immunoglobulin A
-
CPT Code(s):
82784
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: 90 days
-
Clinical Significance:
IgA - Increased IgA is associated with monoclonal IgA myeloma, respiratory and gastrointestinal infections, and malabsorption; decreased IgA is found in selective IgA deficiency and in ataxia telangiectasia.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
IgE
-
Test Name:
IgE
-
Test Code:
R542
-
Alias:
Immunoglobulin E
-
CPT Code(s):
82785
-
Preferred Specimen:
0.3 mL serum
-
Min. Volume:
0.3 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 14 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
IgE - For diagnosis of allergic disease. A normal IgE level does not exclude the possible presence of an allergic disorder.
-
Performing Lab:
Quest Diagnostics-Lenexa 10101 Renner Blvd Lenexa, KS 66219-9752
IGF Binding Protein-3 (IGFBP-3)
-
Test Name:
IGF Binding Protein-3 (IGFBP-3)
-
Test Code:
R34458
-
Alias:
Insulin-Like Growth Factor Binding Protein
-
CPT Code(s):
83520
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 1 year
-
Clinical Significance:
IGF Binding Protein-3 (IGFBP-3) - Insulin-like growth factor binding proteins bind IGF-I and IGF-II with high affinity but do not bind insulin. Of the 6 distinct IGF binding proteins structurally characterized at this time, IGFBP-3 has been shown to be the major carrier of the IGFs, transporting approximately 95% of circulating IGF-I and IGF-II. IGFBP-3 is growth hormone (GH) responsive. Thus, levels are high in acromegaly and low in hypopituitarism, and levels increase in GH-deficient children after GH administration. Other causes of short stature that result in reduced IGFBP-3 levels include poorly controlled diabetes. The IGFBP-3 assay is useful in assessing nutritional status, since IGFBP-3 decreases during both caloric and protein restriction.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
IgG
-
Test Name:
IgG
-
Test Code:
R543
-
Alias:
Immunoglobulin G
-
CPT Code(s):
82784
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: 90 days
-
Clinical Significance:
IgG - Increased IgG is associated with acute and chronic inflammations, monoclonal IgG myeloma, autoimmune diseases; decreased IgG is found in selective IgG deficiency, Bruton's Disease, and acquired immune deficiency.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Immunofixation, Serum
-
Test Name:
Immunofixation, Serum
-
Test Code:
R549
-
Alias:
IFE, Serum,Immunotyping,Immunosubtraction
-
CPT Code(s):
86334
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Immunofixation, Serum - Monoclonal increases in IgG or IgA are often associated with diseases such as multiple myeloma, lymphomas or leukemia. A monoclonal increase in IgM is commonly associated with Waldenström's macroglobulinemia.
-
Performing Lab:
Quest Diagnostics-Lenexa 10101 Renner Blvd Lenexa, KS 66219-9752
Immunoglobulins Panel, Serum
-
Test Name:
Immunoglobulins Panel, Serum
-
Test Code:
R7083
-
Alias:
Quantitative Immunoglobulins
-
CPT Code(s):
82784 (x3)
-
Test Includes:
IgA, IgG, IgM
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Serum separator tube (SST)
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: 90 days
-
Clinical Significance:
Immunoglobulins Panel, Serum - Elevations of IgG, A and/or M are seen in generalized hypergammaglobulinemia, chronic inflammatory conditions and in lymphoproliferative diseases such as multiple myeloma, lymphoma and leukemias. Decreased levels are found in immunodeficiency states, generalized hypogammaglobulinemia and in unrecognized pediatric patients.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
INSULIN
-
Test Name:
INSULIN
-
Test Code:
R561
-
CPT Code(s):
83525
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Unable to add insulin testing unless sample was submitted frozen
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: Unacceptable Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Insulin - For diagnosis and monitoring of diabetes and insulin-secreting tumors.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Insulin Autoantibody
-
Test Name:
Insulin Autoantibody
-
Test Code:
R36178
-
Alias:
Human Insulin Antibody
-
CPT Code(s):
86337
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 28 days Refrigerated: 28 days Frozen: 90 days
-
Clinical Significance:
nsulin Autoantibody - Key clinical use and differentiators Measurement of Insulin Autoantibody (IAA) is used to: 1. Screen for presymptomatic type 1 diabetes (T1D) in individuals with a family history of T1D or those known to have a high-risk HLA genotype, 2. Distinguish between T1D, type 2 diabetes mellitus (T2D), and atypical forms of diabetes such as latent autoimmune diabetes in adults (LADA). [1] Insulin Autoantibody (IAA) is used to help predict the need for insulin treatment in adults with diabetes who have not received treatment with insulin. [1] Intended Clinical Use This test is crucial for differentiating between T1D and T2D. It is important to note that classifying diabetes type can be challenging at the time of presentation, and misdiagnosis can occur in approximately 40% of adults with new T1D. [1] Identifying individuals affected by stage 1 T1D is important for applying eligibility criteria to drugs, such as Teplizumab, which have demonstrated the ability to delay the transition of stage 1 to stage 3 T1D in clinical trials [2,3] IAA has some distinctive features, including that usually it is the first detected autoantibody in young children, [4] its appearance is more common in younger children [5] and its frequency of appearance declines with age. IAA is not informative for individuals treated with insulin, who often develop antibodies in response to injected insulin. [6] Limitations T1D is classified into three stages, with stages 1 and 2 considered presymptomatic. Since the presence of stage 1 and 2 T1D requires at least two islet autoantibodies, relying solely on IAA as a screening test limits the ability to make an accurate diagnosis. Professional organizations, including the American Diabetes Association (ADA), recommend using tests for all four islet cell autoantibodies: IAA, glutamic acid decarboxylase (GAD65), Zinc Transporter 8 (ZnT8), and islet cell antigen 2 antibody (IA-2).[1]
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
IOPHEN-C NR (MEDICATION)
-
Test Name:
IOPHEN-C NR (MEDICATION)
-
Test Code:
501400
IRON
-
Test Name:
IRON
-
Test Code:
FE
-
Alias:
FE
-
CPT Code(s):
83540
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes
-
Transport Temperature:
Refrigerated
-
Schedule:
1-2 Days
-
Clinical Significance:
Alterations in iron and total iron binding capacity levels result from changes in iron intake, absorption, storage, and release mechanisms. Such changes are indicative of a wide range of dysfunctions including anemias, hemochromatosis, nephrosis, cirrhosis, and hepatitis. Both iron and total iron binding capacity measurements are important for definitive diagnosis because they are interrelated.
-
Performing Lab:
Simple Laboratories
IRON/TRANSFERRIN WITH CALCULATED TIBC
-
Test Name:
IRON/TRANSFERRIN WITH CALCULATED TIBC
-
Test Code:
TIBCP
-
Alias:
FE, SIDERPHILIN, TIBC
-
CPT Code(s):
83540, 84466
-
Test Includes:
Iron, Transferrin and calculated TIBC
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 5 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Alterations in iron and TIBC levels result from changes in iron intake, absorption, storage, and release mechanisms. Such changes are indicative of a wide range of dysfunctions including anemias, hemochromatosis, nephrosis, cirrhosis, and hepatitis. Both iron and total iron binding capacity measurements are important for definitive diagnosis because they are interrelated. Transferrin is a plasma protein whose primary function is to transport absorbed iron or stored iron to sites in the body involved in erythropoiesis. The measurement of transferrin aids in the diagnosis of malnutrition, acute inflammation, infection, assessment of renal function, and red blood cell disorders such as iron deficiency anemia.
-
Performing Lab:
Simple Laboratories
j
JAK2 V617F Mutation Analysis
-
Test Name:
JAK2 V617F Mutation Analysis
-
Test Code:
R92473
-
Alias:
Myeloproliferative neoplasm,PMF,MPN,Next-Generation Sequencing,Essential Thrombocythemia (ET),NGS,Janus Kinase 2,Polycythemia Vera (PV),JAK,ET,Primary Myelofibrosis (PMF),PV
-
CPT Code(s):
81270
-
Preferred Specimen:
4 mL whole blood or 3 mL bone marrow aspirate collected in an EDTA (lavender-top) tube
-
Min. Volume:
3 mL whole blood • 1 mL bone marrow aspirate
-
Transport Container:
EDTA (lavender-top) tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: Unacceptable | Extracted DNA Room temperature:7 days Refrigerated: 14 days Frozen: 1 year
-
Clinical Significance:
JAK2 V617F Mutation Analysis - This advanced DNA-based, next-generation sequencing (NGS) assay analyses leukocytes from blood or bone marrow aspirate for mutation at condon 617 of JAK2. The JAK2 V617F mutation is associated with myeloproliferative neoplasms, including polycythemia vera, essential thrombocythemia and primary myelofibrosis.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
Jo-1 Antibody
-
Test Name:
Jo-1 Antibody
-
Test Code:
R5810
-
CPT Code(s):
86235
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Jo-1 Antibody - Jo-1 Antibody occurs most frequently (31%) in patients with polymyositis, but has also been found in patients with dermatomyositis, and the polymyositis/scleroderma "overlap syndrome" (PM/SCL) or polymyositis/systemic lupus erythematosis "overlap syndrome" (PM/SLE).
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
JWH-018 4-HYDROXYPENTYL METABOLITE (MEDICATION)
-
Test Name:
JWH-018 4-HYDROXYPENTYL METABOLITE (MEDICATION)
-
Test Code:
500600
JWH-073 3-HYDROXYBUTYL METABOLITE (MEDICATION)
-
Test Name:
JWH-073 3-HYDROXYBUTYL METABOLITE (MEDICATION)
-
Test Code:
500590
k
KADIAN (MEDICATION)
-
Test Name:
KADIAN (MEDICATION)
-
Test Code:
500650
L
Lactate Dehydrogenase (LD), Body Fluid
-
Test Name:
Lactate Dehydrogenase (LD), Body Fluid
-
Test Code:
R94675
-
CPT Code(s):
83615
-
Preferred Specimen:
1 mL body fluid collected in a sterile plastic transport tube
-
Min. Volume:
0.5 mL
-
Transport Container:
Sterile plastic transport tube
-
Collection Instruction:
Centrifuge to remove any cellular material. Date, time of collection and specimen source are required.
If source Order the following Quest Diagnostics test Peritoneal LD, Peritoneal Fluid (17588) Pleural LD, Pleural Fluid (17589) Synovial LD, Synovial Fluid (17658) Pericardial LD, Pericardial Fluid (17647) CSF LD, CSF (1687) -
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 48 hours Frozen: Unacceptable
-
Clinical Significance:
Lactate Dehydrogenase (LD), Body Fluid
-
Performing Lab:
Mayo Clinical Laboratories 200 1st Street SW Rochester, MN 55905-0001
LAZANDA (MEDICATION)
-
Test Name:
LAZANDA (MEDICATION)
-
Test Code:
501730
LDH (LACTATE DEHYDROGENASE)
-
Test Name:
LDH (LACTATE DEHYDROGENASE)
-
Test Code:
LDH
-
Alias:
LD, LDH
-
CPT Code(s):
83615
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 3 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Elevations in serum lactate dehydrogenase (LD) occur from myocardial infarction, liver disease, pernicious and megaloblastic anemias, pulmonary emboli, malignancies, and muscular dystrophy. A combined analysis of LD and CK (creatine kinase) isoenzymes provides a definite diagnosis of acute myocardial infarction.
-
Performing Lab:
Simple Laboratories
Lead (Venous)
-
Test Name:
Lead (Venous)
-
Test Code:
R599
-
Alias:
PB, Pediatric,Blood Lead,Lead Screen,PB, BL
-
CPT Code(s):
83655
-
Test Includes:
%SBLEADOE, %599
-
Preferred Specimen:
3 mL whole blood collected in a K2 EDTA (tan-top) tube or EDTA (royal blue-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
K2 EDTA (tan-top) tube
-
Collection Instruction:
Collection material such as alcohol swabs should be lead-free. Use powderless gloves. Once washed, fingers must not come into contact with any surface. Clean skin (area for venipuncture) with lead-free alcohol swab prior to puncture. Avoid worksite collection.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 14 days Frozen: 60 days
-
Clinical Significance:
Lead (Venous) - Blood lead level analysis is performed to evaluate the body burden of lead.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Legionella Antigen, EIA, Urine
-
Test Name:
Legionella Antigen, EIA, Urine
-
Test Code:
R8856
-
CPT Code(s):
87449
-
Preferred Specimen:
1 mL urine
-
Min. Volume:
0.5 mL
-
Transport Container:
Sterile screw-cap container
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 24 hours Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Legionella Antigen, EIA, Urine - Legionella urinary antigen is useful in conjunction with other laboratory tests in the diagnosis of Legionnaire's Disease. Legionella urinary antigen may be identified for months after recovery.
-
Performing Lab:
Quest Diagnostics Nichols Institute-Chantilly VA 14225 Newbrook Drive Chantilly, VA 20151-2228
Leukemia/Lymphoma Evaluation
-
Test Name:
Leukemia/Lymphoma Evaluation
-
Test Code:
R35080
-
Alias:
Flow Cytometry Leukemia/Lymphoma,Immunophenotyping,Leukemia Panel,Leukemia/Lymphoma Phenotyping Panel,Lymphoma Panel,Flow
-
CPT Code(s):
88184, 88185 (x21), 88189
-
Test Includes:
Initial markers evaluated: CD2, CD3, CD4, CD5, CD7, CD8, CD10, CD11c, CD13, CD19, CD20, CD23, CD33, CD34, CD38, CD56, CD64, CD117, HLA-DR, sKappa, sLambda. CD45 is used for gating. Additional markers may be performed based on the pathologist review. These markers will be performed at an additional charge (CPT code(s): 88185 for each additional marker).
-
Preferred Specimen:
Peripheral blood: 4 mL collected in a sodium heparin (green-top) tube, ACD-A (yellow-top) tube, or EDTA (lavender-top) tube or Bone marrow: 3 mL collected in a sodium heparin (green-top) tube, ACD-A (yellow-top) tube,or EDTA (lavender-top) tube or Tissue or body fluids: Any type is acceptable
-
Min. Volume:
3 mL peripheral blood • 1 mL bone marrow
-
Transport Container:
See Collection Instructions
-
Collection Instruction:
eripheral blood and bone marrow: The tube must be kept at room temperature and shipped to the lab immediately.
Tissue: Any tissue type is acceptable. Tissue size is dependent upon leukocyte cellularity. (The tissue is disaggregated into single cells so that a minimum of 50,000 cells of interest are harvested.) Ship tissue in a sterile plastic container with RPMI 1640 enriched with FBS (10% FBS RPMI). Absolutely no fixative should be added. Refrigerate and ship immediately.
Body fluids: Any body fluid is acceptable. Sample size is dependent upon cellularity of the sample. (A minimum of 50,000 cells of interest in total volume of fluid). Place fluid in sterile plastic container. Absolutely no fixative should be added. Refrigerate and ship immediately.
A clinical indication and specimen source are required with each specimen. If possible, submit CBC results with differential or an EDTA tube of peripheral blood.
Do not freeze and do not place in fixative.Because of the critical nature of these specimens, the laboratory will attempt to process all specimens received, regardless of age of specimen.
-
Transport Temperature:
Peripheral blood and bone marrow: Room temperature Tissue and body fluids: Refrigerate (cold packs)
-
Stability:
Room temperature: 72 hours (may extend to 5 days depending on cell viability) Refrigerated: Not established Frozen: Not established
-
Clinical Significance:
Leukemia/Lymphoma Evaluation - This panel may be used in the initial evaluation of patients with clinical suspicion of hematologic neoplasms. Immunophenotyping by flow cytometry can aid in the diagnosis and classification of leukemia and lymphoma [1]. Subsequent testing of additional cell surface antigens may be needed to help establish a diagnosis. Leukemias and lymphomas are heterogenous morphologically and clinically. Identification of cell surface markers (T cell, B cell, progenitor, and myeloid markers) by flow cytometry can help assign a cell lineage to neoplastic cells. Accurate immunotyping aids in the diagnosis, classification, and prognosis of hematologic neoplasm and may inform treatment decisions [1]. This immunotyping panel is designed to expedite the evaluation of patients without provisional diagnosis of a certain type of hematologic neoplasm. The results of this panel must be interpreted with cytological, histological, genetic, and clinical findings to generate accurate diagnosis. Additional cell surface markers not included in this panel may be needed to evaluate certain hematologic malignancies (eg, hairy cell leukemia). Because non-viable cells lead to non-specific antibody binding, specimens should be processed as early as possible. The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
Levetiracetam, Immunoassay
-
Test Name:
Levetiracetam, Immunoassay
-
Test Code:
R36330
-
Alias:
Keppra
-
CPT Code(s):
80177
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no-gel)
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 21 days Frozen: 30 days
-
Clinical Significance:
Levetiracetam, Immunoassay - LEV is currently used as an anti-epileptic drug for the treatment of adult partial seizures particularly as an add-on therapy for refractory patients. It also has potential for other anxiety and cognitive disturbances.
-
Performing Lab:
Quest Diagnostics-Lenexa 10101 Renner Blvd Lenexa, KS 66219-9752
LEXUSS 210 (MEDICATION)
-
Test Name:
LEXUSS 210 (MEDICATION)
-
Test Code:
501280
LH (LUTEINIZING HORMONE)
-
Test Name:
LH (LUTEINIZING HORMONE)
-
Test Code:
LH
-
Alias:
hLH ICSH Interstitial Cell Stimulating Hormone Pituitary Gonadotropin
-
CPT Code(s):
83002
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection. If the specimen is collected in an anticoagulant tube, centrifuge and transfer plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 72 hours* Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Concentrations of hLH and hFSH are commonly determined in investigations of menstrual cycle, fertility, and pubertal developmental abnormalities, such as premature ovarian failure, menopause, ovulatory disorders and pituitary failure. The ratio of hLH/hFSH has been used to assist in the diagnosis of polycystic ovary disease. Low concentrations of hLH and hFSH may indicate pituitary failure while elevated concentrations of hLH and hFSH along with decreased concentrations of gonadal steroids may indicate gonadal failure (menopause, ovariectomy, premature ovarian syndrome, Turners Syndrome). Low concentrations of gonadotropin are usually observed in females taking oral steroid based contraceptives. In the male, elevated hLH and hFSH with low concentrations of gonadal steroids may indicate testicular failure or anorchia. In Klinefelter’s syndrome hLH may be elevated due to Sertoli cell failure.
-
Performing Lab:
Simple Laboratories
LIPASE
-
Test Name:
LIPASE
-
Test Code:
LIPA
-
CPT Code(s):
83690
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection. If the specimen is collected in an anticoagulant tube, centrifuge and transfer plasma into a properly labeled transfer tube within two hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Measurements of serum lipase are used in the diagnosis and treatment of acute pancreatitis or pancreatic injury.
-
Performing Lab:
Simple Laboratories
LIPID PANEL RFX DIRECT LDL
-
Test Name:
LIPID PANEL RFX DIRECT LDL
-
Test Code:
LDLR
-
Alias:
Lipid Panel with LDL-Calc (AMA)
-
CPT Code(s):
80061
-
Test Includes:
Total Cholesterol, HDL Cholesterol, LDL Cholesterol (calculated), Triglycerides, Cholesterol/HDL Ratio
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Patient should fast for 12 hours prior to collection, unless instructed differently by physician.
Allow specimen to completely clot. Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within 2 hours from the time of collection. If the specimen is collected in an anticoagulant tube without a gel barrier, centrifuge and transfer plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 72 hours* Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
The tests in a lipid panel are used to determine the risk of coronary heart disease. These tests are good indicators of whether someone is likely to have a heart attack or stroke caused by blockage of blood vessels or hardening of the arteries.
