Evidence map›Paper›PMID 34820609›Full record

ArticleEClinicalMedicine2021

Effect of azithromycin on incidence of acute respiratory exacerbations in children with HIV taking antiretroviral therapy and co-morbid chronic lung disease: a secondary analysis of the BREATHE trial.

Amy Price, Grace McHugh, Victoria Simms, Robina Semphere, Lucky G Ngwira, Tsitsi Bandason, Hilda Mujuru, Jon O Odland, Rashida A Ferrand, Andrea M Rehman

Open access · goldAbstract read
In one paragraph

Article in EClinicalMedicine, 2021. 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
1.1field-weighted citation impact, top 22% 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, 7 citations in OpenAlex.

  1. Trial
  2. HIV-associated lung disease.Nature reviews. Disease primers · 2023
    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

10 authors at 4 institutions in 5 countries.

Amy PriceDepartment of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK.
Grace McHughBiomedical Research and Training Institute, Harare, Zimbabwe.
Victoria SimmsBiomedical Research and Training Institute, Harare, Zimbabwe.
Robina SemphereDepartment of Microbiology & HNTI, College of Medicine, Blantyre, Malawi.
Lucky G NgwiraMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
Tsitsi BandasonBiomedical Research and Training Institute, Harare, Zimbabwe.
Hilda MujuruMalawi-Liverpool-Wellcome Trust Clinical Research Programme, Blantyre, Malawi.
Jon O OdlandFaculty of Health Sciences, UiT, The Arctic University of Norway, Tromsø, Norway.
Rashida A FerrandDepartment of Clinical Research, London School of Hygiene & Tropical Medicine, London, UK.
Andrea M RehmanMRC International Statistics and Epidemiology Group, Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.
London School of Hygiene & Tropical Medicine · GBBiomedical Research and Training Institute · ZWUniversity of Liverpool · GBUniversity of Pretoria · ZA

Funding

Medical Research Council MR/R010161/1
6 · The paper itself

Abstract

backgroundIn the BREATHE trial weekly azithromycin decreased the rate of acute respiratory exacerbations (AREs) compared to placebo among children and adolescents with HIV-associated chronic lung disease (CLD) taking antiretroviral therapy (ART). The aim of this analysis was to identify risk factors associated with AREs and mediators of the effect of azithromycin on AREs.

methodsThe primary outcome of this analysis was the rate of AREs by study arm up to 49 weeks. We analysed rates using Poisson regression with random intercepts. Interaction terms were fitted for potential effect modifiers. Participants were recruited from Zimbabwe and Malawi between15 June 2016 and 4 September 2018.

findingsWe analysed data from 345 participants (171 allocated to azithromycin and 174 allocated to placebo). Rates of AREs were higher among those with an abnormally high respiratory rate at baseline (adjusted rate ratio (aRR) 2.08 95% CI 1.10-3.95 p-value 0.02) and among those with a CD4 cell count <200 cells/mm

interpretationThese may represent subgroups who may benefit the most from treatment with weekly azithromycin, which could help guide targeted treatment.

fundingThere was no funding source for this post hoc analysis.

Identifiers

PMID34820609
PMCPMC8599092
OpenAlexW3213270355

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.