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. Author manuscript; available in PMC: 2024 Mar 19.
Published in final edited form as: Sex Transm Dis. 2020 May;47(5):S8–S12. doi: 10.1097/OLQ.0000000000001123

TABLE 2.

HIV Test Results Obtained at Reference Laboratories and turnaround time for Results in the NAT Referral Program, US, 2016–2019

Year*
2016–2017 2017–2018 2018–2019
No. submitting laboratories 27 28 29
HIV-1 NAT
 No. eligible specimens received and tested at reference laboratories 547 541 643
 No. HIV-1 NAT reactive (% of specimens tested) 77 (14%) 84 (16%) 73 (11%)
HIV-2 NAT
 No. eligible specimens received and tested at reference laboratories 17 11 24
 No. HIV-2 NAT reactive 0 0 0
TAT: median, d
 Specimen collection to receipt in submitting laboratory 1 1 1
 Receipt in submitting laboratory to shipment to reference laboratory 6 5 4
 Shipment to reference laboratory to receipt in reference laboratory 1 1 1
 Receipt in reference laboratory to HIV-1 NAT performed and reported 1 1 1
 Specimen collection to HIV-1 NAT reported 10 9 9
 HIV-1 NAT performed to HIV-2 NAT performed and reported 13 19 10.5
 Specimen collection to HIV-2 NAT reported 22 27 22
 Specimen collection to HIV-1 NAT, % within 1 wk 18% 21% 25%
 Specimen collection to HIV-1 NAT, % within 2 wk 73% 84% 87%
*

Specimens tested in reference laboratories from July 1 to June 30 of indicated years.

Either (1) HIV-1/2 antibody or HIV Ag/Ab reactive (repeatedly) and supplemental antibody negative or indeterminate or (2) BioPlex HIV-1 Ag reactive (repeatedly) only.

Either (1) HIV-1/2 antibody or HIV Ag/Ab reactive (repeatedly), supplemental antibody HIV indeterminate or HIV-2 indeterminate, HIV-1 RNA not detected or (2) BioPlex HIV Undifferentiated or HIV-2 antibody reactive and supplemental antibody nonreactive.