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Mortality rates among patients successfully treated for hepatitis C in the era of interferon-free antivirals: population based cohort study.
Hamill, Victoria; Wong, Stanley; Benselin, Jennifer; Krajden, Mel; Hayes, Peter C; Mutimer, David; Yu, Amanda; Dillon, John F; Gelson, William; Velásquez García, Hector A; Yeung, Alan; Johnson, Philip; Barclay, Stephen T; Alvarez, Maria; Toyoda, Hidenori; Agarwal, Kosh; Fraser, Andrew; Bartlett, Sofia; Aldersley, Mark; Bathgate, Andy; Binka, Mawuena; Richardson, Paul; Morling, Joanne R; Ryder, Stephen D; MacDonald, Douglas; Hutchinson, Sharon; Barnes, Eleanor; Guha, Indra Neil; Irving, William L; Janjua, Naveed Z; Innes, Hamish.
Afiliação
  • Hamill V; School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.
  • Wong S; Public Health Scotland, Glasgow, UK.
  • Benselin J; Joint first authors.
  • Krajden M; British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
  • Hayes PC; Joint first authors.
  • Mutimer D; NIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.
  • Yu A; Nottingham Digestive Diseases Centre, School of Medicine, University of Nottingham, UK.
  • Dillon JF; British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
  • Gelson W; Department of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.
  • Velásquez García HA; Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Yeung A; Liver and Hepatology Unit, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
  • Johnson P; British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
  • Barclay ST; Division of Molecular and Clinical Medicine, School of Medicine, University of Dundee, UK.
  • Alvarez M; Cambridge Liver Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Toyoda H; British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
  • Agarwal K; School of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
  • Fraser A; School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, UK.
  • Bartlett S; Public Health Scotland, Glasgow, UK.
  • Aldersley M; Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
  • Bathgate A; Glasgow Royal Infirmary, Glasgow, UK.
  • Binka M; British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
  • Richardson P; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Morling JR; Institute of Liver Studies, King's College Hospital NHS Foundation Trust, London, UK.
  • Ryder SD; Aberdeen Royal Infirmary, Aberdeen, UK.
  • MacDonald D; Queen Elizabeth University Hospital, Glasgow, UK.
  • Hutchinson S; British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
  • Barnes E; Department of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.
  • Guha IN; Leeds Liver Unit, St James's University Hospital, Leeds, UK.
  • Irving WL; Royal Infirmary of Edinburgh, Edinburgh, UK.
  • Janjua NZ; British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
  • Innes H; Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, UK.
BMJ ; 382: e074001, 2023 08 02.
Article em En | MEDLINE | ID: mdl-37532284
OBJECTIVES: To quantify mortality rates for patients successfully treated for hepatitis C in the era of interferon-free, direct acting antivirals and compare these rates with those of the general population. DESIGN: Population based cohort study. SETTING: British Columbia, Scotland, and England (England cohort consists of patients with cirrhosis only). PARTICIPANTS: 21 790 people who were successfully treated for hepatitis C in the era of interferon-free antivirals (2014-19). Participants were divided into three liver disease severity groups: people without cirrhosis (pre-cirrhosis), those with compensated cirrhosis, and those with end stage liver disease. Follow-up started 12 weeks after antiviral treatment completion and ended on date of death or 31 December 2019. MAIN OUTCOME MEASURES: Crude and age-sex standardised mortality rates, and standardised mortality ratio comparing the number of deaths with that of the general population, adjusting for age, sex, and year. Poisson regression was used to identify factors associated with all cause mortality rates. RESULTS: 1572 (7%) participants died during follow-up. The leading causes of death were drug related mortality (n=383, 24%), liver failure (n=286, 18%), and liver cancer (n=250, 16%). Crude all cause mortality rates (deaths per 1000 person years) were 31.4 (95% confidence interval 29.3 to 33.7), 22.7 (20.7 to 25.0), and 39.6 (35.4 to 44.3) for cohorts from British Columbia, Scotland, and England, respectively. All cause mortality was considerably higher than the rate for the general population across all disease severity groups and settings; for example, all cause mortality was three times higher among people without cirrhosis in British Columbia (standardised mortality ratio 2.96, 95% confidence interval 2.71 to 3.23; P<0.001) and more than 10 times higher for patients with end stage liver disease in British Columbia (13.61, 11.94 to 15.49; P<0.001). In regression analyses, older age, recent substance misuse, alcohol misuse, and comorbidities were associated with higher mortality rates. CONCLUSION: Mortality rates among people successfully treated for hepatitis C in the era of interferon-free, direct acting antivirals are high compared with the general population. Drug and liver related causes of death were the main drivers of excess mortality. These findings highlight the need for continued support and follow-up after successful treatment for hepatitis C to maximise the impact of direct acting antivirals.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite C / Hepatite C Crônica / Doença Hepática Terminal Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatite C / Hepatite C Crônica / Doença Hepática Terminal Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article