Abstract

BackgroundBiannual distribution of azithromycin to children 1–59 months old reduced mortality by 14% in a cluster-randomized trial. The World Health Organization has proposed targeting this intervention to the subgroup of children 1–11 months old to reduce selection for antimicrobial resistance. Here, we describe a trial designed to determine the impact of age-based targeting of biannual azithromycin on mortality and antimicrobial resistance.MethodsAVENIR is a cluster-randomized, placebo-controlled, double-masked, response-adaptive large simple trial in Niger. During the 2.5-year study period, 3350 communities are targeted for enrollment. In the first year, communities in the Dosso region will be randomized 1:1:1 to 1) azithromycin 1–11: biannual azithromycin to children 1–11 months old with placebo to children 12–59 months old, 2) azithromycin 1–59: biannual azithromycin to children 1–59 months old, or 3) placebo: biannual placebo to children 1–59 months old. Regions enrolled after the first year will be randomized with an updated allocation based on the probability of mortality in children 1–59 months in each arm during the preceding study period. A biannual door-to-door census will be conducted to enumerate the population, distribute azithromycin and placebo, and monitor vital status. Primary mortality outcomes are defined as all-cause mortality rate (deaths per 1000 person-years) after 2.5 years from the first enrollment in 1) children 1–59 months old comparing the azithromycin 1–59 and placebo arms, 2) children 1–11 months old comparing the azithromycin 1–11 and placebo arm, and 3) children 12–59 months in the azithromycin 1–11 and azithromycin 1–59 arms. In the Dosso region, 50 communities from each arm will be followed to monitor antimicrobial resistance. Primary resistance outcomes will be assessed after 2 years of distributions and include 1) prevalence of genetic determinants of macrolide resistance in nasopharyngeal samples from children 1–59 months old, and 2) load of genetic determinants of macrolide resistance in rectal samples from children 1–59 months old.DiscussionAs high-mortality settings consider this intervention, the results of this trial will provide evidence to support programmatic and policy decision-making on age-based strategies for azithromycin distribution to promote child survival.Trial registrationThis trial was registered on January 13, 2020 (clinicaltrials.gov: NCT04224987).

Highlights

  • Biannual distribution of azithromycin to children 1–59 months old reduced mortality by 14% in a cluster-randomized trial

  • As high-mortality settings consider this intervention, the results of this trial will provide evidence to support programmatic and policy decision-making on age-based strategies for azithromycin distribution to promote child survival

  • Targeted approaches to azithromycin distribution have been proposed to focus benefits on subgroups at the highest risk of mortality while limiting the amount of antibiotics distributed, theoretically reducing the risks posed by the intervention

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Summary

Introduction

Biannual distribution of azithromycin to children 1–59 months old reduced mortality by 14% in a cluster-randomized trial. With estimates at 108 deaths per 1000 livebirths [1], under-5 mortality in Niger is more than 4 times the SDG target of 25 deaths per 1000 livebirths [3] In such high mortality settings, effective and feasible interventions are urgently needed. Azithromycin distribution has been proposed as a stop-gap intervention to reduce the burden of preventable deaths in high mortality settings while health systems are strengthened. The Macrolides Oraux pour Réduire les Décès avec un Œil sur la Résistance trial (MORDOR) later demonstrated that biannual distribution of oral azithromycin to children 1–59 months of age reduced mortality in this age group by 13.5% in Malawi, Niger, and Tanzania (95% CI 6.7 to 19.8) [9]. The exact mechanism of effect remains unclear, evidence suggests that azithromycin distributions reduce the burden of respiratory infections, diarrhea, and malaria [10], common causes of under-5 mortality in sub-Saharan Africa [1]

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