Back to Search
Start Over
Childhood Mortality After Mass Distribution of Azithromycin
- Source :
- The Pediatric infectious disease journal, vol 37, iss 11
- Publication Year :
- 2018
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2018.
-
Abstract
- BACKGROUND: Mass distributions of azithromycin for trachoma have been associated with secondary benefits, including reductions in child mortality. METHODS: In the Partnership for the Rapid Elimination of Trachoma cluster-randomized trial in Niger, 24 communities were randomized to annual treatment of everyone and 24 communities were randomized to biannual treatment of children under 12 for 3 years (clinicaltrials.gov, NCT00792922). Treatment was a single dose of directly observed oral azithromycin (20 mg/kg up to 1 g in adults). Vital status was assessed during annual census and monitoring visits. In this prespecified secondary analysis, we compared the mortality rate among children 6 months to less than 5 years of age by treatment arm using negative binomial regression. RESULTS: Among children 6 months to less than 5 years of age, 404 deaths occurred during the study period. The mortality rate was 35.6 deaths per 1000 person-years (231 deaths, 95% CI: 30.9-40.9) in the annual arm and 29.0 deaths per 1000 person-years (173 deaths, 95% CI: 24.8-33.8) in the biannual arm. The mortality rate ratio comparing children in the biannual arm to the annual arm was 0.81 (95% CI: 0.66-1.00, P = 0.07; primary outcome). The mortality rate ratio comparing children who died from infectious causes in the biannual arm to the annual arm was 0.73 (95% CI: 0.57-0.94; P = 0.02). No adverse events were reported. CONCLUSIONS: This secondary analysis of a cluster-randomized trial found a nonsignificant 19% decrease in mortality among children 6 months to less than 5 years of age who received biannual azithromycin compared with children who received annual azithromycin. This study was conducted in a high mortality, trachoma-endemic area; thus, results may be specific to this environment only. In addition, the trial was neither designed nor powered to detect a mortality effect, and we cannot rule out the possibility that mortality differences resulted from bias.
- Subjects :
- Male
Comparative Effectiveness Research
Administration, Oral
Azithromycin
Pediatrics
law.invention
0302 clinical medicine
Randomized controlled trial
law
Secondary analysis
Prevalence
Medicine
Niger
030212 general & internal medicine
Cluster randomised controlled trial
Child
Pediatric
mass drug administration
Anti-Bacterial Agents
Infectious Diseases
Trachoma
6.1 Pharmaceuticals
Child, Preschool
Administration
Child Mortality
Public Health and Health Services
Mass Drug Administration
Female
medicine.drug
Oral
Microbiology (medical)
Clinical Trials and Supportive Activities
030231 tropical medicine
Communicable Diseases
Article
Paediatrics and Reproductive Medicine
03 medical and health sciences
Clinical Research
Environmental health
Humans
Preschool
Mass drug administration
business.industry
Extramural
Evaluation of treatments and therapeutic interventions
Infant
cluster-randomized trial
bacterial infections and mycoses
medicine.disease
mortality
eye diseases
Child mortality
Good Health and Well Being
Pediatrics, Perinatology and Child Health
business
Subjects
Details
- ISSN :
- 08913668
- Volume :
- 37
- Database :
- OpenAIRE
- Journal :
- Pediatric Infectious Disease Journal
- Accession number :
- edsair.doi.dedup.....79df571be4cdc73a2a806f8707746148