莱沃西门丹与多布他明治疗急性不补偿性心力衰竭患者:SURVIVE随机试验
Alexandre Mebazaa1, Markku S Nieminen, Milton Packer
1Department of Anesthesiology, Université Paris Diderot and Hospital Lariboisière AP-HP, Paris, France. alexandre.mebazaa@lrb.aphp.fr
JAMA
|May 3, 2007
概括
与多布胺相比,Levosimendan在急性不补偿性心力衰竭患者中没有显著降低180天死亡率. 虽然它降低了B型性尿素水平,但它没有改善其他临床结果.
科学领域:
- 心脏病学 心脏病学
- 药理学 药理学是指药理学的学科.
- 临床试验 临床试验
背景情况:
- 急性不补偿性心力衰竭 (ADHF) 呈现出显著的发病率和死亡率.
- 需要有效的治疗来改善血液动力学和症状,而不会影响生存.
研究的目的:
- 在ADHF患者中,评估短期静脉注射levosimendan与dobutamine的长期生存效应.
主要方法:
- 随机,双盲SURVIVE试验涉及1327名ADHF患者,需要因诺托普支持.
- 患者接受了静脉注射的levosimendan (n=664) 或dobutamine (n=663).
- 主要终点是180天内全因死亡率.
主要成果:
- 在180天的全因死亡率为levosimendan的26%和dobutamine的28% (HR 0.91,P=.40).
- 莱沃西门丹显示B型尿素水平降低更大.
- 在二次临床结局中没有发现显著差异;然而,多布他明的心力衰竭发病率较高,心房动,低血和头痛的发生率较高.
结论:
- 与dobutamine相比,levosimendan没有显著降低180天全因死亡率或改善ADHF患者的二次临床结果.
- 尽管最初B型尿素降低,但levosimendan对生存的临床益处没有被证明.
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