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[捷克和斯洛伐克关于螺普利的干预性研究(CASSIS研究)。一项针对慢性心力衰竭的随机、双盲、多中心、安慰剂对照研究]

[A Czech and Slovak interventional study of spirapril (the CASSIS study). A randomized, double-blind, multicenter, placebo-controlled study in chronic heart failure].

作者信息

Jerie P, Kremer H J, Uhlír O, Widimský J

出版信息

Vnitr Lek. 1997 Jun;43(6):351-8.

PMID:9601863
Abstract

Spirapril, an ACE-inhibitor without the SH group was tested in a randomized double-blind multicentric study in patients with chronic symptomatic heart failure (NYHA II-IV). After a 1-4-week initial stage with placebo the patients were randomized into five groups: the first was given placebo, the second one spirapril 1.5 mg, the third one spirapril 3 mg, the fourth one spirapril 6 mg and the fifth one 5 and later 10 mg for a period of 12 weeks. The number of patients in different groups was in the following order: 48, 48, 53, 51 and 48. The condition for admission into the study was chronic heart failure not responding adequately to treatment with digoxin and diuretics, IHD or dilatation cardiomyopathy with the left ventricular ejection fraction (% tolerating a basic ergometric load for two minutes. The primary criterium was an increment during the period of the load, secondary criteria comprised objective and subjective cardiac symptoms, changes in the left ventricular ejection fraction, cardiothoracic index/heart size and quality of life. The load tolerance increased in all groups, however, no significant differences between groups were found. The authors also found regression of signs of pulmonary congestion during active spirapril treatment and diminution of the cardiac shadow. Moreover the authors proved a significant reduction of the mortality in the actively treated patients as compared with those receiving placebo, a lower frequency of hospital admissions and reduction of serious undesirable cardiovascular symptoms during active treatment. In patients with medium severe and severe cardiac failure with IHD, combination with short acting calcium channel blockers had an unfavourable effect on the load tolerance and clinical parameters. Sprirapril, combined with diuretics and digoxin is a suitable drug also in chronic cardiac failure. Questionable remains the importance of loading tests when verifying the effectiveness of ACE-inhibitors. Treatment with short-time acting calcium antagonists cannot be recommended in symptomatic chronic cardiac failure.

摘要

螺普利是一种不含巯基的血管紧张素转换酶抑制剂,在一项针对慢性症状性心力衰竭(纽约心脏协会II-IV级)患者的随机双盲多中心研究中进行了测试。在为期1至4周的初始阶段服用安慰剂后,患者被随机分为五组:第一组给予安慰剂,第二组给予1.5毫克螺普利,第三组给予3毫克螺普利,第四组给予6毫克螺普利,第五组给予5毫克,之后给予10毫克,为期12周。不同组的患者数量按以下顺序排列:48、48、53、51和48。纳入研究的条件是慢性心力衰竭患者对洋地黄和利尿剂治疗反应不佳、患有缺血性心脏病或扩张型心肌病,左心室射血分数(%)能耐受两分钟的基础运动负荷。主要标准是负荷期间的增加量,次要标准包括客观和主观心脏症状、左心室射血分数的变化、心胸指数/心脏大小和生活质量。所有组的负荷耐受性均有所提高,但各小组之间未发现显著差异。作者还发现,在螺普利积极治疗期间,肺淤血体征有所消退,心脏阴影缩小。此外,作者证明,与接受安慰剂的患者相比,积极治疗的患者死亡率显著降低,住院频率较低,积极治疗期间严重不良心血管症状减少。在患有缺血性心脏病的中度和重度心力衰竭患者中,与短效钙通道阻滞剂联合使用对负荷耐受性和临床参数有不利影响。螺普利与利尿剂和洋地黄联合使用也是慢性心力衰竭的一种合适药物。在验证血管紧张素转换酶抑制剂的有效性时,负荷试验的重要性仍存在疑问。对于有症状的慢性心力衰竭,不建议使用短效钙拮抗剂进行治疗。

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