| Literature DB >> 27458506 |
Yaakov Hasin1, Shimon Shteingart1, Harel Dahari1, Inna Gafanovich1, Sharon Floru1, Marius Braun1, Amir Shlomai1, Anthony Verstandig1, Ilana Dery1, Susan L Uprichard1, Scott J Cotler1, Yoav Lurie1.
Abstract
The United States Food and Drug Administration recently warned that the direct acting antiviral (DAA) combination hepatitis C virus (HCV) treatment of Paritaprevir, Ombitasvir, Dasabuvir, Ritonavir, and Ribavirin (PODr + R) can cause severe liver injury in patients with advanced liver disease. Drug induced liver injury was observed in a small number of patients with decompensated cirrhosis treated with other DAAs, but has not been reported in patients with compensated cirrhosis. We report a case of a 74-year-old woman with chronic HCV and Child-Pugh class A cirrhosis (compensated cirrhosis) treated with PODr + R. The patient presented on day 14 of PODr + R therapy with jaundice and new-onset ascites. Her total bilirubin level increased to 23 mg/dL and international normalized ratio rose to 1.65, while aminotransferase levels remained relatively stable. Hepatitis C treatment was discontinued on day 24 and she gradually recovered. Follow-up testing showed that she achieved a sustained virologic response. In conclusion, hepatic decompensation developed within two weeks of starting treatment with PODr + R in a patient with Child-Pugh class A cirrhosis and was characterized by jaundice and ascites with stable aminotransferase levels. Careful monitoring is warranted in patients with HCV-related cirrhosis treated with PODr + R.Entities:
Keywords: Direct antiviral agent; Drug-induced liver injury; Hepatitis C; Mathematical modeling; Sustained virological response; Viral kinetics
Year: 2016 PMID: 27458506 PMCID: PMC4945506 DOI: 10.4254/wjh.v8.i20.858
Source DB: PubMed Journal: World J Hepatol