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Patient-Reported Outcomes During and After Hepatitis C Virus Direct-Acting Antiviral Treatment Among People Who Inject Drugs.
Cheng, Qinglu; Cunningham, Evan B; Shih, Sophy; Amin, Janaki; Bruneau, Julie; Artenie, Adelina A; Powis, Jeff; Litwin, Alain H; Cooper, Curtis; Dalgard, Olav; Hellard, Margaret; Bruggmann, Philip; Marks, Philippa; Lacombe, Karine; Stedman, Catherine; Read, Phillip; Hajarizadeh, Behzad; Dunlop, Adrian J; Conway, Brian; Feld, Jordan J; Dore, Gregory J; Grebely, Jason.
Afiliação
  • Cheng Q; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia. Electronic address: qcheng@kirby.unsw.edu.au.
  • Cunningham EB; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia.
  • Shih S; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia.
  • Amin J; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia; Department of Health Sciences, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW, Australia.
  • Bruneau J; Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Montréal, QC, Canada; Département de médecine, Université de Montréal, Montréal, QC, Canada.
  • Artenie AA; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, England, UK.
  • Powis J; Infection Prevention and Control, Michael Garron Hospital, Toronto, ON, Canada.
  • Litwin AH; Prisma Health Addiction Medicine Centre, Greenville, SC, USA; School of Medicine - Greenville, University of South Carolina, Greenville, SC, USA; School of Health Research, Clemson University, Clemson, SC, USA.
  • Cooper C; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.
  • Dalgard O; Department of Infectious Diseases, Akershus University Hospital, Oslo, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Hellard M; The Burnet Institute, Melbourne, VIC, Australia; Department of Infectious Disease, The Alfred Hospital, Melbourne, VIC, Australia.
  • Bruggmann P; Arud Centre for Addiction Medicine, Zurich, Switzerland.
  • Marks P; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia.
  • Lacombe K; Faculté de médecine, Sorbonne Université, Paris, France; Infectious Diseases Department, Hôpital Saint-Antoine, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Stedman C; Department of Medicine, University of Otago, Christchurch, New Zealand; Gastroenterology Department, Christchurch Hospital, Christchurch, New Zealand.
  • Read P; Kirketon Road Centre, Sydney, NSW, Australia.
  • Hajarizadeh B; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia.
  • Dunlop AJ; Drug & Alcohol Clinical Services, Hunter New England Local Health District, Newcastle, NSW, Australia; Faculty of Health and Medicine, University of Newcastle, Newcastle, NSW, Australia.
  • Conway B; Vancouver Infectious Diseases Centre, Vancouver, BC, Canada.
  • Feld JJ; Toronto Centre for Liver Disease, University Health Network, Toronto, ON, Canada.
  • Dore GJ; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia; St Vincent's Hospital, Sydney, NSW, Australia.
  • Grebely J; The Kirby Institute, University of New South Wales (UNSW) Sydney, Sydney, NSW, Australia.
Value Health ; 26(6): 883-892, 2023 06.
Article em En | MEDLINE | ID: mdl-36646278
ABSTRACT

OBJECTIVES:

People who inject drugs (PWID) are at a high risk of hepatitis C virus (HCV) infection. HCV cure is associated with improved patient-reported outcomes (PROs), but there are little data among PWID. This study aimed to assess the change in PROs during and after HCV direct-acting antiviral (DAA) treatment.

METHODS:

This analysis used data from 2 clinical trials of DAA treatment in PWID. PROs assessed included health-related quality of life, social functioning, psychological distress, housing, and employment. Generalized estimating equations and group-based trajectory modeling were used to assess changes in PROs over time.

RESULTS:

No significant changes in the 3-level version of EQ-5D scores, EQ visual analogue scale scores, social functioning, psychological distress, and housing were observed over the 108-week study period. There was a significant increase in the proportion of participants employed (18% [95% confidence interval (CI) 12%-23%] at baseline to 28% [95% CI 19%-36%] at the end of the study). Participants were more likely to be employed at 24 weeks and 108 weeks after commencing treatment. Having stable housing increased the odds of being employed (odds ratio 1.70; 95% CI 1.00-2.90). The group-based trajectory modeling demonstrated that most outcomes remained stable during and after DAA treatment.

CONCLUSIONS:

Although no significant improvement was identified in health-related quality of life after HCV DAA treatment, there was a modest but significant increase in employment during study follow-up. The study findings support the need for multifaceted models of HCV care for PWID addressing a range of issues beyond HCV treatment to improve quality of life.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Abuso de Substâncias por Via Intravenosa / Hepatite C / Hepatite C Crônica / Usuários de Drogas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Value Health Assunto da revista: FARMACOLOGIA Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Abuso de Substâncias por Via Intravenosa / Hepatite C / Hepatite C Crônica / Usuários de Drogas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Value Health Assunto da revista: FARMACOLOGIA Ano de publicação: 2023 Tipo de documento: Article