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COST-EFFECTIVENESS OF DIAGNOSTIC AND THERAPEUTIC INTERVENTIONS FOR CHRONIC HEPATITIS C: A SYSTEMATIC REVIEW OF MODEL-BASED ANALYSES
Author
Affilliation
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil / Universidade Federal do Estado do Rio de Janeiro, Instituto de Saúde Coletiva, Rio de Janeiro, RJ, Brasil.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement. ESMI, Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement. ESMI, Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
Fundação Oswaldo Cruz. Centro de Desenvolvimento Tecnológico em Saúde. Rio de Janeiro, RJ, Brasil.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement. ESMI, Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement. ESMI, Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
Fundação Oswaldo Cruz. Centro de Desenvolvimento Tecnológico em Saúde. Rio de Janeiro, RJ, Brasil.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
University of Exeter Medical School. Evidence Synthesis & Modelling for Health Improvement, ESMI. Peninsula Technology Assessment Group. PenTAG, Exeter, UK.
Abstract
Background: Decisions about which subgroup of chronic hepatitis C (CHC) patients should be treated with direct acting anti-viral agents (DAAs) have economic importance due to high drug prices. Treat-all DAA strategies for CHC have gained acceptance despite high drug acquisition costs. However, there are also costs associated with the surveillance of CHC to determine a subgroup of patients with significant impairment. The aim of this systematic
review was to describe the modelling methods used and summarise results in cost-effectiveness analyses (CEAs) of both CHC treatment with DAAs and surveillance of liver disease. Methods: Electronic databases including Embase and Medline were searched from inception to May 2015. Eligible
studies included models predicting costs and/or outcomes for interventions, surveillance, or management of people with CHC. Narrative and quantitative synthesis were conducted. Quality appraisal was conducted using validated checklists. The review was conducted following principles published by NHS Centre for Research and Dissemination. Results: Forty-one CEAs met the eligibility criteria for the review; 37 evaluated an intervention and four evaluated surveillance strategies for targeting DAA treatment to those likely to gain most benefit. Included studies were of variable quality mostly due to reporting omissions. Of the 37 CEAs, eight models that enabled comparative analysis were fully appraised and synthesized. These models provided non-unique cost-effectiveness estimates in a specific DAA comparison in a specific population defined in terms of genotype, prior treatment status, and presence or absence of cirrhosis. Marked heterogeneity in cost-effectiveness estimates was observed despite this stratification. Approximately half of the estimates suggested that DAAs were cost-effective considering a threshold of US$30,000 and 73% with threshold of US$50,000. Two models evaluating surveillance strategies suggested that treating all CHC patients regardless of the staging of liver disease could be cost-effective. Conclusions: CEAs of CHC treatments need to better account for variability in their estimates. This analysis suggested that there are still circumstances where DAAs are not cost-effective. Surveillance in place of a treat-all strategy may still need to be considered as an option for deploying DAAs, particularly where acquisition cost is at the limit of affordability for a given health system.
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