ReviewPLOS global public health2026
Azithromycin mass drug administration to reduce childhood mortality in humanitarian crises.
Review in PLOS global public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Azithromycin mass drug administration (MDA) can reduce under-5 mortality in stable but high-mortality settings, yet its potential in humanitarian crises remains undefined. This review proposes that azithromycin MDA could support existing humanitarian interventions and help address mortality from respiratory and gastrointestinal infections in displaced populations. Mortality rates in crises frequently exceed WHO recommended thresholds for initiating MDA. Operationally, the MDA is feasible, low-cost, and synergises with existing relief efforts like vaccination. While antimicrobial resistance (AMR) is a serious concern, the proposed use, likely a single round or short-term intervention during acute emergencies, may mitigate long-term resistance selection compared to routine biannual dosing. The potential to rapidly reduce excess mortality may outweigh the AMR risks. Azithromycin MDA represents a promising new tool for humanitarian health, though evidence-based protocols and resistance monitoring strategies must be developed through further research.
Identifiers
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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.