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Marked heterogeneity in the diagnosis of compensated cirrhosis of patients with chronic hepatitis C virus infection in a real-world setting: A large, multicenter study from Japan.
Toyoda, Hidenori; Atsukawa, Masanori; Watanabe, Tsunamasa; Nakamuta, Makoto; Uojima, Haruki; Nozaki, Akito; Takaguchi, Koichi; Fujioka, Shinichi; Iio, Etsuko; Shima, Toshihide; Akahane, Takehiro; Fukunishi, Shinya; Asano, Toru; Michitaka, Kojiro; Tsuji, Kunihiko; Abe, Hiroshi; Mikami, Shigeru; Okubo, Hironao; Okubo, Tomomi; Shimada, Noritomo; Ishikawa, Toru; Moriya, Akio; Tani, Joji; Morishita, Asahiro; Ogawa, Chikara; Tachi, Yoshihiko; Ikeda, Hiroki; Yamashita, Naoki; Yasuda, Satoshi; Chuma, Makoto; Tsutsui, Akemi; Hiraoka, Atsushi; Ikegami, Tadashi; Genda, Takuya; Tsubota, Akihito; Masaki, Tsutomu; Iwakiri, Katsuhiko; Kumada, Takashi; Tanaka, Yasuhito; Okanoue, Takeshi.
Afiliación
  • Toyoda H; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Atsukawa M; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Watanabe T; Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
  • Nakamuta M; Department of Hepatology, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
  • Uojima H; Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
  • Nozaki A; Gastroenterology Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Takaguchi K; Department of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
  • Fujioka S; Department of Gastroenterology, Okayama Saiseikai General Hospital, Okayama, Japan.
  • Iio E; Department of Virology and Liver Unit, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
  • Shima T; Department of Gastroenterology and Hepatology, Saiseikai Suita Hospital, Suita, Japan.
  • Akahane T; Department of Gastroenterology, Japanese Red Cross Ishinomaki Hospital, Ishinomaki, Japan.
  • Fukunishi S; Second Department of Internal Medicine, Osaka Medical College, Osaka, Japan.
  • Asano T; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Tokyo Metropolitan Bokuto Hospital, Tokyo, Japan.
  • Michitaka K; Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Japan.
  • Tsuji K; Center for Gastroenterology, Teine Keijinkai Hospital, Sapporo, Japan.
  • Abe H; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Shinmatusdo Central General Hospital, Matsudo, Japan.
  • Mikami S; Department of Internal Medicine, Division of Gastroenterology, Kikkoman General Hospital, Noda.
  • Okubo H; Department of Gastroenterology, Juntendo University Nerima Hospital, Tokyo, Japan.
  • Okubo T; Department of Internal Medicine, Division of Gastroenterology, Nippon Medical School Chiba Hokuso Hospital, Inzai, Japan.
  • Shimada N; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Otakanomori Hospital, Kashiwa, Japan.
  • Ishikawa T; Department of Hepatology, Saiseikai Niigata Hospital, Niigata, Japan.
  • Moriya A; Department of Gastroenterology, Mitoyo General Hospital, Kannonji, Japan.
  • Tani J; Department of Internal Medicine, Yashima General Hospital, Takamatsu, Japan.
  • Morishita A; Department of Gastroenterology, Kagawa University School of Medicine, Takamatsu, Japan.
  • Ogawa C; Department of Gastroenterology and Hepatology, Takamatsu Red Cross Hospital, Takamatsu, Japan.
  • Tachi Y; Department of Gastroenterology and Hepatology, Komaki City Hospital, Komaki, Japan.
  • Ikeda H; Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Japan.
  • Yamashita N; Department of Hepatology, National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.
  • Yasuda S; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Chuma M; Gastroenterology Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Tsutsui A; Department of Hepatology, Kagawa Prefectural Central Hospital, Takamatsu, Japan.
  • Hiraoka A; Gastroenterology Center, Ehime Prefectural Central Hospital, Matsuyama, Japan.
  • Ikegami T; Department of Gastroenterology, Tokyo Medical University Ibaraki Medical Center, Ibaraki, Japan.
  • Genda T; Department of Gastroenterology, Juntendo University, Shizuoka Hospital, Mishima, Japan.
  • Tsubota A; Core Research Facilities for Basic Science, Jikei University School of Medicine, Tokyo, Japan.
  • Masaki T; Department of Gastroenterology and Hepatology, Takamatsu Red Cross Hospital, Takamatsu, Japan.
  • Iwakiri K; Department of Internal Medicine, Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Kumada T; Department of Nursing, Gifu Kyoritsu University, Ogaki, Japan.
  • Tanaka Y; Department of Virology and Liver Unit, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Japan.
  • Okanoue T; Department of Gastroenterology and Hepatology, Saiseikai Suita Hospital, Suita, Japan.
J Gastroenterol Hepatol ; 35(8): 1420-1425, 2020 Aug.
Article en En | MEDLINE | ID: mdl-31950525
BACKGROUND AND AIM: The presence of cirrhosis is an important factor for the management of patients with hepatitis C virus (HCV) infection and it determines the duration of treatment for HCV with the direct-acting antiviral (DAA) regimen of glecaprevir (GLE) and pibrentasvir (PIB), that is, 8 or 12 weeks, if patients do not have a history of DAA failure. However, in real-world settings, determination of cirrhosis depends on the discretion of the attending hepatologists, and it is unclear whether compensated cirrhosis was homogenously diagnosed or not. In this study, we investigated the real-world diagnosis of cirrhosis by characterizing DAA-naïve patients who underwent a 12-week GLE/PIB regimen in whom cirrhosis was diagnosed, comparing their characteristics with those of patients who underwent an 8-week regimen in whom cirrhosis was absent. METHODS: In a large, multicenter cohort study, we compared background characteristics and treatment outcomes among DAA-naïve patients who underwent an 8-week versus a 12-week GLE/PIB regimen. RESULTS: Among 977 patients enrolled, 296 (30.3%) were determined to have cirrhosis and underwent a 12-week regimen. Some patient characteristics largely overlapped between the two groups, including liver fibrosis indices. Sustained viral response rates were similar between groups after adjusting liver fibrosis index with propensity score matching. CONCLUSION: Although adequately diagnosed, the determination of cirrhosis varied widely among institutions or by hepatologists in real-world settings, and the severity of liver fibrosis overlapped significantly between patients in whom compensated cirrhosis was determined to be present and patients in whom cirrhosis was absent. Virologic efficacy was similar after adjusting for the degree of liver fibrosis.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Hepatitis C Crónica / Cirrosis Hepática Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Aged / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: J Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Hepatitis C Crónica / Cirrosis Hepática Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Aged / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: J Gastroenterol Hepatol Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Japón