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[哌唑嗪对慢性心力衰竭的症状及长期血流动力学影响的缺失。为期一年的双盲随机研究]

[Lack of symptomatic and long-term hemodynamic effects of prazosin in chronic heart failure. Double-blind, randomized study over one year].

作者信息

Reifart N, Schmidt-Moritz A D, Nadj M, Kaltenbach M, Bussmann W D

出版信息

Z Kardiol. 1985 Apr;74(4):205-12.

PMID:3923726
Abstract

Long-term treatment of congestive heart failure with prazosin is disputed. Only few controlled trials have been reported so far. Our study is the first randomized double-blind placebo controlled trial over several months that also takes haemodynamic measurements into account. 25 patients with congestive heart failure classes III and IV (NYHA) received either prazosin 20 mg/d orally (n = 12) or placebo (n = 13) and were followed up closely. Before treatment, after 6 and after 12 months we performed echocardiography, heart volume (estimated by chest X-ray) and right heart catheterization at rest and during exercise. No significant differences could be noticed during follow-up concerning the following parameters: symptoms (NYHA), left ventricular end-diastolic diameter, shortening fraction, heart volume and systemic vascular resistance. While diuretics could be reduced in 3 patients with placebo an increasing dose was necessary in 6 out of 12 patients of the prazosin group. Long-term treatment of congestive heart failure with prazosin may be valuable only in exceptional cases.

摘要

关于哌唑嗪用于充血性心力衰竭的长期治疗存在争议。到目前为止,仅有少数对照试验被报道。我们的研究是首个为期数月的随机双盲安慰剂对照试验,该试验还考虑了血流动力学测量。25例纽约心脏协会(NYHA)心功能Ⅲ级和Ⅳ级的充血性心力衰竭患者,分别口服20mg/d哌唑嗪(n = 12)或安慰剂(n = 13),并进行密切随访。在治疗前、治疗6个月后和12个月后,我们进行了超声心动图检查、心脏体积(通过胸部X线估计)以及静息和运动时的右心导管检查。在随访期间,以下参数未发现显著差异:症状(NYHA)、左心室舒张末期直径、缩短分数、心脏体积和体循环血管阻力。安慰剂组有3例患者的利尿剂用量可减少,而哌唑嗪组12例患者中有6例需要增加利尿剂剂量。哌唑嗪用于充血性心力衰竭的长期治疗可能仅在特殊情况下有价值。

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