Distance to Health Centers and Effectiveness of Azithromycin Mass Administration for Children in Niger
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Published:2023-12-15
Issue:12
Volume:6
Page:e2346840
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ISSN:2574-3805
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Container-title:JAMA Network Open
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language:en
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Short-container-title:JAMA Netw Open
Author:
Chao Dennis L.1, Arzika Ahmed M.2, Abdou Amza3, Maliki Ramatou2, Karamba Alio2, Galo Nasser2, Beidi Diallo2, Harouna Nasser2, Abarchi Moustapha2, Root Elisabeth1, Mishra Anu1, Lebas Elodie4, Arnold Benjamin F.45, Oldenburg Catherine E.46, Keenan Jeremy D.45, Lietman Thomas M.4567, O’Brien Kieran S.456
Affiliation:
1. Bill & Melinda Gates Foundation, Seattle, Washington 2. Centre de Recherche et Interventions en Santé Publique, Birni N’Gaoure, Niger 3. Programme Nationale de Santé Oculaire, Niamey, Niger 4. Francis I. Proctor Foundation, University of California, San Francisco 5. Department of Ophthalmology, University of California, San Francisco 6. Department of Epidemiology and Biostatistics, University of California, San Francisco 7. Institute for Global Health Sciences, University of California, San Francisco
Abstract
ImportanceThe MORDOR (Macrolides Oraux pour Réduire les Décès avec un Oeil sur la Résistance) trial demonstrated that mass azithromycin administration reduced mortality by 18% among children aged 1 to 59 months in Niger. The identification of high-risk subgroups to target with this intervention could reduce the risk of antimicrobial resistance.ObjectiveTo evaluate whether distance to the nearest primary health center modifies the effect of azithromycin administration to children aged 1 to 59 months on child mortality.Design, Setting, and ParticipantsThe MORDOR cluster randomized trial was conducted from December 1, 2014, to July 31, 2017; this post hoc secondary analysis was conducted in 2023 among 594 clusters (communities or grappes) in the Boboye and Loga departments in Niger. All children aged 1 to 59 months in eligible communities were evaluated.InterventionsBiannual (twice-yearly) administration of a single dose of oral azithromycin or matching placebo over 2 years.Main Outcomes and MeasuresA population-based census was used to monitor mortality and person-time at risk (trial primary outcome). Community distance to a primary health center was calculated as kilometers between the center of each community and the nearest health center. Negative binomial regression was used to evaluate the interaction between distance and the effect of azithromycin on the incidence of all-cause mortality among children aged 1 to 59 months.ResultsBetween December 1, 2014, and July 31, 2017, a total of 594 communities were enrolled, with 76 092 children (mean [SD] age, 31 [2] months; 39 022 [51.3%] male) included at baseline, for a mean (SD) of 128 (91) children per community. Median (IQR) distance to the nearest primary health center was 5.0 (3.2-7.1) km. Over 2 years, 145 693 person-years at risk were monitored and 3615 deaths were recorded. Overall, mortality rates were 27.5 deaths (95% CI, 26.2-28.7 deaths) per 1000 person-years at risk in the placebo arm and 22.5 deaths (95% CI, 21.4-23.5 deaths) per 1000 person-years at risk in the azithromycin arm. For each kilometer increase in distance in the placebo arm, mortality increased by 5% (adjusted incidence rate ratio, 1.05; 95% CI, 1.03-1.07; P < .001). The effect of azithromycin on mortality varied significantly by distance (interaction P = .02). Mortality reduction with azithromycin compared with placebo was 0% at 0 km from the health center (95% CI, −19% to 17%), 4% at 1 km (95% CI, −12% to 17%), 16% at 5 km (95% CI, 7% to 23%), and 28% at 10 km (95% CI, 17% to 38%).Conclusions and RelevanceIn this secondary analysis of a cluster randomized trial of mass azithromycin administration for child mortality, children younger than 5 years who lived farthest from health facilities appeared to benefit the most from azithromycin administration. These findings may help guide the allocation of resources to ensure that those with the least access to existing health resources are prioritized in program implementation.Trial RegistrationClinicalTrials.gov Identifier: NCT02047981
Publisher
American Medical Association (AMA)
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