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...
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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. |
doi_str_mv | 10.1371/journal.pntd.0009491 |
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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.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0009491</identifier><identifier>PMID: 34237074</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Antibiotics ; Azithromycin ; Bias ; Biology and Life Sciences ; Chlamydia ; Cohort analysis ; Development and progression ; Drug therapy ; Drugs ; Evaluation ; Infections ; Medicine and Health Sciences ; Patient outcomes ; Public health administration ; Regions ; Research and Analysis Methods ; Review ; Reviews ; Sexually transmitted diseases ; STD ; Strains ; Surveillance ; Surveys ; Systematic review ; Trachoma ; Trends ; Tropical diseases</subject><ispartof>PLoS neglected tropical diseases, 2021-07, Vol.15 (7), p.e0009491-e0009491</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Mahmud et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Mahmud et al 2021 Mahmud et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c601t-3c25c94748dbaf1210b8e8a23cfdd99d095a0551383cec0df9312d93875a54ec3</citedby><cites>FETCH-LOGICAL-c601t-3c25c94748dbaf1210b8e8a23cfdd99d095a0551383cec0df9312d93875a54ec3</cites><orcidid>0000-0002-6816-5560 ; 0000-0002-0763-399X ; 0000-0002-7834-8213 ; 0000-0001-8216-0240 ; 0000-0002-1962-5321 ; 0000-0002-5387-783X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266061/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8266061/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids></links><search><contributor>Ngondi, Jeremiah M.</contributor><creatorcontrib>Mahmud, Hamidah</creatorcontrib><creatorcontrib>Landskroner, Emma</creatorcontrib><creatorcontrib>Amza, Abdou</creatorcontrib><creatorcontrib>Aragie, Solomon</creatorcontrib><creatorcontrib>Godwin, William W</creatorcontrib><creatorcontrib>de Hostos Barth, Anna</creatorcontrib><creatorcontrib>O'Brien, Kieran S</creatorcontrib><creatorcontrib>Lietman, Thomas M</creatorcontrib><creatorcontrib>Oldenburg, Catherine E</creatorcontrib><title>Stopping azithromycin mass drug administration for trachoma: A systematic review</title><title>PLoS neglected tropical diseases</title><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.</description><subject>Antibiotics</subject><subject>Azithromycin</subject><subject>Bias</subject><subject>Biology and Life Sciences</subject><subject>Chlamydia</subject><subject>Cohort analysis</subject><subject>Development and progression</subject><subject>Drug therapy</subject><subject>Drugs</subject><subject>Evaluation</subject><subject>Infections</subject><subject>Medicine and Health Sciences</subject><subject>Patient outcomes</subject><subject>Public health administration</subject><subject>Regions</subject><subject>Research and Analysis Methods</subject><subject>Review</subject><subject>Reviews</subject><subject>Sexually transmitted diseases</subject><subject>STD</subject><subject>Strains</subject><subject>Surveillance</subject><subject>Surveys</subject><subject>Systematic review</subject><subject>Trachoma</subject><subject>Trends</subject><subject>Tropical 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azithromycin mass drug administration for trachoma: A systematic review</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c601t-3c25c94748dbaf1210b8e8a23cfdd99d095a0551383cec0df9312d93875a54ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antibiotics</topic><topic>Azithromycin</topic><topic>Bias</topic><topic>Biology and Life Sciences</topic><topic>Chlamydia</topic><topic>Cohort analysis</topic><topic>Development and progression</topic><topic>Drug therapy</topic><topic>Drugs</topic><topic>Evaluation</topic><topic>Infections</topic><topic>Medicine and Health Sciences</topic><topic>Patient outcomes</topic><topic>Public health 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M</au><au>Oldenburg, Catherine E</au><au>Ngondi, Jeremiah M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stopping azithromycin mass drug administration for trachoma: A systematic review</atitle><jtitle>PLoS neglected tropical diseases</jtitle><date>2021-07-01</date><risdate>2021</risdate><volume>15</volume><issue>7</issue><spage>e0009491</spage><epage>e0009491</epage><pages>e0009491-e0009491</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>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.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>34237074</pmid><doi>10.1371/journal.pntd.0009491</doi><orcidid>https://orcid.org/0000-0002-6816-5560</orcidid><orcidid>https://orcid.org/0000-0002-0763-399X</orcidid><orcidid>https://orcid.org/0000-0002-7834-8213</orcidid><orcidid>https://orcid.org/0000-0001-8216-0240</orcidid><orcidid>https://orcid.org/0000-0002-1962-5321</orcidid><orcidid>https://orcid.org/0000-0002-5387-783X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibiotics Azithromycin Bias Biology and Life Sciences Chlamydia Cohort analysis Development and progression Drug therapy Drugs Evaluation Infections Medicine and Health Sciences Patient outcomes Public health administration Regions Research and Analysis Methods Review Reviews Sexually transmitted diseases STD Strains Surveillance Surveys Systematic review Trachoma Trends Tropical diseases |
title | Stopping azithromycin mass drug administration for trachoma: A systematic review |
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