| Literature DB >> 26613201 |
Masataka Tsuge1,2,3, Akira Hiramatsu1,2, Fumi Shinohara1,2, Norihito Nakano1,2, Yuki Nakamura1,2, Masahiro Hatooka1,2, Kei Morio1,2, Reona Morio1,2, Hiromi Kan1,2, Hatsue Fujino1,2, Takuro Uchida1,2, Tomoki Kobayashi1,2, Takayuki Fukuhara1,2, Keiichi Masaki1,2, Takashi Nakahara1,2, Atsushi Ono1,2, Yuko Nagaoki1,2, Daiki Miki1,2,4, Tomokazu Kawaoka1,2, Nobuhiko Hiraga1,2, Michio Imamura1,2, Yoshiiku Kawakami1,2, Hiroshi Aikata1,2, Hidenori Ochi1,2,4, C Nelson Hayes1,2, Kazuaki Chayama1,2,4.
Abstract
Recently, treatments for chronic hepatitis C virus (HCV) infection have been drastically improved by the development of direct-acting antiviral agents. In September 2014, dual oral therapy using daclatasvir (DCV) and asunaprevir (ASV) was approved for the treatment of chronic HCV infection in Japan. We treated a patient with HCV-related liver cirrhosis with severe leg edema due to chronic renal dysfunction using this dual oral therapy. Although serum alanine aminotransferase increased rapidly during the first week of treatment, the antiviral therapy was able to continue, and liver function recovered spontaneously. After 1 month of treatment, serum HCV RNA became continuously undetectable, and serum albumin level gradually increased. Throughout the therapy, serum creatinine level nearly normalized, and leg edema gradually improved. These improvements continued after the combination therapy was completed. HCV RNA remained undetectable following the end of therapy, and sustained virological response at 12 weeks was achieved. It has been reported that chronic HCV infection is associated with renal dysfunction and that HCV eradication can improve it. DCV and ASV combination therapy is safe for patients who have renal dysfunction and may be a suitable therapy for chronic hepatitis C patients with renal dysfunction.Entities:
Keywords: asunaprevir; daclatasvir; hepatitis C virus; liver cirrhosis; renal dysfunction
Year: 2016 PMID: 26613201 DOI: 10.1111/hepr.12629
Source DB: PubMed Journal: Hepatol Res ISSN: 1386-6346 Impact factor: 4.288