Cause-specific mortality of children younger than 5 years in communities receiving biannual mass azithromycin treatment in Niger: verbal autopsy results from a cluster-randomised controlled trial.


Journal

The Lancet. Global health
ISSN: 2214-109X
Titre abrégé: Lancet Glob Health
Pays: England
ID NLM: 101613665

Informations de publication

Date de publication:
02 2020
Historique:
received: 31 05 2019
revised: 31 10 2019
accepted: 03 12 2019
entrez: 26 1 2020
pubmed: 26 1 2020
medline: 4 7 2020
Statut: ppublish

Résumé

The Macrolides Oraux pour Réduire les Décès avec un Oeil sur la Résistance (MORDOR) trial found that biannual mass distribution of azithromycin to children younger than 5 years in Niger reduced the primary outcome of all-cause mortality by 18%. We aimed to determine the causes of mortality among deceased children using verbal autopsy. In this 2-year cluster-randomised controlled trial, 594 community clusters in Niger were randomly allocated (1:1 ratio) to receive biannual mass distributions of either oral azithromycin (approximately 20 mg per kg of bodyweight) or placebo targeted to children aged 1-59 months. Participants, study investigators, and field workers were masked to treatment allocation. Between Nov 23, 2014, and July 31, 2017, 3615 child deaths were recorded by use of biannual house-to-house censuses, and verbal autopsies were done between May 26, 2015, and May 17, 2018, to identify cause of death. Cause-specific mortality, as assessed by verbal autopsy, was a prespecified secondary outcome. This trial is completed and is registered with ClinicalTrials.gov, NCT02047981. Between Nov 23, 2014, and July 31, 2017, 303 communities (n=40 375 children at baseline) in Niger received mass azithromycin and 291 communities (n=35 747 children at baseline) received placebo. Treatment coverage was 90·3% (SD 10·6) in the azithromycin group and 90·4% (10·1) in the placebo group. No communities were lost to follow-up. In total, 1727 child deaths in the azithromycin group and 1888 child deaths in the placebo group were reported from the population censuses. Of these, the cause of death for 1566 (90·7%) children in the azithromycin group and 1735 (91·9%) children in the placebo group were ascertained by verbal autopsy interviews. In the azithromycin group, 437 (27·9%) deaths were due to malaria, 252 (16·1%) deaths were due to pneumonia, and 234 (14·9%) deaths were due to diarrhoea. In the placebo group, 493 (28·4%) deaths were due to malaria, 275 (15·9%) deaths were due to pneumonia, and 251 (14·5%) deaths were due to diarrhoea. Relative to communities that received placebo, child mortality in communities that received azithromycin was lower for malaria (incidence rate ratio 0·78, 95% CI 0·66-0·92; p=0·0029), dysentery (0·65, 0·44-0·94; p=0·025), meningitis (0·67, 0·46-0·97; p=0·036), and pneumonia (0·83, 0·68-1·00; p=0·051). The distribution of causes of death did not differ significantly between the two study groups (p=0·98). Mass azithromycin distribution resulted in approximately a third fewer deaths in children aged 1-59 months due to meningitis and dysentery, and a fifth fewer deaths due to malaria and pneumonia. The lack of difference in the distribution of causes of death between the azithromycin and placebo groups could be attributable to the broad spectrum of azithromycin activity and the study setting, in which most childhood deaths were due to infections. Bill & Melinda Gates Foundation.

Sections du résumé

BACKGROUND
The Macrolides Oraux pour Réduire les Décès avec un Oeil sur la Résistance (MORDOR) trial found that biannual mass distribution of azithromycin to children younger than 5 years in Niger reduced the primary outcome of all-cause mortality by 18%. We aimed to determine the causes of mortality among deceased children using verbal autopsy.
METHODS
In this 2-year cluster-randomised controlled trial, 594 community clusters in Niger were randomly allocated (1:1 ratio) to receive biannual mass distributions of either oral azithromycin (approximately 20 mg per kg of bodyweight) or placebo targeted to children aged 1-59 months. Participants, study investigators, and field workers were masked to treatment allocation. Between Nov 23, 2014, and July 31, 2017, 3615 child deaths were recorded by use of biannual house-to-house censuses, and verbal autopsies were done between May 26, 2015, and May 17, 2018, to identify cause of death. Cause-specific mortality, as assessed by verbal autopsy, was a prespecified secondary outcome. This trial is completed and is registered with ClinicalTrials.gov, NCT02047981.
FINDINGS
Between Nov 23, 2014, and July 31, 2017, 303 communities (n=40 375 children at baseline) in Niger received mass azithromycin and 291 communities (n=35 747 children at baseline) received placebo. Treatment coverage was 90·3% (SD 10·6) in the azithromycin group and 90·4% (10·1) in the placebo group. No communities were lost to follow-up. In total, 1727 child deaths in the azithromycin group and 1888 child deaths in the placebo group were reported from the population censuses. Of these, the cause of death for 1566 (90·7%) children in the azithromycin group and 1735 (91·9%) children in the placebo group were ascertained by verbal autopsy interviews. In the azithromycin group, 437 (27·9%) deaths were due to malaria, 252 (16·1%) deaths were due to pneumonia, and 234 (14·9%) deaths were due to diarrhoea. In the placebo group, 493 (28·4%) deaths were due to malaria, 275 (15·9%) deaths were due to pneumonia, and 251 (14·5%) deaths were due to diarrhoea. Relative to communities that received placebo, child mortality in communities that received azithromycin was lower for malaria (incidence rate ratio 0·78, 95% CI 0·66-0·92; p=0·0029), dysentery (0·65, 0·44-0·94; p=0·025), meningitis (0·67, 0·46-0·97; p=0·036), and pneumonia (0·83, 0·68-1·00; p=0·051). The distribution of causes of death did not differ significantly between the two study groups (p=0·98).
INTERPRETATION
Mass azithromycin distribution resulted in approximately a third fewer deaths in children aged 1-59 months due to meningitis and dysentery, and a fifth fewer deaths due to malaria and pneumonia. The lack of difference in the distribution of causes of death between the azithromycin and placebo groups could be attributable to the broad spectrum of azithromycin activity and the study setting, in which most childhood deaths were due to infections.
FUNDING
Bill & Melinda Gates Foundation.

