Evidence map›Paper›PMID 34481464›Full record

Trial reportBMC infectious diseases2021

Prevalence of undetectable and suppressed viral load in HIV-infected pregnant women initiating Option B+ in Uganda: an observational study nested within a randomized controlled trial.

Grace Gabagaya, Gordon Rukundo, Alexander Amone, Priscilla Wavamunno, Joyce Namale-Matovu, Irene Lubega, Clemensia Nakabiito, Zikulah Namukwaya, Monica Nolan, Samuel S Malamba and 4 more

Registry-linked trialOpen access · goldAbstract readObservational StudyRandomized Controlled Trial
In one paragraph

Trial report in BMC infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02515370 (Using Enhanced Peer Group Strategies to Support Prevention of Mother to Child HIV Transmission), which is not on this map. Cited by 13 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 4 pooled it
1.3field-weighted citation impact, top 17% 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.

NCT02515370 nacompletednot on this map

Using Enhanced Peer Group Strategies to Support Prevention of Mother to Child HIV Transmission (PMTCT) Option B+ in Uganda

TypeinterventionalSponsorMU-JHU CARERan2016 to 2020Enrolled540ConditionsHuman Immunodeficiency VirusArmsFriends for Life Circles (FLCs).
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 4 syntheses or guidelines pooled it, 22 citations in OpenAlex.

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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

14 authors at 5 institutions in 2 countries.

Grace GabagayaMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Gordon RukundoMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Alexander AmoneMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Priscilla WavamunnoMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Joyce Namale-MatovuMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Irene LubegaMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Clemensia NakabiitoMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Zikulah NamukwayaMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Monica NolanMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda.
Samuel S MalambaUganda Virus Research Institute, Entebbe, Uganda.
Rachel KingInstitute for Global Health Sciences, University of California, San Francisco, USA.
Jaco HomsyInstitute for Global Health Sciences, University of California, San Francisco, USA.
Mary Glenn FowlerDepartment of Pathology, Johns Hopkins University, School of Medicine, Baltimore, USA.
Philippa MusokeMakerere University - Johns Hopkins University Research Collaboration, P.O. Box 23491, Kampala, Uganda. pmusoke@mujhu.org.
MUJHU Research Collaboration · UGGlobal Brain Health Institute · USJohns Hopkins University · USMakerere University · UGUganda Virus Research Institute · UG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundViral load (VL) testing is key in monitoring adherence to antiretroviral therapy (ART) and documenting HIV treatment response. As per HIV treatment guidelines in Uganda, the first VL test is recommended 6 months after initiation of ART. Undetectable VL (uVL) at ART initiation may be helpful in detecting elite controllers in the absence of previous ART use. We investigated viral suppression at ART initiation among a cohort of HIV-positive pregnant women enrolled in the Friends for Life Circles (FLC) for Option B+ randomized controlled trial (RCT).

methodsPregnant women ≥ 18 years of age testing positive for HIV at their first antenatal care visit and starting on ART Option B+ as per the National PMTCT Program guidelines were enrolled into the FLC for Option B+ RCT in urban Kampala and rural Mityana districts of Uganda. Each participant had whole blood samples collected at enrolment to assess baseline VL. Plasma HIV-1 RNA was quantified using COBAS Ampliprep /COBAS Taqman. Baseline VL below 400 RNA copies/ml was considered as viral suppression while baseline VL below 20 RNA copies/ml was considered uVL.

resultsThe mean duration from the date of ART initiation to time of sample collection for baseline VL assessment was 4.4 days (SD 3.6). Of the 532 HIV-positive pregnant women enrolled in the FLC for Option B+ study and newly starting Option B+ without a self-reported history of prior ART use, 29 (5.5%) had uVL and 113 (21.4%) had suppressed VL at baseline. There was no association between participants' age, gravidity, marital status, mean monthly income, educational level, disclosure of HIV status to partner, and uVL or viral suppression at baseline. However, non-disclosure of HIV status to any other person was associated with decreased odds of viral suppression at baseline (OR 0.640; 0.416-0.982).

conclusionTwenty-one percent of HIV-positive Ugandan pregnant women initiating ART (Option B+) showed virological suppression at baseline and were presumed to be "elite controllers" or to have misreported being ART-naive. Further studies are needed to better understand the biologic mechanisms of elite controllers among pregnant women as well as to differentiate elite controllers from concealed ART use. Trial Registration The trial was registered as NCT02515370 (04/08/2015) on Clinicaltrials.gov.

Indexed as

Anti-HIV AgentsHIV InfectionsPregnancy Complications, InfectiousFemaleHumansPregnancyPregnant PeoplePrevalenceUgandaViral LoadAnti-HIV AgentsAntiretroviral therapyHIVHIV transmissionOption B+PregnancyUgandaViral loadViral or virological suppression

Identifiers

PMID34481464
PMCPMC8417996
OpenAlexW3198112944

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.