急性失代偿性心力衰竭新疗法的发展。

Heart failure monitor Pub Date : 2002-01-01
John R Teerlink
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引用次数: 0

摘要

1999年有近100万人因心力衰竭住院,比过去20年增加了155%,对这些患者的治疗是一个重要且日益严重的问题。然而,目前可用的治疗方法基于三种基本作用机制(利尿、外源性血管扩张剂和单磷酸环腺苷依赖的正性肌力药物),具有明显的局限性,这鼓励了新药的开发。该适应症的主要药物是三种不同治疗方法的代表,包括内源性血管舒张神经激素(奈西立肽)、钙增敏剂(左西孟旦)和神经激素拮抗剂(替佐生坦)。这三种药物代表了这一重要医学问题的新一代治疗方法,不仅可以治疗症状,还可以改善长期临床结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The development of new medical treatments for acute decompensated heart failure.

There were almost 1 million hospitalizations for heart failure in 1999, representing a 155% increase over the last 20 years, and the treatment of these patients is an important and growing problem. However, currently available therapies, which are based on three basic mechanisms of action (diuresis, exogenous vasodilators, and cyclic adenosine monophosphate-dependent positive inotropes), have significant limitations that have encouraged the development of newer agents. The leading medications for this indication are representatives of three different therapeutic approaches, which include endogenous vasodilatory neurohormones (nesiritide), calcium sensitizers (levosimendan), and neurohormonal antagonists (tezosentan). These three agents represent a new generation of therapeutics for this important medical problem and may provide the means not only to treat symptoms, but also to improve longer-term clinical outcomes.

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