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Stopping azithromycin mass drug administration for trachoma: A systematic review
The World Health Organization (WHO) recommends continuing azithromycin mass drug administration (MDA) for trachoma until endemic regions drop below 5% prevalence of active trachoma in children aged 1–9 years. Azithromycin targets the ocular strains of Chlamydia trachomatis that cause trachoma. Regio...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266061/ https://www.ncbi.nlm.nih.gov/pubmed/34237074 http://dx.doi.org/10.1371/journal.pntd.0009491 |
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author | Mahmud, Hamidah Landskroner, Emma Amza, Abdou Aragie, Solomon Godwin, William W. de Hostos Barth, Anna O’Brien, Kieran S. Lietman, Thomas M. Oldenburg, Catherine E. |
author_facet | Mahmud, Hamidah Landskroner, Emma Amza, Abdou Aragie, Solomon Godwin, William W. de Hostos Barth, Anna O’Brien, Kieran S. Lietman, Thomas M. Oldenburg, Catherine E. |
author_sort | Mahmud, Hamidah |
collection | PubMed |
description | The World Health Organization (WHO) recommends continuing azithromycin mass drug administration (MDA) for trachoma until endemic regions drop below 5% prevalence of active trachoma in children aged 1–9 years. Azithromycin targets the ocular strains of Chlamydia trachomatis that cause trachoma. Regions with low prevalence of active trachoma may have little if any ocular chlamydia, and, thus, may not benefit from azithromycin treatment. Understanding what happens to active trachoma and ocular chlamydia prevalence after stopping azithromycin MDA may improve future treatment decisions. We systematically reviewed published evidence for community prevalence of both active trachoma and ocular chlamydia after cessation of azithromycin distribution. We searched electronic databases for all peer-reviewed studies published before May 2020 that included at least 2 post-MDA surveillance surveys of ocular chlamydia and/or the active trachoma marker, trachomatous inflammation–follicular (TF) prevalence. We assessed trends in the prevalence of both indicators over time after stopping azithromycin MDA. Of 140 identified studies, 21 met inclusion criteria and were used for qualitative synthesis. Post-MDA, we found a gradual increase in ocular chlamydia infection prevalence over time, while TF prevalence generally gradually declined. Ocular chlamydia infection may be a better measurement tool compared to TF for detecting trachoma recrudescence in communities after stopping azithromycin MDA. These findings may guide future trachoma treatment and surveillance efforts. |
format | Online Article Text |
id | pubmed-8266061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-82660612021-07-19 Stopping azithromycin mass drug administration for trachoma: A systematic review Mahmud, Hamidah Landskroner, Emma Amza, Abdou Aragie, Solomon Godwin, William W. de Hostos Barth, Anna O’Brien, Kieran S. Lietman, Thomas M. Oldenburg, Catherine E. PLoS Negl Trop Dis Review The World Health Organization (WHO) recommends continuing azithromycin mass drug administration (MDA) for trachoma until endemic regions drop below 5% prevalence of active trachoma in children aged 1–9 years. Azithromycin targets the ocular strains of Chlamydia trachomatis that cause trachoma. Regions with low prevalence of active trachoma may have little if any ocular chlamydia, and, thus, may not benefit from azithromycin treatment. Understanding what happens to active trachoma and ocular chlamydia prevalence after stopping azithromycin MDA may improve future treatment decisions. We systematically reviewed published evidence for community prevalence of both active trachoma and ocular chlamydia after cessation of azithromycin distribution. We searched electronic databases for all peer-reviewed studies published before May 2020 that included at least 2 post-MDA surveillance surveys of ocular chlamydia and/or the active trachoma marker, trachomatous inflammation–follicular (TF) prevalence. We assessed trends in the prevalence of both indicators over time after stopping azithromycin MDA. Of 140 identified studies, 21 met inclusion criteria and were used for qualitative synthesis. Post-MDA, we found a gradual increase in ocular chlamydia infection prevalence over time, while TF prevalence generally gradually declined. Ocular chlamydia infection may be a better measurement tool compared to TF for detecting trachoma recrudescence in communities after stopping azithromycin MDA. These findings may guide future trachoma treatment and surveillance efforts. Public Library of Science 2021-07-08 /pmc/articles/PMC8266061/ /pubmed/34237074 http://dx.doi.org/10.1371/journal.pntd.0009491 Text en © 2021 Mahmud et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Mahmud, Hamidah Landskroner, Emma Amza, Abdou Aragie, Solomon Godwin, William W. de Hostos Barth, Anna O’Brien, Kieran S. Lietman, Thomas M. Oldenburg, Catherine E. Stopping azithromycin mass drug administration for trachoma: A systematic review |
title | Stopping azithromycin mass drug administration for trachoma: A systematic review |
title_full | Stopping azithromycin mass drug administration for trachoma: A systematic review |
title_fullStr | Stopping azithromycin mass drug administration for trachoma: A systematic review |
title_full_unstemmed | Stopping azithromycin mass drug administration for trachoma: A systematic review |
title_short | Stopping azithromycin mass drug administration for trachoma: A systematic review |
title_sort | stopping azithromycin mass drug administration for trachoma: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266061/ https://www.ncbi.nlm.nih.gov/pubmed/34237074 http://dx.doi.org/10.1371/journal.pntd.0009491 |
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