Prenatal Reflexive Panel
Ordering Recommendation
New York DOH Approval Status
Specimen Required
Lavender (EDTA) or pink (K2EDTA) AND serum separator tube.
Transport One 3 mL EDTA (Min: 0.5 mL) AND one 7 mL EDTA (Min: 3 mL) whole blood in original containers AND Transfer two 2 mL aliquots serum to individual ARUP Standard Transport Tubes (Min: 2 mL each tube)
Whole Blood: Refrigerated.
Serum: Refrigerated.
Frozen whole blood. Clotted whole blood.
Whole Blood: Ambient: 8 hours; Refrigerated: 24 hours; Frozen: Unacceptable
Serum: Ambient: Unacceptable; Refrigerated: 1 week; Frozen; 1 year
Methodology
Automated Cell Count/Differential/Semi-Quantitative Quantitative Charcoal Agglutination/Qualitative Chemiluminescent Immunoassay/Semi-Quantitative Quantitative Chemiluminescent Immunoassay/Hemagglutination/Solid Phase Agglutination
Performed
Mon-Fri
Reported
1-3 days
Reference Interval
Refer to Report.
Interpretive Data
FDA
Note
If RPR is weakly reactive or reactive, then a titer will be added. If Antibody Screen is positive, then Antibody Identification will be added. If results for Hepatitis B Virus Surface Antigen, Prenatal are reactive, then Hepatitis B Virus Surface Antigen Confirmation, Prenatal will be added. Additional charges apply.
Hotline History
CPT Codes
86592; 86762; 86900; 86901; 86850; 85025; 87340; if reflexed, add 86593; 86870; 86880; 86906; 87341
Components
Component Test Code* | Component Chart Name | LOINC |
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Aliases
- Prenatal Panel A