IVF Male Panel, Donor

Test Overview

Test Methodology

Immunoassay (IA) • Hemagglutination • Nucleic Acid Amplification • Transcription Mediated-Amplification (TMA)

Reference Range*

By Report

* Reference ranges may change over time. Please refer to the original patient report when evaluating results.

Test Details

Analytic Time

12 - 14 days

Soft Order Code

QIVFM

MiChart Code

QIVFM

Laboratory

Sendout

Laboratory Reference

Quest Valencia (93306)

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Specimen Requirements

Offsite Collection Instructions

Collect sufficient tubes to ensure required volumes can be obtained once the specimen has been spun and separated. Spin, aliquot (AND label as serum or plasma) into plastic screw capped aliquots. Send to Specimen Processing, along with the urine, refrigerated.

Container

Normal Volume

6 mL serum AND 6 mL plasma AND 2 mL random urine in Aptima

Minimum Volume

4 mL serum AND 4 mL plasma AND 2 mL random urine in Aptima

Additional Information

Test includes: Donor, C. trachomatis/N. gonorrhoeae, RNA, TMA; Donor, HIV-1/-2 plus O Antibody Screen; Donor, Hepatitis B Surface Antigen Reflex to Confirm; Donor, Hepatitis B core Total Antibody; Donor, Hepatitis C Antibody (Anti-HCV); Donor, HIV-1/HBV/HCV NAT Procleix® with Reflex to HIV-1/HBV/HCV Discriminatory; Donor, West Nile Virus NAT; Donor, HTLV-I/II Antibody Screen; Donor, Cytomegalovirus (CMV) Total Antibodies; Donor, Syphilis IgG Antibody

If the Donor, Hepatitis B Surface Antigen is reactive, then Donor, Hepatitis B Surface Antigen, Confirmation will be performed at an additional charge (CPT code: 87341).
If Donor, HIV-1/HBV/HCV/NAT Procleix® with Reflex is reactive, then the Donor, HIV-1 Discriminatory (CPT code: 87535), Donor, HBV Discriminatory (CPT code: 87516), and Donor, HCV Discriminatory (CPT code: 87521) will be performed at an additional charge.