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β肾上腺素能受体阻滞剂内在拟交感活性在心绞痛患者治疗中的评估。

Evaluation of intrinsic sympathomimetic activity of beta-adrenoceptor blocking drugs in the treatment of patients with angina pectoris.

作者信息

Harry J D

出版信息

Bibl Cardiol. 1976(35):172-82.

PMID:10882
Abstract

Beta-adrenoceptor blocking drugs with intrinsic sympathomimetic activity (ISA) may be less effective in the treatment of patients with angina pectoris than some others that lack this property. A review of 14 trials comparing beta-adrenoceptor blocking drug with ISA and those without ISA in angina pectoris has been made. The overall picture emerges from both acute and chronic studies using subjective and objective endpoints, that there is no striking difference in effectiveness between the two kinds of beta-adrenoceptor blocking drugs. The one exception is pindolol (a drug with ISA) which, at higher doses, has been shown to be consistently worse than propranolol (a drug without ISA). The reasons for the similarity between propranolol and other bets-blocking drugs with ISA in the trials cited are either that the trial design was defective (the trials were mainly fixed dose comparisons) or that the stimulant effects of those drugs with ISA is not of sufficient magnitude to make a difference. It is suggested that further carefully constructed clinical trials should be carried out before the second reason can be accepted.

摘要

具有内在拟交感活性(ISA)的β肾上腺素受体阻断药在治疗心绞痛患者时可能不如其他一些缺乏该特性的药物有效。对14项比较具有ISA的β肾上腺素受体阻断药和不具有ISA的β肾上腺素受体阻断药治疗心绞痛的试验进行了综述。从使用主观和客观终点的急性和慢性研究中得出的总体情况是,这两种β肾上腺素受体阻断药在有效性方面没有显著差异。唯一的例外是吲哚洛尔(一种具有ISA的药物),在较高剂量时,已证明其始终比普萘洛尔(一种不具有ISA的药物)效果差。在所引用的试验中,普萘洛尔与其他具有ISA的β受体阻断药之间相似的原因,要么是试验设计有缺陷(试验主要是固定剂量比较),要么是那些具有ISA的药物的刺激作用强度不足以产生差异。建议在接受第二个原因之前应进行进一步精心设计的临床试验。

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