Comparing Azithromycin to Amoxicillin in the Management of Uncomplicated Severe Acute Malnutrition in Burkina Faso: A Pilot Randomized Trial

Author:

O’Brien Kieran1,Sié Ali2,Dah Clarisse2,Ourohiré Millogo2,Ouedraogo Moussa2,Boudo Valentin2,Arzika Ahmed3,Lebas Elodie1,Nyatigo Fanice1,Godwin William1,Kelly John1,Arnold Benjamin14,Oldenburg Catherine145

Affiliation:

1. 1Francis I Proctor Foundation, University of California, San Francisco, California;

2. 2Centre de Recherche en Santé de Nouna, Nouna, Burkina Faso;

3. 3Centre de Recherche et Interventions en Santé Publique, Niamey, Niger;

4. 4Department of Ophthalmology, University of California, San Francisco, California;

5. 5Department of Epidemiology & Biostatistics, University of California, San Francisco, California

Abstract

Azithromycin is a promising alternative to amoxicillin in the management of uncomplicated severe acute malnutrition (SAM) as it can be administered as a single dose and has efficacy against several pathogens causing infectious disease and mortality in children under 5. In this pilot trial, we aimed to establish the feasibility of a larger randomized controlled trial and provide preliminary evidence comparing the effect of azithromycin to amoxicillin on weight gain in children with uncomplicated SAM. We enrolled children 6–59 months old with uncomplicated SAM at six healthcare centers in Burkina Faso. Participants were randomized to a single dose of azithromycin or a 7-day course of amoxicillin and followed weekly until nutritional recovery and again at 8 weeks. Apart from antibiotics, participants received standard of care, which includes ready-to-use therapeutic food. Primary feasibility outcomes included enrollment potential, refusals, and loss to follow-up. The primary clinical outcome was weight gain (g/kg/day) over 8 weeks. Outcome assessors were masked. Between June and October 2020, 312 children were screened, 301 were enrolled with zero refusals, and 282 (93.6%) completed the 8-week visit. Average weight gain was 2.5 g/kg/day (standard deviation [SD] 2.0) in the azithromycin group and 2.6 (SD 1.7) in the amoxicillin group (mean difference −0.1, 95% CI −0.5 to 0.3, P = 0.63). Fewer adverse events were reported in the azithromycin group (risk ratio 0.50, 95% CI 0.31–0.82, P = 0.006). With strong enrollment and follow-up, a fully powered trial in this setting is feasible.

Publisher

American Society of Tropical Medicine and Hygiene

Subject

Virology,Infectious Diseases,Parasitology

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