Azithromycin to Reduce Mortality - An Adaptive Cluster-Randomized Trial
Twice-yearly mass distribution of azithromycin to children is a promising intervention to reduce childhood mortality in sub-Saharan Africa. The World Health Organization recommended restricting distribution to infants 1 to 11 months of age to mitigate antimicrobial resistance, although this more lim...
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Published in | The New England journal of medicine Vol. 391; no. 8; p. 699 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
22.08.2024
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Subjects | |
Online Access | Get more information |
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Abstract | Twice-yearly mass distribution of azithromycin to children is a promising intervention to reduce childhood mortality in sub-Saharan Africa. The World Health Organization recommended restricting distribution to infants 1 to 11 months of age to mitigate antimicrobial resistance, although this more limited treatment had not yet been tested.
We randomly assigned rural communities in Niger to four twice-yearly distributions of azithromycin for children 1 to 59 months of age (child azithromycin group), four twice-yearly distributions of azithromycin for infants 1 to 11 months of age and placebo for children 12 to 59 months of age (infant azithromycin group), or placebo for children 1 to 59 months of age. Census workers who were not aware of the group assignments monitored mortality twice yearly over the course of 2 years. We assessed three primary community-level mortality outcomes (deaths per 1000 person-years), each examining a different age group and pairwise group comparison.
A total of 1273 communities were randomly assigned to the child azithromycin group (1229 were included in the analysis), 773 to the infant azithromycin group (751 included in the analysis), and 954 to the placebo group (929 included in the analysis). Among 382,586 children, 419,440 person-years and 5503 deaths were recorded. Lower mortality among children 1 to 59 months of age was observed in the child azithromycin group (11.9 deaths per 1000 person-years; 95% confidence interval [CI], 11.3 to 12.6) than in the placebo group (13.9 deaths per 1000 person-years; 95% CI, 13.0 to 14.8) (representing 14% lower mortality with azithromycin; 95% CI, 7 to 22; P<0.001). Mortality among infants 1 to 11 months of age was not significantly lower in the infant azithromycin group (22.3 deaths per 1000 person-years; 95% CI, 20.0 to 24.7) than in the placebo group (23.9 deaths per 1000 person-years; 95% CI, 21.6 to 26.2) (representing 6% lower mortality with azithromycin; 95% CI, -8 to 19). Five serious adverse events were reported: three in the placebo group, one in the infant azithromycin group, and one in the child azithromycin group.
Azithromycin distributions to children 1 to 59 months of age significantly reduced mortality and was more effective than treatment of infants 1 to 11 months of age. Antimicrobial resistance must be monitored. (Funded by the Bill and Melinda Gates Foundation; AVENIR ClinicalTrials.gov number, NCT04224987.). |
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AbstractList | Twice-yearly mass distribution of azithromycin to children is a promising intervention to reduce childhood mortality in sub-Saharan Africa. The World Health Organization recommended restricting distribution to infants 1 to 11 months of age to mitigate antimicrobial resistance, although this more limited treatment had not yet been tested.
We randomly assigned rural communities in Niger to four twice-yearly distributions of azithromycin for children 1 to 59 months of age (child azithromycin group), four twice-yearly distributions of azithromycin for infants 1 to 11 months of age and placebo for children 12 to 59 months of age (infant azithromycin group), or placebo for children 1 to 59 months of age. Census workers who were not aware of the group assignments monitored mortality twice yearly over the course of 2 years. We assessed three primary community-level mortality outcomes (deaths per 1000 person-years), each examining a different age group and pairwise group comparison.
