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European Journal of Heart Failure 2000 2(4):447-454; doi:10.1016/S1388-9842(00)00122-7
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© 2000 European Society of Cardiology

Low doses vs. high doses of the angiotensin converting-enzyme inhibitor lisinopril in chronic heart failure: a cost-effectiveness analysis based on the Assessment of Treatment with Lisinopril and Survival (ATLAS) study

Mark J. Sculphera,*, Lynne Pooleb, John Clelandc, Michael Drummonda, Paul W. Armstrongd, John D. Horowitze, Barry M. Massief, Philip A. Poole-Wilsong and Lars Ryden1,h

a Centre for Health Economics, University of York Heslington, York, YO10 5DD, UK
b AstraZeneca, Alderley Park, Macclesfield, UK
c Department of Cardiology, Castle Hill Hospital Cottingham, UK
d Department of Medicine, University of Alberta Edmonton, Canada
e University of Adelaide Adelaide, Australia
f University of California San Francisco, CA, USA
g Imperial College School of Medicine London, UK
h Karolinska Institutet Stockholm, Sweden

* Corresponding author. Tel.: +1904-433-641; fax: +1904-433-644. E-mail addressmjs23{at}york.ac.uk (M.J. Sculpher).


   Abstract

Objective: A cost-effectiveness analysis of high and low doses of the angiotensin-converting enzyme (ACE) inhibitor lisinopril in the treatment of chronic heart failure.

Methods: A cost-effectiveness analysis using data from a randomized controlled trial, ATLAS, where 3164 patients with chronic heart failure were allocated to a high-dose (daily target dose 32.5–35 mg) or low-dose strategy (daily target dose 2.5–5.0 mg) of lisinopril. Differential costs were based on resource use data collected in the trial costed using UK unit costs. Cost-effectiveness analysis related differential costs to differential life-years during a 4-year trial follow-up.

Results: The mean total number of hospital in-patient days per patient was 18.5 in the high dose group and 22.5 in the low dose group. Over the whole duration of the trial, the mean (S.D.) daily dose of lisinopril in the high-dose group was 22.5 mg (15.7mg) compared to 3.2 mg (2.5 mg) in the low-dose group. The mean difference in cost per patient was £397 lower in the high-dose group [95% CI (high-dose–low-dose) –£1263 to £436]. Mean life-years per patient were 0.085 years higher in the high-dose group [95% CI (high-dose–low-dose) –0.0074 to 0.1706). Based on mean costs and life-years, high-dose therapy dominates low-dose (less costly and more effective). Allowing for uncertainty in mean costs and life-years, the probability of high-dose therapy being less costly than low dose was 82%. If a decision maker is willing to pay at least £3600 per life-year gained, the probability of high-dose being more cost-effective was 92%.

Conclusions: The ATLAS Study showed that the treatment of heart failure with high-doses of lisinopril has a high probability of being more cost-effective than low-dose therapy.

Key Words: Cost-effectiveness • Heart failure • Angiotensin converting-enzyme inhibitor

Received June 30, 2000; Accepted July 3, 2000


1 On behalf of the ATLAS Study Group.


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