Pravastatin reduced the risk of stroke from any cause compared to placebo (3.7% vs 4.5%; RRR 19%, 95% CI 0-34%; P=0.05) in patients with previous myocardial infarction or unstable angina.
RCT (n=9,014)
Double-blind
Effect estimate: RRR 19% (95% CI 0 to 34)
Absolute Event Rate: 3.7% vs 4.5%
p-value: p=0.05
BACKGROUND: Several epidemiologic studies have concluded that there is no relation between total cholesterol levels and the risk of stroke. In some studies that classified strokes according to cause, there was an association between increasing cholesterol levels and the risk of ischemic stroke and a possible association between low cholesterol levels and the risk of hemorrhagic stroke. Recent reviews of trials of 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors have suggested that these agents may reduce the risk of stroke. METHODS: In a double-blind trial (the Long-Term Intervention with Pravastatin in Ischaemic Disease study), we compared the effects of pravastatin on mortality due to coronary heart disease (the primary end point) with the effects of placebo among 9014 patients with a history of myocardial infarction or unstable angina and a total cholesterol level of 155 to 271 mg per deciliter (4.0 to 7.0 mmol per liter). Our goal in the present study was to assess effects on stroke from any cause and nonhemorrhagic stroke, which were secondary end points. RESULTS: There were 419 strokes among 373 patients over a follow-up period of six years. A total of 309 strokes were classified as ischemic, 31 as hemorrhagic, and 79 as of unknown type. Among the patients given placebo, the risk of stroke was 4.5 percent, as compared with 3.7 percent among those given pravastatin (relative reduction in risk, 19 percent; 95 percent confidence interval, 0 to 34 percent; P=0.05). Non-hemorrhagic stroke occurred in 4.4 percent of the patients given placebo, as compared with 3.4 percent of those given pravastatin (reduction in risk, 23 percent; 95 percent confidence interval, 5 to 38 percent; P=0.02). Pravastatin had no effect on hemorrhagic stroke (incidence, 0.2 percent in the placebo group vs. 0.4 percent in the pravastatin group; P=0.28). CONCLUSIONS: Pravastatin has a moderate effect in reducing the risk of stroke from any cause and the risk of nonhemorrhagic stroke in patients with previous myocardial infarction or unstable angina.
White et al. (Thu,) conducted a rct in History of myocardial infarction or unstable angina (n=9,014). Pravastatin vs. Placebo was evaluated on Stroke from any cause (RRR 19%, 95% CI 0 to 34, p=0.05). Pravastatin reduced the risk of stroke from any cause compared to placebo (3.7% vs 4.5%; RRR 19%, 95% CI 0-34%; P=0.05) in patients with previous myocardial infarction or unstable angina.
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