Long-Term Liver Disease, Treatment, and Mortality Outcomes Among 17,000 Persons Diagnosed with Chronic Hepatitis C Virus Infection: Current Chronic Hepatitis Cohort Study Status and Review of Findings
- PMID:29778254
- PMCID: PMC6211170
- DOI: 10.1016/j.idc.2018.02.002
Long-Term Liver Disease, Treatment, and Mortality Outcomes Among 17,000 Persons Diagnosed with Chronic Hepatitis C Virus Infection: Current Chronic Hepatitis Cohort Study Status and Review of Findings
Abstract
Chronic Hepatitis Cohort Study (CHeCS) publications using data from "real-world" patients with hepatitis C virus (HCV) have described demographic disparities in access to care; rates of advanced liver disease, morbidity, and mortality (2.5%-3.5% per year during 2006-10, although only 19% of all CHeCS decedents, and just 30% of those with deaths attributed to liver disease, had HCV listed on death certificate); substantial comorbidities, such as diabetes, advanced liver fibrosis (29% prevalence), renal disease, and depression, and partial reversal of all these with successful antiviral therapy; patient risk behaviors; and use of noninvasive markers to assess liver disease.
Keywords: Cirrhosis; Comorbidities; Direct-acting antiviral; Hepatitis C; Mortality; Real-world cohort; Sustained viral response.
Published by Elsevier Inc.
Conflict of interest statement
Conflict of Interest: The authors have made the following disclosures: S.C. Gordon receives grant/research support from AbbVie Pharmaceuticals (M15–410, M13–576, M15–942, M14–222, M13–590, M14–227, M14–868), Conatus (IDN-6556–14, IDN-6556–120), CymaBay (CB8025–21629, CB8025–31731), Gilead Pharmaceuticals (GS-US-330–1508, GS-US-320–4018, GS-US-367–1170, GS-US-367–1171, GS-US-367–1172, GS-US-367–1173, GS-US-334–0154, GS-US-337–4063, IN-US-337–3957), Intercept Pharmaceuticals (747–303, 747–301, 747–302, 747–207, [Master agreement dated Nov 9, 2015, with Statements of Work 1–3 for Fibrotic Liver Diseases (FOLD) study]), and Merck (MK5172–017, MK5172–062, MK3682–035, MK3682–041, MK3682–012, MK3682–021). He is also a consultant/advisor for Abbvie, Gilead, Intercept, and Merck. L.B. Rupp, M. Lu, J.A. Boscarino, M.A. Schmidt, and Y.G. Daida receive research grant support from Gilead Pharmaceuticals (IN-US-337–3957) and Intercept (Master agreement dated Nov 9, 2015, with Statements of Work 1–3 for Fibrotic Liver Diseases (FOLD) study).
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