-
Performing Lab:
Simple Laboratories
Lipoprotein (a)
-
Test Name:
Lipoprotein (a)
-
Test Code:
R34604
-
Alias:
Lp (a)
-
CPT Code(s):
83695
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 90 days
-
Clinical Significance:
Lipoprotein (a) - Elevated concentrations of Lp(a) are associated with increased risk of coronary artery disease.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Lipoprotein Fractionation, NMR with Lipid Panel (Triglycerides/HDL-C)
-
Test Name:
Lipoprotein Fractionation, NMR with Lipid Panel (Triglycerides/HDL-C)
-
Test Code:
R37849
-
CPT Code(s):
83704, 80061
-
Test Includes:
37847 - Lipoprotein Fractionation, NMR 37848 - Lipid Panel with Triglycerides/HDL-Cholesterol
-
Preferred Specimen:
2 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
1.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
1. Gently invert draw tube 5X (DO NOT SHAKE).
2. Let blood clot for 30-60 minutes at room temperature.
3. Centrifuge for 10 minutes.
4. Aliquot top layer from red-top draw tube and place SERUM in transport tube and dispose of draw tube. Label the transport tube as “No Additive Serum Red”. ONLY ship No Additive Serum in transport tube.
5. Store and transport refrigerated. Specimen is stable at -20° for 10 days and -70° for 28 days but CANNOT BE SHIPPED ON DRY ICE.Note: Adults without other risk factors for heart disease should receive a lipid panel once every five years. Individuals who have had an abnormal lipid panel, or those who have other cardiovascular risk factors, may be tested more frequently.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: Unacceptable Refrigerated: 7 days Frozen -20° C: Unacceptable Frozen -70° C: Unacceptable
-
Clinical Significance:
Lipoprotein Fractionation, NMR with Lipid Panel (Triglycerides/HDL-C) - The Lipoprotein Fractionation, NMR test is used to help assess the risk for cardiovascular disease (CVD) in patients with intermediate or high risk based on traditional or emerging risk factors, and to assess therapeutic response in patients undergoing lipid-lowering therapy. The lipid panel is used to determine an individual's risk of developing cardiovascular disease and to monitor the efficacy of therapy or lifestyle changes.
-
Performing Lab:
Cleveland HeartLab, Inc 6701 Carnegie Avenue, Suite 500 Cleveland, OH 44103-4623
Lithium
-
Test Name:
Lithium
-
Test Code:
R613
-
CPT Code(s):
80178
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 10 days Refrigerated: 10 days Frozen: Not established
-
Clinical Significance:
Lithium - Lithium is used to treat manic-depressive disorders and the manic phase of affective disorders, including mania. The therapeutic window is relatively small. Therapeutic drug monitoring is useful to optimize dose and avoid toxicity.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Liver Fibrosis, FibroTest-ActiTest Panel
-
Test Name:
Liver Fibrosis, FibroTest-ActiTest Panel
-
Test Code:
R92688
-
Alias:
FibroSure Panel
-
CPT Code(s):
81596
-
Test Includes:
Fibrosis Score, Fibrosis Stage, Fibrosis Interpretation Necroinflammat Act Score, Necroinflammat Act Grade, Necroinflammat Interpretation Alpha-2-Macroglobulin Haptoglobin Apolipoprotein A1 Total Bilirubin GGT ALT
-
Preferred Specimen:
3.5 mL serum
-
Min. Volume:
2 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Serum should be separated from the cells as soon as possible after visible clot formation (usually 15-30 minutes after collection). Avoid freezing and thawing.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: 24 hours Refrigerated: 72 hours Frozen -20° C: 5 days Frozen -70° C: 28 days
-
Clinical Significance:
Liver Fibrosis, FibroTest-ActiTest Panel - FibroTest and ActiTest permit the non-invasive evaluation of Hepatitis C (or B) individuals for the presence of liver fibrosis and liver inflammation, respectively. The FibroTest and ActiTest scores are calculated based on patient age, gender and concentrations of serum of y-glutamyl transferase (GGT), total bilirubin (TB), a-2 macroglobulin, haptoglobin, apolipoprotein A1 and alanine aminotransferase (ActiTest). Fibrotest and ActiTest Scores, on a scale of 0.0 to 1.0, are assigned a Metavir scale indicating the level of fibrosis or inflammation present.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
LONSYS (MEDICATION)
-
Test Name:
LONSYS (MEDICATION)
-
Test Code:
501710
LORABENZ (MEDICATION)
-
Test Name:
LORABENZ (MEDICATION)
-
Test Code:
501870
LORCET (MEDICATION)
-
Test Name:
LORCET (MEDICATION)
-
Test Code:
501740
LOW DENSITY LIPOPROTEIN (LDL), DIRECT MEASUREMENT
-
Test Name:
LOW DENSITY LIPOPROTEIN (LDL), DIRECT MEASUREMENT
-
Test Code:
LDLD
-
Alias:
LDL Cholesterol, Direct
-
CPT Code(s):
83721
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 m SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Patient should fast for 12 hours prior to collection, unless instructed differently by physician.
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-Hep tube, centrifuge for 15 minutes.
The serum should be physically separated from contact with cells within two hours from the time of collection. -
Transport Temperature:
Refrigerated
-
Schedule:
1-2 Days
-
Clinical Significance:
LDL cholesterol is directly related to the risk of developing coronary heart disease. A low HDL/LDL cholesterol ratio is directly related to the risk of developing coronary artery disease. Elevated LDL cholesterol is the primary target of cholesterol-lowering therapy.
-
Performing Lab:
Simple Laboratories
Lupus Anticoagulant Evaluation with Reflex
-
Test Name:
Lupus Anticoagulant Evaluation with Reflex
-
Test Code:
R7079
-
CPT Code(s):
85613, 85730
-
Test Includes:
PTT-LA and dRVVT with Reflex Confirmations If PTT-LA Screen is prolonged (>40 seconds), then Hexagonal Phase Confirmation will be performed at an additional charge (CPT code(s): 85598). If Hexagonal Phase Confirmation is positive or weakly positive, then Thrombin Clotting Time will be performed at an additional charge (CPT code(s): 85670). If dRVVT Screen is prolonged (>45 seconds), then dRVVT Confirm will be performed at an additional charge (CPT code(s): 85597). If dRVVT Confirm is positive, then dRVVT 1:1 Mixing Study will be performed at an additional charge (CPT code(s): 85613).
-
Preferred Specimen:
3 mL frozen, platelet-poor plasma collected in a 3.2% sodium citrate (light blue-top) tube
-
Min. Volume:
2 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Platelet-poor plasma: Centrifuge light blue-top tube for 15 minutes at approximately 1500 g within 60 minutes of collection. Using a plastic pipette, remove plasma, taking care to avoid the WBC/platelet buffy layer and place into a plastic vial. Centrifuge a second time and transfer platelet-poor plasma into a new plastic vial. Plasma must be free of platelets (<10,000/mcL). Freeze immediately and ship on dry ice.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: Unacceptable Refrigerated: Unacceptable Frozen: 30 days
-
Clinical Significance:
Lupus Anticoagulant Evaluation with Reflex - Lupus anticoagulants (LA) are members of a family of antibodies with phospholipid-protein specificity. LA may be defined as an immunoglobulin, IgG or IgM or a mixture of both, that interferes with one or more of the in-vitro phospholipid (PL) dependent tests of coagulation. These antibodies are not associated with a hemorrhagic diathesis, but rather have been linked to thrombotic events. In addition to thrombosis other clinical complications have been associated with the presence of LA. These include strokes, nonbacterial thrombotic endocarditis, livedo reticularis and a variety of obstetrical complications such as intrauterine fetal death, recurrent spontaneous abortion, fetal growth retardation, early onset preeclampsia and chorea gravidarum.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Lyme Disease Antibodies (IgG, IgM), Immunoblot
-
Test Name:
Lyme Disease Antibodies (IgG, IgM), Immunoblot
-
Test Code:
R8593
-
Alias:
Borrelia burgdorferi
-
CPT Code(s):
86617 (x2)
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. For patients receiving STRENSIQ, consideration should be given to using alternate methods.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Lyme Disease Antibodies (IgG, IgM), Immunoblot - Lyme disease is transmitted by a tick vector carrying Borrelia burgdorferi. Immunoblot testing qualitatively examines, with high specificity, antibodies in a patient's specimen. Immunoblot testing is appropriate for confirming a detected EIA or IFA test result.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Lymphocyte Subset Panel 1
-
Test Name:
Lymphocyte Subset Panel 1
-
Test Code:
R7197
-
Alias:
Flow
-
CPT Code(s):
86355,86357, 86359, 86360
-
Test Includes:
% CD3 (Mature T Cells), Absolute CD3+ Cells, % CD4, Absolute CD4+ Cells, % CD8, Absolute CD8+ Cells, CD4/CD8 Ratio, % CD16+CD56 (NK Cells), Abs NKCell(CD16+CD56+Cell), % CD19 (B Cells), Absolute CD19+ Cells, Absolute Lymphocytes
-
Preferred Specimen:
5 mL whole blood collected in an EDTA (lavender-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
Room temperature
-
Collection Instruction:
If a CBC is also required, a separate EDTA (lavender-top) tube must be submitted
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: Unacceptable Frozen: Uacceptable
-
Clinical Significance:
Lymphocyte Subset Panel 1 - Immunophenotypic analysis may assist in evaluating cellular immunocompetency in suspected cases of primary and secondary immunodeficiency states.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Lymphocyte Subset Panel 4
-
Test Name:
Lymphocyte Subset Panel 4
-
Test Code:
R7924
-
Alias:
Flow
-
CPT Code(s):
86360
-
Test Includes:
% CD4, Absolute CD4+ Cells, % CD8, Absolute CD8+ Cells, CD4/CD8 Ratio, Absolute Lymphocytes
-
Preferred Specimen:
5 mL whole blood collected in an EDTA (lavender-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
5 mL (or 3 mL pediatric) EDTA (lavender-top) tube
-
Collection Instruction:
If a CBC is also required, a separate EDTA (lavender-top) tube must be submitted.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: Unacceptable Frozen: Unacceptable
-
Clinical Significance:
Lymphocyte Subset Panel 4 - This panel separately reports CD4+ T cells (CD4) and CD8+ T cells (CD8) in the blood, as well as a calculated CD4/CD8 ratio. This panel may provide information of the immune status of individuals living with HIV. It can be used to help establish baseline values and track antiretroviral (ARV)-related treatment progress. It can also be used to evaluate helper and suppressor cell immune status in individuals with other immunodeficiency diseases. The CD4 count is the most valuable indicator of immune status in HIV-infected individuals. It can help determine the need for prophylaxis for opportunistic infections and the urgency of ARV initiation. The CD8 count reflects the level of immune activation in response to HIV. In the early stages of infection, CD4 levels and the CD4/CD8 ratio typically decline after seroconversion occurs. However, after seroconversion, CD8 cells increase in an attempt to mount a response against HIV. In ARV-treated patients with controlled viral load, CD8 counts. Post-therapy, persistently elevated CD8 counts have been linked to increased risk of non--AIDS-defining diseases, independent of CD4 count, including cardiovascular, renal, respiratory, metabolic diseases, and cancer [1-3]. This panel can be used to establish baseline CD4 and CD8 levels, as well as percentages and ratios, which help determine how long the virus has been present in the blood and the overall prognosis. During ARV treatment, this panel can help assess CD4 recovery and CD8 response to treatment [1,2]. During the first 2 years of ARV therapy, The National Institutes of Health recommends testing CD4 every 3 to 6 months. Patients who develop viremia while on therapy or whose CD4 count stays below 300 cells/µL. should also have their CD4 levels tested every 3 to 6 months. After 2 years of ARV therapy, with consistently suppressed viral load and a CD4 count of 300 to 500 cells/µL, CD4 counts should be tested every 12 months. CD4 testing should also be conducted if therapy fails. Note that CD4 testing is optional when CD4 counts are >500 cells/µL [1].
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Lymphocyte Subset Panel 5
-
Test Name:
Lymphocyte Subset Panel 5
-
Test Code:
R8360
-
Alias:
Flow
-
CPT Code(s):
86361
-
Test Includes:
% CD4, Absolute CD4+ Cells, Absolute Lymphocytes
-
Preferred Specimen:
5 mL whole blood collected in an EDTA (lavender-top) tube
-
Min. Volume:
0.5 mL
-
Transport Container:
5 mL (or 3 mL pediatric) EDTA (lavender-top ) tube
-
Collection Instruction:
If a CBC is also required, a separate EDTA (lavender-top) tube must be submitted.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: Unacceptable Frozen: Unacceptable
-
Clinical Significance:
Lymphocyte Subset Panel 5 - This panel is used to measure CD4+ T cells (CD4) in the blood (absolute CD4 cell count, %CD4, absolute lymphocytes). The CD4+ T-cell (CD4) count is the most valuable indicator of immune status in HIV-infected individuals. This panel can be used to establish a baseline CD4 level and to monitor treatment progress. It can also be used to facilitate differential diagnoses between congenital and acquired immunodeficiency diseases [1]. A significant reduction in CD4 count can lead to opportunistic infections, and the CD4 cell count/percentage can he used to make decisions regarding opportunistic infection prophylaxis as per guidelines [1]. During the first 2 years of antiretroviral (ARV) therapy, CD4 levels should be tested every 3 to 6 months. Patients who develop viremia while on therapy or whose CD4 count stays below 300 cells/µL should also have their CD4 levels tested every 3 to 6 months. After 2 years of ARV therapy, with consistently suppressed viral load and a CD4 count of 300 to 500 cells/µL, CD4 counts should be tested every 12 months. Note that when CD4 counts are > 500 cells/ µL, CD4 testing is optional [1]. CD4 testing should also be conducted if therapy fails. Refer to current HIV management guidelines for further information on recommended testing frequency [1].
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
M
M-END MAX D (MEDICATION)
-
Test Name:
M-END MAX D (MEDICATION)
-
Test Code:
501350
Magnesium, RBC
-
Test Name:
Magnesium, RBC
-
Test Code:
R623
-
Alias:
RBC Magnesium,MG (RBC),MG RBC,MG++ (RBC),RBC MG
-
CPT Code(s):
83735
-
Preferred Specimen:
0.5 mL packed RBC cells collected in an EDTA (lavender-top) tube or sodium heparin (royal blue-top) tube
-
Min. Volume:
0.2 mL RBCs • 0.5 mL whole blood
-
Transport Container:
Trace-element and metal-free transport tube
-
Collection Instruction:
Packed RBCs: Centrifuge specimen and discard plasma within two hours of collection. Transfer RBCs to a plastic transfer vial.
Whole blood: Do not centrifuge whole blood.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Packed RBC cells Room temperature: 7 days Refrigerated: 7 days Frozen: Unacceptable Whole blood Room temperature: 4 days Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Magnesium, RBC - Magnesium is an essential trace element. Deficiency leads to irritability, neuromuscular abnormalities, cardiac and renal damage. Its salts are used as antacids and cathartics. Excessive amount may cause CNS depression, loss of muscle tone, respiratory and cardiac arrest.
-
Performing Lab:
Quest Diagnostics Nichols Institute-Chantilly VA 14225 Newbrook Drive Chantilly, VA 20151-2228
MAGNESIUM, SERUM
-
Test Name:
MAGNESIUM, SERUM
-
Test Code:
MG
-
Alias:
MG, MAG
-
CPT Code(s):
83735
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection. If the specimen is collected in an anticoagulant tube, centrifuge and transfer plasma into a properly labeled transfer tube within two hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Magnesium measurements are used in the diagnosis and treatment of hypomagnesemia (abnormally low) and hypermagnesemia (abnormally high).Decreased serum magnesium levels have been observed in cases of diabetes, alcoholism, diuresis, hyperthyroidism, hypoparathyroidism, malabsorption, hyperalimentation, myocardial infarction, congestive heart failure and liver cirrhosis. Increased serum magnesium levels have been found in cases of renal failure, dehydration, severe diabetic acidosis and Addison’s Disease.
-
Performing Lab:
Simple Laboratories
MAR-COF BP (MEDICATION)
-
Test Name:
MAR-COF BP (MEDICATION)
-
Test Code:
501220
Maternal Serum AFP
-
Test Name:
Maternal Serum AFP
-
Test Code:
R5059
-
Alias:
Alpha-Fetoprotein, Maternal Serum,Neural Tube Defect Screen,AFP Single Screen,MSS1
-
CPT Code(s):
82105
-
Test Includes:
AFP Maternal Risk Interpretation
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
For manual orders use “Maternal Serum Screen Requisition”
The maternal serum AFP test in pregnant women should be performed between 15.0 and 22.9 weeks gestational age, although the optimal period is 15.0-16.9 weeks. This time frame allows sufficient opportunity for further diagnostic studies if the initial MSAFP results are abnormal. Specimens submitted before 15.0 weeks or after 22.9 weeks gestation cannot be properly evaluated.
The Maternal Serum Screen Requisition designed to obtain patient data and the patient’s informed consent must be utilized when ordering the maternal serum AFP test. Because the maternal serum AFP test results are influenced by certain patient characteristics, the following data must be provided with the specimen in order to permit accurate interpretation of results: Date of collection, patient’s (maternal) date of birth, patient’s estimated date of delivery, patient’s weight, patient’s race, patient diabetic status (is patient insulin dependent prior to pregnancy), number of fetuses, and whether this is a repeat sample.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 14 days Refrigerated: 14 days Frozen: 45 days
-
Clinical Significance:
Maternal Serum AFP - Maternal serum alpha-fetoprotein (MSAFP) is used for prenatal screening. Maternal serum Alpha-Fetoprotein (AFP) elevation is associated with open neural tube defects, multiple gestation, placental anomalies, ventral abdominal wall defects, congenital nephrosis, and oligohydramnios. Follow-up for abnormal AFP results include genetic counseling, level II or III ultrasound examination and consideration of amniocentesis for chromosome and AFP analysis. MSAFP is not to be used as a screening test for chromosomal abnormalities.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
MAXIPHEN CD (MEDICATION)
-
Test Name:
MAXIPHEN CD (MEDICATION)
-
Test Code:
501430
MAXIPHEN CDX (MEDICATION)
-
Test Name:
MAXIPHEN CDX (MEDICATION)
-
Test Code:
501440
MDPV (MEDICATION)
-
Test Name:
MDPV (MEDICATION)
-
Test Code:
500560
MEASLES AB (IGG), IMMUNE STATUS
-
Test Name:
MEASLES AB (IGG), IMMUNE STATUS
-
Test Code:
R964
-
Alias:
MEASLES
-
CPT Code(s):
86765
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Measles Antibody (IgG), Immune Status - Measles, also known as rubeola, causes fever, irritability, respiratory illness, and the characteristic skin rash. Immunization has greatly diminished the incidence of measles. The presence of IgG is consistent with immunity or prior exposure. IgM is consistent with current or recent infection. IgM tests can generate false positive results and low levels of IgM can persist for longer than 12 months.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Measles, Mumps, and Rubella (MMR) Antibodies (IgG) Panel, Immune Status
-
Test Name:
Measles, Mumps, and Rubella (MMR) Antibodies (IgG) Panel, Immune Status
-
Test Code:
R5259
-
Alias:
Mumps Virus Antibody,IgG,Serum,Anti-Rubella Ab IgG,Measles,German,Anti-German Measles Ab IgG,Rubella Antibody Index,German Measles Antibody,Rubella Titer,Rubella IgG,Rubella Screen
-
CPT Code(s):
86735, 86765, 86762
-
Test Includes:
Measles Antibody (IgG), Immune Status Mumps Virus Antibody (IgG), Immune Status Rubella Antibody (IgG), Immune Status
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
1 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Measles, Mumps, and Rubella (MMR) Antibodies (IgG) Panel, Immune Status - This panel provides presumptive evidence of immunity to measles, mumps, and rubella for purposes of routine vaccination, for students at post-high school educational institutions, and for international travelers.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
MEPHEDRONE (MEDICATION)
-
Test Name:
MEPHEDRONE (MEDICATION)
-
Test Code:
500570
METHADOSE (MEDICATION)
-
Test Name:
METHADOSE (MEDICATION)
-
Test Code:
501650
Methylmalonic Acid
-
Test Name:
Methylmalonic Acid
-
Test Code:
R34879
-
Alias:
MMA
-
CPT Code(s):
83921
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
1 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 10 months
-
Clinical Significance:
Methylmalonic Acid - The Methylmalonic Acid (MMA) test is used in the diagnosis of acquired cobalamin (vitamin B12) deficiency in adults and to screen for inherited organic acidemia in neonates and infants. Elevated MMA in either blood or urine indicates vitamin B12 deficiency in adults, with MMA acting as a functional biomarker for vitamin B12 status. In neonates and infants, elevated MMA is associated with inborn errors of metabolism. Adults with signs and symptoms of cobalamin deficiency, including peripheral neuropathy, ataxia, memory impairment, depression, behavioral changes, and anemia, should be tested for MMA, especially if they are elderly or have experienced intestinal malabsorption or digestive disorders [1]. In the United States all newborns should be screened for MMA as part of the Department of Health and Human Services (HHS) Recommended Universal Newborn Screening Panel [1]. MMA can be acquired due to underlying medical conditions that lead to B-vitamin deficiencies or inherited as an autosomal recessive inborn error of metabolism. If a neonate or infant has elevated MMA suggestive of an organic acidemia, the parents may elect to undergo carrier testing, or have their other children undergo genetic testing. Siblings of a child with MMA-related mutation have a 25% chance of being affected and a 50% chance of being a carrier [2].
