-受体阻滞剂治疗心力衰竭的持续作用。

Heart failure monitor Pub Date : 2006-01-01
Dariusz P Korczyk, Robert N Doughty
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引用次数: 0

摘要

在世界范围内,新诊断的心力衰竭患者数量持续增长,这在一定程度上反映了急性冠状动脉综合征后生存率的提高和人口老龄化。寻找新的有效的治疗方法仍然是21世纪的首要任务。β受体阻滞剂的使用现已在轻度和中度收缩期心力衰竭的临床背景下得到很好的确立。β -阻断剂对死亡率的影响与血管紧张素转换酶抑制剂治疗的影响是附加的。最近完成的大型随机试验提供了强有力的证据,证明β受体阻滞剂用于严重(NYHA功能级IV)心力衰竭和无症状左心室收缩功能障碍和近期心肌梗死患者。显然,患者选择仍然是心衰患者安全使用-受体阻滞剂的关键。来自临床试验的进一步数据支持在死亡率和发病率、良好的安全记录和极端年龄(儿童和>70岁的成人)和特定临床情况(包括糖尿病、慢性阻塞性气道疾病、肾衰竭和心房纤颤)患者的耐受性方面具有类似的益处。最近在心力衰竭和保留收缩功能(所谓的舒张性心力衰竭)患者中使用具有血管舒张特性的β受体阻滞剂似乎很有希望,但在广泛临床应用之前,需要大规模、长期的试验。
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A continued role for beta-blocker therapy in heart failure.

The number of patients with newly diagnosed heart failure continues to grow worldwide, to some extent reflecting the increase in survival after acute coronary syndromes and the aging of the population. The search for new and effective therapies for this condition remains a priority in the 21st century. The use of beta-blockers is now well established in the clinical context of mild and moderate systolic heart failure. The effects of beta-blockade on mortality are additive to those with angiotensin-converting enzyme inhibitor therapy. Recently completed, large, randomized trials provided strong evidence for the use of beta-blockers in severe (NYHA functional class IV) heart failure and in asymptomatic patients with left ventricular systolic dysfunction and recent myocardial infarction. Obviously, patient selection still remains the key to the safe use of beta-blockers in patients with heart failure. Further data from clinical trials have emerged to support similar benefits in terms of mortality and morbidity, a good safety record, and tolerability in patients at extremes of age (children and adults >70 years of age) and in specific clinical circumstances (including diabetes, chronic obstructive airways disease, renal failure, and atrial fibrillation). Recent use of beta-blockers with vasodilatory properties in patients with heart failure and preserved systolic function (so-called diastolic heart failure) appears promising but will require large-scale, long-term trials prior to widespread clinical use.

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