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[培哚普利与慢性心力衰竭]

[Perindopril and chronic heart failure].

作者信息

Bounhoure J P

机构信息

Service de cardiologie, hôpital de Rangueil, Toulouse.

出版信息

Arch Mal Coeur Vaiss. 1991 Dec;84 Spec No 4:89-92.

PMID:1793331
Abstract

Haemodynamic studies performed in patients with cardiac failure have shown that perindopril decreases right and left ventricular filling pressures, systemic blood pressure and peripheral resistances, slightly reduces the heart rate and increases cardiac output. Flammang showed that these haemodynamic changes are sustained after 12 months' treatment. A randomised double blind multicenter trial versus placebo was carried out over 3 months following a 15 days pre-inclusion period in 125 patients with NYHA Stage II and III cardiac failure stabilised by digitalis and diuretic therapy. Perindopril was administered at a dosage of 2 or 4 mg according to initial systolic blood pressure and efficacy was evaluated at 1 and 3 months according to the NYHA classification, a score of clinical severity, the duration of two exercise stress tests on a bicycle ergometer or treadmill and the cardiothoracic ratio. There were no cases of cardiac decompensation (NYHA Stage IV) in the group of perindopril whilst 3 cases were observed in the placebo group. Significant improvements in the clinical scores and effort capacity were observed in the perindopril group. The duration of exercise on the treadmill was 778 seconds with perindopril compared to 544 seconds in the placebo group. Systolic blood pressure did not change and there was a slight decrease in standing diastolic pressures. No significant increases in blood urea or creatinine levels were observed. To study the effects on blood pressure, a major factor in the management of a patient with cardiac failure, McFadyen compared the changes in blood pressure after a single dose of perindopril, enalapril, captopril and placebo.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对心力衰竭患者进行的血流动力学研究表明,培哚普利可降低左右心室充盈压、体循环血压和外周阻力,轻度降低心率并增加心输出量。弗拉芒指出,经过12个月的治疗后,这些血流动力学变化仍持续存在。在125例经洋地黄和利尿剂治疗病情稳定的纽约心脏协会(NYHA)Ⅱ级和Ⅲ级心力衰竭患者中,在15天的预入选期后,进行了一项为期3个月的随机双盲多中心试验,与安慰剂进行对比。根据初始收缩压给予培哚普利2或4毫克的剂量,并在1个月和3个月时根据NYHA分级、临床严重程度评分、在自行车测力计或跑步机上进行的两次运动应激试验的时长以及心胸比率来评估疗效。培哚普利组未出现心脏失代偿(NYHAⅣ级)病例,而安慰剂组观察到3例。培哚普利组的临床评分和运动能力有显著改善。使用培哚普利时在跑步机上的运动时长为778秒,而安慰剂组为544秒。收缩压未改变,站立时舒张压略有下降。未观察到血尿素或肌酐水平有显著升高。为研究对血压(心力衰竭患者管理中的一个主要因素)的影响,麦克法登比较了单剂量培哚普利、依那普利、卡托普利和安慰剂后的血压变化。(摘要截选于250词)

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