Quality of life in patients with chronic hepatitis C infection: Severe comorbidities and disease perception matter more than liver-disease stage.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 09 11 2018
accepted: 24 03 2019
entrez: 4 5 2019
pubmed: 6 5 2019
medline: 15 1 2020
Statut: epublish

Résumé

This study evaluated the clinical and non-clinical determinants of health-related quality of life (HRQoL) associated with untreated chronic hepatitis C (CHC) in France. From 01/2014 to 01/2015, untreated CHC patients were invited to complete a questionnaire including EQ-5D utility instrument and two visual analogue scales (VAS) measuring overall health and fatigue in three French centers (Paris, Lille and Montpellier). Answers were analyzed in mixed models (taking into account the clustering effects of centers and physicians). Five hundreds and five patients were enrolled: 52% males; the mean age was 54; 41% had BMI>25; 64% had genotype 1; 36% were at the stage of severe fibrosis (F3-F4); 38% had severe comorbidities other than liver-related. In the univariate analysis, EQ-5D utility was associated with socio-demographic variables as age, place of birth, education, and employment; CHC-related variables as conditions of HCV screening and severity of fibrosis; CHC-unrelated variables as comorbidities other than CHC, being overweight, and psychiatric disorders; feelings about CHC disease as perception of progression, lack of information on CHC and its treatments, and entourage's feeling. In multivariate analysis, EQ-5D utility was affected by not being in employment (0.72 vs. 0.80), having severe comorbidities other than CHC (0.72 vs. 0.79), being overweight (0.73 vs. 0.78), and feeling worried about CHC progression (0.66 vs. 0.72-0.84). Similar results were found for the VAS. The presence of severe comorbidities and worrying about CHC progression, but not stage of fibrosis, seem to alter significantly EQ-5D health utility in CHC French patients.

Sections du résumé

BACKGROUND AND AIMS
This study evaluated the clinical and non-clinical determinants of health-related quality of life (HRQoL) associated with untreated chronic hepatitis C (CHC) in France.
METHODS
From 01/2014 to 01/2015, untreated CHC patients were invited to complete a questionnaire including EQ-5D utility instrument and two visual analogue scales (VAS) measuring overall health and fatigue in three French centers (Paris, Lille and Montpellier). Answers were analyzed in mixed models (taking into account the clustering effects of centers and physicians).
RESULTS
Five hundreds and five patients were enrolled: 52% males; the mean age was 54; 41% had BMI>25; 64% had genotype 1; 36% were at the stage of severe fibrosis (F3-F4); 38% had severe comorbidities other than liver-related. In the univariate analysis, EQ-5D utility was associated with socio-demographic variables as age, place of birth, education, and employment; CHC-related variables as conditions of HCV screening and severity of fibrosis; CHC-unrelated variables as comorbidities other than CHC, being overweight, and psychiatric disorders; feelings about CHC disease as perception of progression, lack of information on CHC and its treatments, and entourage's feeling. In multivariate analysis, EQ-5D utility was affected by not being in employment (0.72 vs. 0.80), having severe comorbidities other than CHC (0.72 vs. 0.79), being overweight (0.73 vs. 0.78), and feeling worried about CHC progression (0.66 vs. 0.72-0.84). Similar results were found for the VAS.
CONCLUSIONS
The presence of severe comorbidities and worrying about CHC progression, but not stage of fibrosis, seem to alter significantly EQ-5D health utility in CHC French patients.

Identifiants

pubmed: 31050687
doi: 10.1371/journal.pone.0215596
pii: PONE-D-18-32239
pmc: PMC6499434
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0215596

Déclaration de conflit d'intérêts

Sabrina Cossais has no conflict of interest. Michaël Schwarzinger has received research funding from Abbvie. Stanislas Pol has served as a speaker for BMS, Boehringer Ingelheim, Janssen, Gilead, Roche, MSD, Sanofi, Novartis, Vertex, Abbvie; an advisory board member for Bristol-Myers Squibb, Boehringer Ingelheim, Janssen, Vertex, Gilead, Roche, MSD, Novartis, AbbVie, Sanofi, and Glaxo Smith Kline; and has received research funding from BMS, Gilead, Roche, and MSD. Hélène Fontaine as served as an advisory board member for BMS, Gilead, Janssen, Abbvie, and MSD. Dominique Larrey has served as an advisory board member for BMS, Gilead, Janssen, Abbvie, and MSD. Georges-Philippe Pageaux has served as an advisory board member for Gilead, BMS, Janssen, and MSD. Valérie Canva has served as a speaker and as a consultant for Abbvie, Bristol-Myers Squibb, Janssen, Gilead and MSD. Philippe Mathurin as served as a speaker for Roche, MSD, Bristol-Myers Squibb, Gilead, Bayer; an advisory board member for Roche, MSD, Bristol-Myers Squibb, Gilead, Janssen, Norgine; and has received research funding from Roche, Janssen. Yazdan Yazdanpanah has served as a speaker and as a consultant for Abbott, Bristol-Myers Squibb, Gilead, MSD, Roche, Tibotec and ViiV Healthcare. Sylvie Deuffic-Burban has served as a speaker for Bristol-Myers Squibb, Gilead and Janssen; a consultant for Abbvie, Bristol-Myers Squibb, Gilead, HEVA, Janssen, MSD and Public Health Expertise; and has received research funding from Janssen and MSD.

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Auteurs

Sabrina Cossais (S)

Inserm, IAME, UMR 1137, Paris, France; Université Paris Nord, Sorbonne Paris Cité, Paris, France.

Michaël Schwarzinger (M)

Inserm, IAME, UMR 1137, Paris, France; Université Paris Nord, Sorbonne Paris Cité, Paris, France.
THEN (Translational Health Economics Network), Paris, France.

Stanislas Pol (S)

Unité hépatologie, Groupe Hospitalier Cochin Hôtel-Dieu, Paris, France.
Inserm U1223, Institut Pasteur; Université Paris Descartes, Paris, France.

Hélène Fontaine (H)

Unité hépatologie, Groupe Hospitalier Cochin Hôtel-Dieu, Paris, France.
Inserm U1223, Institut Pasteur; Université Paris Descartes, Paris, France.

Dominique Larrey (D)

Service des maladies de l'appareil digestif, Hôpital Saint Eloi, IBR- Inserm Montpellier, France.

Georges-Philippe Pageaux (GP)

Service des maladies de l'appareil digestif, Hôpital Saint Eloi, IBR- Inserm Montpellier, France.

Valérie Canva (V)

Service des Maladies de l'Appareil digestif et de la Nutrition, Hôpital Huriez, Lille, France.

Philippe Mathurin (P)

Service des Maladies de l'Appareil digestif et de la Nutrition, Hôpital Huriez, Lille, France.
Université Lille, Inserm, CHU Lille, U995-LIRIC-Lille Inflammation Research International Center, Lille, France.

Yazdan Yazdanpanah (Y)

Inserm, IAME, UMR 1137, Paris, France; Université Paris Nord, Sorbonne Paris Cité, Paris, France.
Service des Maladies Infectieuses et Tropicales, Hôpital Bichat Claude Bernard, Paris, France.

Sylvie Deuffic-Burban (S)

Inserm, IAME, UMR 1137, Paris, France; Université Paris Nord, Sorbonne Paris Cité, Paris, France.
Université Lille, Inserm, CHU Lille, U995-LIRIC-Lille Inflammation Research International Center, Lille, France.

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