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Effectiveness of azithromycin mass drug administration on trachoma: a systematic review
Azithromycin mass drug administration (MDA) is a key part of the strategy for controlling trachoma. This systematic review aimed to comprehensively summarize the present studies of azithromycin MDA on trachoma; provide an overview of the impact of azithromycin MDA on trachoma in different districts;...
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Published in: | Chinese medical journal 2021-09, Vol.134 (24), p.2944-2953 |
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creator | Xiong, Tao Yue, Yan Li, Wen-Xing Choonara, Imti Qazi, Shamim Chen, Hong-Ju Tang, Jun Shi, Jing Wang, Hua Zeng, Li-Nan Xia, Bin Qiao, Li-Na Qu, Yi Mu, De-Zhi |
description | Azithromycin mass drug administration (MDA) is a key part of the strategy for controlling trachoma. This systematic review aimed to comprehensively summarize the present studies of azithromycin MDA on trachoma; provide an overview of the impact of azithromycin MDA on trachoma in different districts; and explore the possible methods to enhance the effectiveness of azithromycin MDA in hyperendemic districts.
PubMed, Embase, the Cochrane Central Register of Controlled Trials, Web of Science, and ClinicalTrials.gov were searched up to February 2021 with no language restriction. Studies reporting the effect of azithromycin MDA on trachoma were included. Mathematical modeling studies, animal studies, case reports, and reviews were excluded. The trachomatous inflammation-follicular (TF) |
doi_str_mv | 10.1097/CM9.0000000000001717 |
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PubMed, Embase, the Cochrane Central Register of Controlled Trials, Web of Science, and ClinicalTrials.gov were searched up to February 2021 with no language restriction. Studies reporting the effect of azithromycin MDA on trachoma were included. Mathematical modeling studies, animal studies, case reports, and reviews were excluded. The trachomatous inflammation-follicular (TF) <5.0% was used to judge the effect of azithromycin MDA on eliminating trachoma as a public health problem. Two researchers independently conducted the selection process and risk of bias assessment.
A total of 1543 studies were screened, of which 67 studies including 13 cluster-randomized controlled trials and 54 non-randomized studies were included. The effect of azithromycin MDA on trachoma was closely related to the baseline prevalence in districts. For the districts with baseline prevalence between 5.0% and 9.9%, a single round of MDA achieved a TF <5.0%. For the districts with baseline between 10.0% and 29.9%, annual MDA for 3 to 5 years reduced TF <5.0%. However, for the districts with high level of baseline prevalence (TF >30.0%), especially with baseline TF >50.0%, annual MDA was unable to achieve the TF <5.0% even after 5 to 7 years of treatment. Quarterly MDA is more effective in controlling trachoma in these hyperendemic districts.
Azithromycin MDA for controlling trachoma depends on the baseline prevalence. The recommendation by the World Health Organization that annual MDA for 3 to 5 years in the districts with TF baseline >10.0% is not appropriate for all eligible districts.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.1097/CM9.0000000000001717</identifier><identifier>PMID: 34665571</identifier><language>eng</language><publisher>China: Lippincott Williams & Wilkins</publisher><subject>Anti-Bacterial Agents - therapeutic use ; Antibiotics ; Azithromycin - therapeutic use ; Bias ; Children & youth ; Drug dosages ; Humans ; Infant ; Infections ; Infectious diseases ; Mass Drug Administration ; Prevalence ; Public health ; Systematic Review ; Trachoma - drug therapy ; Trachoma - epidemiology</subject><ispartof>Chinese medical journal, 2021-09, Vol.134 (24), p.2944-2953</ispartof><rights>Lippincott Williams & Wilkins</rights><rights>Copyright © 2021 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license.