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
METHYLONE (MEDICATION)
-
Test Name:
METHYLONE (MEDICATION)
-
Test Code:
500580
MICROALBUMIN WITH CREATININE RATIO, RANDOM URINE
-
Test Name:
MICROALBUMIN WITH CREATININE RATIO, RANDOM URINE
-
Test Code:
MAP
-
Alias:
Albumin:Creatinine ratio, random urine
-
CPT Code(s):
82570, 82043
-
Test Includes:
Microalbumin Creatinine Microalbumin/creatinine ratio
-
Preferred Specimen:
RANDOM URINE
-
Min. Volume:
1.0 mL RANDOM URINE
-
Transport Container:
STERILE CUP
-
Collection Instruction:
Collect random urine in a sterile urine cup. Transfer to a BD Non-Additive Urine Collection tube. Label it with patient’s name and the date and time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 72 hours Freezing is not recommended
-
Schedule:
1-2 Days
-
Clinical Significance:
Refer to individual tests.
-
Performing Lab:
Simple Laboratories
MS CONTIN (MEDICATION)
-
Test Name:
MS CONTIN (MEDICATION)
-
Test Code:
500620
MSIR (MEDICATION)
-
Test Name:
MSIR (MEDICATION)
-
Test Code:
500630
Mumps Virus Antibody (IgG), Immune Status
-
Test Name:
Mumps Virus Antibody (IgG), Immune Status
-
Test Code:
R8624
-
CPT Code(s):
86735
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Mumps Virus Antibody (IgG), Immune Status - Mumps is an acute, usually self-limited systemic illness characterized by parotiditis, high fever and fatigue. One third of infections are asymptomatic.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Mycobacteria, Culture, with Fluorochrome Smear
-
Test Name:
Mycobacteria, Culture, with Fluorochrome Smear
-
Test Code:
R4554
-
Alias:
Acid Fast Bacilli,AFB (Acid Fast Bacilli),Tuberculosis,TB
-
CPT Code(s):
87116, 87206
-
Test Includes:
Mycobacteria Culture, Acid-Fast Bacilli Stain An additional charge for Concentration (CPT code(s): 87015) will be added as appropriate. Identification will be performed at an additional charge for each organism CPT code(s) 87118: Matrix Assisted Laser Desorption/Ionization-Time of Flight or CPT code(s) 87153: AFB Sequencing If TB is isolated for the first time or after three months after the first isolate from a patient, susceptibilities will be performed at an additional charge (CPT code(s): 87190 per drug. Methodology
-
Preferred Specimen:
10 mL body fluids or lower respiratory tract specimens or 10 mL gastric lavage or 2 mL CSF or 2 grams fresh (unfixed) tissue or 40 mL urine collected in a sterile leak-proof container or 1 mL exudate, aspirate, lesion material, ocular specimen collected in a sterile leak-proof container or 1 gram or 1 mL stool collected in a sterile leak-proof container See the alphabetical listing in the Microbiology section of Specimen Collection & Transport Guide for further instructions.
-
Min. Volume:
2 mL body fluids or lower respiratory tract specimens • 2 mL gastric lavage • 1 mL CSF • 1 gram fresh (unfixed) tissue • 20 mL urine collected in a sterile leak-proof container • 1 mL exudate, aspirate, lesion material, ocular specimen collected in a sterile leak-proof container • 1 gram or 1 mL stool
-
Transport Container:
Refer to Preferred Specimen(s) and Collection Instructions
-
Collection Instruction:
Tissue and biopsy material: Sterile leak-proof container with small amount of saline, no fixative or preservative.
Gastric lavage fluid: Sterile leak-proof container. Must be neutralized with sodium bicarbonate within 4 hours of collection.
Expectorated sputum: Instruct patient to gargle with water and cough deeply. Three separate early morning collections on at least three consecutive days are recommended. -
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: Unacceptable Refrigerated: 5 days Frozen: Unacceptable
-
Clinical Significance:
Mycobacteria, Culture, with Fluorochrome Smear - There are more than 70 species of mycobacteria of which the primary pathogen is M. tuberculosis. Tuberculosis is a chronic, granulomatous disease caused by M. tuberculosis. Identification, and, if appropriate, antibiotic sensitivity, is required to initiate necessary therapy.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
MYCOPLASMA GENITALIUM, GENITAL
-
Test Name:
MYCOPLASMA GENITALIUM, GENITAL
-
Test Code:
LS5013
-
CPT Code(s):
87563
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA MULTI-TEST SWAB (ORANGE)
-
Collection Instruction:
Follow the instructions in the collection kits from GenProbe for each specific collection kit
-
Transport Temperature:
ROOM TEMPERATURE
-
Stability:
After collection, swab specimens in transport tubes can be stored for up to 60 days.
-
Schedule:
1-3 Days
-
Clinical Significance:
The Aptima Mycoplasma genitalium assay is an in vitro nucleic acid amplification test (NAAT) for the qualitative detection of ribosomal RNA (rRNA) from Mycoplasma genitalium. It is intended for use as an aid in the diagnosis of M. genitalium urogenital infections in male and female patients.
-
Performing Lab:
Simple Laboratories
MYCOPLASMA GENITALIUM, URINE
-
Test Name:
MYCOPLASMA GENITALIUM, URINE
-
Test Code:
LS5014
-
CPT Code(s):
87563
-
Preferred Specimen:
MALE OR FEMALE URINE
-
Transport Container:
APTIMA URINE TRANSPORT TUBE (YELLOW)
-
Collection Instruction:
Follow the instructions in the collection kits from GenProbe for each specific collection kit
-
Transport Temperature:
ROOM TEMPERATURE
-
Stability:
After collection, swab specimens in transport tubes can be stored for up to 60 days.
-
Schedule:
1-3 Days
-
Clinical Significance:
The Aptima Mycoplasma genitalium assay is an in vitro nucleic acid amplification test (NAAT) for the qualitative detection of ribosomal RNA (rRNA) from Mycoplasma genitalium. It is intended for use as an aid in the diagnosis of M. genitalium urogenital infections in male and female patients.
-
Performing Lab:
Simple Laboratories
Mycoplasma pneumoniae Antibodies (IgG, IgM)
-
Test Name:
Mycoplasma pneumoniae Antibodies (IgG, IgM)
-
Test Code:
R34127
-
CPT Code(s):
86738
-
Test Includes:
659, 21130
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Mycoplasma pneumoniae Antibodies (IgG, IgM) - This test helps detect Mycoplasma pneumoniae infections. Respiratory tract infections including community-acquired pneumonia are common reasons for testing for M pneumoniae, especially in children [3,4].Clinical presentations of M pneumoniae infection are generally mild, but can vary widely across individuals, and are most often characterized by tracheobronchitis with upper respiratory tract symptoms. Approximately one-third of people with M pneumoniae infection develop pneumonia that was previously considered "atypical." Extrapulmonary complications may include encephalitis, hemolytic anemia, renal dysfunction, gastrointestinal complaints, erythema multiforme, and Stevens-Johnson syndrome [1,2].M pneumoniae infection is diagnosed by culture, serology, or nucleic acid amplification tests. Serologic tests may be useful when the possibility of Mycoplasma infection is high. A positive IgG result indicates previous or recent infection. Testing children who have suspected community-acquired pneumonia for M pneumoniae may help guide antibiotic selection [3,4].Clinical false-negative results for IgG- and IgM-based serologic tests can occur due to compromised immunity, testing before an antibody response has started, or the presence of interfering substances in host serum.Real-time polymerase chain reaction testing for M pneumoniae DNA is more sensitive than serology testing and can provide timely results to inform patient management [2]. IgA antibodies to M pneumoniae appear early; testing IgA antibodies may aid in identifying acute infection [1].The results of this test should be interpreted in the context of pertinent clinical history and physical examination findings.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Myoglobin, Serum
-
Test Name:
Myoglobin, Serum
-
Test Code:
R660
-
CPT Code(s):
83874
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 35 days
-
Clinical Significance:
Myoglobin, Serum - Assessment of skeletal muscle breakdown (rhabdomyolysis).
-
Performing Lab:
Quest Diagnostics Nichols Institute-Chantilly VA 14225 Newbrook Drive Chantilly, VA 20151-2228
Myositis Specific 11 Antibody Panel
-
Test Name:
Myositis Specific 11 Antibody Panel
-
Test Code:
R94777
-
CPT Code(s):
84182 (x6), 86235 (x5)
-
Test Includes:
Jo-1 Ab, Pl-7 Ab, Pl-12 Ab, EJ Ab, OJ Ab, SRP Ab, Mi-2 Alpha Ab, Mi-2 Beta Ab, MDA5 Ab, TIF1 Gamma Ab, NXP-2 Ab
-
Preferred Specimen:
0.5 mL serum
-
Min. Volume:
0.3 mL serum
-
Transport Container:
Transport tube
-
Collection Instruction:
Collect serum in a red-top or SST tube. Separate serum from cells within 4 hours of collection. Transfer to a transport tube and ship by overnight courier.
Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. For patients receiving STRENSIQ, consideration should be given to using alternate methods.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 28 days
-
Clinical Significance:
Myositis Specific 11 Antibody Panel - Myositis-specific autoantibodies (MSAs) are highly selective, usually exclusive and are associated with particular clinical phenotypes within the myositis spectrum. Myositis-specific autoantibodies to cytoplasmic enzymes that catalyze the binding of specific amino acids to their cognate tRNA define the anti-synthetase syndrome characterized by myositis and lung inflammation, and include autoantibodies to Jo-1 (antihistidyl-tRNA synthetase), PL-7 (threonyl), PL-12 (alanyl), EJ (glycyl), and OJ (isoleucyl). A further subset of myositis patients is characterized by the presence of autoantibodies directed against the signal recognition particle (SRP). Autoantibodies to Mi-2 (Mi-2/nucleosome remodeling and deacetylase (NuRD) complex) are detected in patients with hallmark dermatomyositis features. Autoantibody to a cytoplasmic 140-kDa protein, melanoma-differentiation associated gene 5 (MDA5), also known as anti-CADM140, identified patients with clinically amyopathic dermatomyositis (CADM) and rapidly progressive lung disease. Autoantibodies to transcriptional intermediary factor 1-gamma (TIF-1 y), a p155/140 nuclear protein involved in cellular differentiation, have been reported in adult and juvenile dermatomyositis; in adults, it is associated with malignancy. Autoantibodies to nuclear matrix protein NXP-2, another 140-kDa protein, is found in juvenile dermatomyositis (JDM). Anti-TIF-1 y and anti-NXP-2, two novel serological subsets in JDM, occur collectively in >40% of children and appear to identify those with more severe disease.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
N
NASOTUSS (MEDICATION)
-
Test Name:
NASOTUSS (MEDICATION)
-
Test Code:
501240
NEISSERIA GONORRHOEAE, GENITAL, PCR
-
Test Name:
NEISSERIA GONORRHOEAE, GENITAL, PCR
-
Test Code:
LS5007
-
Alias:
GC N. gonorroeae
-
CPT Code(s):
87591
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA SWAB (UNI-SEX OR VAGINAL SWAB)
-
Collection Instruction:
For endocervical swab, vaginal swab or male urethral swab: Collect specimen according to printed instructions on APTIMA unisex swab collection kit packaging
-
Transport Temperature:
Refrigerated
-
Stability:
60 days - after testing, specimens are stored in the lab for 7 days
-
Schedule:
1-3 Days
-
Clinical Significance:
This assay may be used to test specimens from symptomatic and asymptomatic individuals to aid in the diagnosis of gonococcal urogenital disease.
-
Performing Lab:
Simple Laboratories
NEISSERIA GONORRHOEAE, URINE, PCR
-
Test Name:
NEISSERIA GONORRHOEAE, URINE, PCR
-
Test Code:
LS5009
-
Alias:
GC N. gonorroeae
-
CPT Code(s):
87951
-
Preferred Specimen:
MALE OR FEMALE URINE
-
Transport Container:
APTIMA URINE TRANSPORT TUBE (YELLOW)
-
Collection Instruction:
For male or female urine specimen: Patient should not have urinated for at least one hour prior to sampling. Patient should provide first-catch urine sample (approximately 20-30mL of initial urine stream) into a sterile urine collection cup. Specimen may be sent to lab in primary collection sterile urine cup, transferred to yellow cap vacutainer tube or transferred to Aptima urine transport tube according to printed instructions on APTIMA urine specimen collection kit packaging.
-
Transport Temperature:
Refrigerated
-
Stability:
Urine, sterile container: Room temperature or refrigerated 24 hour APTIMA urine specimen tube: Room temperature or refrigerated 30 days (Note: after testing, specimens are saved in the lab for 7 days.)
-
Schedule:
1-3 Days
-
Clinical Significance:
This assay may be used to test specimens from symptomatic and asymptomatic individuals to aid in the diagnosis of gonococcal urogenital disease.
-
Performing Lab:
Simple Laboratories
NEO AC (MEDICATION)
-
Test Name:
NEO AC (MEDICATION)
-
Test Code:
501560
NORCO (MEDICATION)
-
Test Name:
NORCO (MEDICATION)
-
Test Code:
501750
NORTRIPTYLINE HCL (MEDICATION)
-
Test Name:
NORTRIPTYLINE HCL (MEDICATION)
-
Test Code:
500460
NOTUSS-NX (MEDICATION)
-
Test Name:
NOTUSS-NX (MEDICATION)
-
Test Code:
501230
NOTUSS-NXD (MEDICATION)
-
Test Name:
NOTUSS-NXD (MEDICATION)
-
Test Code:
501260
NOTUSS-PE (MEDICATION)
-
Test Name:
NOTUSS-PE (MEDICATION)
-
Test Code:
501490
NUCOFED (MEDICATION)
-
Test Name:
NUCOFED (MEDICATION)
-
Test Code:
501470
NUCOFED EXPECTORANT (MEDICATION)
-
Test Name:
NUCOFED EXPECTORANT (MEDICATION)
-
Test Code:
501550
O
O-DESMETHYLTRAMADOL (MEDICATION)
-
Test Name:
O-DESMETHYLTRAMADOL (MEDICATION)
-
Test Code:
500390
ORAMORPH SR (MEDICATION)
-
Test Name:
ORAMORPH SR (MEDICATION)
-
Test Code:
500610
Osmolality, Serum
-
Test Name:
Osmolality, Serum
-
Test Code:
R677
-
CPT Code(s):
83930
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 5 days Frozen: 14 days
-
Clinical Significance:
Osmolality, Serum - For the evaluation of fluid and electrolyte balance.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Osmolality, Urine
-
Test Name:
Osmolality, Urine
-
Test Code:
R678
-
CPT Code(s):
83935
-
Preferred Specimen:
2 mL random urine
-
Min. Volume:
0.5 mL
-
Transport Container:
Plastic urine container
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Osmolality, Urine - For assessing the concentrating ability of the kidney.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Ova and Parasites, Concentrate and Permanent Smear
-
Test Name:
Ova and Parasites, Concentrate and Permanent Smear
-
Test Code:
R681
-
Alias:
O and P with Permanent Stain
-
CPT Code(s):
87177, 87209
-
Test Includes:
Ova and Parasite Concentrate Result, Trichrome Result
-
Preferred Specimen:
10 grams or 10 mL fresh stool preserved in 1 single Total-Fix® transport vial or 10% formalin and polyvinyl alcohol transport vials
-
Min. Volume:
5 grams or 5 mL stool • 10 mL urine (unpreserved) • 2 mL sputum or BAL
-
Transport Container:
Total-Fix transport vial 10% formalin and polyvinyl alcohol transport vials Urine submitted in a sterile screw-cap container Sputum or BAL submitted in a sterile screw-cap container or with 10% formalin
-
Collection Instruction:
Note: Tissue samples should be sent to pathology. Stool: Place fresh stool in a single Total-Fix transport vial or 10% formalin transport vial, as well as PVA transport medium, within 30 minutes of collection. Add stool to bring the liquid level to the “fill to here” line on the vial. Mix well. Send specimen(s) at room temperature in the same shipping container.
If parasite infestation is strongly suspected, collect at least 3 stool specimens every other day, since a single specimen can be negative. If Giardia is strongly suspected, please see Giardia Antigen, EIA, Stool, Test Code 8625.Urine: Urine may be submitted unpreserved for exam for Schistosoma. Collect at mid-day. Peak egg secretion occurs between noon and 3 p.m. Do not submit first morning specimen. In patients with hematuria, eggs may be found trapped in blood and mucous in the terminal portion (last-voided portion) of the urine specimen. Trichrome Stain is not performed on non-stool samples.
Sputum: The specimen should be a deep expectorated sputum, preferably collected in the early morning. A 24-hour sputum collection is also acceptable. Submit in a sterile screw-cap container, unpreserved or in 10% formalin to increase stability. Trichrome Stain is not performed on non-stool samples.
-
Transport Temperature:
Stool, sputum, and BAL (preserved): Room temperature Urine, sputum, and BAL (unpreserved): Refrigerated (cold packs)
-
Stability:
Stool (preserved) Room temperature: 30 days Refrigerated: 30 days Frozen: Unacceptable Urine, Sputum, BAL (unpreserved) Room temperature: Unacceptable Refrigerated: 48 hours Frozen: Unacceptable Sputum, BAL (preserved) Room temperature: 30 days Refrigerated: 30 days Frozen: Unacceptable
-
Clinical Significance:
Ova and Parasites, Concentrate and Permanent Smear - Diseases caused by human parasites remain on a worldwide basis among the principle causes of morbidity and mortality. Correct diagnosis of intestinal parasitic infection depends on proper collection, transport, detection and identification of parasites in stool specimens. Symptoms range from malaise to death. Treatment is dependent upon examining multiple stool specimens due to the erratic shed rates of some parasites.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Oxcarbazepine Metabolite
-
Test Name:
Oxcarbazepine Metabolite
-
Test Code:
R36637
-
Alias:
Trileptal,Hydroxycarbazepine,10-Hydroxycarbazepine
-
CPT Code(s):
80183
-
Test Includes:
10-Hydroxycarbazepine
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.25 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 72 hours Refrigerated: 14 days Frozen: 60 days
-
Clinical Significance:
Oxcarbazepine Metabolite - Oxcarbazepine (trileptal) is an anti-convulsant used for treating generalized tonic-clonic and partial seizures. It can be administered alone or as an adjunct to other anti-convulsants. Clinically significant effects of oxcarbazepine are observed when plasma levels of its active metabolite, 10-OH-carbazepine, are between 15 and 35 ug/mL. Toxic symptoms may occur when plasma levels exceed 35 ug/mL. The therapeutic monitoring of oxcarbazepine and its active metabolite are important for achieving proper serum/plasma concentration to inhibit epileptic seizures and avoid adverse effects. The precise mechanism of the action by which oxcarbazepine and its active metabolite exert their antiseizure effect is unknown. However, in vitro electro-physiological studies indicate that they produce blockade of voltage-sensitive sodium channels, resulting in the stabilization of hyperexcited neural membranes, inhibition of repetitive neuronal firing, and diminution of propagation of synaptic impulses. These are important in prevention of seizure spread in the brain. In addition, the increased potassium conduction and calcium channel activities may contribute to the antiseizure treatment effects. After oral administration, oxcarbazepine is readily absorbed in the body, followed by rapid and almost complete metabolization to 10-OH-carbazepine, active metabolite. The half-life of oxcarbazepine is only 1 to 2.5 hours, while that of 10-OH-carbazepine is 11 to 15 hours. The protein binding of oxcarbazepine is about 67%, whereas that of the metabolite is about 38%. The clearance of oxcarbazepine and its active metabolite from the body is mainly through ketone reduction and O-site conjugation with glucuronic acid rather than oxidative processes via cytochrome P450 system. More than 95% of the treatment dosage is excreted by the kidneys. Fecal excretion only accounts for less than 4%.
