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Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial

BACKGROUND: It is widely thought that widespread antibiotic use selects for community antibiotic resistance, though this has been difficult to prove in the setting of a community-randomized clinical trial. In this study, we used a randomized clinical trial design to assess whether macrolide resistan...

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Autores principales: Skalet, Alison H., Cevallos, Vicky, Ayele, Berhan, Gebre, Teshome, Zhou, Zhaoxia, Jorgensen, James H., Zerihun, Mulat, Habte, Dereje, Assefa, Yared, Emerson, Paul M., Gaynor, Bruce D., Porco, Travis C., Lietman, Thomas M., Keenan, Jeremy D.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001893/
https://www.ncbi.nlm.nih.gov/pubmed/21179434
http://dx.doi.org/10.1371/journal.pmed.1000377
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author Skalet, Alison H.
Cevallos, Vicky
Ayele, Berhan
Gebre, Teshome
Zhou, Zhaoxia
Jorgensen, James H.
Zerihun, Mulat
Habte, Dereje
Assefa, Yared
Emerson, Paul M.
Gaynor, Bruce D.
Porco, Travis C.
Lietman, Thomas M.
Keenan, Jeremy D.
author_facet Skalet, Alison H.
Cevallos, Vicky
Ayele, Berhan
Gebre, Teshome
Zhou, Zhaoxia
Jorgensen, James H.
Zerihun, Mulat
Habte, Dereje
Assefa, Yared
Emerson, Paul M.
Gaynor, Bruce D.
Porco, Travis C.
Lietman, Thomas M.
Keenan, Jeremy D.
author_sort Skalet, Alison H.
collection PubMed
description BACKGROUND: It is widely thought that widespread antibiotic use selects for community antibiotic resistance, though this has been difficult to prove in the setting of a community-randomized clinical trial. In this study, we used a randomized clinical trial design to assess whether macrolide resistance was higher in communities treated with mass azithromycin for trachoma, compared to untreated control communities. METHODS AND FINDINGS: In a cluster-randomized trial for trachoma control in Ethiopia, 12 communities were randomized to receive mass azithromycin treatment of children aged 1–10 years at months 0, 3, 6, and 9. Twelve control communities were randomized to receive no antibiotic treatments until the conclusion of the study. Nasopharyngeal swabs were collected from randomly selected children in the treated group at baseline and month 12, and in the control group at month 12. Antibiotic susceptibility testing was performed on Streptococcus pneumoniae isolated from the swabs using Etest strips. In the treated group, the mean prevalence of azithromycin resistance among all monitored children increased from 3.6% (95% confidence interval [CI] 0.8%–8.9%) at baseline, to 46.9% (37.5%–57.5%) at month 12 (p = 0.003). In control communities, azithromycin resistance was 9.2% (95% CI 6.7%–13.3%) at month 12, significantly lower than the treated group (p<0.0001). Penicillin resistance was identified in 0.8% (95% CI 0%–4.2%) of isolates in the control group at 1 year, and in no isolates in the children-treated group at baseline or 1 year. CONCLUSIONS: This cluster-randomized clinical trial demonstrated that compared to untreated control communities, nasopharyngeal pneumococcal resistance to macrolides was significantly higher in communities randomized to intensive azithromycin treatment. Mass azithromycin distributions were given more frequently than currently recommended by the World Health Organization's trachoma program. Azithromycin use in this setting did not select for resistance to penicillins, which remain the drug of choice for pneumococcal infections. TRIAL REGISTRATION: www.ClinicalTrials.gov NCT00322972 Please see later in the article for the Editors' Summary
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spelling pubmed-30018932010-12-21 Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial Skalet, Alison H. Cevallos, Vicky Ayele, Berhan Gebre, Teshome Zhou, Zhaoxia Jorgensen, James H. Zerihun, Mulat Habte, Dereje Assefa, Yared Emerson, Paul M. Gaynor, Bruce D. Porco, Travis C. Lietman, Thomas M. Keenan, Jeremy D. PLoS Med Research Article BACKGROUND: It is widely thought that widespread antibiotic use selects for community antibiotic resistance, though this has been difficult to prove in the setting of a community-randomized clinical trial. In this study, we used a randomized clinical trial design to assess whether macrolide resistance was higher in communities treated with mass azithromycin for trachoma, compared to untreated control communities. METHODS AND FINDINGS: In a cluster-randomized trial for trachoma control in Ethiopia, 12 communities were randomized to receive mass azithromycin treatment of children aged 1–10 years at months 0, 3, 6, and 9. Twelve control communities were randomized to receive no antibiotic treatments until the conclusion of the study. Nasopharyngeal swabs were collected from randomly selected children in the treated group at baseline and month 12, and in the control group at month 12. Antibiotic susceptibility testing was performed on Streptococcus pneumoniae isolated from the swabs using Etest strips. In the treated group, the mean prevalence of azithromycin resistance among all monitored children increased from 3.6% (95% confidence interval [CI] 0.8%–8.9%) at baseline, to 46.9% (37.5%–57.5%) at month 12 (p = 0.003). In control communities, azithromycin resistance was 9.2% (95% CI 6.7%–13.3%) at month 12, significantly lower than the treated group (p<0.0001). Penicillin resistance was identified in 0.8% (95% CI 0%–4.2%) of isolates in the control group at 1 year, and in no isolates in the children-treated group at baseline or 1 year. CONCLUSIONS: This cluster-randomized clinical trial demonstrated that compared to untreated control communities, nasopharyngeal pneumococcal resistance to macrolides was significantly higher in communities randomized to intensive azithromycin treatment. Mass azithromycin distributions were given more frequently than currently recommended by the World Health Organization's trachoma program. Azithromycin use in this setting did not select for resistance to penicillins, which remain the drug of choice for pneumococcal infections. TRIAL REGISTRATION: www.ClinicalTrials.gov NCT00322972 Please see later in the article for the Editors' Summary Public Library of Science 2010-12-14 /pmc/articles/PMC3001893/ /pubmed/21179434 http://dx.doi.org/10.1371/journal.pmed.1000377 Text en Skalet et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Skalet, Alison H.
Cevallos, Vicky
Ayele, Berhan
Gebre, Teshome
Zhou, Zhaoxia
Jorgensen, James H.
Zerihun, Mulat
Habte, Dereje
Assefa, Yared
Emerson, Paul M.
Gaynor, Bruce D.
Porco, Travis C.
Lietman, Thomas M.
Keenan, Jeremy D.
Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial
title Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial
title_full Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial
title_fullStr Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial
title_full_unstemmed Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial
title_short Antibiotic Selection Pressure and Macrolide Resistance in Nasopharyngeal Streptococcus pneumoniae: A Cluster-Randomized Clinical Trial
title_sort antibiotic selection pressure and macrolide resistance in nasopharyngeal streptococcus pneumoniae: a cluster-randomized clinical trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001893/
https://www.ncbi.nlm.nih.gov/pubmed/21179434
http://dx.doi.org/10.1371/journal.pmed.1000377
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