</rights><rights>Copyright © 2021 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2021 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5476-a59efb7315207c54bae6ea054c53c5cb2355361e7b4b39fc7276908af59368cb3</citedby><cites>FETCH-LOGICAL-c5476-a59efb7315207c54bae6ea054c53c5cb2355361e7b4b39fc7276908af59368cb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8710348/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2612724163?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34665571$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xiong, Tao</creatorcontrib><creatorcontrib>Yue, Yan</creatorcontrib><creatorcontrib>Li, Wen-Xing</creatorcontrib><creatorcontrib>Choonara, Imti</creatorcontrib><creatorcontrib>Qazi, Shamim</creatorcontrib><creatorcontrib>Chen, Hong-Ju</creatorcontrib><creatorcontrib>Tang, Jun</creatorcontrib><creatorcontrib>Shi, Jing</creatorcontrib><creatorcontrib>Wang, Hua</creatorcontrib><creatorcontrib>Zeng, Li-Nan</creatorcontrib><creatorcontrib>Xia, Bin</creatorcontrib><creatorcontrib>Qiao, Li-Na</creatorcontrib><creatorcontrib>Qu, Yi</creatorcontrib><creatorcontrib>Mu, De-Zhi</creatorcontrib><title>Effectiveness of azithromycin mass drug administration on trachoma: a systematic review</title><title>Chinese medical journal</title><addtitle>Chin Med J (Engl)</addtitle><description>Azithromycin mass drug administration (MDA) is a key part of the strategy for controlling trachoma. This systematic review aimed to comprehensively summarize the present studies of azithromycin MDA on trachoma; provide an overview of the impact of azithromycin MDA on trachoma in different districts; and explore the possible methods to enhance the effectiveness of azithromycin MDA in hyperendemic districts.
PubMed, Embase, the Cochrane Central Register of Controlled Trials, Web of Science, and ClinicalTrials.gov were searched up to February 2021 with no language restriction. Studies reporting the effect of azithromycin MDA on trachoma were included. Mathematical modeling studies, animal studies, case reports, and reviews were excluded. The trachomatous inflammation-follicular (TF) <5.0% was used to judge the effect of azithromycin MDA on eliminating trachoma as a public health problem. Two researchers independently conducted the selection process and risk of bias assessment.
A total of 1543 studies were screened, of which 67 studies including 13 cluster-randomized controlled trials and 54 non-randomized studies were included. The effect of azithromycin MDA on trachoma was closely related to the baseline prevalence in districts. For the districts with baseline prevalence between 5.0% and 9.9%, a single round of MDA achieved a TF <5.0%. For the districts with baseline between 10.0% and 29.9%, annual MDA for 3 to 5 years reduced TF <5.0%. However, for the districts with high level of baseline prevalence (TF >30.0%), especially with baseline TF >50.0%, annual MDA was unable to achieve the TF <5.0% even after 5 to 7 years of treatment. Quarterly MDA is more effective in controlling trachoma in these hyperendemic districts.
Azithromycin MDA for controlling trachoma depends on the baseline prevalence. The recommendation by the World Health Organization that annual MDA for 3 to 5 years in the districts with TF baseline >10.0% is not appropriate for all eligible districts.