Evidence map›Paper›PMID 37092059›Full record

Trial reportAfrican health sciences2022

HIV genotypic resistance among pregnant women initiating ART in Uganda: a baseline evaluation of participants in the Option B+ clinical trial.

Alexander Amone, Priscilla Wavamunno, Grace Gabagaya, Gordon Rukundo, Joyce Namale-Matovu, Samuel S Malamba, Irene Lubega, Jaco Homsy, Rachel King, Clemensia Nakabiito and 3 more

Open access · diamondAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in African health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Trial
  2. Review
  3. 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

13 authors at 5 institutions in 2 countries.

Alexander AmoneMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Priscilla WavamunnoMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Grace GabagayaMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Gordon RukundoMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Joyce Namale-MatovuMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Samuel S MalambaUganda Virus Research Institute, Entebbe, Uganda.
Irene LubegaMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Jaco HomsyInstitute for Global Health Sciences, University of California, San Francisco, CA, USA.
Rachel KingInstitute for Global Health Sciences, University of California, San Francisco, CA, USA.
Clemensia NakabiitoMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Monica NolanMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Mary Glenn FowlerMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
Philippa MusokeMakerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
MUJHU Research Collaboration · UGUniversity of California, San Francisco · USJohns Hopkins University · USMakerere University · UGUganda Virus Research Institute · UG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pre-treatment HIV drug resistance is a threat to elimination of mother to child HIV transmission and could lead to virological failure among HIV-positive pregnant women. We analysed genotypic HIV drug resistance (HIVDR) of baseline samples of participants enrolled in the Option B+ clinical trial in Uganda. Methods: HIV-infected pregnant women attending antenatal care were enrolled from Uganda's National Referral Hospital (Mulago) and Mityana District general hospital and surrounding health centers (HCs). Genotypic HIV testing was performed on blood samples from the first 135 enrolled women out of a subset of 136 participants (25%) who had a baseline VL>1000 copies/mL as one sample failed to amplify. Results: 159/540 (29.4%) had a VL < 1000 copies/ml and 381/540 (70.6%) had a VL >1,000 copies/ml. Of the women with VL>1000 copies/ml, 32 (23.7%) had resistance mutations including 29/135 (21.5%) NNRTI mutations, 6/135 (4.4%) NRTI mutations and 3/135 (2.2%) had both NNRTI and NRTI mutations. The most common NNRTI resistance mutations were: K103KN (5), K103N (5), V179T (4) and E138A (4). Conclusions: One quarter of the HIV-infected pregnant women in this trial at baseline had NNRTI genotypic resistance mutations. Our findings support new WHO guidelines for first-line ART that were changed to dolutegravir-based regimens.

Indexed as

Anti-HIV AgentsDrug Resistance, ViralHIV-1HIV InfectionsInfectious Disease Transmission, VerticalPregnancy Complications, InfectiousFemaleHumansMutationPregnancyPrenatal CareUgandaViral LoadAnti-HIV Agents

Identifiers

PMID37092059
PMCPMC10117495
OpenAlexW4323059701

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.