Evidence map›Paper›PMID 32852361›Full record

Trial reportJournal of acquired immune deficiency syndromes (1999)2020

Brief Report: Cessation of Long-Term Cotrimoxazole Prophylaxis in HIV-Infected Children Does Not Alter the Carriage of Antimicrobial Resistance Genes.

Freddy Francis, Ethan K Gough, Thaddeus J Edens, Chipo Berejena, Mutsawashe Bwakura-Dangarembizi, Annie Shonhai, Kusum J Nathoo, Magdalena Glass, Diana M Gibb, Andrew J Prendergast and 1 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of acquired immune deficiency syndromes (1999), 2020. 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 39% 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, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

11 authors at 6 institutions in 4 countries.

Freddy FrancisDepartment of Medicine, Experimental Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Ethan K GoughDepartment of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Thaddeus J EdensDevil's Staircase Consulting, BC Centre for Disease Control, West Vancouver, British Columbia, Canada.
Chipo BerejenaUniversity of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
Mutsawashe Bwakura-DangarembiziUniversity of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
Annie ShonhaiUniversity of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
Kusum J NathooUniversity of Zimbabwe College of Health Sciences, Harare, Zimbabwe.
Magdalena GlassSchool of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
Diana M GibbMRC Clinical Trials Unit at University College London, London, United Kingdom.
Andrew J PrendergastBlizard Institute, Queen Mary University of London, London, United Kingdom.
Amee R MangesSchool of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
University of Zimbabwe · ZWBC Centre for Disease Control · CAUniversity of British Columbia · CAJohns Hopkins University · USMRC Clinical Trials Unit at UCL · GBZvitambo Institute for Maternal and Child Health Research · ZW

Funding

CIHRMedical Research Council G0300400Medical Research Council G1001190Medical Research Council MC_UU_12023/26Wellcome TrustWellcome Trust 093768/Z/10/ZWellcome Trust 108065/Z/15/Z
6 · The paper itself

Abstract

backgroundCotrimoxazole (CTX) is a broad-spectrum antimicrobial, combining trimethoprim and sulfamethoxazole. CTX prophylaxis reduces mortality and morbidity among people living with HIV in regions with high prevalence of bacterial infections and malaria. The Antiretroviral research for Watoto trial evaluated the effect of stopping versus continuing CTX prophylaxis in sub-Saharan Africa.

methodsIn this study, 72 HIV-infected Zimbabwean children, on antiretroviral therapy, provided fecal samples at 84 and 96 weeks after randomization to continue or stop CTX. DNA was extracted for whole metagenome shotgun sequencing, with sequencing reads mapped to the Comprehensive Antibiotic Resistance Database to identify CTX and other antimicrobial resistance genes.

resultsThere were minimal differences in the carriage of CTX resistance genes between groups. The dfrA1 gene, conferring trimethoprim resistance, was significantly higher in the continue group (P = 0.039) and the tetA(P) gene conferring resistance to tetracycline was significantly higher in the stop group (P = 0.013). CTX prophylaxis has a role in shaping the resistome; however, stopping prophylaxis does not decrease resistance gene abundance.

conclusionsNo differences were observed in resistance gene carriage between the stop and continue groups. The previously shown multi-faceted protective effects of CTX in antiretroviral research for Watoto trial clinical outcomes are not outweighed by the risk of multi-drug resistance gene selection due to prophylaxis. These findings are reassuring, given current recommendations for long-term CTX prophylaxis among children living with HIV in sub-Saharan Africa to decrease mortality and morbidity.

Indexed as

Anti-Bacterial AgentsAnti-Infective AgentsChildChild, PreschoolDrug Resistance, MicrobialFemaleGastrointestinal MicrobiomeHIV InfectionsHumansMaleTrimethoprim, Sulfamethoxazole Drug CombinationZimbabweAnti-Bacterial AgentsAnti-Infective AgentsTrimethoprim, Sulfamethoxazole Drug Combination

Identifiers

PMID32852361
PMCPMC7654951
OpenAlexW3080141863

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.