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  Vol. 302 No. 9, September 2, 2009 TABLE OF CONTENTS
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Effect of Mass Distribution of Azithromycin for Trachoma Control on Overall Mortality in Ethiopian Children

A Randomized Trial

Travis C. Porco, PhD, MPH; Teshome Gebre, MBA; Berhan Ayele, MSc; Jenafir House, MPH; Jeremy Keenan, MD; Zhaoxia Zhou, BS; Kevin Cyrus Hong, BS; Nicole Stoller, MPH; Kathryn J. Ray, MA; Paul Emerson, PhD; Bruce D. Gaynor, MD; Thomas M. Lietman, MD

JAMA. 2009;302(9):962-968.

Context  Mass oral azithromycin distribution to affected communities is a cornerstone of the World Health Organization's trachoma elimination program. Antibiotics are provided to target the ocular strains of chlamydia that cause trachoma, but may also be efficacious against respiratory disease, diarrhea, and malaria—frequent causes of childhood mortality in trachoma-endemic areas.

Objective  To compare mortality rates of participants aged 1 to 9 years in treated communities with those in untreated communities.

Design, Setting, and Participants  We conducted a cluster-randomized clinical trial of mass azithromycin administration for trachoma control. Forty-eight communities (known as subkebeles) were randomized into 1 of 3 treatment schedules (annual treatment of all residents [15 902 participants], biannual treatment of all residents [17 288 participants], or quarterly treatment of children only [14 716 participants]) or into 1 group for which treatment was delayed by 1 year (control, 18 498 participants). Twelve subkebeles were randomized to each of the 4 schedules with all children in each of the 3 communities being eligible for treatment. The trial was conducted in a field setting in rural Ethiopia, May 2006 to May 2007.

Interventions  A single dose of oral azithromycin (adults, 1 g; children, 20 mg/kg) was administered for treatment of ocular Chlamydia trachomatis infection. Antibiotic coverage levels for children aged 1 to 9 years exceeded 80% at all visits.

Main Outcome Measure  The main outcome measure was the community-specific mortality risk for children aged 1 to 9 years over the course of 1 year. Mortality was measured by enumerative census at baseline and again after 1 year. Comparison of the risk of mortality was a prespecified outcome for the clinical trial.

Results  The odds ratio for childhood mortality in the intervention communities was 0.51 (95% confidence interval, 0.29-0.90; P = .02; clustered logistic regression) compared with the control group. In the treated communities, the estimated overall mortality rate during this period for children aged 1 to 9 years in the untreated group was 8.3 per 1000 person-years (95% confidence interval, 5.3-13.1), while among the treated communities, the estimated overall mortality rate was 4.1 per 1000 person-years (95% confidence interval, 3.0-5.7) for children aged 1 to 9 years.

Conclusion  In a trachoma-endemic area, mass distribution of oral azithromycin was associated with reduced mortality in children.

Trial Registration  clinicaltrials.gov Identifier: NCT00322972


Author Affiliations: F.I. Proctor Foundation (Drs Porco, Gaynor, Keenan, and Lietman, Mss House, Zhou, Stoller, and Ray and Mr Hong), Departments of Ophthalmology (Drs Porco, Gaynor, Keenan, and Lietman, and Ms Zhou) and Epidemiology and Biostatistics (Drs Porco and Lietman), Institute for Global Health (Dr Lietman), University of California, San Francisco; Carter Center, Ethiopia-USA (Messrs Gebre and Ayele and Dr Emerson).



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