Improved health-related quality of life after hepatitis C viraemic clearance among people who inject drugs may not be durable.


Journal

Addiction (Abingdon, England)
ISSN: 1360-0443
Titre abrégé: Addiction
Pays: England
ID NLM: 9304118

Informations de publication

Date de publication:
07 2023
Historique:
received: 11 08 2022
accepted: 07 02 2023
medline: 14 6 2023
pubmed: 23 2 2023
entrez: 22 2 2023
Statut: ppublish

Résumé

Chronic infection with the hepatitis C virus (HCV) has a detrimental impact on health-related quality of life (QoL). Scale-up of HCV direct-acting antiviral (DAA) therapy among people who inject drugs (PWID) is underway in several countries since the introduction of interferon-free regimens. This study aimed to assess the impact of DAA treatment success on QoL for PWID. Cross-sectional study using two rounds of the Needle Exchange Surveillance Initiative, a national anonymous bio-behavioural survey and a longitudinal study involving PWID who underwent DAA therapy. The setting for the cross-sectional study was Scotland (2017-2018, 2019-2020). The setting for the longitudinal study was the Tayside region of Scotland (2019-2021). In the cross-sectional study PWID were recruited from services providing injecting equipment (n = 4009). In the longitudinal study, participants were PWID on DAA therapy (n = 83). In the cross-sectional study, the association between QoL (measured using the EQ-5D-5L quality of life instrument) and HCV diagnosis and treatment was assessed using multilevel linear regression. In the longitudinal study, QoL was compared at four timepoints using multilevel regression, from treatment commencement until 12 months following commencement. In the cross-sectional study, 41% (n = 1618) were ever chronically HCV infected, of whom 78% (n = 1262) were aware of their status and of whom 64% (n = 704) had undergone DAA therapy. There was no evidence for a marked QoL improvement associated with viral clearance among those treated for HCV (B = 0.03; 95% CI, -0.03 to 0.09). In the longitudinal study, improved QoL was observed at the sustained virologic response test timepoint (B = 0.18; 95% CI, 0.10-0.27), but this was not maintained at 12 months following start of treatment (B = 0.02; 95% CI, -0.05 to 0.10). Successful direct-acting antiviral therapy for hepatitis C infection may not lead to a durable improvement in quality of life among people who inject drugs, although there may be a transient improvement around the time of sustained virologic response. Economic models of the impact of scaling-up treatment may need to include more conservative quality of life benefits over and above reductions in mortality, disease progression and transmission of infection.

Sections du résumé

BACKGROUND AND AIMS
Chronic infection with the hepatitis C virus (HCV) has a detrimental impact on health-related quality of life (QoL). Scale-up of HCV direct-acting antiviral (DAA) therapy among people who inject drugs (PWID) is underway in several countries since the introduction of interferon-free regimens. This study aimed to assess the impact of DAA treatment success on QoL for PWID.
DESIGN
Cross-sectional study using two rounds of the Needle Exchange Surveillance Initiative, a national anonymous bio-behavioural survey and a longitudinal study involving PWID who underwent DAA therapy.
SETTING
The setting for the cross-sectional study was Scotland (2017-2018, 2019-2020). The setting for the longitudinal study was the Tayside region of Scotland (2019-2021).
PARTICIPANTS
In the cross-sectional study PWID were recruited from services providing injecting equipment (n = 4009). In the longitudinal study, participants were PWID on DAA therapy (n = 83).
MEASUREMENTS
In the cross-sectional study, the association between QoL (measured using the EQ-5D-5L quality of life instrument) and HCV diagnosis and treatment was assessed using multilevel linear regression. In the longitudinal study, QoL was compared at four timepoints using multilevel regression, from treatment commencement until 12 months following commencement.
FINDINGS
In the cross-sectional study, 41% (n = 1618) were ever chronically HCV infected, of whom 78% (n = 1262) were aware of their status and of whom 64% (n = 704) had undergone DAA therapy. There was no evidence for a marked QoL improvement associated with viral clearance among those treated for HCV (B = 0.03; 95% CI, -0.03 to 0.09). In the longitudinal study, improved QoL was observed at the sustained virologic response test timepoint (B = 0.18; 95% CI, 0.10-0.27), but this was not maintained at 12 months following start of treatment (B = 0.02; 95% CI, -0.05 to 0.10).
CONCLUSIONS
Successful direct-acting antiviral therapy for hepatitis C infection may not lead to a durable improvement in quality of life among people who inject drugs, although there may be a transient improvement around the time of sustained virologic response. Economic models of the impact of scaling-up treatment may need to include more conservative quality of life benefits over and above reductions in mortality, disease progression and transmission of infection.

Identifiants

pubmed: 36808787
doi: 10.1111/add.16169
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1340-1350

Subventions

Organisme : Medical Research Council
ID : MR/N00616X/1
Pays : United Kingdom
Organisme : Department of Health
ID : RP-PG-0616-20 008
Pays : United Kingdom

Informations de copyright

© 2023 The Authors. Addiction published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction.

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Auteurs

Scott A McDonald (SA)

School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, G4 0BA, UK.
Public Health Scotland, Meridian Court, Glasgow, G2 6QE, UK.

Gareth Myring (G)

University of Bristol, Bristol, BS8 1TL, UK.

Norah E Palmateer (NE)

School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, G4 0BA, UK.
Public Health Scotland, Meridian Court, Glasgow, G2 6QE, UK.

Andrew McAuley (A)

School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, G4 0BA, UK.
Public Health Scotland, Meridian Court, Glasgow, G2 6QE, UK.

Lewis Beer (L)

University of Dundee, Dundee, UK.

John F Dillon (JF)

University of Dundee, Dundee, UK.

William Hollingworth (W)

University of Bristol, Bristol, BS8 1TL, UK.

Rory Gunson (R)

West of Scotland Specialist Virology Centre, Glasgow Royal Infirmary, Glasgow, UK.

Matthew Hickman (M)

Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, BS8 1TL, UK.

Sharon J Hutchinson (SJ)

School of Health and Life Sciences, Glasgow Caledonian University, Glasgow, G4 0BA, UK.
Public Health Scotland, Meridian Court, Glasgow, G2 6QE, UK.

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