Evidence map›Paper›PMID 40257829›Full record

Trial reportThe Journal of infectious diseases2025

Impact of Macrolide Resistance on Azithromycin for Prevention of Rehospitalization or Death Among Children Discharged From Hospitals in Western Kenya.

Polycarp Mogeni, John Benjamin Ochieng, Hannah E Atlas, Kirkby D Tickell, Doreen Rwigi, Kevin Kariuki, Laura Riziki Aluoch, Catherine Sonye, Evans Apondi, Lilian Ambila and 8 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02414399 (Azithromycin to Prevent Post-discharge Morbidity and Mortality in Kenyan Children), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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.

NCT02414399 phase4unknown statusnot on this map

Azithromycin to Prevent Post-discharge Morbidity and Mortality in Kenyan Children

TypeinterventionalSponsorUniversity of WashingtonRan2016 to 2025Enrolled1,400ConditionsPneumonia, Diarrhea, Malaria, Co-infectionArmsAzithromycin, Placebo
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  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

18 authors.

Polycarp MogeniCenter for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.ORCID 0000-0003-1926-7576
John Benjamin OchiengCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Hannah E AtlasDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Kirkby D TickellDepartment of Global Health, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-4108-1236
Doreen RwigiCenter for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.ORCID 0000-0002-0215-1887
Kevin KariukiCenter for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.ORCID 0000-0001-6586-1504
Laura Riziki AluochCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.ORCID 0009-0006-9956-7737
Catherine SonyeCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Evans ApondiCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Lilian AmbilaCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Mame M DiakhateDepartment of Global Health, University of Washington, Seattle, Washington, USA.
Benson O SingaCenter for Clinical Research, Kenya Medical Research Institute, Nairobi, Kenya.
Jie LiuSchool of Public Health, Qingdao University, Qingdao, China.ORCID 0000-0003-2658-5249
James A Platts-MillsDivision of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia, USA.ORCID 0000-0002-4956-0418
Ferric C FangDivision of Allergy and Infectious Diseases, Department of Medicine, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-3243-110X
Judd L WalsonDepartment of Global Health, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-4836-720X
Eric R HouptDivision of Infectious Diseases and International Health, Department of Medicine, University of Virginia, Charlottesville, Virginia, USA.
Patricia B PavlinacDepartment of Global Health, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-0051-9131

Funding

Mechanisms of post-discharge morbidity and mortality in HIV-infected and HIV-exposed uninfected childrenR01HD079695 · NICHD · UNIVERSITY OF WASHINGTON · PI WALSON, JUDD L. · 2015 to 2019
$3.8M
The role of enteric pathogens and antimicrobial resistance in driving clinical and nutritional deterioration, and azithromycin's potential effect, among children discharged from hospital in KenyaR01AI150978 · NIAID · UNIVERSITY OF WASHINGTON · PI PAVLINAC, PATRICIA · 2020 to 2024
$3.7M
Eunice Kennedy Shriver National Institute of Child Health and Human DevelopmentNational Institute of Allergy and Infectious DiseasesNIAID NIH HHS R01 AI150978NICHD NIH HHS R01 HD079695NIH HHS 1R01AI150978NIH HHS R01HD079695
6 · The paper itself

Abstract

backgroundThe Toto Bora trial tested whether a 5-day course of azithromycin reduced the risk of rehospitalization or death in the 6 months following hospitalization among Kenyan children and found no overall benefit. We hypothesized that macrolide resistance in gut microbes could modify azithromycin's effect.

methodsFrom June 2016 to November 2019, Kenyan children aged 1-59 months were enrolled at hospital discharge and randomized to azithromycin or placebo. DNA from fecal samples and Escherichia coli isolates was analyzed for common macrolide resistance genes. Cox proportional hazards regression models, including interaction terms between randomization arm and individual macrolide resistance genes, were used to analyze time to rehospitalization or death, with Bonferroni correction applied to account for multiple comparisons.

resultsAmong 1393 children tested, 94.7% had at least 1 macrolide resistance gene in their fecal DNA at hospital discharge, most commonly mph(A) (68.6% [955/1393]), followed by msr(D) (67.3% [937/1393]) and erm(B) (60.7% [846/1393]). Mef(A) (23.7% [330/1393]) was the only macrolide resistance gene that modified azithromycin's effect on rehospitalization or death (interaction P = .008). In children without the mef(A) gene, azithromycin reduced the hazard of rehospitalization or death by a third (hazard ratio [HR], 0.66 [95% confidence interval {CI}, .45-.99]) whereas among children with the mef(A) gene, there was a higher risk in those randomized to azithromycin (HR, 2.72 [95% CI, 1.21-6.09]). The effect size of azithromycin's impact on mortality and rehospitalization as separate outcomes in children with and without mef(A) were consistent but underpowered.

conclusionsMacrolide resistance in the gut microbiome may influence the efficacy of azithromycin in children discharged from the hospital. Clinical Trials Registration. NCT02414399.

Indexed as

Anti-Bacterial AgentsAzithromycinDrug Resistance, BacterialMacrolidesPatient ReadmissionChild, PreschoolEscherichia coliFecesFemaleGastrointestinal MicrobiomeHumansInfantKenyaMalePatient DischargeAnti-Bacterial AgentsAzithromycinMacrolidesazithromycingut microbiomehospitalmacrolide resistancemortalitypostdischarge

Identifiers

PMID40257829
PMCPMC12349937

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.