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Uptake of interferon-free DAA therapy among HCV-infected decompensated cirrhosis patients and evidence for decreased mortality.
McDonald, Scott A; Barclay, Stephen T; Innes, Hamish A; Fraser, Andrew; Hayes, Peter C; Bathgate, Andrew; Dillon, John F; Went, April; Goldberg, David J; Hutchinson, Sharon J.
Afiliación
  • McDonald SA; School of Health and Life Sciences, Glasgow Caledonian University and Health Protection Scotland, Glasgow, UK.
  • Barclay ST; Glasgow Royal Infirmary, Glasgow, UK.
  • Innes HA; School of Health and Life Sciences, Glasgow Caledonian University and Health Protection Scotland, Glasgow, UK.
  • Fraser A; Aberdeen Royal Infirmary, Aberdeen, UK.
  • Hayes PC; Queen Elizabeth University Hospital, Glasgow, UK.
  • Bathgate A; Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Dillon JF; Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Went A; School of Medicine, University of Dundee, Dundee, UK.
  • Goldberg DJ; Health Protection Scotland, Glasgow, UK.
  • Hutchinson SJ; School of Health and Life Sciences, Glasgow Caledonian University and Health Protection Scotland, Glasgow, UK.
J Viral Hepat ; 28(9): 1246-1255, 2021 09.
Article en En | MEDLINE | ID: mdl-34002914
ABSTRACT
Interferon-free DAA therapies have recently been licensed for patients infected with hepatitis C virus (HCV) who have decompensated cirrhosis (DC). Our aim was to describe factors associated with uptake of IFN-free DAAs in DC patients and to compare mortality risk and hospital admission rates between pre-DAA and DAA eras. This observational study used record-linkage between Scotland's HCV Clinical Database and national inpatient hospitalization and mortality registers. For the DAA uptake analysis, the study population (n = 297) was restricted to patients alive on 1 November 2014, and Cox regression was used to estimate uptake associated with various covariates. For the Cox regression of mortality comparing pre-DAA and DAA eras, the study population (n = 624) comprised those diagnosed with DC in 2005-2018; follow-up was censored at two years. DAA uptake was 63% overall and was significantly higher for treatment-experienced patients (adjusted hazard ratio (aHR) = 1.64, 95% CI1.14-2.34), genotype 1 vs. other genotypes (aHR = 1.55. 95% CI1.15-2.10) and lower for persons diagnosed with DC pre-2014 (0.47, 95% CI0.33-0.68) and in Greater Glasgow (0.64, 95% CI0.47-0.88). The intention-to-treat SVR rate was 89% (95% CI83-93%). All-cause and liver-related mortality risk were significantly reduced among patients diagnosed with DC in the DAA era (November 2014-December 2018) compared with the pre-DAA era (2005-October 2014) (aHRs of 0.68, 95% CI0.49-0.93; 0.69, 95% CI0.50-0.95, respectively); in contrast, hospital admission rates were higher in the DAA era (aRR = 1.14, 95% CI1.04-1.26). The majority of HCV-infected DC patients engaged with specialist services can be treated with IFN-free DAAs. Improved survival among patients diagnosed with DC in the DAA era supports the beneficial impact of IFN-free therapies among those with advanced liver disease.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hepatitis C / Hepatitis C Crónica Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Viral Hepat Asunto de la revista: GASTROENTEROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hepatitis C / Hepatitis C Crónica Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Viral Hepat Asunto de la revista: GASTROENTEROLOGIA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido