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dc.contributor.authorLin, Shang-Yien_US
dc.contributor.authorChiu, Yi-Wenen_US
dc.contributor.authorLu, Po-Liangen_US
dc.contributor.authorHwang, Shang-Jyhen_US
dc.contributor.authorChen, Tun-Chiehen_US
dc.contributor.authorHsieh, Min-Hanen_US
dc.contributor.authorChen, Yen-Hsuen_US
dc.date.accessioned2019-04-02T05:58:11Z-
dc.date.available2019-04-02T05:58:11Z-
dc.date.issued2019-02-01en_US
dc.identifier.issn1684-1182en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.jmii.2018.05.003en_US
dc.identifier.urihttp://hdl.handle.net/11536/148871-
dc.description.abstractThe consequences of once-weekly rifapentine plus isoniazid for 3 months (3HP) against latent tuberculosis infections in hemodialysis patients have not been studied before. This is the first study to evaluate the safety and tolerability of 3HP in this population and revealed a completion rate of 65.4%. The therapy was not associated with hepatotoxicity, but with high rates of adverse events (69.2%). Copyright (C) 2018, Taiwan Society of Microbiology. Published by Elsevier Taiwan LLC.en_US
dc.language.isoen_USen_US
dc.subjectRifapentineen_US
dc.subject3HPen_US
dc.subjectLatent tuberculosisen_US
dc.subjectLTBIen_US
dc.subjectHemodialysisen_US
dc.titleThree months of rifapentine and isoniazid for latent tuberculosis infection in hemodialysis patients: High rates of adverse eventsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jmii.2018.05.003en_US
dc.identifier.journalJOURNAL OF MICROBIOLOGY IMMUNOLOGY AND INFECTIONen_US
dc.citation.volume52en_US
dc.citation.spage158en_US
dc.citation.epage162en_US
dc.contributor.department生醫工程研究所zh_TW
dc.contributor.departmentInstitute of Biomedical Engineeringen_US
dc.identifier.wosnumberWOS:000458620500019en_US
dc.citation.woscount0en_US
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