• Jeremy D Keenan, Ahmed M Arzika, Ramatou Maliki, Nameywa Boubacar, Sanoussi Elh Adamou, Maria Moussa Ali, Catherine Cook, Elodie Lebas, Ying Lin, Kathryn J Ray, Kieran S O'Brien, Thuy Doan, Catherine E Oldenburg, E Kelly Callahan, Paul M Emerson, Travis C Porco, and Thomas M Lietman.
• From the Francis I. Proctor Foundation (J.D.K., C.C., E.L., Y.L., K.J.R., K.S.O., T.D., C.E.O., T.C.P., T.M.L.), the Departments of Ophthalmology (J.D.K., T.D., C.E.O., T.C.P., T.M.L.) and Epidemiology and Biostatistics (K.J.R., C.E.O., T.C.P., T.M.L.), and the Institute for Global Health Sciences (C.E.O., T.M.L.), University of California, San Francisco, San Francisco, and the University of California, Berkeley, School of Public Health, Berkeley (K.S.O.) - both in California; and the Carter Center (A.M.A., R.M., N.B., S.E.A., M.M.A., E.K.C.) and Emory University (P.M.E.), Atlanta, and the International Trachoma Initiative, Decatur (P.M.E.) - all in Georgia.
• N. Engl. J. Med. 2019 Jun 6; 380 (23): 2207-2214.

BackgroundThe MORDOR I trial (Macrolides Oraux pour Réduire les Décès avec un Oeil sur la Résistance) showed that in Niger, mass administration of azithromycin twice a year for 2 years resulted in 18% lower postneonatal childhood mortality than administration of placebo. Whether this benefit could increase with each administration or wane owing to antibiotic resistance was unknown.MethodsIn the Niger component of the MORDOR I trial, we randomly assigned 594 communities to four twice-yearly distributions of either azithromycin or placebo to children 1 to 59 months of age. In MORDOR II, all these communities received two additional open-label azithromycin distributions. All-cause mortality was assessed twice yearly by census workers who were unaware of participants' original assignments.ResultsIn the MORDOR II trial, the mean (±SD) azithromycin coverage was 91.3±7.2% in the communities that received twice-yearly azithromycin for the first time (i.e., had received placebo for 2 years in MORDOR I) and 92.0±6.6% in communities that received azithromycin for the third year (i.e., had received azithromycin for 2 years in MORDOR I). In MORDOR II, mortality was 24.0 per 1000 person-years (95% confidence interval [CI], 22.1 to 26.3) in communities that had originally received placebo in the first year and 23.3 per 1000 person-years (95% CI, 21.4 to 25.5) in those that had originally received azithromycin in the first year, with no significant difference between groups (P = 0.55). In communities that had originally received placebo, mortality decreased by 13.3% (95% CI, 5.8 to 20.2) when the communities received azithromycin (P = 0.007). In communities that had originally received azithromycin and continued receiving it for an additional year, the difference in mortality between the third year and the first 2 years was not significant (-3.6%; 95% CI, -12.3 to 4.5; P = 0.50).ConclusionsWe found no evidence that the effect of mass administration of azithromycin on childhood mortality in Niger waned in the third year of treatment. Childhood mortality decreased when communities that had originally received placebo received azithromycin. (Funded by the Bill and Melinda Gates Foundation; ClinicalTrials.gov number, NCT02047981.).Copyright © 2019 Massachusetts Medical Society.

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