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Targeted Antibiotics for Trachoma: A Cluster-Randomized Trial.
Melo, Jason S; Aragie, Solomon; Chernet, Ambahun; Tadesse, Zerihun; Dagnew, Adane; Hailu, Dagnachew; Haile, Mahteme; Zeru, Tàye; Wittberg, Dionna M; Nash, Scott D; Callahan, E Kelly; Arnold, Benjamin F; Porco, Travis C; Lietman, Thomas M; Keenan, Jeremy D.
Afiliação
  • Melo JS; Francis I. Proctor Foundation, University of California San Francisco, San Francisco, California, USA.
  • Aragie S; The Carter Center Ethiopia, Addis Ababa, Ethiopia.
  • Chernet A; The Carter Center Ethiopia, Addis Ababa, Ethiopia.
  • Tadesse Z; The Carter Center Ethiopia, Addis Ababa, Ethiopia.
  • Dagnew A; The Carter Center Ethiopia, Addis Ababa, Ethiopia.
  • Hailu D; The Carter Center Ethiopia, Addis Ababa, Ethiopia.
  • Haile M; Amhara Public Health Institute, Bahir Dar, Ethiopia.
  • Zeru T; Amhara Public Health Institute, Bahir Dar, Ethiopia.
  • Wittberg DM; Francis I. Proctor Foundation, University of California San Francisco, San Francisco, California, USA.
  • Nash SD; The Carter Center, Atlanta, Georgia, USA.
  • Callahan EK; The Carter Center, Atlanta, Georgia, USA.
  • Arnold BF; Francis I. Proctor Foundation, University of California San Francisco, San Francisco, California, USA.
  • Porco TC; Department of Ophthalmology, University of California San Francisco, San Francisco, California, USA.
  • Lietman TM; Francis I. Proctor Foundation, University of California San Francisco, San Francisco, California, USA.
  • Keenan JD; Department of Epidemiology and Biostatistics, University of California San Francisco, San Francisco, California, USA.
Clin Infect Dis ; 73(6): 979-986, 2021 09 15.
Article em En | MEDLINE | ID: mdl-33674869
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gonorreia / Tracoma Tipo de estudo: Clinical_trials / Guideline / Prevalence_studies / Risk_factors_studies Limite: Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gonorreia / Tracoma Tipo de estudo: Clinical_trials / Guideline / Prevalence_studies / Risk_factors_studies Limite: Child / Child, preschool / Humans / Infant Idioma: En Ano de publicação: 2021 Tipo de documento: Article