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Extensive Drug Resistance Acquired During Treatment of Multidrug-Resistant Tuberculosis

DC Field Value Language
dc.contributor.author조상래-
dc.date.accessioned2015-01-06T17:31:26Z-
dc.date.available2015-01-06T17:31:26Z-
dc.date.issued2014-
dc.identifier.issn1058-4838-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/100138-
dc.description.abstractBACKGROUND: Increasing access to drugs for the treatment of multidrug-resistant (MDR) tuberculosis is crucial but could lead to increasing resistance to these same drugs. In 2000, the international Green Light Committee (GLC) initiative began to increase access while attempting to prevent acquired resistance. METHODS: To assess the GLC's impact, we followed adults with pulmonary MDR tuberculosis from the start to the end of treatment with monthly sputum cultures, drug susceptibility testing, and genotyping. We compared the frequency and predictors of acquired resistance to second-line drugs (SLDs) in 9 countries that volunteered to participate, 5 countries that met GLC criteria, and 4 countries that did not apply to the GLC. RESULTS: In total, 832 subjects were enrolled. Of those without baseline resistance to specific SLDs, 68 (8.9%) acquired extensively drug-resistant (XDR) tuberculosis, 79 (11.2%) acquired fluoroquinolone (FQ) resistance, and 56 (7.8%) acquired resistance to second-line injectable drugs (SLIs). The relative risk (95% confidence interval [CI]) of acquired resistance was lower at GLC-approved sites: 0.27 (.16-.47) for XDR tuberculosis, 0.28 (.17-.45) for FQ, and 0.15 (.06-.39) to 0.60 (.34-1.05) for 3 different SLIs. The risk increased as the number of potentially effective drugs decreased. Controlling for baseline drug resistance and differences between sites, the odds ratios (95% CIs) were 0.21 (.07-.62) for acquired XDR tuberculosis and 0.23 (.09-.59) for acquired FQ resistance. CONCLUSIONS: Treatment of MDR tuberculosis involves substantial risk of acquired resistance to SLDs, increasing as baseline drug resistance increases. The risk was significantly lower in programs documented by the GLC to meet specific standards. Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US.-
dc.description.statementOfResponsibilityopen-
dc.format.extent1049~1063-
dc.relation.isPartOfCLINICAL INFECTIOUS DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdolescent-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAntitubercular Agents/therapeutic use*-
dc.subject.MESHCohort Studies-
dc.subject.MESHDrug Resistance, Multiple, Bacterial*-
dc.subject.MESHFemale-
dc.subject.MESHGenotyping Techniques-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMicrobial Sensitivity Tests-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMycobacterium tuberculosis/drug effects*-
dc.subject.MESHMycobacterium tuberculosis/isolation & purification-
dc.subject.MESHProspective Studies-
dc.subject.MESHSelection, Genetic-
dc.subject.MESHSputum/microbiology-
dc.subject.MESHTuberculosis, Multidrug-Resistant/drug therapy*-
dc.subject.MESHTuberculosis, Multidrug-Resistant/microbiology*-
dc.subject.MESHTuberculosis, Pulmonary/drug therapy*-
dc.subject.MESHTuberculosis, Pulmonary/microbiology*-
dc.subject.MESHYoung Adult-
dc.titleExtensive Drug Resistance Acquired During Treatment of Multidrug-Resistant Tuberculosis-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Microbiology (미생물학)-
dc.contributor.googleauthorJ. Peter Cegielski-
dc.contributor.googleauthorTracy Dalton-
dc.contributor.googleauthorMartin Yagui-
dc.contributor.googleauthorWanpen Wattanaamornkiet-
dc.contributor.googleauthorGrigory V. Volchenkov-
dc.contributor.googleauthorLaura E. Via-
dc.contributor.googleauthorMartie Van Der Walt-
dc.contributor.googleauthorThelma Tupasi-
dc.contributor.googleauthorSarah E. Smith-
dc.contributor.googleauthorRonel Odendaal-
dc.contributor.googleauthorVaira Leimane-
dc.contributor.googleauthorCharlotte Kvasnovsky-
dc.contributor.googleauthorTatiana Kuznetsova-
dc.contributor.googleauthorEkaterina Kurbatova-
dc.contributor.googleauthorTiina Kummik-
dc.contributor.googleauthorLiga Kuksa-
dc.contributor.googleauthorKai Kliiman-
dc.contributor.googleauthorElena V. Kiryanova-
dc.contributor.googleauthorHeeJin Kim-
dc.contributor.googleauthorChang-ki Kim-
dc.contributor.googleauthorBoris Y. Kazennyy-
dc.contributor.googleauthorRuwen Jou-
dc.contributor.googleauthorWei-Lun Huang-
dc.contributor.googleauthorJulia Ershova-
dc.contributor.googleauthorVladislav V. Erokhin-
dc.contributor.googleauthorLois Diem-
dc.contributor.googleauthorCarmen Contreras-
dc.contributor.googleauthorSang Nae Cho-
dc.contributor.googleauthorLarisa N. Chernousova-
dc.contributor.googleauthorMichael P. Chen-
dc.contributor.googleauthorJanice Campos Caoili-
dc.contributor.googleauthorJaime Bayona-
dc.contributor.googleauthorSomsak Akksilp-
dc.identifier.doi10.1093/cid/ciu572-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA03824-
dc.relation.journalcodeJ00581-
dc.identifier.eissn1537-6591-
dc.identifier.pmid25057101-
dc.identifier.urlhttp://cid.oxfordjournals.org/content/59/8/1049.long-
dc.subject.keywordGreen Light Committee-
dc.subject.keywordextensively drug-resistant tuberculosis-
dc.subject.keywordmultidrug-resistant tuberculosis-
dc.subject.keywordtuberculosis-
dc.contributor.alternativeNameCho, Sang Nae-
dc.contributor.affiliatedAuthorCho, Sang Nae-
dc.rights.accessRightsfree-
dc.citation.volume59-
dc.citation.number8-
dc.citation.startPage1049-
dc.citation.endPage1063-
dc.identifier.bibliographicCitationCLINICAL INFECTIOUS DISEASES, Vol.59(8) : 1049-1063, 2014-
dc.identifier.rimsid51701-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers

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