-
Performing Lab:
Quest Diagnostics Nichols Institute-Chantilly VA 14225 Newbrook Drive Chantilly, VA 20151-2228
P
PARATHYROID HORMONE (PTH), INTACT
-
Test Name:
PARATHYROID HORMONE (PTH), INTACT
-
Test Code:
PTH
-
Alias:
PARATHYRIM
-
CPT Code(s):
83970
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 4 hours (serum) 8 hours (plasma) Refrigerated: 8 hours (serum) 48 hours (plasma) Frozen: 6 months (serum or plasma)
-
Schedule:
1-2 Days
-
Clinical Significance:
In patients with disorders of calcium metabolism, quantitative determination of circulating PTH may assist in the differential diagnosis of hypercalcemia and hypocalcemia. In hypercalcemia due to primary hyperparathyroidism or ectopic PTH secretion (pseudo hyperparathyroidism), most patients have increased PTH levels. By contrast in hypercalcemia due to malignancy or other causes, the concentration of PTH in the circulation is typically low, either below or towards the low end of the reference range for apparently healthy individuals.
-
Performing Lab:
Simple Laboratories
Parvovirus B19 Antibodies (IgG, IgM)
-
Test Name:
Parvovirus B19 Antibodies (IgG, IgM)
-
Test Code:
R8946
-
CPT Code(s):
86747
-
Test Includes:
8945, 8948
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
1 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Parvovirus B19 Antibodies (IgG, IgM) - Parvovirus B19 is also known as Fifth Disease. It primarily affects children and causes a rash on the face, trunk, and limbs. Joint pain and swelling is more common in adults. Although one-fifth of those affected have only mild disease, patients with sickle cell anemia or similar types of chronic anemia can suffer from acute anemia. Infection during pregnancy can lead to complications.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
PENTOBARBITAL (MEDICATION)
-
Test Name:
PENTOBARBITAL (MEDICATION)
-
Test Code:
500540
Phenobarbital
-
Test Name:
Phenobarbital
-
Test Code:
R708
-
Alias:
Quandrinal™,Donnatal®,Luminal®
-
CPT Code(s):
80184
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Phenobarbital - Phenobarbital is an anticonvulsant used for the long-term treatment of generalized tonic-clonic (grand mal) seizures and cortical focal seizures. Phenobarbital levels are monitored to assure adequate therapeutic levels are achieved and to avoid toxicity.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
PHENOBARBITAL (MEDICATION)
-
Test Name:
PHENOBARBITAL (MEDICATION)
-
Test Code:
500530
PHENYLHISTINE DH (MEDICATION)
-
Test Name:
PHENYLHISTINE DH (MEDICATION)
-
Test Code:
501340
PHOSPHORUS
-
Test Name:
PHOSPHORUS
-
Test Code:
PHOS
-
Alias:
Inorganic phosphorus Phos Phosphate PO4
-
CPT Code(s):
84100
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 7 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Measurements of inorganic phosphorus are used in the diagnosis and treatment of various disorders including parathyroid gland and kidney diseases, and vitamin D imbalance.
-
Performing Lab:
Simple Laboratories
PHYSEPTONE (MEDICATION)
-
Test Name:
PHYSEPTONE (MEDICATION)
-
Test Code:
501660
POLYHIST NC (MEDICATION)
-
Test Name:
POLYHIST NC (MEDICATION)
-
Test Code:
501570
POTASSIUM
-
Test Name:
POTASSIUM
-
Test Code:
K
-
Alias:
K K+ LAB114
-
CPT Code(s):
84132
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL serum This volume may not allow for repeat testing.
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-Hep tube, centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 48 hours Longer stability if frozen
-
Schedule:
1-2 Days
-
Clinical Significance:
Electrolytes affect most metabolic processes. They serve to maintain osmotic pressure and hydration of various body fluids, proper body pH and regulation of appropriate heart and muscle functions. Electrolytes are also involved in oxidation-reduction reactions and participate as essential parts or, cofactors, in enzyme reactions.
-
Performing Lab:
Simple Laboratories
Prealbumin
-
Test Name:
Prealbumin
-
Test Code:
R4847
-
Alias:
Transthyretin,Thyroxine Binding Prealbumin
-
CPT Code(s):
84134
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 14 days
-
Clinical Significance:
Prealbumin - Prealbumin is decreased in protein-calorie malnutrition, liver disease, and acute inflammation. It may be used as an indicator of nutritional requirements and response to therapy during total parenteral nutrition and as a biochemical marker of nutritional adequacy in premature infants.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Pregnenolone, LC/MS
-
Test Name:
Pregnenolone, LC/MS
-
Test Code:
R31493
-
CPT Code(s):
84140
-
Preferred Specimen:
0.5 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Collect blood in a Vacutainer® with no additives. Allow blood to clot (30 minutes) at room temperature, 18-25° C. Centrifuge and separate the serum from the cells. Freeze as soon as possible.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: Unacceptable Refrigerated: 72 hours Frozen -20° C: 14 days Frozen -70° C: 30 days
-
Clinical Significance:
pregnenolone, LC/MS - This test may be useful in differentiating among different types of congenital adrenal hyperplasia (CAH). This test may also be used to monitor progress and treatment after diagnosis [1]. CAH is a group of autosomal recessive diseases characterized by deficiencies of enzymes in steroid hormone production. These deficiencies cause imbalances of steroid intermediates and hormones. Clinical manifestations of CAH vary and depend upon the type of defect and severity of the impairment. Therefore, measurement of different steroid hormones can help in diagnosing CAH [1,2]. Pregnenolone is a precursor to all steroid hormones. It can be elevated in some rare types of CAH, including deficiencies of 3-beta-hydroxysteroid dehydrogenase, 17-alpha-hydroxylase, and P450 oxidoreductase. Levels of pregnenolone (and all other steroids) can be low in lipoid adrenal hyperplasia [2]. This test is generally ordered after evaluation of 17-hydroxyprogesterone (test code 17180). 17-hydroxyprogesterone testing, included in newborn screening, is used to detect 21-hydroxylase deficiency (the cause of 95% of CAH). When symptoms and signs suggest CAH, but 21-hydroxylase deficiency and 11-beta-hydroxylase deficiency are ruled out, pregnenolone can be measured to assist in diagnosing other types of CAH [1,2]. Pregnenolone degrades rapidly at refrigerator temperature. Specimens should be frozen immediately after collection and remain frozen until analysis [3]. This test should be interpreted in the context of pertinent clinical and family history as well as physical examination findings.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
PRO-CLEAR AC (MEDICATION)
-
Test Name:
PRO-CLEAR AC (MEDICATION)
-
Test Code:
501580
PRO-RED AC (MEDICATION)
-
Test Name:
PRO-RED AC (MEDICATION)
-
Test Code:
501510
PROGESTERONE
-
Test Name:
PROGESTERONE
-
Test Code:
PROG
-
CPT Code(s):
84144
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in an anticoagulant tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube. Specify specimen type (serum or plasma) on transfer tube.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 1 day Refrigerated: 2 days Freeze sample for longer stability. Specimens should not be stored in SST.
-
Schedule:
1-2 Days
-
Clinical Significance:
Progesterone levels are indicative of viable pregnancies. Ultrasonography is required to confirm viability at low progesterone levels. Serum concentrations are relatively constant at 8-10 weeks gestation, unless the pregnancy is failing, which can be signaled by decreasing progesterone values. After 10-12 weeks, levels increase more rapidly, but serum progesterone determinations are not considered useful for diagnoses in late pregnancy. Ovulation, and the presence of a functioning corpus luteum, can be demonstrated with serial determinations of serum progesterone. Luteal phase dysfunction may be diagnosed when ovulation has occurred and there is inadequate luteinization and reduced progesterone secretion.
-
Performing Lab:
Simple Laboratories
PROLACTIN
-
Test Name:
PROLACTIN
-
Test Code:
PROL
-
CPT Code(s):
84146
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Fasting specimens are preferred.
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in an anticoagulant tube without a gel barrier, centrifuge and transfer plasma into a properly labeled transfer tube.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 48 hours
-
Schedule:
1-2 Days
-
Clinical Significance:
Prolactin is secreted by the anterior pituitary gland and is required for normal breast development and lactation in women. Prolactin levels will rise throughout gestation. In the absence of breast feeding, prolactin levels will return to normal within three weeks after birth. Abnormally high levels of prolactin are often associated with female infertility, impotence and infertility in males, primary hypothyroidism, and pituitary tumors.
-
Performing Lab:
Simple Laboratories
PROMETHAZINE VC WC (MEDICATION)
-
Test Name:
PROMETHAZINE VC WC (MEDICATION)
-
Test Code:
501500
PROMETHAZINE WC (MEDICATION)
-
Test Name:
PROMETHAZINE WC (MEDICATION)
-
Test Code:
501540
PROSTATE SPECIFIC ANTIGEN (PSA), TOTAL
-
Test Name:
PROSTATE SPECIFIC ANTIGEN (PSA), TOTAL
-
Test Code:
PSA
-
CPT Code(s):
84153
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 24 hours
-
Schedule:
1-2 Days
-
Clinical Significance:
Prostate Specific Antigen (PSA) levels in human serum aid in the detection of prostate cancer in men aged 50 years or older. Prostate biopsy is required for the diagnosis of cancer. It is also used for further indicatetions for the serial measurement of PSA to aid in the prognosis and management of patients with prostate cancer.
-
Performing Lab:
Simple Laboratories
Protein Electrophoresis and Total Protein, Random Urine
-
Test Name:
Protein Electrophoresis and Total Protein, Random Urine
-
Test Code:
R8525
-
Alias:
UPEP
-
CPT Code(s):
82570, 84156, 84166
-
Test Includes:
Protein, Total, Random Urine with Creatinine Protein Electrophoresis
-
Preferred Specimen:
25 mL random urine - no preservative
-
Min. Volume:
15 mL
-
Transport Container:
Plastic urine container
-
Collection Instruction:
Note: Submit a first morning voided specimen whenever possible
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 5 days Frozen: 30 days
-
Clinical Significance:
Protein Electrophoresis and Total Protein, Random Urine - This test is used to analyze the protein content in urine. The proteins are separated into 5 major components: albumin, alpha-1, alpha-2, beta, and gamma. Interpretation of elevations, decreases, or visual changes in different components and/or associated patterns can provide information on various disease states, including inflammatory diseases, autoimmune diseases, different types of kidney injury, plasma cell disorders, and cancers [1,2]. UPEP is used to evaluate an individual with symptoms associated with potential monoclonal gammopathy, or when an individual has abnormally high total protein, albumin, or immunoglobulin levels. This test can help with initial diagnosis, as well as monitoring disease progression and treatment effectiveness [1,2]. Although a 24-hour UPEP (test code 750) is recommended for diagnosis and monitoring, sometimes a random UPEP (test code 8525) is ordered at the discretion of the clinician to help guide the diagnostic process in the right direction. One advantage of a UPEP is that no special handling is required, which may be an important factor depending on clinical conditions. NOTE: The results of this test should not be used in isolation; these results alone are not enough to make a diagnosis or for monitoring. UPEP results should be evaluated along with other laboratory, clinical, and imaging findings as appropriate. Additional testing, such as bone marrow studies, serum protein electrophoresis (SPEP), and immunofixation (IFE), may be required for comprehensive evaluation [1,2].
-
Performing Lab:
Quest Diagnostics-Lenexa 10101 Renner Blvd Lenexa, KS 66219-9752
PROTEIN, TOTAL SERUM
-
Test Name:
PROTEIN, TOTAL SERUM
-
Test Code:
TP
-
CPT Code(s):
84155
-
Preferred Specimen:
1.0 ML SERUM
-
Min. Volume:
0.5 ML SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection. If the specimen is collected in an anticoagulant tube without a gel barrier, centrifuge and transfer plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
REFRIGERATED
-
Stability:
Room temperature: 7 days Refrigerated: 30 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Measurements of Total Protein are used in the diagnosis and treatment of a variety of diseases involving the liver, kidney, or bone marrow as well as other metabolic and nutritional disorders. The total serum protein is the sum of all circulating proteins and is a major component of blood. It is often useful, however, in interpreting the significance of the total protein concentration to have more specific knowledge of individual fractions such as albumins and globulins.
-
Performing Lab:
Simple Laboratories
PROTHROMBIN TIME (PT)(PROTIME)
-
Test Name:
PROTHROMBIN TIME (PT)(PROTIME)
-
Test Code:
LS5090
-
CPT Code(s):
85610
-
Preferred Specimen:
1 - full (see fill line on tube) Sodium Citrate (lt blue)
-
Min. Volume:
1 - full (see fill line on tube) Sodium Citrate (lt blue) tube or 1.0 mL frozen platelet-poor plasma
-
Transport Container:
SODIUM CITRATE (LT BLUE TOP)
-
Collection Instruction:
Invert tube 5 to 10 times immediately after filling and transport at room temperature (stable for 24 hours). To increase stability, send frozen platelet-poor plasma.
For frozen platelet-poor specimens: Centrifuge the specimen for 15 minutes within 1 hour of collection. Using a plastic pipette, remove the plasma taking care to avoid the WBC/platelet buffy layer and transfer the plasma into a properly labeled transfer tube. Centrifuge the transferred plasma a second time and transfer platelet-poor plasma into a new properly labeled transfer tube. Label tube as “platelet-poor”. Freeze immediately and transport to the lab frozen.
-
Transport Temperature:
Room temperature or frozen (refer to stability times)
-
Stability:
Room temperature: 24 hoursRefrigerated: unacceptableFrozen: 14 days (platelet-poor plasma only)
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Prothrombin time is used for the evaluation of the extrinsic coagulation pathway and the monitoring of oral anticoagulant therapy (OAT).
-
Performing Lab:
Simple Laboratories
PSA, Free and Total
-
Test Name:
PSA, Free and Total
-
Test Code:
R31348
-
Alias:
PSA, Free,Fractionated PSA,PSA II,Prostate Specific Antigen Free and Total,Free PSA and Total PSA
-
CPT Code(s):
84153, 84154
-
Test Includes:
PSA, Total PSA, Free PSA, % Free
-
Preferred Specimen:
2 mL frozen serum
-
Min. Volume:
0.6 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Do not collect specimen after a transrectal biopsy, results may be falsely elevated.
Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. For patients receiving STRENSIQ, consideration should be given to using alternate methods.
-
Transport Temperature:
Frozen • Room temperature acceptable if received within 72 hours
-
Stability:
Room temperature: 72 hours Refrigerated: 72 hours Frozen: 5 months
-
Clinical Significance:
PSA, Free and Total - In men over 50 years with total PSA between 4.0 and 10.0 ng/mL, the percent (%) free PSA gives an estimate of the probability of cancer. In these circumstances the measurement of the % free PSA may aid in avoiding unnecessary biopsies. Elevated levels of Prostate Specific Antigen (PSA) have been associated with benign and malignant prostatic disorders. Studies indicate that in men 50 years or older measurement of PSA is a useful addition to the digital rectal exam in the early detection of prostate cancer. In addition, PSA decreases to undetectable levels following complete resection of the tumor and may rise again with recurrent disease or persist with residual disease. Thus, PSA levels may be of assistance in the management of prostate cancer patients.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
PTH-Related Protein (PTH-rP)
-
Test Name:
PTH-Related Protein (PTH-rP)
-
Test Code:
R34478
-
CPT Code(s):
83519
-
Preferred Specimen:
0.5 mL plasma collected in a sodium heparin (green-top) tube
-
Min. Volume:
0.3 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Sodium heparin tubes: Centrifuge the specimen as soon as possible.
Transfer the plasma to a transport tube.
Do not submit unspun tubes. -
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
PTH-Related Protein (PTH-rP) - Differential diagnosis of hypercalcemia; manage patients with solid tumors and hypercalcemia.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
PTT, ACTIVATED (APTT)
-
Test Name:
PTT, ACTIVATED (APTT)
-
Test Code:
LS0961
-
CPT Code(s):
85730
-
Preferred Specimen:
1 - full (see line on tube) Sodium Citrate (lt blue) tube
-
Min. Volume:
1 - full (see line on tube) Sodium Citrate (lt blue) tube or 1.0 mL frozen platelet-poor plasma
-
Transport Container:
SODIUM CITRATE (LT BLUE TOP)
-
Collection Instruction:
Invert tube 5 to 10 times immediately after filling and transport at room temperature (stable for 24 hrs). NOTE: For patients on heparin, specimen must be centrifuged within 1 hour of collection and tested within 4 hours if kept at room temperature. To increase stability send frozen platelet-poor plasma.
For frozen platelet-poor specimens: Centrifuge the specimen for 15 minutes within 1 hour of collection. Using a plastic pipette, remove the plasma taking care to avoid the WBC/platelet buffy layer and transfer the plasma into a properly labeled transfer tube. Centrifuge the transferred plasma a second time and transfer platelet-poor plasma into a new properly labeled transfer tube. Label tube as “platelet-poor”. Freeze immediately and transport to the lab frozen. -
Transport Temperature:
Room Temperature
-
Stability:
Room temperature: 24 hours (patients on heparin: 4 hours room temperature) Frozen: 14 days (platelet-poor plasma)
-
Schedule:
1-2 DAYS
-
Clinical Significance:
General screening procedure for the evaluation of the intrinsic coagulation pathway and to monitor patients receiving heparin anticoagulant therapy.
-
Performing Lab:
Simple Laboratories
Q
QNATAL(R) ADVANCED
-
Test Name:
QNATAL(R) ADVANCED
-
Test Code:
R92777
-
Alias:
NIPT
-
CPT Code(s):
81420
-
Preferred Specimen:
10 mL whole blood collected in a Streck cell-free (black/tan tiger-top) glass tube
-
Min. Volume:
8 mL
-
Transport Container:
Cell-free DNA Streck tube
-
Collection Instruction:
Do not draw before 10 weeks gestation. Sample collection using a straight needle (not a butterfly needle) is preferred. Use Streck tubes only.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerate: Unacceptable Frozen: Unacceptable
-
Clinical Significance:
QNatal® Advanced - QNatal® Advanced is a cell-free DNA test that screens for increased risk of certain fetal chromosomal abnormalities that may cause birth defects, including Trisomy 21 (Down Syndrome), Trisomy 18 (Edwards Syndrome), Trisomy 13 (Patau Syndrome) and certain sex chromosome abnormalities (i.e., 45,X, 47,XXY, 47,XXX, and 47,XYY). In addition, if selected as an option, QNatal Advanced can screen for certain microdeletions (i.e., 22q, 5p, 1p36, 15q, 11q, 8q, and 4p) that may cause birth defects, and/or for fetal sex. This test does not assess the risk of fetal anomalies such as neural tube defects or ventral wall defects. QNatal Advanced is not recommended before 10 weeks of gestation due to a significantly increased risk of a failed result. QNatal Advanced is a screening test, not a diagnostic test, and therefore all positive/increased risk results should be followed by genetic counseling and further diagnostic testing and procedures, when clinically indicated. Pregnancy management decisions should not be based on the results of this screening test alone. As with any test, there may be false positives or false negatives. All results should be interpreted in the context of pertinent clinical findings, relevant obstetric history and laboratory data based on a clear understanding of the value and limitations of the test data. The positive predictive value varies by patient risk factors as well as by genetic marker, and may be lower for rare conditions. Performance data for QNatal® Advanced may be obtained by contacting Quest Diagnostics at 1.866.GENE.INFO (1.866.436.3463).
