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Cost effectiveness of perindopril in reducing cardiovascular events in patients with stable coronary artery disease using data from the EUROPA study
  1. Andrew Briggs1,
  2. Borislava Mihaylova2,
  3. Mark Sculpher3,
  4. Alistair Hall4,
  5. Jane Wolstenholme2,
  6. Maarten Simoons5,
  7. Jaap Deckers5,
  8. Roberto Ferrari6,
  9. Willem J Remme7,
  10. Michel Bertrand8,
  11. Kim Fox9,
  12. on behalf of the EUROPA Trial Investigators
  1. 1Public Health and Health Policy, University of Glasgow, Glasgow, UK
  2. 2Health Economics Research Centre, Department of Public Health, University of Oxford, Old Road Campus, Headington, Oxford, UK
  3. 3Centre for Health Economics, University of York, Heslington, York, UK
  4. 4BHF Heart Research Centre, University of Leeds, Leeds, UK
  5. 5Department of Cardiology Thoraxcenter, Erasmus University Medical Centre, Rotterdam, The Netherlands
  6. 6University of Ferrara, Ferrara, and Fondazione S Maugeri IRCCS, Pavia, Italy
  7. 7Sticares Cardiovascular Research Institute, Rhoon, The Netherlands
  8. 8Hôpital Cardiologique de Lille, Lille, France
  9. 9Cardiology Department, Royal Brompton Hospital, London, UK
  1. Correspondence to:
    Professor A Briggs
    Public Health and Health Policy, University of Glasgow, Glasgow G12 8RZ, UK; a.briggs{at}clinmed.gla.ac.uk

Abstract

Background: The EUropean trial on Reduction Of cardiac events with Perindopril in stable coronary Artery disease (EUROPA) trial has recently reported.

Objective: To assess the cost effectiveness of perindopril in stable coronary heart disease in the UK.

Methods: Clinical and resource use data were taken from the EUROPA trial. Costs included drugs and hospitalisations. Health-related quality of life values were taken from published sources. A cost-effectiveness analysis is presented as a function of the risk of a primary event (non-fatal myocardial infarction, cardiac arrest or cardiovascular death) in order to identify people for whom treatment offers greatest value for money.

Results: The median incremental cost of perindopril for each quality-adjusted life year (QALY) gained across the heterogeneous population of EUROPA was estimated as £9700 (interquartile range £6400–£14 200). Overall, 88% of the EUROPA population had an estimated cost per QALY below £20 000 and 97% below £30 000. For a threshold value of cost effectiveness of £30 000 per QALY gained, treatment of people representing the 25th, 50th (median) and 75th centiles of the cost effectiveness distribution for perindopril has a probability of 0.999, 0.99 and 0.93 of being cost effective, respectively. Cost effectiveness was strongly related to higher risk of a primary event under standard care.

Conclusions: Whether the use of perindopril can be considered cost effective depends on the threshold value of cost effectiveness of healthcare systems. For the large majority of patients included in EUROPA, the incremental cost per QALY gained was lower than the apparent threshold used by the National Institute for Health and Clinical Excellence in the UK.

  • EUROPA, EUropean trial on Reduction Of cardiac events with Perindopril in stable coronary Artery disease
  • HOPE, Heart Outcomes Prevention Evaluation
  • HRQL, health-related quality of life
  • QALY, quality-adjusted life year; PEACE, Prevention of Events with Angiotensin Converting Enzyme Inhibition
  • cost–benefit analysis
  • hypertension
  • cardiovascular diseases

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Footnotes

  • Published Online First 29 November 2006

  • Conflict of interest: All authors have some potential conflicts of interest through research grants, consultancy arrangements, speaker’s fees, honoraria and other activities funded by the sponsor. AB and MS hold a minority shareholding in Oxford Outcomes Ltd, the company contracted to undertake the analysis.

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