Evidence map›Paper›PMID 31876868›Full record

ArticleSexually transmitted diseases2020

Three Years of Shared Service HIV Nucleic Acid Testing for Public Health Laboratories: Worthwhile for HIV-1 but Not for HIV-2.

Linda M Styer, Anne M Gaynor, Monica M Parker, S Berry Bennett, Laura G Wesolowski, Steven Ethridge, Pollyanna R Chavez, Timothy J Sullivan, Salvacion Fordan, Kelly Wroblewski

Open access · greenAbstract read
In one paragraph

Article in Sexually transmitted diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Linda M StyerFrom the Wadsworth Center, New York State Department of Health, Albany, NY.
Anne M GaynorAssociation of Public Health Laboratories, Silver Spring, MD.
Monica M ParkerFrom the Wadsworth Center, New York State Department of Health, Albany, NY.
S Berry BennettFlorida Department of Health, Bureau of Public Health Laboratories, Jacksonville, FL.
Laura G WesolowskiDivision of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, GA.
Steven EthridgeDivision of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, GA.
Pollyanna R ChavezDivision of HIV/AIDS Prevention, Centers for Disease Control and Prevention, Atlanta, GA.
Timothy J SullivanFrom the Wadsworth Center, New York State Department of Health, Albany, NY.
Salvacion FordanFlorida Department of Health, Bureau of Public Health Laboratories, Jacksonville, FL.
Kelly WroblewskiAssociation of Public Health Laboratories, Silver Spring, MD.
Centers for Disease Control and Prevention · USAssociation of Public Health Laboratories · USFlorida Department of Health · USNew York State Department of Health · USWadsworth Center · US

Funding

Intramural CDC HHS CC999999OSELS CDC HHS U60 OE000103
6 · The paper itself

Abstract

backgroundIn 2016, HIV-2 nucleic acid testing (NAT) was added to a shared service program that conducts HIV-1 NAT for public health laboratories performing the recommended algorithm for diagnosing HIV. Here, we evaluate the usefulness of HIV-2 NAT in this program as compared with HIV-1 NAT.

methodsSpecimens eligible for HIV-1 NAT were reactive on an HIV-1/2 antibody or antigen/antibody initial test and nonreactive or indeterminate on a supplemental antibody test or were reactive for HIV-1 antigen-only on an HIV-1/2 antigen/antibody initial test. Specimens eligible for HIV-2 NAT were reactive on an initial test, HIV-2 indeterminate or HIV indeterminate on a supplemental antibody test and had no detectable HIV-1 RNA or were reactive for HIV-2 antibody on an HIV-1/2 antigen/antibody test, and this reactivity was not confirmed with a supplemental antibody assay. All specimens were tested in a reference laboratory using APTIMA HIV-1 qualitative RNA and/or a validated qualitative HIV-2 RNA real-time PCR assay.

resultsDuring 2016 to 2019, HIV-1 RNA was detected in 234 (14%) of 1731 specimens tested. HIV-2 RNA was not detected in 52 specimens tested. Median time from specimen collection to reporting of HIV-1 and HIV-2 NAT results by year ranged from 9 to 10 days and from 22 to 27 days, respectively. Two specimens with HIV-2 indeterminate results on a supplemental antibody test had detectable HIV-1 RNA.

conclusionsA shared service model for HIV-1 NAT is both feasible and beneficial for public health laboratories. However, because no HIV-2 infections were detected, our data suggest that this program should reconsider the usefulness of HIV-2 NAT testing.

Indexed as

AlgorithmsDiagnostic Tests, RoutineHIV-1HIV-2HIV InfectionsHumansLaboratoriesMass ScreeningNucleic Acid Amplification TechniquesPublic HealthReal-Time Polymerase Chain ReactionRNA, ViralSensitivity and SpecificityVirologyRNA, Viral

Identifiers

PMID31876868
PMCPMC10949347
OpenAlexW2998731471

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.