Childhood mortality in a cohort treated with mass azithromycin for trachoma
- PMID: 21427395
- PMCID: PMC3106233
- DOI: 10.1093/cid/cir069
Childhood mortality in a cohort treated with mass azithromycin for trachoma
Abstract
Background: Mass azithromycin distributions are used to clear ocular strains of chlamydia that cause trachoma, but treatments may also affect respiratory infections, diarrhea, and malaria. Here, we monitor a large cohort in which almost 90% of individuals received azithromycin. We assess whether receiving treatment is associated with reduced all-cause and infectious childhood mortality.
Methods: As part of a clinical trial for trachoma, a census was conducted in 24 communities in rural Ethiopia. All individuals ≥1 year of age were eligible for single-dose oral azithromycin, although antibiotic coverage was not universal. A follow-up census was performed 26 months after treatment to estimate all-cause mortality among children 1-5 years of age, and verbal autopsies were performed to identify infectious mortality.
Results: The cohort included 35,052 individuals ≥1 year of age and 5507 children 1-5 years of age, of whom 4914 received a dose of azithromycin. All-cause mortality was significantly lower among those 1-5-year-old children who received azithromycin (odds ratio [OR]=0.35 [95% confidence interval {CI}, 0.17-0.74]), as was infectious mortality (OR=0.20 [95% CI, 0.07-0.58]). When individuals were compared only with members of the same household, azithromycin treatment was still associated with reduced all-cause mortality in children 1-5 years of age (OR=0.40 [95% CI, 0.16-0.96]), although this relationship was not statistically significant for infectious mortality (OR=0.35 [95% CI, 0.10-1.28]).
Conclusions: This study demonstrated an association between mass oral azithromycin treatment and reduced all-cause and infectious childhood mortality. This relationship could not be attributed to bias at the level of the household. Mass azithromycin distributions may have benefits unrelated to trachoma.
Trial registration: ClinicalTrials.gov NCT00322972.
© The Author 2011. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved.
Comment in
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Thinking deeper about important mass treatment trials.Clin Infect Dis. 2012 Jun;54(11):1674-5. doi: 10.1093/cid/cis241. Epub 2012 Mar 19. Clin Infect Dis. 2012. PMID: 22431805 Free PMC article. No abstract available.
References
-
- Solomon A, Zondervan M, Kuper H, Buchan J, Mabey D, Foster A. Trachoma control: a guide for programme managers. Geneva, Switzerland: World Health Organization; 2006.
-
- Wright HR, Turner A, Taylor HR. Trachoma. Lancet. 2008;371:1945–54. - PubMed
-
- Schachter J, West SK, Mabey D, et al. Azithromycin in control of trachoma. Lancet. 1999;354:630–5. - PubMed
-
- Chidambaram JD, Alemayehu W, Melese M, et al. Effect of a single mass antibiotic distribution on the prevalence of infectious trachoma. JAMA. 2006;295:1142–6. - PubMed
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