Effect of a single dose of oral azithromycin on malaria parasitaemia in children: a randomized controlled trial.


Journal

Malaria journal
ISSN: 1475-2875
Titre abrégé: Malar J
Pays: England
ID NLM: 101139802

Informations de publication

Date de publication:
31 Aug 2021
Historique:
received: 09 03 2021
accepted: 25 08 2021
entrez: 1 9 2021
pubmed: 2 9 2021
medline: 5 11 2021
Statut: epublish

Résumé

Azithromycin has recently been shown to reduce all-cause childhood mortality in sub-Saharan Africa. One potential mechanism of this effect is via the anti-malarial effect of azithromycin, which may help treat or prevent malaria infection. This study evaluated short- and longer-term effects of azithromycin on malaria outcomes in children. Children aged 8 days to 59 months were randomized in a 1:1 fashion to a single oral dose of azithromycin (20 mg/kg) or matching placebo. Children were evaluated for malaria via thin and thick smear and rapid diagnostic test (for those with tympanic temperature ≥ 37.5 °C) at baseline and 14 days and 6 months after treatment. Malaria outcomes in children receiving azithromycin versus placebo were compared at each follow-up timepoint separately. Of 450 children enrolled, 230 were randomized to azithromycin and 220 to placebo. Children were a median of 26 months and 51% were female, and 17% were positive for malaria parasitaemia at baseline. There was no evidence of a difference in malaria parasitaemia at 14 days or 6 months after treatment. In the azithromycin arm, 20% of children were positive for parasitaemia at 14 days compared to 17% in the placebo arm (P = 0.43) and 7.6% vs. 5.6% in the azithromycin compared to placebo arms at 6 months (P = 0.47). Azithromycin did not affect malaria outcomes in this study, possibly due to the individually randomized nature of the trial. Trial registration This study is registered at clinicaltrials.gov (NCT03676751; registered 19 September 2018).

Sections du résumé

BACKGROUND BACKGROUND
Azithromycin has recently been shown to reduce all-cause childhood mortality in sub-Saharan Africa. One potential mechanism of this effect is via the anti-malarial effect of azithromycin, which may help treat or prevent malaria infection. This study evaluated short- and longer-term effects of azithromycin on malaria outcomes in children.
METHODS METHODS
Children aged 8 days to 59 months were randomized in a 1:1 fashion to a single oral dose of azithromycin (20 mg/kg) or matching placebo. Children were evaluated for malaria via thin and thick smear and rapid diagnostic test (for those with tympanic temperature ≥ 37.5 °C) at baseline and 14 days and 6 months after treatment. Malaria outcomes in children receiving azithromycin versus placebo were compared at each follow-up timepoint separately.
RESULTS RESULTS
Of 450 children enrolled, 230 were randomized to azithromycin and 220 to placebo. Children were a median of 26 months and 51% were female, and 17% were positive for malaria parasitaemia at baseline. There was no evidence of a difference in malaria parasitaemia at 14 days or 6 months after treatment. In the azithromycin arm, 20% of children were positive for parasitaemia at 14 days compared to 17% in the placebo arm (P = 0.43) and 7.6% vs. 5.6% in the azithromycin compared to placebo arms at 6 months (P = 0.47).
CONCLUSIONS CONCLUSIONS
Azithromycin did not affect malaria outcomes in this study, possibly due to the individually randomized nature of the trial. Trial registration This study is registered at clinicaltrials.gov (NCT03676751; registered 19 September 2018).

Identifiants

pubmed: 34465327
doi: 10.1186/s12936-021-03895-9
pii: 10.1186/s12936-021-03895-9
pmc: PMC8407066
doi:

Substances chimiques

Antimalarials 0
Azithromycin 83905-01-5

Banques de données

ClinicalTrials.gov
['NCT03676751']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

360

Subventions

Organisme : Bill and Melinda Gates Foundation
ID : OPP1187628
Organisme : Research to Prevent Blindness
ID : Research to Prevent Blindness

Informations de copyright

© 2021. The Author(s).

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Auteurs

Boubacar Coulibaly (B)

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

Ali Sié (A)

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

Clarisse Dah (C)

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

Mamadou Bountogo (M)

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

Mamadou Ouattara (M)

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

Adama Compaoré (A)

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

Moustapha Nikiema (M)

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

Jérôme Nankoné Tiansi (JN)

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

Nestor Dembélé Sibiri (ND)

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

Jessica M Brogdon (JM)

Francis I Proctor Foundation, University of California, San Francisco, 490 Illinois St, Floor 2, San Francisco, CA, 94143, USA.

Elodie Lebas (E)

Francis I Proctor Foundation, University of California, San Francisco, 490 Illinois St, Floor 2, San Francisco, CA, 94143, USA.

Thuy Doan (T)

Francis I Proctor Foundation, University of California, San Francisco, 490 Illinois St, Floor 2, San Francisco, CA, 94143, USA.
Department of Ophthalmology, University of California, San Francisco, San Francisco, CA, USA.

Travis C Porco (TC)

Francis I Proctor Foundation, University of California, San Francisco, 490 Illinois St, Floor 2, San Francisco, CA, 94143, USA.
Department of Ophthalmology, University of California, San Francisco, San Francisco, CA, USA.

Thomas M Lietman (TM)

Francis I Proctor Foundation, University of California, San Francisco, 490 Illinois St, Floor 2, San Francisco, CA, 94143, USA.
Department of Ophthalmology, University of California, San Francisco, San Francisco, CA, USA.
Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, USA.

Catherine E Oldenburg (CE)

Francis I Proctor Foundation, University of California, San Francisco, 490 Illinois St, Floor 2, San Francisco, CA, 94143, USA. catherine.oldenburg@ucsf.edu.
Department of Ophthalmology, University of California, San Francisco, San Francisco, CA, USA. catherine.oldenburg@ucsf.edu.
Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, USA. catherine.oldenburg@ucsf.edu.

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Classifications MeSH