Increased Carriage of Macrolide-Resistant Fecal E. coli Following Mass Distribution of Azithromycin for Trachoma Control
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2014/08/01
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Description:Background: Mass drug treatment with azithromycin (MDA) is part of the WHO-endorsed 'SAFE' strategy for trachoma control in endemic communities. MDA has been associated with reduced trachoma prevalence and short-term reductions in other bacterial infections, but can also lead to increased circulation of macrolide-resistant bacteria. Methods: We prospectively monitored macrolide resistance in fecal E. coli collected from young children participating in the PRETþ Study in rural Tanzania. MDA was administered in four villages with >10% trachoma prevalence. Four nearby communities with lower trachoma prevalence served as controls. Rectal swabs were collected during cross-sectional surveys performed at baseline, 1, 3 and 6 months after MDA. Fecal E. coli isolates were screened for macrolide susceptibility using disc diffusion and minimum inhibitory concentration methods. Cross-sectional and longitudinal differences in resistance prevalence by MDA exposure were compared using t-tests and logistic regression. Results: There was no difference in the proportion of individuals carrying azithromycin-resistant E. coli at baseline (0.21 vs 0.16, P>0.05). Azithromycin resistance carriage prevalence remained stable over follow-up in non-MDA villages but increased sharply in MDA villages (0.61 at 1 month, 0.42 at 3 months and 0.31 at 6 months). MDA exposure was highly associated with azithromycin resistance carriage at 1 month post-MDA (OR 15.27, P<0.001) and subsequent surveys. Younger age and recent diarrhoea were also associated with increased odds of resistance (P<0.01). Conclusions: MDA resulted in significantly increased prevalence of macrolide resistance in E. coli. Although MDA is effective for trachoma elimination, it has costs; it is essential to monitor antimicrobial resistance following MDA. [Description provided by NIOSH]
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ISSN:0300-5771
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Volume:43
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Issue:4
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NIOSHTIC Number:nn:20051841
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Citation:Int J Epidemiol 2014 Aug; 43(4):1105-1113
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Contact Point Address:Jessica C. Seidman, Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, 615 N. Wolfe Street, Baltimore, MD 21205, USA
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Email:jseidman@jhsph.edu
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Federal Fiscal Year:2014
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Performing Organization:Johns Hopkins University - Baltimore
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Peer Reviewed:True
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Start Date:20090901
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Source Full Name:International Journal of Epidemiology
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End Date:20150831
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Main Document Checksum:urn:sha-512:2167a3f8046e92ee42b63a1b7cd30202f02b8f2b122f3f04de983f4e92b52648c40a21be9f2ca68bd8996fba413f3bb02d9d12019458403de53772d14cd922f9
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