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Key Trials Linking CHD and Cardiovascular Diseases
to Dyslipidaemias
Primary Prevention Trials
- World Health Organization Cooperative Trial
in the Primary Prevention of Ischaemic Heart Disease using Clofibrate
- The Lipid Research Clinics Coronary Primary
Prevention Trial (LRC-CPPT)
- West of Scotland Coronary Prevention
Study (WOSCOPS)
- Air Force/Texas Coronary Atherosclerosis
Prevention Study (AFCAPS/TexCAPS)
Secondary Prevention Trials
- Coronary Drug Project
- Stockholm Ischaemic Heart Disease Secondary
Prevention Study
- Scandinavian Simvastatin Survival Study
(4S)
- Cholesterol and Recurrent Events (CARE)
trial
- Long-term Intervention with Pravastatin
in Ischaemic Disease (LIPID) study
The results of the clinical trials (which were carried out at different
times and in different settings) have been expressed in the standardised
and comparable terms of evidence-based medicine. The following outcome
indicators have been calculated for major end points in each trial.
Absolute risk (AR) = number of events/number
of patients in group
Absolute risk reduction (ARR) = absolute
risk in control group (ARC) - absolute risk in treatment group (ART)
%ARR = 100 x ARR
Relative risk reduction (RRR) = ARR/ARC
%RRR = 100 x RRR
Number needed to treat to prevent one event (NNT)
= 1/ARR
Number needed to harm (one event) = 1/(ART
- ARC)
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