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Mass azithromycin distribution and nutritional status among children aged 1-59 months: a secondary analysis of a cluster randomized trial

Ouattara, M.; Hu, H.; Bountogo, M.; Coulibaly, B.; Boudo, V.; Compaore, G.; Dah, C.; Lebas, E.; O'Brien, K. S.; Arnold, B. F.; Lietman, T. M.; Sie, A.; Oldenburg, C. E.

2025-08-19 pediatrics
10.1101/2025.08.17.25333846 medRxiv
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BackgroundTwice yearly distribution of azithromycin has been shown to reduce all-cause child mortality in several contexts. Azithromycin likely reduces mortality via reduction in clinical or subclinical infections. Treating infections may improve child nutritional status to further reduce mortality risk. Here, we used data from a placebo-controlled cluster randomized trial of azithromycin for prevention of child mortality in Burkina Faso to evaluate the effects of twice-yearly azithromycin on mid-upper arm circumference (MUAC) in children aged 1-59 months and weight-for-age Z-score (WAZ) in infants aged 1-11 months. MethodsThe Child Health with Azithromycin Trial (CHAT) was a 1:1 cluster randomized trial of twice-yearly azithromycin compared to matching placebo for prevention of all-cause mortality in children aged 1-59 months. MUAC measurements were collected in all children at the time of treatment. Weight measurements were collected in infants aged 1-11 months to calculate weight-based dosing. We evaluated MUAC and WAZ at the community level and longitudinally at the individual child level, accounting for the cluster randomized design of the trial. Results80,282 children aged 1-59 months and 26,983 infants aged 1-11 months in 284 communities were included in analyses. At the community level, we found no evidence of a difference in mean MUAC or WAZ after 36 months or over time. There was no evidence of a difference in change over time in MUAC (P-value for interaction = 0.94) or WAZ (P=0.18) at the individual level. ConclusionsWe found no evidence to support an effect of twice-yearly mass azithromycin distribution on measures of undernutrition in children in this setting in Burkina Faso. Trial RegistrationClinicalTrials.gov NCT03676764

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