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
QuantiFERON®-TB Gold Plus, 1 Tube
-
Test Name:
QuantiFERON®-TB Gold Plus, 1 Tube
-
Test Code:
R36970
-
Alias:
QFT Gold Plus,IGRA,QFT Plus,TB Gold,QFT TB
-
CPT Code(s):
86480
-
Test Includes:
The Centers for Disease Control and Prevention (CDC) has provided guidance on clinical considerations for tuberculosis (TB) testing such as QuantiFERON®-TB Gold Plus in conjunction with COVID-19 mRNA vaccines. Please refer to the QuantiFERON®-TB Gold Plus FAQ link under Test Resources for more detailed information on the latest CDC guidelines regarding TB testing and COVID-19 vaccines.
-
Preferred Specimen:
6 mL whole blood collected in a no gel lithium heparin (green-top) tube
-
Min. Volume:
6 mL
-
Transport Container:
Lithium heparin (green-top) tube
-
Collection Instruction:
Collect a minimum of 6 mL of blood by venipuncture into a lithium heparin (green-top) tube. Gently mix by inverting the tube several times to dissolve the heparin.
Refrigerate at 2-8° C. -
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: Unacceptable Refrigerate: 48 hours Frozen: Unacceptable
-
Clinical Significance:
QuantiFERON®-TB Gold Plus, 1 Tube - This test is a blood-based interferon-gamma release assay (IGRA) used as an aid in the diagnosis of Mycobacterium tuberculosis infection. It is an immune response-based, indirect test for M tuberculosis infection (including disease) and is intended for use in conjunction with risk assessment, radiography, and other medical and diagnostic evaluations. Additional testing is needed to determine if a person who has tested positive has latent tuberculosis (TB) infection or TB disease. This in vitro diagnostic test uses a peptide cocktail simulating ESAT-6, CFP-10, and TB7.7 proteins to stimulate cells in heparinized whole blood. Detection of interferon-γ (IFN-γ) by ELISA is used to identify in vitro responses to those peptide antigens that are associated with Mycobacterium tuberculosis infection. For the four-tube QFT-Plus testing option, see test code #36971. Guidelines recommend testing for individuals who 1) have been exposed to a person with latent or active TB, including the general population and healthcare workers; 2) are from TB-endemic countries, which include most countries in Latin America, the Caribbean, Africa, Asia, and Eastern Europe, and Russia; 3) work in high-risk settings, such as correctional facilities, long-term care (LTC) facilities, nursing homes, and homeless shelters; or 4) have HIV or have an injection drug substance use disorder [1]. All of these individuals can be tested with either a traditional tuberculin skin test (TST) or an IGRA. However, the American Thoracic Society (ATS), the Infectious Disease Society of America (IDSA), and the Centers for Disease Control and Prevention (CDC) jointly prefer an IGRA test for individuals who have been vaccinated against bacillus Calmette-Guérin (BCG) or are not likely to return for the follow-up portion of the TST (and in both cases are at least 5 years old and likely to have TB infection and are at low or moderate risk of disease progression, or in whom it has been determined that TB testing is necessary [1]. The QuantiFERON-TB Gold test has specificity >99% in low-risk individuals and sensitivity of 92% in individuals with active disease [2]. In contrast to the TST, IGRA testing for TB requires only 1 patient visit (instead of 2). Also, IGRAs are not associated with the booster phenomenon, in which previously infected individuals generate a false-positive on a TST. In addition, prior BCG vaccination does not generate a false-positive result. Note that for children aged 2 and above, either TST or IGRA can be used [3,4] The CDC does not recommend dual testing with both a TST and an IGRA, unless the goal is to confirm a positive result, or when a high-risk individual’s test results are negative and there is clinical suspicion of TB. In this clinical situation, dual testing is used for confirmatory purposes [4]. For more information about TST versus IGRA testing, please visit the QuantiFERON®-TB Gold FAQs page. Note that when using QuantiFERON®-TB Gold Plus, blood samples must be processed within 16 to 48 hours after collection while white blood cells are still viable.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
QuantiFERON®-TB Gold Plus, 4 Tubes, Draw Site Incubated
-
Test Name:
QuantiFERON®-TB Gold Plus, 4 Tubes, Draw Site Incubated
-
Test Code:
R36971
-
Alias:
TB Gold,QFT Gold Plus,QFT TB,QFT Plus,IGRA
-
CPT Code(s):
86480
-
Test Includes:
The Centers for Disease Control and Prevention (CDC) has provided guidance on clinical considerations for tuberculosis (TB) testing such as QuantiFERON®-TB Gold Plus in conjunction with COVID-19 mRNA vaccines. Please refer to the QuantiFERON®-TB Gold Plus FAQ link under Test Resources for more detailed information on the latest CDC guidelines regarding TB testing and COVID-19 vaccines.
-
Preferred Specimen:
1 mL whole blood collected in each of the following tubes: QFT-Nil control (gray cap, white or gold ring) tube QFT-TB1 antigen (green cap, white or gold ring) tube QFT-TB2 antigen (yellow cap, white or gold ring) tube QFT-Mitogen control (purple cap, white or gold ring) tube
-
Min. Volume:
0.8 mL in each tube
-
Transport Container:
QFT-Nil control (gray cap, white or gold ring) tube QFT-TB1 antigen (green cap, white or gold ring) tube QFT-TB2 antigen (yellow cap, white or gold ring) tube QFT-Mitogen control (purple cap, white or gold ring) tube
-
Collection Instruction:
Note: Specimen collection locations >3350 feet above sea level should use the QuantiFERON® collection kit designed for “High Altitude” (tubes with a gold ring on tube top)
For each patient, collect 1 mL of blood by venipuncture directly into each of the 4 QFT-PLUS blood collection tubes. These tubes should be at 17-25° C at the time of draw.
If a “butterfly needle” is being used, a “purge” tube should be used to ensure that the tubing is filled with blood prior to the QFT-PLUS tubes being used.
Immediately after filling the tubes, shake them 10 times just firmly enough to ensure the entire surface of the tube is coated with blood, to solubilize antigens on tube walls.
Each of the four tubes must be transferred to a 37° C +/- 1° C incubator as soon as possible and within 16 hours of collection for 16-24 hours. If the blood is not incubated immediately after collection, re-mixing of the tubes by inverting 10 times must be performed immediately prior to incubation. The specimen rack should sit off the floor of the incubator and the tubes should be upright.
Following incubation either:
A. Centrifuge each of the 4 incubated collection tubes for 15 minutes at 2000-3000 RCF(G). Label with patient name, identification number, and date of collection. Deliver to Quest Diagnostics at 2-8° C. Samples will be stable for 28 days at 2-8° C (refrigerated).
*OR*
B. Immediately transport the 4 collection tubes to Quest Diagnostics between 4 and 27° C. Samples will be stable for 72 hours at 4-27° C (refrigerated or at room temperature).The Centers for Disease Control and Prevention (CDC) has provided guidance on clinical considerations for tuberculosis (TB) testing such as QuantiFERON®-TB Gold Plus in conjunction with COVID-19 mRNA vaccines. Please refer to the QuantiFERON®-TB Gold Plus FAQ link (https://education.questdiagnostics.com/faq/FAQ204) for more detailed information on the latest CDC guidelines regarding TB testing and COVID-19 vaccines.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Uncentrifuged specimens Room temperature: 72 hours after incubation Refrigerated: 72 hours after incubation Frozen: Unacceptable Centrifuged specimens Room temperature: Unacceptable Refrigerated: 28 days Frozen: Unacceptable
-
Clinical Significance:
QuantiFERON®-TB Gold Plus, 4 Tubes, Draw Site Incubated - This test is a blood-based interferon-gamma release assay (IGRA) used as an aid in the diagnosis of Mycobacterium tuberculosis infection. It is an immune response-based, indirect test for M tuberculosis infection (including disease) and is intended for use in conjunction with risk assessment, radiography, and other medical and diagnostic evaluations. Additional testing is needed to determine if a person who has tested positive has latent tuberculosis (TB) infection or TB disease. This in vitro diagnostic test uses a peptide cocktail simulating ESAT-6, CFP-10, and TB7.7 proteins to stimulate cells in heparinized whole blood. Detection of interferon-γ (IFN-γ) by ELISA is used to identify in vitro responses to those peptide antigens that are associated with Mycobacterium tuberculosis infection. This test uses a 4-tube blood collection method, which requires incubation before submitting to the lab. For the single-tube QFT-Plus testing option, see test code #36970. Guidelines recommend testing for individuals who 1) have been exposed to a person with latent or active TB, including the general population and healthcare workers; 2) are from TB-endemic countries, which include most countries in Latin America, the Caribbean, Africa, Asia, and Eastern Europe, and Russia; 3) work in high-risk settings, such as correctional facilities, long-term care (LTC) facilities, nursing homes, and homeless shelters; or 4) have HIV or have an injection drug substance use disorder [1]. All of these individuals can be tested with either a traditional tuberculin skin test (TST) or an IGRA. However, the American Thoracic Society (ATS), the Infectious Disease Society of America (IDSA), and the Centers for Disease Control and Prevention (CDC) jointly prefer an IGRA test for individuals who have been vaccinated against bacillus Calmette-Guérin (BCG) or are not likely to return for the follow-up portion of the TST (and in both cases are at least 5 years old and likely to have TB infection and are at low or moderate risk of disease progression, or in whom it has been determined that TB testing is necessary [1]. The QuantiFERON-TB Gold test has specificity >99% in low-risk individuals and sensitivity of 92% in individuals with active disease [2]. In contrast to the TST, IGRA testing for TB requires only 1 patient visit (instead of 2). Also, IGRAs are not associated with the booster phenomenon, in which previously infected individuals generate a false-positive on a TST; and prior BCG vaccination does not generate a false-positive result. Note that for children aged 2 and above, either TST or IGRA can be used [3,4]. The CDC does not recommend dual testing with both a TST and an IGRA, unless the goal is to confirm a positive result, or when a high-risk individual’s test results are negative and there is clinical suspicion of TB. In this clinical situation, dual testing is used for confirmatory purposes [4]. For more information about TST versus IGRA testing, please visit the QuantiFERON®-TB Gold FAQs page. Note: Specimens collected for this test must be transferred to a 37 °C incubator as soon as possible (within 16 hours of collection). An alternative, single-tube test option (QuantiFERON®-TB Gold Plus, 1 Tube; test code 36970) allows the specimen to be stabilized for up to 48 hours before incubation.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
QuestAssureD™ 25-Hydroxyvitamin D (D2, D3)
-
Test Name:
QuestAssureD™ 25-Hydroxyvitamin D (D2, D3)
-
Test Code:
R92888
-
Alias:
Vitamin D3, 25-hydroxy,D2 Vitamin,D3 Vitamin,25-Hydroxycholecalciferol (25OHD3),25-Hydroxyergocalciferol (25OHD2),25-Hydroxyvitamin D2,25-Hydroxyvitamin D3,25-OH-D2,25-OH-D3,Vit D, LC/MS/MS,Vitamin D2, 25-hydroxy
-
CPT Code(s):
82306
-
Test Includes:
Vitamin D, 25-OH, Total Vitamin D, 25-OH, D3 Vitamin D, 25-OH, D2
-
Preferred Specimen:
0.5 mL serum
-
Min. Volume:
0.3 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Collect blood in a standard red-top serum Vacutainer® tube. Allow blood to clot at room temperature. Centrifuge and separate the serum from the cells immediately.
Alternatively, collect blood in a serum separator tube (SST), allow to clot at room temperature. Centrifuge and remove from the gel within 48 hours. -
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 21 days Refrigerated: 21 days Frozen: 21 days
-
Clinical Significance:
QuestAssureD™ 25-Hydroxyvitamin D (D2, D3) - Measurement of serum 25-OH vitamin D concentrations provide a good index of circulating vitamin D activity in patients not suffering from renal disease. Lower than normal 25-OH vitamin D levels can result from a dietary deficiency, poor absorption of the vitamin or impaired metabolism of the sterol in the liver. A 25-OH vitamin D deficiency can lead to bone diseases such as rickets and osteomalacia. Above normal levels can lead to hypercalcemia. This assay employs liquid chromatography tandem mass spectrometry to independently measure and report the two common forms of 25-hydroxy vitamin D: 25-OH D3 - the endogenous form of the vitamin and 25-OH D2 - the analog form used to treat 25-OH Vitamin D3 deficiency.
-
Performing Lab:
med fusion 2501 South State Hwy 121, Suite 1100 Lewisville, TX 75067-8188
R
RAPID FLU A/B
-
Test Name:
RAPID FLU A/B
-
Test Code:
LS5018
-
Test Includes:
Influenza A, Influenza B
-
Preferred Specimen:
Nasopharyngeal or nasal swab
-
Transport Container:
RED CAP VIRAL PBS SWAB
-
Performing Lab:
Simple Laboratories
RENAL/KIDNEY FUNCTION PANEL
-
Test Name:
RENAL/KIDNEY FUNCTION PANEL
-
Test Code:
RENAL
-
Alias:
KIDNEY FUNCTION PANEL, KFP, RFP
-
CPT Code(s):
80069
-
Test Includes:
ALBUMIN, BUN (BLOOD UREA NITROGEN), CALCIUM, TOTAL, CHLORIDE, CO2, CREATININE, GLUCOSE
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Patient should fast 8 hours prior to collection unless instructed differently by a physician.
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 72 hours Refrigerated: 4 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
The kidney performs many physiological and excretory functions. The renal function panel evaluates the functional state of the kidney.
-
Performing Lab:
Simple Laboratories
RF (RHEUMATOID FACTOR) QUANTITATIVE
-
Test Name:
RF (RHEUMATOID FACTOR) QUANTITATIVE
-
Test Code:
RA
-
Alias:
RF, RHEUMATOID
-
CPT Code(s):
86431
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 24 hours Refrigerated: 8 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Rheumatoid factors (RF) are antibodies directed against antigenic determinants on the Fc fragment of IgG. These are usually IgM antibodies, but may be IgG, IgA or IgE.
-
Performing Lab:
Simple Laboratories
Rheumatoid Factor
-
Test Name:
Rheumatoid Factor
-
Test Code:
R4418
-
Alias:
RF
-
CPT Code(s):
86431
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Serum separator tube (SST)
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 7 days Frozen: 90 days
-
Clinical Significance:
Rheumatoid Factor - Elevated RF is found in collagen vascular diseases such as SLE, rheumatoid arthritis, scleroderma, Sjogren's syndrome, and in other conditions such as leprosy, tuberculosis, syphilis, malignancy, thyroid disease and in a significant percentage of otherwise normal elderly patients.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
RIVOTRIL (MEDICATION)
-
Test Name:
RIVOTRIL (MEDICATION)
-
Test Code:
500700
ROBITUSSIN-AC (MEDICATION)
-
Test Name:
ROBITUSSIN-AC (MEDICATION)
-
Test Code:
501390
RPR SCREEN WITH REFLEX TO TITER
-
Test Name:
RPR SCREEN WITH REFLEX TO TITER
-
Test Code:
RPR
-
Alias:
Non-Treponemal Syphilis serology
-
CPT Code(s):
86592
-
Test Includes:
RPR Screening *Note: This test is meant for screening purposes of known Syphilis patients. There is no confirmation test associated with this order.
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 5 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
RPR test is used for the rapid detection and the qualitative determination of syphilis in serum or plasma.
-
Performing Lab:
Simple Laboratories
RUBELLA ANTIBODY IGG
-
Test Name:
RUBELLA ANTIBODY IGG
-
Test Code:
RUB
-
Alias:
3 Day Measles German Measles
-
CPT Code(s):
86762
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM (This volume does not allow for repeat testing.)
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 2 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Rubella is a viral illness. The infection is usually benign or even unapparent in children or adults. Clinical manifestations include a generalized skin rash over the entire body, a low-grade fever, headache, and sometimes a sore throat. Infections in utero, particularly during the first four months of pregnancy, can lead to can lead to congenital defects such as deafness, cardiac problems, cataracts or glaucoma, and sometimes fetal death. Demonstration of rubella IgG antibody in a pregnant woman prior to conception provides assurance of fetal protection from possible rubella viral infection during pregnancy. Vaccination efficiency is demonstrated by detection of rubella IgG antibody in serum following immunization.
-
Performing Lab:
Simple Laboratories
S
Sarcoptes scabiei (Scabies) Examination
-
Test Name:
Sarcoptes scabiei (Scabies) Examination
-
Test Code:
R8628
-
Alias:
Mites,Itch Mites,Scabies Mite Exam
-
CPT Code(s):
87220
-
Preferred Specimen:
Dry skin scrapings or submit scrapings between two microscopic slides rubber-banded together in a screw-cap tube or plastic vial
-
Transport Container:
Plastic screw-cap container
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: Indefinite Refrigerated: Indefinite Frozen: Unacceptable
-
Clinical Significance:
Sarcoptes scabiei (Scabies) Examination - Sarcoptes scabiei causes scabies which is recognized by a nocturnal itch occurring primarily on the webbing between the fingers spreading to the wrists, elbows, buttocks, breasts and external genitalia. This itch and accompanying skin eruptions are delayed for several weeks after the initial infection. The rash represents a sensitization to the bite which does not necessarily correspond to the location of the active adult female.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
SARS-COV-2 (COVID-19) DETECTION
-
Test Name:
SARS-COV-2 (COVID-19) DETECTION
-
Test Code:
LS5004
-
CPT Code(s):
87635
-
Preferred Specimen:
Nasopharyngeal or nasal swab
-
Transport Container:
RED CAP VIRAL PBS SWAB
-
Performing Lab:
Simple Laboratories
Scleroderma Antibody (Scl-70)
-
Test Name:
Scleroderma Antibody (Scl-70)
-
Test Code:
R4942
-
CPT Code(s):
86235
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Scleroderma Antibody (Scl-70) - Scl-70 antibody is present in approximately 40% of patients with progressive systemic sclerosis (PSS).
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
SECOBARBITAL (MEDICATION)
-
Test Name:
SECOBARBITAL (MEDICATION)
-
Test Code:
500550
SICKLE CELL SCREEN
-
Test Name:
SICKLE CELL SCREEN
-
Test Code:
SC
Sjogren’s Antibodies (SS-A, SS-B)
-
Test Name:
Sjogren’s Antibodies (SS-A, SS-B)
-
Test Code:
R7832
-
Alias:
SS-A & SS-B
-
CPT Code(s):
86235 (x2)
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Sjogren's Antibodies (SS-A, SS-B) - Sjögren's antibodies (SS-B) is detected in approximately 15% of patients with Sjögren's Syndrome. Sjögren's antibody (SS-B) is present only if Sjögren's antibody (SS-A) is also detected. The presence of both antibodies (SS-A and SS-B) strengthen the diagnosis of Sjögren's Syndrome and conveys prognostic information.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Sjogren’s Antibody (SS-A)
-
Test Name:
Sjogren’s Antibody (SS-A)
-
Test Code:
R38568
-
Alias:
Sjogrens
-
CPT Code(s):
86235
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Sjogren's Antibody (SS-A) - Sjögren's Antibodies (SS-B) is detected in approximately 15% of patients with Sjögren's Syndrome. Sjögren's Antibody (SS-B) is present only if Sjögren's Antibody (SS-A) is also detected. The presence of both antibodies (SS-A and SS-B) strengthen the diagnosis of Sjögren's Syndrome and conveys prognostic information.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Sm Antibody
-
Test Name:
Sm Antibody
-
Test Code:
R37923
-
Alias:
Sm or Smith Antibody
-
CPT Code(s):
86235
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Sm Antibody - Smith Antibody (Sm) is highly specific for systemic lupus erythematosus (SLE). Smith Antibody is also detected in approximately 15% of patients with SLE. Smith Antibody is detected in more than half of young African-American women with SLE.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
SODIUM, SERUM
-
Test Name:
SODIUM, SERUM
-
Test Code:
NA
-
Alias:
NA
-
CPT Code(s):
84295
-
Preferred Specimen:
1.0 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 14 days Refrigerated: 14 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Sodium measurements are used in the diagnosis and treatment of aldosteronism (excessive secretion of the hormone aldosterone), diabetes insipidus, adrenal hypertension, Addison's disease, dehydration, inappropriate antidiuretic hormone secretion, or other disease involving electrolyte imbalance.
