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10.1056/NEJMoa1715474

http://scihub22266oqcxt.onion/10.1056/NEJMoa1715474
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C5849140!5849140!29694816
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suck abstract from ncbi


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pmid29694816      N+Engl+J+Med ä ; 378 (17): 1583-92
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  • Mass azithromycin distribution for reducing childhood mortality in sub-Saharan Africa #MMPMID29694816
  • Keenan JD; Bailey RL; West SK; Arzika AM; Hart J; Weaver J; Kalua K; Mrango Z; Ray KJ; Cook C; Lebas E; O'Brien KS; Emerson PM; Porco TC; Leitman TM
  • N Engl J Med ä[]; 378 (17): 1583-92 PMID29694816show ga
  • Background.Interventions to reduce under-5 mortality can either target the vulnerable or include all children regardless of state of health. Here, we assess whether mass distribution of a broad-spectrum antibiotic to pre-school children reduces mortality in sub-Saharan Africa. Methods.MORDOR was a large simple trial that randomized communities in Malawi, Niger, and Tanzania to 4 biannual mass distributions of either oral azithromycin or placebo. Children aged 1-59 months were enumerated and offered treatment. Vital status was assessed at the subsequent biannual census. The primary outcome was aggregate all-cause mortality, with country-specific rates as pre-specified subgroup analyses. Results.In total, 1533 communities were randomized, 190,238 children censused at baseline, and 323,302 person-years monitored. Mean antibiotic coverage over the 4 biannual distributions was 90.4% (SD 10.4%) of the censused population. The overall annual mortality rate in placebo- treated communities was 16.5 per 1000 person-years (9.6 per 1000 person-years in Malawi, 27.5 in Niger, and 5.5 in Tanzania). Antibiotic-treated communities had an estimated 13.5% lower mortality overall (95% CI 6.7%?19.8%, P<0.001). Mortality was 5.7% lower in Malawi (CI - 9.7%?18.9%, P=0.45), 18.1% lower in Niger (CI 10.0%?25.5%, P<0.001), and 3.4% lower in Tanzania (CI -21.2%?23.0%, P=0.77). The greatest reduction was observed in 1-5 month-old children (24.9% lower, CI 10.6%?37.0%, P=0.001). Conclusions.Mass azithromycin distribution to post-neonatal, pre-school children may reduce childhood mortality in sub-Saharan Africa, particularly in high mortality areas such as Niger. Any implementation would need to consider selection for antibiotic resistance.
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