(Circulation. 1996;93:1774-1776.)
© 1996 American Heart Association, Inc.
Articles |
From the Division of Cardiology and Preventive Cardiology and Therapeutics Program, Hamilton Civic Hospitals Research Centre, McMaster University, Hamilton, Ontario, Canada.
Correspondence to Dr Salim Yusuf, Hamilton General Hospital, 237 Barton St E, Hamilton, Ontario, Canada L8L 2X2. E-mail yusufs@fhs.mcmaster.csu.ca.
Key Words: Editorials cost-benefit analysis epidemiology prevention cholesterol
| Introduction |
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The first generation of lipid-lowering trials (Helsinki [gemfibrozil],2 WHO [clofibrate],3 LRC-CPPT [cholestyramine]4 ) used drugs that lowered cholesterol only modestly (about 10%); some of these drugs produced side effects, so that compliance with treatment was suboptimal, and the studies were consequently inadequately powered to provide reliable estimation of the effects of lipid lowering on mortality. Although at first glance, the results of these trials appeared to be inconclusive or even contradictory, a comprehensive overview of these trials in an epidemiological context1 provided a coherent result: the gains in CHD reduction were related to the degree of cholesterol lowering and the duration of the intervention.
More recently, with
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