Targeted Antibiotics for Trachoma: A Cluster-Randomized Trial

Autor: E. Kelly Callahan, Ambahun Chernet, Travis C. Porco, Benjamin F. Arnold, Solomon Aragie, Dagnachew Hailu, Adane Dagnew, Scott D. Nash, Jeremy D. Keenan, Thomas M. Lietman, Zerihun Tadesse, Dionna M Wittberg, Taye Zeru, Mahteme Haile, Jason S Melo
Rok vydání: 2021
Předmět:
Antibiotics
Chlamydia trachomatis
antibacterial agents
chlamydia
Azithromycin
Medical and Health Sciences
Gonorrhea
0302 clinical medicine
Prevalence
030212 general & internal medicine
Child
Pediatric
mass drug administration
education.field_of_study
Chlamydia
Absolute risk reduction
Biological Sciences
Anti-Bacterial Agents
Infectious Diseases
Trachoma
Child
Preschool

6.1 Pharmaceuticals
HIV/AIDS
Infection
medicine.drug
Microbiology (medical)
medicine.medical_specialty
medicine.drug_class
Clinical Trials and Supportive Activities
030231 tropical medicine
Population
Microbiology
03 medical and health sciences
Clinical Research
Internal medicine
medicine
Humans
Preschool
education
Mass drug administration
Eye Disease and Disorders of Vision
business.industry
Infant
medicine.disease
Confidence interval
Major Articles and Commentaries
Africa
Sexually Transmitted Infections
business
Zdroj: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, vol 73, iss 6
Clin Infect Dis
ISSN: 1537-6591
1058-4838
Popis: Background Current guidelines recommend community-wide mass azithromycin for trachoma, but a targeted treatment strategy could reduce the volume of antibiotics required. Methods In total, 48 Ethiopian communities were randomized to mass, targeted, or delayed azithromycin distributions. In the targeted arm, only children aged 6 months to 5 years with evidence of ocular chlamydia received azithromycin, distributed thrice over the following year. The primary outcome was ocular chlamydia at months 12 and 24, comparing the targeted and delayed arms (0–5 year-olds, superiority analysis) and the targeted and mass azithromycin arms (8–12 year-olds, noninferiority analysis, 10% noninferiority margin). Results At baseline, the mean prevalence of ocular chlamydia in the 3 arms ranged from 7% to 9% among 0–5 year-olds and from 3% to 9% among 8–12 year-olds. Averaged across months 12–24, the mean prevalence of ocular chlamydia among 0–5 year-olds was 16.7% (95% confidence interval [CI]: 9.0%–24.4%) in the targeted arm and 22.3% (95% CI: 11.1%–33.6%) in the delayed arm (P = .61). The final mean prevalence of ocular chlamydia among 8–12 year-olds was 13.5% (95% CI: 7.9%–19.1%) in the targeted arm and 5.5% (95% CI: 0.3%–10.7%) in the mass treatment arm (adjusted risk difference 8.5 percentage points [pp] higher in the targeted arm, 95% CI: 0.9 pp–16.1 pp higher). Conclusions Antibiotic treatments targeted to infected preschool children did not result in significantly less ocular chlamydia infections compared with untreated communities and did not meet noninferiority criteria relative to mass azithromycin distributions. Targeted approaches may require treatment of a broader segment of the population in areas with hyperendemic trachoma.
Databáze: OpenAIRE