Cleland John G F, McGowan James
Department of Cardiology, Castle Hill Hospital, University of Hull, Cottingham, Kingston upon Hull, United Kingdom.
Curr Opin Cardiol. 2002 May;17(3):257-65. doi: 10.1097/00001573-200205000-00008.
Levosimendan is a new inotropic and vasodilator agent. The inotropic effect is mediated by calcium concentration-dependent conformational changes in troponin C during systole leading to sensitization of the contractile apparatus to calcium ions. The vasodilator effect is mediated by opening potassium channels on vascular smooth muscle. It has a complex pharmacokinetic profile, with a long-acting metabolite that has hemodynamic effects persisting for approximately 1 week. Although it is absorbed orally, it has been developed only for intravenous use thus far. The hemodynamic effects are not reduced and may be enhanced in the presence of beta-blockers, possibly an important attribute when dealing with exacerbation of heart failure caused by or in the presence of beta-blockers. More patients with heart failure have participated in randomized controlled trials of levosimendan than of any other intravenous inotropic agent. Experience with its use after cardiac surgery is limited. Preliminary observations suggest that hemodynamic changes are associated with symptomatic benefit and a reduction in morbidity and mortality in patients with severe heart failure caused by left ventricular systolic dysfunction, compared with placebo in one study and dobutamine in another. Levosimendan may be the first inotropic agent that it is both safe and effective in altering clinical outcomes relevant for patients. Part of this benefit may be achieved because levosimendan allows other inotropic agents that may have adverse effects on patient outcome to be avoided. Further research is required to confirm whether levosimendan reduces mortality and morbidity compared with a placebo and when administered repetitively. If it does, it may become routine therapy for the treatment of severe heart failure.
左西孟旦是一种新型的强心和血管扩张剂。其强心作用是由收缩期肌钙蛋白C中钙浓度依赖性的构象变化介导的,导致收缩装置对钙离子敏感。血管扩张作用是通过打开血管平滑肌上的钾通道介导的。它具有复杂的药代动力学特征,有一种长效代谢产物,其血流动力学效应可持续约1周。虽然它可口服吸收,但迄今为止仅开发了静脉制剂。在使用β受体阻滞剂的情况下,其血流动力学效应不会降低,反而可能增强,这在处理由β受体阻滞剂引起或存在β受体阻滞剂时的心力衰竭加重情况时可能是一个重要特性。参与左西孟旦随机对照试验的心力衰竭患者比参与任何其他静脉用强心剂试验的患者都多。其在心脏手术后的使用经验有限。初步观察表明,与一项研究中的安慰剂和另一项研究中的多巴酚丁胺相比,对于由左心室收缩功能障碍引起的严重心力衰竭患者,血流动力学变化与症状改善以及发病率和死亡率降低相关。左西孟旦可能是第一种在改变与患者相关的临床结局方面既安全又有效的强心剂。部分益处可能是因为左西孟旦可以避免使用其他可能对患者预后有不良影响的强心剂。需要进一步研究来证实左西孟旦与安慰剂相比以及重复给药时是否能降低死亡率和发病率。如果能,它可能会成为治疗严重心力衰竭的常规疗法。