-
Performing Lab:
Simple Laboratories
STATUSS GREEN (MEDICATION)
-
Test Name:
STATUSS GREEN (MEDICATION)
-
Test Code:
501250
STIMULANTS
-
Test Name:
STIMULANTS
-
Test Code:
411102
STREP A, RAPID MOLECULAR
-
Test Name:
STREP A, RAPID MOLECULAR
-
Test Code:
LS5022
-
CPT Code(s):
87651
-
Preferred Specimen:
THROAT SPECIMEN
-
Transport Container:
E-SWAB
-
Collection Instruction:
NULL
-
Transport Temperature:
Refrigerated
-
Stability:
Room temp: 48 hours Refrigerated: 6 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Group A strep is a bacterial pathogen that commonly cause infections in the throat. Treating an infected person with an appropriate antibiotic generally reduces the spread of the infection and reduces the risk of post-infection complications, such as rheumatic fever and acute glomerular nephritis.
-
Performing Lab:
Simple Laboratories
Streptococcus Group B Culture
-
Test Name:
Streptococcus Group B Culture
-
Test Code:
R5617
-
Alias:
Culture, Group B Strep
-
CPT Code(s):
87081
-
Test Includes:
If culture is positive, identification will be performed at an additional charge (CPT code(s): 87077 or 87140 or 87143 or 87147 or 87149). Antibiotic susceptibilities are only performed when appropriate (CPT code(s): 87181 or 87184 or 87185 or 87186).
-
Preferred Specimen:
Vaginal-rectal swab submitted in Amies liquid transport swab, Amies gel transport swab, Amies liquid elution swab (ESwab) or equivalent
-
Min. Volume:
One transport swab
-
Transport Container:
Transport swab
-
Collection Instruction:
For prenatal cultures obtain specimens from both the vaginal introitus and anorectum utilizing one or two swabs. Cervical cultures are not acceptable for prenatal screening; a speculum should not be used. After culture collection place swab(s) into one bacterial transport medium.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 48 hours Refrigerated: 48 hours Frozen: Unacceptable
-
Clinical Significance:
Streptococcus Group B Culture - Group B streptococci can be one of the most significant pathogens in the neonatal period. The organism is transmitted to the newborn through the birth canal. Prepartum vaginal introitus and anorectal cultures are important to determine carriage.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
SUBLIMAZE (MEDICATION)
-
Test Name:
SUBLIMAZE (MEDICATION)
-
Test Code:
501720
SYMORON (MEDICATION)
-
Test Name:
SYMORON (MEDICATION)
-
Test Code:
501620
T
T3 FREE
-
Test Name:
T3 FREE
-
Test Code:
FT3
-
Alias:
FT3 Triiodothyronine Unbound T3
-
CPT Code(s):
84481
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 ML SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 2 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
With normal levels of thyroid binding proteins, free T3 levels correlate with total T3. Measuring free T3 is useful when altered levels of total T3 occur due to changes in thyroid hormone binding proteins, especially in cases with altered TBG or low albumin concentrations. Free T3 is elevated alone (T3 toxicosis) in about 5% of hyperthyroids.
-
Performing Lab:
Simple Laboratories
T3 Reverse, LC/MS/MS
-
Test Name:
T3 Reverse, LC/MS/MS
-
Test Code:
R90963
-
CPT Code(s):
84482
-
Preferred Specimen:
0.5 mL serum
-
Min. Volume:
0.3 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Serum: Allow blood to clot at room temperature for 30 minutes. Centrifuge to separate serum from the cells within 24 hours of collection and immediately pour serum into a plastic transport tube.
Plasma: Centrifuge to separate plasma from the cells within 24 hours of collection and immediately pour plasma into a plastic transport tube.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
T3 Reverse, LC/MS/MS - 3,3',5'-Triiodothyronine (reverse T3, rT3) is, along with 3,3,5'-Triiodothyronine (T3) a deiodinated metabolite of thyroxine (T4), the major secretory product of the thyroid gland and is secreted into the bloodstream. Unlike T3, however, rT3 is thought to be metabolically inert. The process of 5'-monodeiodination that converts T4 to T3, and rT3 to diiodothyronine (DTT) is inhibited in a wide variety of conditions, collectively referred to as nonthyroidal illnesses (NTI) or the 'euthyroid sick' state. These conditions include fasting, malnutrition, poorly controlled diabetes mellitus, trauma, surgery, and systemic illness. Consequently, in patients with NTI the serum T3 level typically decreases, and the rT3 often, but not always, increases.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
T3 UPTAKE
-
Test Name:
T3 UPTAKE
-
Test Code:
T3
-
Alias:
Hanolsky Uptake Tes Resin Uptake Resin Uptake (T3) T3 Index T3 Resin Uptake Triiodothyronine
-
CPT Code(s):
84479
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 2 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
The thyroid hormone thyroxine (T4) is physiologically part of the regulating circuit of the thyroid gland and has an effect on general metabolism. The determination of total thyroxine only provides correct information when the thyroxine-binding capacity in serum is normal. The performance of a T-uptake or TBC assay provides a measure of the available thyroxine-binding sites.
-
Performing Lab:
Simple Laboratories
T3, TOTAL
-
Test Name:
T3, TOTAL
-
Test Code:
84480
-
Alias:
T3 Hormone Triiodothyronine
-
CPT Code(s):
84480
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 ML SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 2 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
The clinical importance of total T3 determination is in the diagnosis of thyroid disorders. Elevated levels of T3 occur in Graves’ disease, and most other classical causes of hyperthyroidism. Decreased levels occur in primary hypothyroid diseases such as Hashimoto’s thyroiditis and neonatal hypothyroidism or secondary hypothyroidism due to defects at the hypothalamo-hypophyseal level.
-
Performing Lab:
Simple Laboratories
Testosterone, Free (Dialysis) and Total, MS
-
Test Name:
Testosterone, Free (Dialysis) and Total, MS
-
Test Code:
R36170
-
Alias:
F Testo,Free & Total Testosterone, LC/MS/MS,Testosterone Index,Testosterone,Total/Free, Pediatric,Dialyzable Testosterone,Fractionated Testosterone,Free and Unbound Testosterone
-
CPT Code(s):
84402, 84403
-
Test Includes:
Testosterone, Total, MS and Testosterone, Free (Dialysis)
-
Preferred Specimen:
1.8 mL serum
-
Min. Volume:
0.9 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Specify age and sex on test request form.
Red-top tube (no gel): Allow blood to clot at room temperature. Centrifuge to separate the serum from the cells and immediately pour serum into a plastic transport tube.
Serum separator tube: Allow blood to clot at room temperature, centrifuge, and remove serum from the gel immediately (not to exceed 48 hours) by pouring serum into a plastic transport tube. -
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 21 days Frozen: 2 years
-
Clinical Significance:
Testosterone, Free (Dialysis) and Total, MS - Helpful in assessing testicular function in prepubescent hypogonadal males and in managing hirsutism, virilization in females.
-
Performing Lab:
med fusion 2501 South State Hwy 121, Suite 1100 Lewisville, TX 75067-8188
TESTOSTERONE, TOTAL
-
Test Name:
TESTOSTERONE, TOTAL
-
Test Code:
TESTOS
-
CPT Code(s):
84403
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 48 hours
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Testosterone in males is secreted by adult Leydig cells and is controlled principally by lutenizing hormone (LH). The majority of serum testosterone is bound to sex hormone binding globulin (SHBG), but it also exists loosely bound to albumin and in the free state. An abnormally low total testosterone level in males can be indicative of hypogonadism, hypopituitarism, hyperprolactinemia, renal failure, hepatic cirrhosis, or Kleinfelter’s syndrome. High total testosterone values in males can be caused by adrenal and testicular tumors, congenital adrenal hyperplasia or abnormalities of the hypothalamic-pituitary-testicular axis.
-
Performing Lab:
Simple Laboratories
ThinPrep® Automated Pap and HPV mRNA E6/E7 with Reflex to HPV 16,18/45
-
Test Name:
ThinPrep® Automated Pap and HPV mRNA E6/E7 with Reflex to HPV 16,18/45
-
Test Code:
R91414
-
CPT Code(s):
88175 (HCPCS: G0145), 87624
-
Test Includes:
ThinPrep® Automated Pap HPV mRNA E6/E7 with Reflex to HPV Genotypes 16, 18/45 If the ThinPrep® Automated Pap is Normal and the HPV mRNA E6/E7 is Detected, then HPV Genotypes 16,18/45 will be performed at an additional charge (CPT code(s): 87625).
-
Preferred Specimen:
Pap sample collected in 1 ThinPrep® pap vial
-
Min. Volume:
1 ThinPrep vial
-
Transport Container:
1 ThinPrep vial
-
Transport Temperature:
Room temperature
-
Stability:
Pap Room temperature: 42 days Refrigerated: Unacceptable Frozen: Unacceptable HPV ThinPrep Pap vial Room temperature: 30 days Refrigerated: 105 days Frozen: Unacceptable ThinPrep in Aptima® transfer tube Room temperature: 60 days Refrigerated: 60 days Frozen: 2 years Refer to local service area for specimen retention
-
Clinical Significance:
ThinPrep® Automated Pap and HPV mRNA E6/E7 with Reflex to HPV 16,18/45
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
THYROGLOBULIN ANTIBODY
-
Test Name:
THYROGLOBULIN ANTIBODY
-
Test Code:
THYROG
-
CPT Code(s):
86800
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-Heparin tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 days Refrigerated: 2 days Frozen: 1 Month
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Circulating thyroid antibodies have been widely implicated in the etiology of autoimmune thyroid disease and both thyroglobulin and microsomal antibodies are measured routinely in clinical practice. Thyroglobulin autoantibodies are detected at high titers, mainly in autoimmune thyroiditis and Grave’s disease. Serum autoantibodies to thyroglobulin/colloid have been found in 40-70% of patients with chronic thyroiditis and in smaller percentages of patients with thyrotoxicosis and nontoxic goiters.
-
Performing Lab:
Simple Laboratories
THYROGLOBULIN ANTIBODY
-
Test Name:
THYROGLOBULIN ANTIBODY
-
Test Code:
THYROG
Thyroglobulin Panel
-
Test Name:
Thyroglobulin Panel
-
Test Code:
R30278
-
Alias:
ATG and TG,TG and ATG
-
CPT Code(s):
84432,86800
-
Test Includes:
Thyroglobulin Antibodies and Quantitative Thyroglobulin
-
Preferred Specimen:
2 mL serum
-
Min. Volume:
1 mL
-
Transport Container:
Serum separator tube (SST)
-
Collection Instruction:
Administration of STRENSIQ may interfere in certain assays and may falsely elevate values. For patients receiving STRENSIQ, consideration should be given to using alternate methods.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Thyroglobulin Panel - Thyroglobulin (TG) is a secretory product only of the thyroid gland. The major clinical use of serum TG measurement is to monitor, but not to diagnose, patients with well-differentiated thyroid cancers. The measurement of thyroglobulin, after thyroidectomy and ablation of the thyroid gland, is useful to determine metastasis. Deficient TG synthesis is observed in infants with goitrous hypo-thyroidism. Most patients with thyroid autoimmune disease have thyroglobulin antibody. With immunometric assays (sandwich assays), TGAB interference typically produces inappropriately low TG results, most likely caused by endogenous TG immune complexes that block one or more of the reagent antibodies from binding endogenous TG.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Thyroglobulin, LC/MS/MS
-
Test Name:
Thyroglobulin, LC/MS/MS
-
Test Code:
R90810
-
CPT Code(s):
84432
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 6 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Thyroglobulin, LC/MS/MS - Measurement of thyroglobulin (Tg) is useful in the detection of residual or recurrent thyroid cancer. Many individuals develop auto-antibodies to Tg (Tg Ab) and the presence of Tg Ab interferes with the measurement of immunoassay Tg. The LC/MS/MS assay will provide quantitative measurement of Tg in the presence of Tg Ab.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
THYROID PROFILE WITH TSH
-
Test Name:
THYROID PROFILE WITH TSH
-
Test Code:
T
-
Alias:
THYROID PANEL W/TSH
-
CPT Code(s):
84436; 84479; 84443
-
Test Includes:
TSH, T3 Uptake, T4 (Thyroxine) Total Free T4 Index (T7)
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a Li-Heparin tube, centrifuge for 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 7 days Refrigerated: 7 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Thyroid Panel - For diagnosis of hypothyroidism and hyperthyroidism.
-
Performing Lab:
Simple Laboratories
THYROXINE (T4)
-
Test Name:
THYROXINE (T4)
-
Test Code:
T4
-
Alias:
T4 Total Tetraiodothyronine
-
CPT Code(s):
84436
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 mL serum or plasma
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 8 hours Refrigerated: 48 hours
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Thyroxine is commonly measured in serum as total T4, measuring both bound and free T4. It is used as a thyroid screening test alone or in conjunction with other thyroid tests. Measurement of total T4 gives a reliable reflection of clinical thyroid status in the absence of binding abnormalities. However, changes in binding proteins can occur which affect the level of total T4, but leave the level of unbound hormone unchanged. The clinical importance of total T4 determination is in the diagnosis and confirmation of thyroid disorders. Elevated levels of T4 occur in Graves’ disease, subacute thyroiditis, toxic nodule, or secondary (pituitary) hyperthyroidism. Decreased levels occur primarily due to defects at the hypothalamic-pituitary level.
-
Performing Lab:
Simple Laboratories
THYROXINE (T4), FREE
-
Test Name:
THYROXINE (T4), FREE
-
Test Code:
FT4
-
Alias:
FT4, UNBOUND T4
-
CPT Code(s):
84439
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 mL serum or plasma
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room Temperature: 8 hours Refrigerated: 48 hours Freeze samples for longer stability
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Elevated free T4 levels support the clinical findings of a diagnosis of hyperthyroidism while clearly low freeT4 levles coupled with appropriate clinical findings, can establish a diagnosis of hypothyroidism. Measurment of free T4 levels along with other thyroid tests and clinical findings can establish borderline hyperthyroid and hypothyroid diagnoses.
-
Performing Lab:
Simple Laboratories
Tissue Transglutaminase (tTG) Antibody (IgA)
-
Test Name:
Tissue Transglutaminase (tTG) Antibody (IgA)
-
Test Code:
R8821
-
Alias:
Celiac Disease,tTG Antibody,Transglutaminase, Tissue Antibody IgA,Dermatitis Herpetiformis,tTG IgA
-
CPT Code(s):
86364
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 30 days
-
Clinical Significance:
Tissue Transglutaminase (tTG) Antibody (IgA) - Tissue Transglutaminase Antibody, IgA, is useful in diagnosing gluten-sensitive enteropathies, such as Celiac Sprue Disease, and an associated skin condition, dermatitis herpetiformis.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Tissue, Pathology Report
-
Test Name:
Tissue, Pathology Report
-
Test Code:
R3542
-
Alias:
Biopsy and Tissue Pathology
-
CPT Code(s):
88300 Surg Path Level I, Gross Examination Only 88302 Surg Path Level II, Gross and Microscopic Examination 88304 Surg Path Level III, Gross and Microscopic Examination 88305 Surg Path Level IV, Gross and Microscopic Examination 88307 Surg Path Level V, Gross and Microscopic Examination 88309 Surg Path Level VI, Gross and Microscopic Examination
-
Test Includes:
Preparation of each submitted sample and microscopic interpretation by a pathologist. The fee for service will vary depending upon the number of specimens submitted, the size and complexity of the specimen and difficulty of diagnosis. Specimens requiring a decalcification procedure will be performed at an additional charge (CPT code(s): 88311). Special stains (CPT code(s): 88312 (each stain) or 88313 (each stain)) and/or IHC immunohistochemistry stains (CPT code(s): 88342 (each antibody)) may be ordered at the discretion of the pathologist. These services will be performed at an additional charge.
-
Preferred Specimen:
See Collection Instructions
-
Min. Volume:
See Collection Instructions
-
Transport Container:
See Collection Instructions
-
Collection Instruction:
Provide all patient information using the Tissue Pathology requisition form.
For instructions refer to
https://www.questdiagnostics.com/content/dam/corporate/restricted/documents/test-directory/Specimen_Collection_and_Transport_Guide_2019.pdf -
Transport Temperature:
See Collection Instructions
-
Stability:
See Collection Instructions
-
Clinical Significance:
Tissue, Pathology Report - The nature of possible underlying disease states can often be detected by microscopically visualizing histologic changes in tissue biopsies.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Tobramycin
-
Test Name:
Tobramycin
-
Test Code:
R888
-
CPT Code(s):
80200
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 7 days
-
Clinical Significance:
Tobramycin - Tobramycin is an aminoglycoside antibiotic used in the treatment of gram-negative bacterial infections, especially Pseudomonas, Proteus, Klebsiella and also Staphylococcus. Tobramycin is potentially nephrotoxic and ototoxic and serial monitoring of peak and trough serum levels may provide the clinician with information to maintain safe and therapeutic levels.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Toxoplasma Antibody (IgM)
-
Test Name:
Toxoplasma Antibody (IgM)
-
Test Code:
R37207
-
CPT Code(s):
86778
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Toxoplasma Antibody (IgM) - T. gondii IgM is typically detected within a few days of infection, peaks within a few weeks, and usually falls to undetectable levels within a few months. In some patients, however, T. gondii IgM persists for more than a year; Thus, detection of T. gondii IgM does not necessarily indicate recent or ongoing toxoplasmosis.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
TPO (THYROPEROXIDASE) ANTIBODY
-
Test Name:
TPO (THYROPEROXIDASE) ANTIBODY
-
Test Code:
TPO
-
Alias:
Antimicrosomal Antibody Antithyroid Microsomal Antibody Anti-TPO Thyroid Peroxidase Autoantibodies TPO Autoantibodies
-
CPT Code(s):
86376
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM OR PLASA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 48 hours
-
Schedule:
1-2 DAYS
-
Clinical Significance:
The determination of TPOAb levels is the most sensitive test for detecting autoimmune thyroid disease. The highest TPOAb levels are observed in patients suffereing from Hashimoto's thyroiditis. In this disease, the prevalence of TPOAb is about 90% of cases confirming the autoimmune origin of the disease. These autoantibodies also frequently occur (60%-80%) in the course of Graves' disease.
-
Performing Lab:
Simple Laboratories
TRAb (TSH Receptor Binding Antibody)
-
Test Name:
TRAb (TSH Receptor Binding Antibody)
-
Test Code:
R38683
-
Alias:
Thyrotropin Receptor Antibody,TSH Receptor Binding Antibody,Thyrotropin Binding (TBII),TBII
-
CPT Code(s):
83520
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Allow serum to clot at room temperature. Serum must be separated from the cells or gel barrier within 1 hour of collection and poured into a transport vial.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 14 days Frozen: 21 days
-
Clinical Significance:
TRAb (TSH Receptor Binding Antibody) - Measurement of TRAb is used to diagnose and manage Graves' disease, neonatal hypothyroidism, and postpartum thyroid dysfunction. TRAb, which measures the ability of antibodies to inhibit TSH binding to its receptor, reflects the presence of either or both the stimulatory and inhibitory immunoglobulin classes.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
TRANSFERRIN
-
Test Name:
TRANSFERRIN
-
Test Code:
TRANS
-
Alias:
SIDEROPHILIN
-
CPT Code(s):
84466
-
Preferred Specimen:
1.0 ML SERUM
-
Min. Volume:
0.5 ML SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge 15 minutes.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 5 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Transferrin levels rise with iron deficiency and fall in cases of iron overload. An increase in transferrin is seen in iron deficiency anemia. It may also be increased late in pregnancy and in women on oral contraceptives. It is decreased in conditions associated with increased protein loss, such as nephrotic syndrome, chronic renal failure, severe burns, and protein-deficiency states and in severe liver disease. Transferrin is a negative acute-phase protein and will be decreased during any inflammatory state or severe illness
-
Performing Lab:
Simple Laboratories
TRAZODONE HCL (MEDICATION)
-
Test Name:
TRAZODONE HCL (MEDICATION)
-
Test Code:
500500
TREPONEMA PALLIDUM WITH REFLEX
-
Test Name:
TREPONEMA PALLIDUM WITH REFLEX
-
Test Code:
013005
-
Alias:
Agglutination (TP-PA) Test T. pallidum Ab TP-PA
-
CPT Code(s):
86780
-
Test Includes:
Reflex to qualitative rapid plasma reagin (RPR) on positives. May carry additional CPT codes
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
1.0 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimens to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum or plasma should be physically separated from contact with cells within 2 hours from the time of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
If T. Pallidum antibody is equivocal or reactive, RPR screen with reflex to titer will be performed at an additional charge (CPT code 86592). If RPR screen is reactive, RPR titer will be performed at an additional charge (CPT code 86593). If RPR screen is non-reactive, it will reflex to another treponemal test for confirmation (FTA-ABS) at an additional charge (CPT code 86780).