Identifiants

pubmed: 31981558
pii: S2214-109X(19)30540-6
doi: 10.1016/S2214-109X(19)30540-6
pmc: PMC7025321
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Antimalarials 0
Azithromycin 83905-01-5

Banques de données

ClinicalTrials.gov
['NCT02047981']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e288-e295

Investigateurs

Paul M Emerson (PM)
Jerusha Weaver (J)
Sheila K West (SK)
Robin L Bailey (RL)
John Hart (J)
Amza Abdou (A)
Boubacar Kadri (B)
Nassirou Beido (N)
E Kelly Callahan (EK)
Aisha E Stewart (AE)
Ahmed M Arzika (AM)
Sanoussi Elh Adamou (S)
Nana Fatima Galo (NF)
Fatima Ibrahim (F)
Salissou Kane (S)
Mariama Kiemago (M)
Ramatou Maliki (R)
Catherine Cook (C)
Sun Y Cotter (SY)
Thuy Doan (T)
Dionna M Fry (DM)
Jeremy D Keenan (JD)
Elodie Lebas (E)
Thomas M Lietman (TM)
Ying Lin (Y)
Kieran S O'Brien (KS)
Catherine E Oldenburg (CE)
Travis C Porco (TC)
Kathryn J Ray (KJ)
Philip J Rosenthal (PJ)
George W Rutherford (GW)
Benjamin Vanderschelden (B)
Nicole E Varnado (NE)
Lina Zhong (L)
Zhaoxia Zhou (Z)

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Jeremy D Keenan (JD)

Francis I Proctor Foundation, University of California, San Francisco, CA, USA; Department of Ophthalmology, University of California, San Francisco, CA, USA. Electronic address: jeremy.keenan@ucsf.edu.

Ahmed M Arzika (AM)

The Carter Center Niger, Niamey, Niger.

Ramatou Maliki (R)

The Carter Center Niger, Niamey, Niger.

Sanoussi Elh Adamou (S)

The Carter Center Niger, Niamey, Niger.

Fatima Ibrahim (F)

The Carter Center Niger, Niamey, Niger.

Mariama Kiemago (M)

The Carter Center Niger, Niamey, Niger.

Nana Fatima Galo (NF)

The Carter Center Niger, Niamey, Niger.

Elodie Lebas (E)

Francis I Proctor Foundation, University of California, San Francisco, CA, USA.

Catherine Cook (C)

Francis I Proctor Foundation, University of California, San Francisco, CA, USA.

Benjamin Vanderschelden (B)

Francis I Proctor Foundation, University of California, San Francisco, CA, USA.

Robin L Bailey (RL)

London School of Hygiene & Tropical Medicine, London, UK.

Sheila K West (SK)

Dana Center for Preventive Ophthalmology, Wilmer Eye Institute, Johns Hopkins University, Baltimore, MD, USA.

Travis C Porco (TC)

Francis I Proctor Foundation, University of California, San Francisco, CA, USA; Department of Ophthalmology, University of California, San Francisco, CA, USA; Department of Epidemiology & Biostatistics, University of California, San Francisco, CA, USA; Institute for Global Health Sciences, University of California, San Francisco, CA, USA.

Thomas M Lietman (TM)

Francis I Proctor Foundation, University of California, San Francisco, CA, USA; Department of Ophthalmology, University of California, San Francisco, CA, USA; Department of Epidemiology & Biostatistics, University of California, San Francisco, CA, USA; Institute for Global Health Sciences, University of California, San Francisco, CA, USA.

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Classifications MeSH