Who to screen for hepatitis C? A cost-effectiveness study in Belgium of comprehensive hepatitis C screening in four target groups.


Journal

Acta gastro-enterologica Belgica
ISSN: 1784-3227
Titre abrégé: Acta Gastroenterol Belg
Pays: Belgium
ID NLM: 0414075

Informations de publication

Date de publication:
Historique:
entrez: 1 10 2019
pubmed: 1 10 2019
medline: 23 10 2019
Statut: ppublish

Résumé

Hepatitis C virus (HCV) infection often causes asymptomatic disease and patients are frequently diagnosed at an advanced stage. Oral direct acting antivirals (DAAs) are successful in treating HCV with high sustained virologic response (SVR) and excellent tolerability. The aim of this study is to evaluate cost-effectiveness of a broad screening strategy proposing screening to all undiagnosed members of a population (comprehensive HCV screening), in the general adult population, emergency department (ED) attendees, men who have sex with men (MSM) and people who inject drugs (PWID). We populated a theoretical model with Belgian data. A decision tree model simulating HCV screening and diagnosis was combined with a Markov state transition model simulating treatment. There was one screening round per year during five years. In the ED population only one screening round was considered. The model calculated that more HCV patients could be detected and treated with comprehensive screening compared to the current situation. Incremental cost per incremental quality adjusted life years (QALY) gained was lower than 10.000€/QALY for one and for five screening rounds in the general population (5.139 and 5.200 respectively), in ED attendees (one screening round 5.967), in MSMs (4.292 and 4.302 respectively) and in PWIDs (3.504 and 3.524 respectively). A broad screening strategy combined with treatment is likely to be a cost-effective strategy to detect and treat HCV infected patients and diminish the HCV burden in Belgium.

Sections du résumé

BACKGROUND AND STUDY AIMS OBJECTIVE
Hepatitis C virus (HCV) infection often causes asymptomatic disease and patients are frequently diagnosed at an advanced stage. Oral direct acting antivirals (DAAs) are successful in treating HCV with high sustained virologic response (SVR) and excellent tolerability. The aim of this study is to evaluate cost-effectiveness of a broad screening strategy proposing screening to all undiagnosed members of a population (comprehensive HCV screening), in the general adult population, emergency department (ED) attendees, men who have sex with men (MSM) and people who inject drugs (PWID).
PATIENTS AND METHODS METHODS
We populated a theoretical model with Belgian data. A decision tree model simulating HCV screening and diagnosis was combined with a Markov state transition model simulating treatment. There was one screening round per year during five years. In the ED population only one screening round was considered.
RESULTS RESULTS
The model calculated that more HCV patients could be detected and treated with comprehensive screening compared to the current situation. Incremental cost per incremental quality adjusted life years (QALY) gained was lower than 10.000€/QALY for one and for five screening rounds in the general population (5.139 and 5.200 respectively), in ED attendees (one screening round 5.967), in MSMs (4.292 and 4.302 respectively) and in PWIDs (3.504 and 3.524 respectively).
CONCLUSION CONCLUSIONS
A broad screening strategy combined with treatment is likely to be a cost-effective strategy to detect and treat HCV infected patients and diminish the HCV burden in Belgium.

Identifiants

pubmed: 31566325

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

379-387

Subventions

Organisme : Gilead

Informations de copyright

© Acta Gastro-Enterologica Belgica.

Auteurs

L Opstaele (L)

ANZ Medical Writing, Middenlaan 75, 8400 Oostende, Belgium.

R Bielen (R)

UHasselt, Limburg Clinical Research Program, Ziekenhuis Oost-Limburg, Belgium.

S Bourgeois (S)

Ziekenhuis Netwerk Antwerpen, Belgium.

C Moreno (C)

CUB Hôpital Erasme, Université libre de Bruxelles, Belgium.

F Nevens (F)

University Hospital Gasthuisberg, Belgium.

G Robaeys (G)

UHasselt, Limburg Clinical Research Program, University Hospital Gasthuisberg Leuven, Ziekenhuis Oost-Limburg, Belgium.

G Robaeys (G)

UHasselt, Limburg Clinical Research Program, University Hospital Gasthuisberg Leuven, Ziekenhuis Oost-Limburg, Belgium.

H Van Vlierberghe (H)

University Hospital Ghent, Belgium.

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