Health economic modelling in Cystic Fibrosis: A systematic review

Mohindru, Bishal, Turner, David ORCID: https://orcid.org/0000-0002-1689-4147, Sach, Tracey ORCID: https://orcid.org/0000-0002-8098-9220, Bilton, Diana, Carr, Siobhan, Archangelidi, Olga, Bhadhuri, Arjun and Whitty, Jennifer A. ORCID: https://orcid.org/0000-0002-5886-1933 (2019) Health economic modelling in Cystic Fibrosis: A systematic review. Journal of Cystic Fibrosis, 18 (4). pp. 452-460. ISSN 1569-1993

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Abstract

Introduction: Cystic Fibrosis (CF) is a heritable chronic condition. Due to the genetic and progressive nature of CF, a number of interventions are available for the condition. In the United Kingdom (U.K.) average annual cost of CF treatment is between €49,000 to €76,000 (2012) per patient [1]. A review of health economic modelling studies is warranted to provide decision makers and researchers with an in depth understanding of modelling practices in CF and guidance for future research. Methods: Online searches were performed in the 5 databases, studies were included if they were: a) Model based economic evaluation for management of Cystic Fibrosis. Articles were restricted to English language only, but no restriction was applied on publication year. Results: Nine studies were reviewed, most were Markov cohort models. Models evaluated pharmaceutical interventions and drug adherence. Modelling structure was consistent across most articles and a range of sources were used to populate the models. Cost and utility data were based on different sources and elicitation methods respectively. The majority of models failed to incorporate significant health events which impact both cost and disease progression. Conclusion: In our review we observed a lack of, application of European Medicines Agency (EMA) guidelines for clinical trial endpoints, model structure justifications and lastly, health-related quality of life derived utility information around important clinical events. Future work around conceptual modelling of CF progression, utility valuation of significant health events and meeting EMA guidelines for trial reporting is encouraged.

Item Type: Article
Uncontrolled Keywords: cost-effectiveness analysis,cystic fibrosis,health economics,modelling,pediatrics, perinatology, and child health,pulmonary and respiratory medicine ,/dk/atira/pure/subjectarea/asjc/2700/2735
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
UEA Research Groups: Faculty of Medicine and Health Sciences > Research Groups > Health Economics
Faculty of Medicine and Health Sciences > Research Groups > Public Health and Health Services Research (former - to 2023)
Faculty of Medicine and Health Sciences > Research Groups > Norwich Clinical Trials Unit
Faculty of Medicine and Health Sciences > Research Groups > Health Services and Primary Care
Faculty of Medicine and Health Sciences > Research Groups > Respiratory and Airways Group
Faculty of Medicine and Health Sciences > Research Centres > Population Health
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Depositing User: LivePure Connector
Date Deposited: 28 Feb 2019 15:30
Last Modified: 19 Oct 2023 02:22
URI: https://ueaeprints.uea.ac.uk/id/eprint/70053
DOI: 10.1016/j.jcf.2019.01.007

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