-
Performing Lab:
Simple Laboratories
TRICHOMONAS VAGINALIS, GENITAL, PCR
-
Test Name:
TRICHOMONAS VAGINALIS, GENITAL, PCR
-
Test Code:
LS5023
-
Alias:
Trichomonas NAT, TV
-
CPT Code(s):
87661
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA SWAB (UNI-SEX OR VAGINAL SWAB)
-
Collection Instruction:
For endocervical swab, vaginal swab or male urethral swab: Collect specimen according to printed instructions on APTIMA unisex swab collection kit packaging
-
Transport Temperature:
Refrigerated
-
Stability:
60 days - after testing, specimens are stored in the lab for 7 days
-
Schedule:
1-3 Days
-
Clinical Significance:
Trichomonas vaginalis infections cause vaginitis, urethritis and cervicitis. Discharge and small hemorrhagic lesions may be present in the genitourinary tract. Complications can include premature labor, low-birth-weight offspring, premature rupture of membranes and post-abortion or post-hysterectomy infection. An association with pelvic inflammatory disease, tubal infertility, and cervical cancer with previous episodes of trichomoniasis has been reported. Symptomatic women with trichomoniasis usually complain of vaginal discharge, vulvovaginal soreness and/or irritation. Dysuria is also common. However, it has been estimated that 10-50% of T. vaginalis infections in women are asymptomatic.
-
Performing Lab:
Simple Laboratories
TRICHOMONAS VAGINALIS, URINE, PCR
-
Test Name:
TRICHOMONAS VAGINALIS, URINE, PCR
-
Test Code:
LS5024
-
Alias:
Trichomonas NAT, TV
-
CPT Code(s):
87661
-
Preferred Specimen:
APTIMA YELLOW URINE
-
Transport Container:
APTIMA URINE TRANSPORT TUBE (YELLOW)/STERILE CUP
-
Collection Instruction:
For male or female urine specimen: Patient should not have urinated for at least one hour prior to sampling. Patient should provide first-catch urine sample (approximately 20-30mL of initial urine stream) into a sterile urine collection cup. Specimen may be sent to lab in primary collection sterile urine cup, transferred to yellow cap vacutainer tube or transferred to Aptima urine transport tube according to printed instructions on APTIMA urine specimen collection kit packaging.
-
Transport Temperature:
Refrigerated
-
Stability:
Urine, sterile container: Room temperature or refrigerated 24 hour APTIMA urine specimen tube: Room temperature or refrigerated 30 days (Note: after testing, specimens are saved in the lab for 7 days.)
-
Schedule:
1-3 Days
-
Clinical Significance:
Trichomonas vaginalis infections cause vaginitis, urethritis and cervicitis. Discharge and small hemorrhagic lesions may be present in the genitourinary tract. Complications can include premature labor, low-birth-weight offspring, premature rupture of membranes and post-abortion or post-hysterectomy infection. An association with pelvic inflammatory disease, tubal infertility, and cervical cancer with previous episodes of trichomoniasis has been reported. Symptomatic women with trichomoniasis usually complain of vaginal discharge, vulvovaginal soreness and/or irritation. Dysuria is also common. However, it has been estimated that 10-50% of T. vaginalis infections in women are asymptomatic.
-
Performing Lab:
Simple Laboratories
TRIDAL (MEDICATION)
-
Test Name:
TRIDAL (MEDICATION)
-
Test Code:
501420
TRIGLYCERIDES
-
Test Name:
TRIGLYCERIDES
-
Test Code:
TRIG
-
CPT Code(s):
84478
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Patient should fast for 12 hours prior to collection, unless instructed differently by physician.
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 7 days Frozen: 3 months
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Triglyceride measurements are used in the diagnosis and treatment of patients with diabetes mellitus, nephrosis, liver obstruction, other diseases involving lipid metabolism, or various endocrine disorders.
-
Performing Lab:
Simple Laboratories
TRIMIPRAMINE (MEDICATION)
-
Test Name:
TRIMIPRAMINE (MEDICATION)
-
Test Code:
500480
Tryptase
-
Test Name:
Tryptase
-
Test Code:
R34484
-
CPT Code(s):
83520
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Samples should be obtained between 15 minutes and 3 hours after the event suspected of causing mast cell activation. When sample is drawn, separate serum from cells within 3 hours of collection.
-
Transport Temperature:
Refrigerated (cold-packs)
-
Stability:
Room temperature: Unacceptable Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Tryptase - This test may be used as a marker of mast cell activity. Tryptase is a serine protease released by mast cells constitutively (alpha-tryptase) and during activation (beta-tryptase). Serum measurement detects both forms and does not differentiate them [1]. Elevated basal tryptase levels are not uncommon and in most cases are due to hereditary alpha tryptasemia [2]. They are also seen in mastocytosis, other myeloid disorders, allergic disorders, chronic renal failure and some chronic infections [3]. Using tryptase to confirm anaphylaxis may require drawing the sample within 30 minutes - 6 hours of the suspected event and comparison with baseline levels drawn at least 24 hours after all signs and symptoms have resolved [4].
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
TSH (THYROID STIMULATING HORMONE)
-
Test Name:
TSH (THYROID STIMULATING HORMONE)
-
Test Code:
TSH
-
Alias:
Third Generation TSH Thyrotropin, Htsh
-
CPT Code(s):
84443
-
Preferred Specimen:
2.0 mL serum
-
Min. Volume:
.5 mL serum or plasma
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 18 hours Refrigerated: 7 days Frozen: 1 month
-
Schedule:
1-2 DAYS
-
Clinical Significance:
The principal clinical use for hTSH measurement is for the assessment of thyroid status. hTSH is measured to: 1) Exclude hypothyroidism (elevated levels of hTSH) or hyperthyroidism (depressed or nondetectable levels of hTSH). 2) Monitor T4 replacement treatment in primary hypothyroidism or antithyroid treatment in hyperthyroidism. 3) Follow T4 suppression of the trophic influence of hTSH is “cold nodules†and non-toxic goiter. 4) Assess the response to TRH stimulating testing. As more sensitive and precise methods become available, hTSH measurements are also increasingly used to identify subclinical or latent hypothyroidism or hyperthyroidism.
-
Performing Lab:
Simple Laboratories
TSH, REFLEX FREE T4
-
Test Name:
TSH, REFLEX FREE T4
-
Test Code:
013009
-
Alias:
hTSH Third Generation TSH Thyrotropin
-
CPT Code(s):
84443
-
Preferred Specimen:
2.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
Free T4: Will automatically run if the TSH is < 0.30 µIU/mL or > 5.33 µIU/mL
Additional charge/CPT code (84439) will apply. -
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: 1 month
-
Schedule:
1-2 DAYS
-
Clinical Significance:
The principal clinical use for hTSH measurement is for the assessment of thyroid status. hTSH is measured to: 1) Exclude hypothyroidism (elevated levels of hTSH) or hyperthyroidism (depressed or nondetectable levels of hTSH). 2) Monitor T4 replacement treatment in primary hypothyroidism or antithyroid treatment in hyperthyroidism. 3) Follow T4 suppression of the trophic influence of hTSH is “cold nodules” and non-toxic goiter. 4) Assess the response to TRH stimulating testing. As more sensitive and precise methods become available, hTSH measurements are also increasingly used to identify subclinical or latent hypothyroidism or hyperthyroidism.
-
Performing Lab:
Simple Laboratories
TSI (Thyroid Stimulating Immunoglobulin)
-
Test Name:
TSI (Thyroid Stimulating Immunoglobulin)
-
Test Code:
R30551
-
Alias:
Long Acting Thyroid Stimulator,Thyroid Stimulating Antibody,TSIG,Thyretain™,(LATS)
-
CPT Code(s):
84445
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: Unacceptable Refrigerated: 21 days Frozen: 60 days
-
Clinical Significance:
TSI (Thyroid Stimulating Immunoglobulin) - Graves' disease is a classic form of hyperthyroid disease, affecting approximately 0.4% of the population of the United States. It is caused by IgG immunoglobulins, collectively known as thyroid stimulating immunoglobulins (TSI). Patients who are candidates for antithyroid drug therapy may not respond to this treatment when TSI levels are markedly elevated. The determination of TSI can also assist in predicting hyperthyroidism in neonates, due to placental transmission of the immunoglobulins from a mother with hyperthyroidism.
-
Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
TYLENOL #3 (MEDICATION)
-
Test Name:
TYLENOL #3 (MEDICATION)
-
Test Code:
501590
TYLENOL #4 (MEDICATION)
-
Test Name:
TYLENOL #4 (MEDICATION)
-
Test Code:
501600
U
U/A (URINALYSIS WITH MICROSCOPIC) REFLEX CULTURE
-
Test Name:
U/A (URINALYSIS WITH MICROSCOPIC) REFLEX CULTURE
-
Test Code:
LS9006
-
Alias:
UA w/Micro, Reflex Culture
-
CPT Code(s):
81001
-
Test Includes:
Color, appearance, glucose, protein, bilirubin, pH, blood, ketones, nitrite, leukocytes, specific gravity, urobilinogen, and microscopic examination of urine
-
Preferred Specimen:
10.0 mL URINE
-
Min. Volume:
2.0 mL urine in urine preservative tube (speckled) and 3.0 mL urine in urine culture tube (gray)
-
Transport Container:
STERILE URINE CUP
-
Collection Instruction:
Collect urine using “clean catch” method into sterile container. Transfer specimen first into a urine culture tube (gray) and then into the urine preservative tube (speckled). Label all containers with the patient’s name, birthdate, date and time of collection. Please refer to separate patient instructions for “clean catch” urine instructions.
-
Transport Temperature:
Refrigerated
-
Stability:
Urine Preservative Tube (speckled): Refrigerated/Room Temp: 48 hours Urine Culture Tube (gray): Room temperature or refrigerated: 48 hours Urine Non-Preservative tube: 48 Hours
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Test results from a routine urinalysis may provide information regarding the status of carbohydrate metabolism, kidney and liver function, acid-base balance and urinary tract infection.
-
Performing Lab:
Simple Laboratories
UREA NITROGEN (BUN)
-
Test Name:
UREA NITROGEN (BUN)
-
Test Code:
BUN
-
Alias:
Blood Urea Nitrogen BUN
-
CPT Code(s):
84520
-
Preferred Specimen:
1.0 ML SERUM
-
Min. Volume:
0.5 ML SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 24 hours Refrigerated: 3 days Frozen: 2-3 months
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Measurements of urea nitrogen are used in the diagnosis and treatment of certain renal and metabolic disorders. Blood Urea Nitrogen (BUN) levels are a measure of kidney function and also of prerenal and postrenal conditions. Prerenal causes of elevated BUN include cardiac decompensation, water depletion or increased protein catabolism. Among the renal causes of increased levels are acute glomerulonephritis, chronic nephritis, polycystic kidney, nephrosclerosis, and tubular necrosis. Any type of obstruction of the urinary tract is a postrenal cause for elevated BUN levels. Both urea and creatinine are cleared by the renal glomeruli, however, urea is subsequently partially reabsorbed by the renal tubules, while creatinine is not. Consequently, serum urea nitrogen and serum creatinine determinations are frequently performed together in the differential diagnosis of kidney function.
-
Performing Lab:
Simple Laboratories
URIC ACID
-
Test Name:
URIC ACID
-
Test Code:
UA
-
CPT Code(s):
84550
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL SERUM OR PLASMA
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Refrigerated: 5 days
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Measurements of Uric Acid are used in the diagnosis and treatment of numerous renal and metabolic disorders, including renal failure, gout, leukemia, psoriasis, starvation or other wasting conditions, and of patients receiving cytotoxic drugs.
-
Performing Lab:
Simple Laboratories
URINALYSIS (UA)
-
Test Name:
URINALYSIS (UA)
-
Test Code:
LS5038
-
Alias:
U/A (URINALYSIS WITH MICROSCOPIC)
-
CPT Code(s):
81001
-
Test Includes:
Color, Appearance, glucose, protein, bilirubin, pH, blood, ketones, nitrite, leukocytes, specific gravity, urobilinogen, and microscopic examination of urine sediment
-
Preferred Specimen:
10.0 mL URINE
-
Min. Volume:
2.0 mL URINE
-
Transport Container:
STERILE URINE CUP
-
Collection Instruction:
Collect urine using “clean catch” method into sterile urine cup. Transfer specimen to urine non-preservative tube (yellow). Label container with the patient’s name, birthdate, date and time of collection. Refrigerate urine specimen collected in sterile cup if testing cannot be immediately performed.
Please refer to separate patient instructions for “clean catch” method instructions. -
Transport Temperature:
Refrigerated
-
Stability:
Sterile Cup: 48 hours refrigerated
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Routine urinalysis may provide information regarding the status of carbohydrate metabolism, kidney and liver function, acid-base balance and urinary tract infection.
-
Performing Lab:
Simple Laboratories
URINALYSIS W/ REFLEX TO UPP
-
Test Name:
URINALYSIS W/ REFLEX TO UPP
-
Test Code:
LS9004
-
CPT Code(s):
81001
-
Preferred Specimen:
10.0 mL URINE
-
Min. Volume:
2.0 mL URINE
-
Transport Container:
STERILE CUP
-
Collection Instruction:
Collect urine using “clean catch” method into sterile container. Transfer specimen first into a urine culture tube (gray) and then into the urine preservative tube (speckled) and the BD non-additive tube. Label all containers with the patient’s name, birthdate, date and time of collection. Please refer to separate patient instructions for “clean catch” urine instructions.
-
Transport Temperature:
Refrigerated
-
Schedule:
1-2 Days
-
Performing Lab:
Simple Laboratories
URINALYSIS W/ REFLEX TO UPP AND CULTURE
-
Test Name:
URINALYSIS W/ REFLEX TO UPP AND CULTURE
-
Test Code:
LS9005
-
CPT Code(s):
81001
-
Preferred Specimen:
10.0 mL URINE
-
Min. Volume:
2.0 mL URINE
-
Transport Container:
STERILE CUP
-
Collection Instruction:
Collect urine using “clean catch” method into sterile container. Transfer specimen first into a urine culture tube (gray) and then into the urine preservative tube (speckled) and the BD non-additive tube. Label all containers with the patient’s name, birthdate, date and time of collection. Please refer to separate patient instructions for “clean catch” urine instructions.
-
Transport Temperature:
Refrigerated
-
Schedule:
1-2 Days
-
Performing Lab:
Simple Laboratories
URINE PATHOGEN PANEL (PCR)
-
Test Name:
URINE PATHOGEN PANEL (PCR)
-
Test Code:
LS9002
-
Alias:
MOLECULAR UTI
-
CPT Code(s):
87481, 87640, 87653, 87150 x13, 87641, 87500, 87798 x13
-
Test Includes:
Staphylococcus aureus Acinetobacter baumannii Enterococcus faecalis Escherichia coli Klebsiella oxytoca Klebsiella pneumoniae Pseudomonas aeruginosa Enterobacter cloacae Proteus mirabilis Morganella morganii Citrobacter freundii Proteus vulgaris Klebsiella aerogenes Enterococcus faecium Mycoplasma hominis Ureaplasma urealyticun Providencia stuartii Serratia marcescens Staphylococcus saprophyticus Streptococcus agalactiae Candida tropicalis Candida krusei Candida albicans Candida glabrata Candida auris Candida lusitaniae Candida parapsilosis ampC mecA femA aph2 QnrB QnrA vanA1, vanA2 vanB NDM KPC OXA-48 VIM, IMP-7 SHV TEM CTX-M group 1 CTX-M group 2 mefA ErmA ErmB ant2 DfrA DfrA1 DfrA5 TetO Sul1 Sul2 GyrA ParC TetM TetB Antla
-
Preferred Specimen:
URINE
-
Transport Container:
STERILE CUP
-
Collection Instruction:
Don gloves and follow one of the sample collection methods below based upon the type of wound:
• Decubitus ulcer and other open wounds:
a. Roll the swab directly across the affected area until saturated.
b. Proceed to step 2.
• Abscess with intact skin:
a. Disinfect the area. Using a sterile needle/syringe, aspirate purulent material from abscess.
b. Transfer 0.3-0.5 mL of purulent material directly into molecular transport tube.
c. Proceed to step 5.
• Abscess with open skin/sinus tract:
a. Roll sterile swab within abscess/sinus with purulent material and ensure the swab is fully saturated.
b. Proceed to step 2.
• Joint Fluid:
a. Disinfect the area. Using a sterile needle/syringe, aspirate joint fluid.
b. Eject 0.3-0.5 mL of joint fluid directly into molecular transport tube.
c. Proceed to step 5.
• Vesicular dermatitis lesions:
a. Carefully open the lesion with a scalpel blade.
b. Collect fluid contents on the swab.
c. Thoroughly swab the base. The ‘roof tissue’ of the vesicle can be carefully removed, and submitted in
same MTM tube.
d. Place all material in the molecular collection tube.
e. Snap off excess handle and securely tighten tube cap.
f. Keep the tube in an upright position for 10 – 15 minutes.
• Cellulitis/Skin Rashes:
a. Preferred/Optional: Gently scrape the affected area with a sterile scalpel blade (not provided).
b. Vigorously swab the scraped/affected area with the swab.
c. Using the same swab, collect any material on the scalpel blade.
d. Proceed to step 2.
2. Place the swab in the molecular transport tube.
3. Swirl the swab in the solution 5 times.
4. Break the swab handle at the indentation mark and recap the tube retaining the swab in the tube.
5. Snap off excess handle and securely tighten top of the transport tube.
6. Keep the tube in an upright position for 10 – 15 minutes. -
Performing Lab:
Simple Laboratories
V
VAGINITIS PANEL
-
Test Name:
VAGINITIS PANEL
-
Test Code:
LS9009
-
CPT Code(s):
81513; 87661; 87481 (X2)
-
Test Includes:
Bacterial vaginosis (BV) Candida vaginitis (CV) Trichomonas vaginalis (TV)
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA MULTI-TEST SWAB (ORANGE)
-
Collection Instruction:
1. Open Aptima Multitest swab package (orange) and remove the swab. Do not touch the soft tip.
2. Hold the swab in the middle of the shaft at the score line.
3. Inser t the swab into the vagina about 2 inches and gently rotate the swab clockwise for 10-30 seconds.
4. While holding the swab, remove the cap from the tube. Do not spill the contents. If the contents of the tube are spilled, use a new Aptima Multitest kit.
5. Place the swab n the transport tube and break the swab shaft at the score line.
6. Tightly screw the cap onto the tube.
-
Transport Temperature:
Room Temperature or Refrigerated
-
Stability:
After collection, swab specimens in transport tubes can be stored at 2ºC to 30ºC for up to 30 days.
