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rosuvastatin and primary cardiovascular prevention New Indication Continue to use pravastatin or simvastatin

机译:罗苏伐他汀和心血管一级预防新适应症继续使用普伐他汀或辛伐他汀

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摘要

When a patient who has never had a cardiovascular event, i.e. primary cardiovascular prevention, requires cholesterol-lowering drug therapy, pravastatin and simvastatin are first-choice drugs (1). Rosuvastatin (Crestor0, AstraZeneca) is now authorised in this setting, based on unplanned subgroup analyses of a placebo-controlled trial (the Jupiter study) involving 17 802 patients with no prior cardiovascular history (1 -3).In February 2009 we concluded that the risk-benefit balance of rosuvastatin was uncertain in the overall Jupiter study population (1). Since then, new results for cardiovascular mortality (0.4% with rosuvastatin and 0.5% with placebo; p=0.315) have not challenged our earlier conclusions (2). Retrospective subgroup analyses, which are inherently unreliable, suggest that rosuvastatin reduced the incidence of an endpoint combining various cardiovascular events in "high-risk" patients, but not overall mortality (3).
机译:当从未发生过心血管事件(即主要的心血管疾病预防)的患者需要降低胆固醇的药物治疗时,普伐他汀和辛伐他汀是首选药物(1)。 Rosuvastatin(Crestor0,AstraZeneca)在这种情况下已获授权,基于一项安慰剂对照试验(Jupiter研究)的计划外亚组分析,该试验涉及17 802名既往无心血管病史的患者(1-3)。2009年2月,我们得出结论在整个Jupiter研究人群中,瑞舒伐他汀的风险收益平衡尚不确定(1)。从那时起,心血管死亡率的新结果(瑞舒伐他汀组为0.4%,安慰剂组为0.5%; p = 0.315)并未挑战我们先前的结论(2)。追溯性亚组分析本质上是不可靠的,提示瑞舒伐他汀降低了结合“高危”患者各种心血管事件的终点发生率,但并未降低整体死亡率(3)。

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