A total of 1273 communities were randomly assigned to the child azithromycin group (1229 were included in the analysis), 773 to the infant azithromycin group (751 included in the analysis), and 954 to the placebo group (929 included in the analysis). Among 382,586 children, 419,440 person-years and 5503 deaths were recorded. Lower mortality among children 1 to 59 months of age was observed in the child azithromycin group (11.9 deaths per 1000 person-years; 95% confidence interval [CI], 11.3 to 12.6) than in the placebo group (13.9 deaths per 1000 person-years; 95% CI, 13.0 to 14.8) (representing 14% lower mortality with azithromycin; 95% CI, 7 to 22; P<0.001). Mortality among infants 1 to 11 months of age was not significantly lower in the infant azithromycin group (22.3 deaths per 1000 person-years; 95% CI, 20.0 to 24.7) than in the placebo group (23.9 deaths per 1000 person-years; 95% CI, 21.6 to 26.2) (representing 6% lower mortality with azithromycin; 95% CI, -8 to 19). Five serious adverse events were reported: three in the placebo group, one in the infant azithromycin group, and one in the child azithromycin group.
Azithromycin distributions to children 1 to 59 months of age significantly reduced mortality and was more effective than treatment of infants 1 to 11 months of age. Antimicrobial resistance must be monitored. (Funded by the Bill and Melinda Gates Foundation; AVENIR ClinicalTrials.gov number, NCT04224987.). |
Author | Galo, Nasser Maliki, Ramatou Doan, Thuy Porco, Travis C Arnold, Benjamin F Aichatou, Bawa Keenan, Jeremy D Bello, Ismael Mamane Le, Victoria Liu, Zijun Colby, Emily Lietman, Thomas M Beidi, Diallo Abarchi, Moustapha Ibrahim, Almou Amza, Abdou Oldenburg, Catherine E Karamba, Alio M O'Brien, Kieran S Mahamadou, Sani Peterson, Brittany Harouna, Naser Lebas, Elodie Arzika, Ahmed M |
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Contributor | Hocking, Frances Zakari, Amadou Arnold, Benjamin Chen, Cindi Hightower, Allen Colby, Emily Mhirsi, Zied Zhong, Lina Bagna, Hamidou Amadou Haroun, Laminou Maliki Tomko, Sheena Nameywa, Boubacar Ali, Djibo Jackson, Brian Amouzou, Agbessi Youssoufou Souley, Abdoul Salam Mariama, Boubacar Abdou, Amza Brander, Rebecca Issa, Ibrahima Russell, Fiona Ousmane, Sani Sakina, Ocquet Keenan, Jeremy D Oumarou, Amadou Bello, Ismael Mamane Brandt, Carolyn Le, Victoria Emerson, Paul Roos, David Lebas, Elodie Zhou, Zhaoxia Ruder, Kevin Beido, Nassirou Moustapha, Abarchi Hamadou, Karamatoulaye Keimago, Mariama Oumarou, Farissatou Seyfoulaye, Amina Labbo, Rabiou Knirsch, Charles Mahamadou, Sani Harouna, Naser Oron, Assaf Gallo, Nasser Boubacar, Ousseini Cook, Catherine Yahaya, Mahamadou Liu, Zijun Maiga, Salamatou Kyane, Sandrine Nguyen, William Djatao, Idi Moussa Jambou, Ronan Arzika, Ahmed Hooper, P J Lamine, S'Hooshim N Izadnegahdar, Rasa Porco, Travis C Rajaram, Surabhi Assao, Mourtala Mounkala, Aida Kadri, Boubacar Lindsay, Brianna O'Brien, Kieran S Peterson, Brit |
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Snippet | Twice-yearly mass distribution of azithromycin to children is a promising intervention to reduce childhood mortality in sub-Saharan Africa. The World Health... |
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SubjectTerms | Anti-Bacterial Agents - administration & dosage Anti-Bacterial Agents - adverse effects Azithromycin - administration & dosage Azithromycin - adverse effects Bacterial Infections - mortality Bacterial Infections - prevention & control Chemoprevention - adverse effects Chemoprevention - statistics & numerical data Child Mortality Child, Preschool Drug Resistance, Bacterial Female Humans Infant Infant Mortality Male Mass Drug Administration - adverse effects Mass Drug Administration - statistics & numerical data Niger - epidemiology Rural Population - statistics & numerical data |
Title | Azithromycin to Reduce Mortality - An Adaptive Cluster-Randomized Trial |
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