Risk factors for non-haemorrhagic stroke in patients with coronary heart disease and the effect of lipid-modifying therapy with pravastatin

被引:7
|
作者
West, MJ [1 ]
White, HD
Simes, RJ
Kirby, A
Watson, JD
Anderson, NE
Hankey, GJ
Wonders, S
Hunt, D
Tonkin, AM
机构
[1] Univ Queensland, Prince Charles Hosp, Dept Med, Brisbane, Qld 4032, Australia
[2] Green Lane Hosp, Auckland 3, New Zealand
[3] NHMRC, Clin Trials Ctr, Sydney, NSW, Australia
[4] Auckland Med Sch, Auckland, New Zealand
[5] Royal Prince Alfred Hosp, Sydney, NSW, Australia
[6] Royal Perth Hosp, Perth, WA, Australia
[7] Royal Melbourne Hosp, Melbourne, Vic, Australia
[8] Natl Heart Fdn Australia, Melbourne, Vic, Australia
关键词
coronary heart disease; non-haemorrhagic stroke; pravastatin; risk factors; transient ischaemic attack;
D O I
10.1097/00004872-200212000-00032
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objective To determine the relative importance of recognised risk factors for non-haemorrhagic stroke, including serum cholesterol and the effect of cholesterol-lowering therapy, on the occurrence of non-haemorrhagic stroke in patients enrolled in the LIPID (Long-term Intervention with Pravastatin in Ischaemic Disease) study. Design The LIPID study was a placebo-controlled, double-blind trial of the efficacy on coronary heart disease mortality of pravastatin therapy over 6 years in 9014 patients with previous acute coronary syndromes and baseline total cholesterol of 4-7 mmol/l. Following identification of patients who had suffered non-haemorrhagic stroke, a pre-specified secondary end point, multivariate Cox regression was used to determine risk in the total population. Time-to-event analysis was used to determine the effect of pravastatin therapy on the rate of non-haemorrhagic stroke. Results There were 388 non-haemorrhagic strokes in 350 patients. Factors conferring risk of future non-haemorrhagic stroke were age, atrial fibrillation, prior stroke, diabetes, hypertension, systolic blood pressure, cigarette smoking, body mass index, male sex and creatinine clearance. Baseline lipids did not predict non-haemorrhagic stroke. Treatment with pravastatin reduced non-haemorrhagic stroke by 23% (P= 0.016) when considered alone, and 21% (P= 0.024) after adjustment for other risk factors. Conclusions The study confirmed the variety of risk factors for non-haemorrhagic stroke. From the risk predictors, a simple prognostic index was created for nonhaemorrhagic stroke to identify a group of patients at high risk. Treatment with pravastatin resulted in significant additional benefit after allowance for risk factors. (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:2513 / 2517
页数:5
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