</description><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibiotics</subject><subject>Azithromycin - therapeutic use</subject><subject>Bias</subject><subject>Children & youth</subject><subject>Drug dosages</subject><subject>Humans</subject><subject>Infant</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Mass Drug Administration</subject><subject>Prevalence</subject><subject>Public health</subject><subject>Systematic Review</subject><subject>Trachoma - drug therapy</subject><subject>Trachoma - epidemiology</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkt9rFDEQxxdRbK3-ByILvviyNb-z8UGQo2qh4oviY5jNTe5y7m5qsnvH-deb82ptGwIZJt_5ZGYyVfWSknNKjH67-GLOyZ1FNdWPqlMmBWukEvRxdUq4Uo0yxpxUz3LeEMKk1OppdcKFUsWkp9WPC-_RTWGLI-ZcR1_D7zCtUxz2Loz1AMW5TPOqhuUQxpCnBFOIY112Md06DvCuhjrv84RDuXJ1wm3A3fPqiYc-44ub86z6_vHi2-Jzc_X10-Xiw1XjpNCqAWnQd5pTyYgurg5QIRApnOROuo5xKbmiqDvRceOdZloZ0oKXhqvWdfysujxylxE29jqFAdLeRgj2ryOmlYVU0urRSl-apEzrgROBJdyb8ubSgSO66wAK6_2RdT13Ay4djqXE_h70_s0Y1nYVt7bVlHDRFsCbG0CKv2bMkx1Cdtj3MGKcs2Wy5UKo1sgiff1AuolzGkurLFOUaSao4kUljiqXYs4J_W0ylNjDFNgyBfbhFJSwV3cLuQ369-3_ubvYT5jyz37eYbJrhH5aH3jMcE4aRhiljBHSHNCK_wF5lr2Q</recordid><startdate>20210916</startdate><enddate>20210916</enddate><creator>Xiong, Tao</creator><creator>Yue, Yan</creator><creator>Li, Wen-Xing</creator><creator>Choonara, Imti</creator><creator>Qazi, Shamim</creator><creator>Chen, Hong-Ju</creator><creator>Tang, Jun</creator><creator>Shi, Jing</creator><creator>Wang, Hua</creator><creator>Zeng, Li-Nan</creator><creator>Xia, Bin</creator><creator>Qiao, Li-Na</creator><creator>Qu, Yi</creator><creator>Mu, De-Zhi</creator><general>Lippincott Williams & Wilkins</general><general>Lippincott Williams & Wilkins Ovid Technologies</general><general>Wolters Kluwer</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20210916</creationdate><title>Effectiveness of azithromycin mass drug administration on trachoma: a systematic review</title><author>Xiong, Tao ; 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This systematic review aimed to comprehensively summarize the present studies of azithromycin MDA on trachoma; provide an overview of the impact of azithromycin MDA on trachoma in different districts; and explore the possible methods to enhance the effectiveness of azithromycin MDA in hyperendemic districts.
PubMed, Embase, the Cochrane Central Register of Controlled Trials, Web of Science, and ClinicalTrials.gov were searched up to February 2021 with no language restriction. Studies reporting the effect of azithromycin MDA on trachoma were included. Mathematical modeling studies, animal studies, case reports, and reviews were excluded. The trachomatous inflammation-follicular (TF) <5.0% was used to judge the effect of azithromycin MDA on eliminating trachoma as a public health problem. Two researchers independently conducted the selection process and risk of bias assessment.
A total of 1543 studies were screened, of which 67 studies including 13 cluster-randomized controlled trials and 54 non-randomized studies were included. The effect of azithromycin MDA on trachoma was closely related to the baseline prevalence in districts. For the districts with baseline prevalence between 5.0% and 9.9%, a single round of MDA achieved a TF <5.0%. For the districts with baseline between 10.0% and 29.9%, annual MDA for 3 to 5 years reduced TF <5.0%. However, for the districts with high level of baseline prevalence (TF >30.0%), especially with baseline TF >50.0%, annual MDA was unable to achieve the TF <5.0% even after 5 to 7 years of treatment. Quarterly MDA is more effective in controlling trachoma in these hyperendemic districts.
Azithromycin MDA for controlling trachoma depends on the baseline prevalence. The recommendation by the World Health Organization that annual MDA for 3 to 5 years in the districts with TF baseline >10.0% is not appropriate for all eligible districts.</abstract><cop>China</cop><pub>Lippincott Williams & Wilkins</pub><pmid>34665571</pmid><doi>10.1097/CM9.0000000000001717</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Bacterial Agents - therapeutic use Antibiotics Azithromycin - therapeutic use Bias Children & youth Drug dosages Humans Infant Infections Infectious diseases Mass Drug Administration Prevalence Public health Systematic Review Trachoma - drug therapy Trachoma - epidemiology |
title | Effectiveness of azithromycin mass drug administration on trachoma: a systematic review |
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