...
首页> 外文期刊>The annals of pharmacotherapy >Levosimendan: a novel inotropic agent for treatment of acute, decompensated heart failure.
【24h】

Levosimendan: a novel inotropic agent for treatment of acute, decompensated heart failure.

机译:左西孟旦:一种新型的正性肌力药,用于治疗急性失代偿性心力衰竭。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

OBJECTIVE: To review the literature on a novel calcium sensitizer, levosimendan. DATA SOURCES: Articles were identified through searches of MEDLINE (1966-June 2005), International Pharmaceutical Abstracts (1970-June 2005), and EMBASE (1992-June 2005) using the key words levosimendan, simendan, calcium sensitizer, calcium sensitiser, and congestive heart failure. STUDY SELECTION AND DATA EXTRACTION: Clinical trials and pharmacokinetic studies evaluating the safety and efficacy of levosimendan were selected. DATA SYNTHESIS: Levosimendan 6-24 mug/kg intravenous bolus followed by a 24-hour continuous infusion of 0.05-0.2 mug/kg/min improved cardiac output and reduced pulmonary capillary wedge pressure in a dose-dependent manner. Dose-ranging and randomized clinical trials have demonstrated improvement in symptoms and hemodynamics and short-term survival outcomes in the treatment of acute, decompensated heart failure. Clinical trials evaluating retrospective mortality data and combined endpoints (mortality,rehospitalization) have demonstrated better outcomes with levosimendan compared with dobutamine. The incidence of hypotension with levosimendan is not significantly different than with dobutamine, but there is a dose-related increase in heart rate. CONCLUSIONS: Levosimendan is useful in moderate to severe low-output heart failure in patients who have failed to respond to diuretics and vasodilators. Based on current studies, levosimendan appears to be a safe alternative to dobutamine for treatment of acute, decompensated heart failure. Prospective clinical trials are needed to confirm the effect of levosimendan on long-term survival and its role in heart failure in the setting of myocardial infarction.
机译:目的:回顾有关新型钙敏化剂左西孟旦的文献。资料来源:通过检索MEDLINE(1966年-2005年6月),International Pharmaceutical Abstracts(1970年-2005年6月)和EMBASE(1992年6月-2005年)来检索文章,关键词是左西孟旦,西门丹,钙敏化剂,钙敏化剂和充血性心力衰竭。研究选择和数据提取:选择评价左西孟旦安全性和有效性的临床试验和药代动力学研究。数据合成:左西孟旦6-24杯/千克静脉推注,然后24小时连续输注0.05-0.2杯/千克/分钟,以剂量依赖性方式改善心输出量并降低肺毛细血管楔压。剂量范围和随机临床试验表明,在急性,代偿性心力衰竭的治疗中,症状和血液动力学以及短期生存结局得到改善。评估回顾性死亡率数据和综合终点(死亡率,再次住院)的临床试验表明,左西孟旦比多巴酚丁胺的疗效更好。左西孟旦低血压的发生率与多巴酚丁胺无显着差异,但是心率与剂量相关。结论:左西孟旦可用于对利尿剂和血管扩张药无效的患者的中度至重度低输出心力衰竭。根据目前的研究,左西孟旦似乎是多巴酚丁胺治疗急性失代偿性心力衰竭的安全替代品。需要进行前瞻性临床试验,以确认左西孟旦对长期生存的影响及其在心肌梗死中在心力衰竭中的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号