-
Schedule:
1-3 Days
-
Clinical Significance:
The Aptima BV assay is an in vitro nucleic acid amplification test that utilizes real time transcription-mediated amplification (TMA) for detection and quantitation of ribosomal RNA from bacteria associated with bacterial vaginosis (BV), including Lactobacillus (L. gasseri, L. crispatus, and L. jensenii), Gardnerella vaginalis, and Atopobium vaginae. The Aptima CV/TV assay is an in vitro nucleic acid amplification test for the detection of RNA from microorganisms associated with vulvovaginal candidiasis and trichomoniasis. The assay utilizes real time transcription-mediated amplification (TMA) to detect and qualitatively report results for the following organisms: • Candida species group (C. albicans, C. tropicalis, C. parapsilosis, C. dubliniensis) • Candida glabrata • Trichomonas vaginalis
-
Performing Lab:
Simple Laboratories
VAGINITIS PLUS (CT,GC,BV,CV,TV)
-
Test Name:
VAGINITIS PLUS (CT,GC,BV,CV,TV)
-
Test Code:
LS9008
-
CPT Code(s):
81513; 87481 (X2); 87661; 87491; 87591
-
Test Includes:
Bacterial vaginosis (BV) Candida vaginitis (CV) Trichomonas vaginalis (TV) Chlamydia trachomatis (CT) Neisseria gonorrhoeae (GC)
-
Preferred Specimen:
Vaginal swab using Aptima Multitest swab (orange) - Clinician-collected or self-collected Female endocervical swab in Aptima Unisex swab (white) Male urethral swab in Aptima Unisex swab (white) Male self collected urethral meatal swab in Aptima Multitest swab
-
Transport Container:
APTIMA MULTI-TEST SWAB (ORANGE)
-
Collection Instruction:
1. Open Aptima Multitest swab package (orange) and remove the swab. Do not touch the soft tip.
2. Hold the swab in the middle of the shaft at the score line.
3. Insert the swab into the vagina about 2 inches and gently rotate the swab clockwise for 10-30 seconds.
4. While holding the swab, remove the cap from the tube. Do not spill the contents. If the contents of the tube are spilled, use a new Aptima Multitest kit.
5. Place the swab n the transport tube and break the swab shaft at the score line.
6. Tightly screw the cap onto the tube.
-
Transport Temperature:
Room Temperature or Refrigerated
-
Stability:
After collection, swab specimens in transport tubes can be stored at 2-30C for up to 30 days
-
Schedule:
1-3 Days
-
Clinical Significance:
See Individual Tests
-
Performing Lab:
Simple Laboratories
VALIUM (MEDICATION)
-
Test Name:
VALIUM (MEDICATION)
-
Test Code:
501610
Valproic Acid
-
Test Name:
Valproic Acid
-
Test Code:
R916
-
CPT Code(s):
80164
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Collection Instruction:
Do not use gel barrier tubes. Centrifuge and immediately separate serum or plasma specimens from the cells into clean transport tube.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Valproic Acid - Valproic acid is used as an anticonvulsant to treat certain types of seizures, to prevent migraine headaches and to treat various psychiatric illnesses such as bipolar disorder and aggression. Drugs that compete for protein-binding sites with valproic acid can increase the concentration of valproic acid. Therapeutic drug monitoring is useful to optimize dose. Measurement of the free concentration is useful if toxicity is suspected.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
VANACOF CD (MEDICATION)
-
Test Name:
VANACOF CD (MEDICATION)
-
Test Code:
501360
Vancomycin
-
Test Name:
Vancomycin
-
Test Code:
R917
-
Alias:
Dipropylacetic Acid,Vanocin,Vancocin,Vancocine
-
CPT Code(s):
80202
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Vancomycin - Vancomycin is an antibiotic used in the treatment of serious bacterial infections, especially methicillin-resistant staphylococci. Vancomycin is also used in treatment for penicillin-allergic patients who cannot receive or have failed to respond to other drugs, including the penicillins and/or cephalosporins and for other infections caused by vancomycin-susceptible organisms.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Vancomycin, Trough
-
Test Name:
Vancomycin, Trough
-
Test Code:
R8579
-
Alias:
Dipropylacetic Acid,Vanocin,Vancocin,Vancocine
-
CPT Code(s):
80202
-
Preferred Specimen:
1 mL serum collected in a red-top tube (no gel)
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 72 hours Refrigerated: 7 days Frozen: Unacceptable
-
Clinical Significance:
Vancomycin, Trough - Vancomycin is an antibiotic used in the treatment of bacterial infections, especially methicillin-resistant staphylococci. Vancomycin is also used in treatment for penicillin-allergic patients who cannot receive or have failed to respond to other drugs, including the penicillins and/or cephalosporins and for other infections caused by vancomycin-susceptible organisms.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Varicella-Zoster Virus Antibodies (IgG, IgM)
-
Test Name:
Varicella-Zoster Virus Antibodies (IgG, IgM)
-
Test Code:
R34128
-
Alias:
Chicken Pox IgG and IgM Ab,Herpes Zoster IgG and IgM Ab,VZV Ab IgG and IgM
-
CPT Code(s):
86787
-
Test Includes:
4439, 8683
-
Preferred Specimen:
1.5 mL serum
-
Min. Volume:
1 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Varicella-Zoster Virus Antibodies (IgG, IgM)
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Varicella-Zoster Virus Antibody (IgG)
-
Test Name:
Varicella-Zoster Virus Antibody (IgG)
-
Test Code:
R4439
-
Alias:
Herpes Zoster IgG Ab,Varicella IgG Antibodies,VZV Antibody IgG,VZV IgG,Shingles,Chicken Pox
-
CPT Code(s):
86787
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Varicella-Zoster Virus Antibody (IgG) - Varicella-Zoster Virus (VZV) causes chicken pox and when reactivated, potentially decades later, causes shingles. Twenty percent of adults will develop shingles, a rash or blister of the skin that may cause severe pain. Varicella-Zoster IgG, EIA reliably measures immunity due to previous infection, but is unsuitable for detection of post-vaccination immune status.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
Varicella-Zoster Virus Antibody (IgM)
-
Test Name:
Varicella-Zoster Virus Antibody (IgM)
-
Test Code:
R8683
-
Alias:
Shingles,Herpes Zoster IgM,Chicken Pox IgM
-
CPT Code(s):
86787
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.2 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 4 days Refrigerated: 7 days Frozen: 30 days
-
Clinical Significance:
Varicella-Zoster Virus Antibody (IgM) - Varicella-Zoster Virus (VZV) causes chicken pox and when reactivated, potentially decades later, causes shingles. Twenty percent of adults will develop shingles, a rash or blister of the skin that may cause severe pain.
-
Performing Lab:
Quest Diagnostics - Great Lakes Region
VICODIN (MEDICATION)
-
Test Name:
VICODIN (MEDICATION)
-
Test Code:
501760
VICOPROFEN (MEDICATION)
-
Test Name:
VICOPROFEN (MEDICATION)
-
Test Code:
501770
Vitamin A (Retinol)
-
Test Name:
Vitamin A (Retinol)
-
Test Code:
R921
-
Alias:
Retinol
-
CPT Code(s):
84590
-
Preferred Specimen:
2 mL serum protected from light
-
Min. Volume:
0.7 mL
-
Transport Container:
Amber transport tube
-
Collection Instruction:
Allow blood to clot at room temperature for 30 minutes. Centrifuge to separate serum from the cells within 24 hours of collection and immediately pour serum into a plastic transport tube.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 24 hours Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Vitamin A (Retinol) - Vitamin A is critical for vision, growth, and many cell functions. High concentrations of Vitamin A are seen with renal failure, but this is not associated with toxicity and excessive ingestion. High concentrations are associated with bone fractures. Low concentrations of Vitamin A are consistent with fat malabsorption and are rarely due to inadequate diet.
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Performing Lab:
med fusion 2501 South State Hwy 121, Suite 1100 Lewisville, TX 75067-8188
Vitamin B1 (Thiamine), Blood, LC/MS/MS
-
Test Name:
Vitamin B1 (Thiamine), Blood, LC/MS/MS
-
Test Code:
R5042
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Alias:
Thiamine,B1
-
CPT Code(s):
84425
-
Preferred Specimen:
2 mL whole blood collected in an EDTA (lavender-top) tube - protected from light
-
Min. Volume:
1 mL
-
Transport Container:
Amber transport tube
-
Collection Instruction:
Transfer whole blood to amber transport tube. If amber tube is not available, wrap tube in aluminum foil to protect from light. Freeze immediately.
-
Transport Temperature:
Frozen
-
Stability:
Room temperature: 8 hours Refrigerated: 5 days Frozen: 35 days
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Clinical Significance:
Vitamin B1 (Thiamine), Blood, LC/MS/MS - Vitamin B1 is required for branched-chain amino acid and carbohydrate metabolism. Vitamin B1 deficiency is most often due to alcoholism or chronic illness. In the early stage, patients with vitamin B1 deficiency exhibit anorexia, irritability, apathy, and generalized weakness. Prolonged deficiency causes beriberi.
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Performing Lab:
med fusion 2501 South State Hwy 121, Suite 1100 Lewisville, TX 75067-8188
VITAMIN B12
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Test Name:
VITAMIN B12
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Test Code:
B12
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Alias:
B12 Cobalamin, True
-
CPT Code(s):
82607
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Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.5 mL serum or plasma This volume does not allow for repeat testing.
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
A fasting specimen is preferred. Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. The serum should be physically separated from contact with cells within two hours from the time of collection. If the specimen is collected in an anticoagulant tube, centrifuge and transfer plasma into a properly labeled transfer tube within 2 hours of collection.
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Transport Temperature:
Refrigerated
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Stability:
Room temperature: 8 hours Refrigerated: 5 days
-
Schedule:
1-2 Days
-
Clinical Significance:
Vitamin B12 is a coenzyme that is involved in two very important metabolic functions vital to normal cell growth and DNA synthesis. Deficiency of this vitamin can lead to megaloblastic anemia and ultimately to severe neurological problems. Vitamin B12 and folate are linked by the reaction pathway for methionine synthesis; a deficiency in either will disrupt this metabolic pathway and lead to the same symptoms and medical problems. It is usually necessary to measure both vitamins in a clinical work-up, with the treatment depending on which of the two is deficient.
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Performing Lab:
Simple Laboratories
Vitamin B6, Plasma
-
Test Name:
Vitamin B6, Plasma
-
Test Code:
R926
-
Alias:
Pyridoxal™,B6 Vitamin,Pyridoxal Phosphate
-
CPT Code(s):
84207
-
Preferred Specimen:
1 mL frozen plasma collected in an EDTA (lavender-top) tube - protected from light
-
Min. Volume:
0.5 mL
-
Transport Container:
Amber transport tube
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Collection Instruction:
Separate cells within 24 hours by centrifugation for 5-10 minutes. Transfer plasma to an amber polypropylene or polyethylene transport tube to protect from light. Alternately, neutral color polypropylene or polyethylene tube can be used if wrapped in aluminum foil. Freeze the tubes at -10 to -30° C. Ship frozen.
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Transport Temperature:
Frozen
-
Stability:
Room temperature: 72 hours Refrigerated: 5 days Frozen: 14 days Frozen -70° C: 42 days
-
Clinical Significance:
Vitamin B6, Plasma - Test is used to determine vitamin B6 deficiency or overdosage, for monitoring treatment, and to evaluate wellness and health.
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Performing Lab:
med fusion 2501 South State Hwy 121, Suite 1100 Lewisville, TX 75067-8188
VITAMIN D, 25-OH (TOTAL D2/D3)
-
Test Name:
VITAMIN D, 25-OH (TOTAL D2/D3)
-
Test Code:
VITADH
-
Alias:
Vitamin D 25-OH, 25-Hydroxycalciferol, 25-OH-D, Cholecalciferol Metabolite, Vitamin D, Vitamin D3 Metabolite
-
CPT Code(s):
82306
-
Preferred Specimen:
1.0 mL SERUM
-
Min. Volume:
0.3 mL SERUM
-
Transport Container:
SST (GOLD/TIGER)
-
Collection Instruction:
Allow specimen to completely clot (this can take up to 60 minutes). Centrifuge for 15 minutes. If the specimen is collected in a tube without a gel barrier, centrifuge and transfer the plasma into a properly labeled transfer tube within 2 hours of collection.
-
Transport Temperature:
Refrigerated
-
Stability:
Room temperature: 72 Hours Refrigerated: 7 days Frozen: 1 YEAR
-
Schedule:
1-2 DAYS
-
Clinical Significance:
Vitamin D 25(OH) determines the total 25-hydroxyvitamin D [25(OH) vitamin D] levels in human serum and plasma which is then used as an aid in the assessment of vitamin D sufficiency.
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Performing Lab:
Simple Laboratories
Vitamin E (Tocopherol)
-
Test Name:
Vitamin E (Tocopherol)
-
Test Code:
R931
-
Alias:
Tocopherol
-
CPT Code(s):
84446
-
Test Includes:
Vitamin E, Alpha-Tocopherol and Vitamin E, Beta-Gamma-Tocopherol
-
Preferred Specimen:
2 mL serum - protected from light
-
Min. Volume:
0.7 mL
-
Transport Container:
Amber transport tube
-
Collection Instruction:
Allow blood to clot at room temperature for 30 minutes. Centrifuge to separate serum from the cells within 24 hours of collection and immediately pour serum into a plastic transport tube.
-
Transport Temperature:
Refrigerated (cold packs)
-
Stability:
Room temperature: 24 hours Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Vitamin E (Tocopherol) - Deficiency of vitamin E may cause extensive neuropathy in young children and, in addition, is suspect as a possible cause of motor and sensory neuropathy in older children and in adults. One likely cause of vitamin E deficiency is intestinal malabsorption, resulting from bowel disease, pancreatic disease, or chronic cholestasis. Other causes of malabsorption of vitamin E include celiac disease, cystic fibrosis, and intestinal lymphangiectasia.
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Performing Lab:
med fusion 2501 South State Hwy 121, Suite 1100 Lewisville, TX 75067-8188
W
WHITE BLOOD CELLS (WBC), STOOL
-
Test Name:
WHITE BLOOD CELLS (WBC), STOOL
-
Test Code:
LS5046
-
Alias:
Fecal Leukocyte Stain Stool for White Cells WBC, Stool White Cells, Stool
-
CPT Code(s):
89055
-
Test Includes:
Evaluation of fecal material for the presence of WBC by direct smear and stain. CPT coding for microbiology and virology procedures often cannot be determined before the culture is performed.
-
Preferred Specimen:
STOOL
-
Transport Container:
STERILE CUP
-
Collection Instruction:
NULL
-
Transport Temperature:
Room Temperature
-
Performing Lab:
Simple Laboratories
WOUND PATHOGEN PANEL (PCR)
-
Test Name:
WOUND PATHOGEN PANEL (PCR)
-
Test Code:
LS9007
-
Alias:
MOLECULAR WOUND
-
CPT Code(s):
87150 (X10); 87798 (X13); 87653; 87641; 87500; 87651
-
Test Includes:
Acinetobacter baumannii Bacteroides fragilis Citrobacter freundii Clostridium novyi Clostridium perfringens Clostridium septicum Enterobacter cloacae Enterococcus faecalis Enterococcus faecium Escherichia coli Group A Strep Group B Strep Group C Strep Group G Strep Kingella kingae Klebsiella aerogenes Klebsiella oxytoca Klebsiella pneumoniae Morganella morganii Proteus mirabilis Proteus vulgaris Pseudomonas aeruginosa Staphylococcus aureus Staphylococcus aureus Staphylococcus epidermidis AmpC Resistance Marker (ampC) Methicillin Resistance Marker (mecA, femA) Quinolone and fluoroquinolone Resistance Marker (QnrB, QnrA) Vancomycin Resistance Marker (vanA1, vanA2, vanB) Carbapenem Resistance Marker (NDM, KPC, OXA-48, VIM, IMP-7) ESBL Resistance Marker (SHV, TEM, CTX-M Group 1, CTX M Group 2) Macrolide Resistance Marker ((mefA, ErmA, ErmB) Gentamicin Resistance Marker (aph2, ant2) Trimethaprim Resistance Marker (DfrA, DfrA1, DfrA5) Bactrim Resistance Marker (Sul1, Sul2) Quinolone Resistance Marker (GyrA, ParC) Aminoglycoside Resistance Marker (Antla, aph3)
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Preferred Specimen:
E-SWAB
-
Transport Container:
E-SWAB
-
Performing Lab:
Simple Laboratories
x
XANAX (MEDICATION)
-
Test Name:
XANAX (MEDICATION)
-
Test Code:
500710
Z
Z-TUSS (MEDICATION)
-
Test Name:
Z-TUSS (MEDICATION)
-
Test Code:
501290
Zinc
-
Test Name:
Zinc
-
Test Code:
R945
-
Alias:
ZN, Plasma
-
CPT Code(s):
84630
-
Preferred Specimen:
2 mL plasma collected in an EDTA or sodium heparin (royal blue-top) tube
-
Min. Volume:
0.7 mL
-
Transport Container:
Acid-washed or metal-free vial
-
Collection Instruction:
Separate plasma or serum from cells within 2 hours. Transfer separated plasma/serum to a plastic acid-washed or metal-free vial.
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 5 days Refrigerated: 10 days Frozen: 30 days
-
Clinical Significance:
Zinc - Zinc is an essential element involved in a myriad of enzyme systems including wound healing, immune function, and fetal development. Zinc measurements are used to detect and monitor industrial, dietary, and accidental exposure to zinc. Also, zinc measurements may be used to evaluate health and monitor response to treatment.
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Performing Lab:
Quest Diagnostics - Great Lakes Region
Zinc Transporter 8 (ZnT8) Antibody
-
Test Name:
Zinc Transporter 8 (ZnT8) Antibody
-
Test Code:
R93022
-
CPT Code(s):
86341
-
Preferred Specimen:
1 mL serum
-
Min. Volume:
0.5 mL
-
Transport Container:
Transport tube
-
Transport Temperature:
Room temperature
-
Stability:
Room temperature: 7 days Refrigerated: 7 days Frozen: 28 days
-
Clinical Significance:
Zinc Transporter 8 (ZnT8) Antibody - Key clinical use and differentiators Measurement of Zinc transporter type 8 (ZnT8) is used to: 1. Screen for presymptomatic T1D in individuals with a family history of type 1 diabetes (T1D) or those known to have a high-risk HLA genotype, 2. Distinguish between T1D, type 2 diabetes mellitus (T2D), and atypical forms of diabetes such as latent autoimmune diabetes in adults (LADA). Zinc transporter type 8 (ZnT8) is a transmembrane protein in the beta cell granule which is attacked by the ZnT8 antibody in patients with T1D. Intended Clinical Use This test is crucial for differentiating between T1D and T2D. It is important to note that classifying diabetes type can be challenging at the time of presentation, and misdiagnosis can occur in approximately 40% of adults with new T1D. [1] Identifying individuals affected by stage 1 T1D is important for applying eligibility criteria to drugs, such as Teplizumab, which have demonstrated the ability to delay the transition of stage 1 to stage 3 T1D in clinical trials. [2,3] ZnT8 has some distinctive features, including that its presence can improve risk stratification in individuals with single GADA+, IAA+ or IA-2A+ status. In one study, half of the children who developed ZnT8 developed diabetes within 5 years.[4] Limitations T1D is classified into three stages, with stages 1 and 2 considered presymptomatic. Since the presence of stage 1 and 2 T1D requires at least two islet autoantibodies, relying solely on ZnT8 as a screening test limits the ability to make an accurate diagnosis. Professional organizations, including the American Diabetes Association (ADA), recommend using tests for all four islet cell autoantibodies: IAA, glutamic acid decarboxylase (GAD65), Zinc Transporter 8 (ZnT8), and islet cell antigen 2 antibody (IA-2).[1]
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Performing Lab:
Quest Diagnostics Nichols Institute-San Juan Capistrano, CA 33608 Ortega Highway San Juan Capistrano, CA 92675-2042
ZOTEX-C (MEDICATION)
-
Test Name:
ZOTEX-C (MEDICATION)
-
Test Code:
501530