Publication

Trimethoprim-Sulfamethoxazole Prophylaxis and Antibiotic Nonsusceptibility in Invasive Pneumococcal Disease

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Last modified
  • 03/05/2025
Type of Material
Authors
    Heidi M. Soeters, Emory UniversityAnne von Gottberg, National Institute for Communicable DiseasesCheryl Cohen, National Institute for Communicable DiseasesVanessa Quan, National Institute for Communicable DiseasesKeith Klugman, Emory University
Language
  • English
Date
  • 2012-03-01
Publisher
  • American Society for Microbiology
Publication Version
Copyright Statement
  • Copyright © 2012, American Society for Microbiology. All Rights Reserved.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0066-4804
Volume
  • 56
Issue
  • 3
Start Page
  • 1602
End Page
  • 1605
Grant/Funding Information
  • The contents of this work are solely the responsibility of the authors and do not necessarily represent the official views of CDC.
  • This work was supported by the Rollins School of Public Health Global Field Experience Global Frameworks Grant (to H.M.S.); the Rollins School of Public Health Student Initiative Fund (to H.M.S.); the United States Agency for International Development's Antimicrobial Resistance Initiative, transferred via a cooperative agreement (number U60/CCU022088) from the Centers for Disease Control and Prevention (CDC), Atlanta, GA (2003 to 2006); and the CDC, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Global AIDS Program (GAP) cooperative agreement U62/PSO022901(2005 to 2007).
Abstract
  • Among 5,043 invasive pneumococcal disease (IPD) isolates identified through South African national surveillance from 2003 to 2007, we estimated the effect of trimethoprim-sulfamethoxazole (TMP-SMX) prophylaxis on antimicrobial resistance. Patients on TMP-SMX prophylaxis were more likely to have a pneumococcal isolate nonsusceptible to TMP-SMX, penicillin, and rifampin. TMP-SMX nonsusceptibility was associated with nonsusceptibility to penicillin, erythromycin, and rifampin and multidrug resistance. This study informs empirical treatment of suspected IPD in patients with a history of TMP-SMX use.
Author Notes
  • Address correspondence to Heidi M. Soeters, hsoeters@email.unc.edu Present address: Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Keywords
Research Categories
  • Health Sciences, Pharmacology
  • Health Sciences, Medicine and Surgery

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