Treating Idiopathic Pulmonary Fibrosis with the addition of co-trimoxazole: an economic evaluation alongside a randomised controlled trial

Wilson, Edward C. F., Shulgina, Ludmila, Cahn, Anthony P., Chilvers, Edwin R., Parfrey, Helen, Clark, Allan B., Twentyman, Orion P. and Wilson, Andrew M. (2014) Treating Idiopathic Pulmonary Fibrosis with the addition of co-trimoxazole: an economic evaluation alongside a randomised controlled trial. PharmacoEconomics, 32 (1). pp. 87-99. ISSN 1170-7690

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Abstract

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a fibrotic disease of the lungs of unknown origin with a poor prognosis. A small trial of co-trimoxazole demonstrated improvements in symptoms and functional parameters over a 3-month period. We therefore conducted a larger trial with a concurrent economic evaluation to investigate this antibiotic further. METHODS: We report an economic evaluation alongside a multi-centre, randomised, placebo-controlled, double-blind trial of 12 months therapy with 960 mg co-trimoxazole daily in 181 patients with fibrotic idiopathic interstitial pneumonia (IIP). Patients were recruited from 28 university and district hospitals in the UK and were aged over 40 years with fibrotic IIP. We report costs to the National Health Service (NHS) and society, change in forced vital capacity (primary endpoint) and quality-adjusted life-years (QALYs) gained, incremental cost effectiveness and cost utility ratios over 12 months. RESULTS: From the perspective of society, mean cost per patient in the co-trimoxazole arm was approximately £1177 higher than in the placebo arm, but mean QALYs were 0.053 higher yielding an incremental cost-effectiveness ratio of £22,012 per QALY gained with a 54.44 % probability of being below £30,000. The cost of IPF to UK society in 2011 is tentatively estimated at £124 million, of which 13 % is NHS costs, 1 % social services, 2 % patient out-of-pocket costs and 84 % lost productivity. CONCLUSIONS: Given commonly employed thresholds in the UK NHS, on balance co-trimoxazole may be a cost-effective treatment for IPF, although there is substantial decision uncertainty. However, recent guidance on the use of immunosuppressive therapy in IPF patients should be taken into account prior to any policy decision.

Item Type: Article
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Depositing User: Pure Connector
Date Deposited: 25 Jul 2014 12:42
Last Modified: 19 Oct 2020 23:36
URI: https://ueaeprints.uea.ac.uk/id/eprint/49423
DOI: 10.1007/s40273-013-0112-z

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