Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/6142
Title: The cost-effectiveness of exercise referral schemes
Authors: Anokye, NK
Trueman, P
Green, C
Pavey, TG
Hillsdon, M
Taylor, RS
Issue Date: 2011
Publisher: BioMed Central Ltd
Citation: BMC Public Health, 11: 954, Dec 2011
Abstract: Background: Exercise referral schemes (ERS) aim to identify inactive adults in the primary care setting. The primary care professional refers the patient to a third party service, with this service taking responsibility for prescribing and monitoring an exercise programme tailored to the needs of the patient. This paper examines the cost-effectiveness of ERS in promoting physical activity compared with usual care in primary care setting. Methods: A decision analytic model was developed to estimate the cost-effectiveness of ERS from a UK NHS perspective. The costs and outcomes of ERS were modelled over the patient's lifetime. Data were derived from a systematic review of the literature on the clinical and cost-effectiveness of ERS, and on parameter inputs in the modelling framework. Outcomes were expressed as incremental cost per quality-adjusted life-year (QALY). Deterministic and probabilistic sensitivity analyses investigated the impact of varying ERS cost and effectiveness assumptions. Sub-group analyses explored the cost-effectiveness of ERS in sedentary people with an underlying condition. Results: Compared with usual care, the mean incremental lifetime cost per patient for ERS was GBP169 and the mean incremental QALY was 0.008, generating a base-case incremental cost-effectiveness ratio (ICER) for ERS at GBP20,876 per QALY in sedentary individuals without a diagnosed medical condition. There was a 51% probability that ERS was cost-effective at GBP20,000 per QALY and 88% probability that ERS was cost-effective at GBP30,000 per QALY. In sub-group analyses, cost per QALY for ERS in sedentary obese individuals was GBP14,618, and in sedentary hypertensives and sedentary individuals with depression the estimated cost per QALY was GBP12,834 and GBP8,414 respectively. Incremental lifetime costs and benefits associated with ERS were small, reflecting the preventative public health context of the intervention, with this resulting in estimates of cost-effectiveness that are sensitive to variations in the relative risk of becoming physically active and cost of ERS. Conclusions: ERS is associated with modest increase in lifetime costs and benefits. The cost-effectiveness of ERS is highly sensitive to small changes in the effectiveness and cost of ERS and is subject to some significant uncertainty mainly due to limitations in the clinical effectiveness evidence base.
Description: This article is made available through the Brunel Open Access Publishing Fund - Copyright @ 2011 Anokye et al.
URI: http://www.biomedcentral.com/1471-2458/11/954/abstract
http://bura.brunel.ac.uk/handle/2438/6142
DOI: http://dx.doi.org/10.1186/1471-2458-11-954
ISSN: 1471-2458
Appears in Collections:Publications
Brunel OA Publishing Fund
Health Economics Research Group (HERG)

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