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EFFICACY AND SAFETY OF TREATMENT WITH DACLATASVIR AND ASUNAPREVIR FOR HEPATITIS C VIRUS GENOTYPE 1
https://doi.org/10.20569/00003587
https://doi.org/10.20569/0000358727bd5697-50e1-4428-8a68-4b451faaf23f
名前 / ファイル | ライセンス | アクション |
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2018-07-05 | |||||
タイトル | ||||||
タイトル | EFFICACY AND SAFETY OF TREATMENT WITH DACLATASVIR AND ASUNAPREVIR FOR HEPATITIS C VIRUS GENOTYPE 1 | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | hepatitis C virus | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | interferon free | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | daclatasvir | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | asunaprevir | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | α fetoprotein | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
ID登録 | ||||||
ID登録 | 10.20569/00003587 | |||||
ID登録タイプ | JaLC | |||||
著者 |
AJIMINE, Takuma
× AJIMINE, Takuma× OHSHIMA, Shigetoshi× GOTO, Takashi× KOMATSU, Masafumi× NAKANE, Kunio× YAGISAWA, Hitoshi× Goto, Mitsuo× NAKAJIMA, Kou× Miura, Masato× FUNAOKA, Masato× HOSHINO, Takao× KURAMITSU, Tomoyuki× FUJISHIMA, Yuukou× WATANABE, Daisuke× Segawa, Daisuke× Inomata, Masaaki× IIJIMA, Katsunori |
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内容記述(抄録) | ||||||
内容記述タイプ | Other | |||||
内容記述 | AIM : To assesse the efficacy and safety of therapy with daclatasvir (DCV) and asunaprevir (ASV) for HCV genotype 1. METHOD : The study population was 253 patients who were enrolled in the Akita hepatitis C study group from 2015 to 2016. We followed them until 24 weeks after the end of treatment. RESULT : The sustained virological response (SVR) at 24 weeks after the end of treatment rates were 84.2%. In univariate analyses, the Y93 mutation and a history of triple therapy with protease inhibitor reduced the SVR 24 rate. In multivariate analyses, the Y93H mutation, a history of triple therapy with protease inhibitor, and LC status reduced the SVR 24 rate. The most frequently reported adverse event was ALT elevation, noted in 25.7% of patients. 10.7% of patients had T-Bil elevation, 7.1% experienced drug rush, 11.5% experienced respiratory symptoms, 10.3% developed a fever, and 7.1% experienced digestive symptom. Only 9 (3.6%) patients stopped taking the drugs due to drug-related severe adverse events. CONCLUSION : DCV and ASV therapy showed a high efficacy and low rate of adverse events. |
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著者版フラグ | ||||||
出版タイプ | VoR | |||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
書誌情報 |
秋田医学 en : AKITA JOURNAL OF MEDICINE 巻 44, 号 3/4, p. 101-109, 発行日 2018-03 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 03866106 | |||||
NCID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN00009294 | |||||
出版者 | ||||||
出版者 | 秋田医学会 |