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维拉帕米对肥厚型心肌病患者血流动力学功能及心肌代谢的影响。

Effects of verapamil on haemodynamic function and myocardial metabolism in patients with hypertrophic cardiomyopathy.

作者信息

Wilmshurst P T, Thompson D S, Juul S M, Jenkins B S, Webb-Peploe M M

出版信息

Br Heart J. 1986 Dec;56(6):544-53. doi: 10.1136/hrt.56.6.544.

Abstract

The effect of 20 mg dose of intravenous verapamil was studied over a range of heart rates in 12 patients with hypertrophic cardiomyopathy. Six patients had an appreciable left ventricular outflow tract gradient and six did not. The drug reduced myocardial oxygen consumption in proportion to a reduction in the development of left ventricular pressure. The negative inotropic effect of verapamil was counteracted by the drug's non-specific vasodilator activity, so that cardiac index was unaltered at any heart rate and as a result myocardial efficiency was unaffected by the drug. Verapamil did not consistently alter myocardial metabolism. Some patients showed improvement in anaerobic myocardial metabolism after verapamil but an equal number showed impairment of lactate metabolism. It was not possible to predict from clinical features, echocardiographic findings, or haemodynamic variables measured before administration of verapamil which patients would demonstrate haemodynamic or metabolic improvement after the drug. In this short term study no mechanism was demonstrated by which patients with hypertrophic cardiomyopathy might obtain a consistent improvement from treatment with verapamil.

摘要

对12例肥厚型心肌病患者在一系列心率水平下研究了静脉注射20mg维拉帕米的效果。6例患者有明显的左心室流出道压差,6例没有。该药物使心肌氧耗量的减少与左心室压力上升幅度的降低成比例。维拉帕米的负性肌力作用被其非特异性血管舒张活性抵消,因此在任何心率下心脏指数均未改变,结果心肌效率不受该药物影响。维拉帕米并未持续改变心肌代谢。一些患者在使用维拉帕米后无氧心肌代谢有所改善,但同样数量的患者乳酸代谢出现受损。根据维拉帕米给药前测量的临床特征、超声心动图表现或血流动力学变量,无法预测哪些患者在用药后会出现血流动力学或代谢改善。在这项短期研究中,未证实肥厚型心肌病患者通过维拉帕米治疗能持续改善的机制。

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本文引用的文献

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Hypertrophic cardiomyopathy--therapy with slow channel inhibiting agents.
Prog Cardiovasc Dis. 1982 Nov-Dec;25(3):193-210. doi: 10.1016/0033-0620(82)90016-0.
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The frontiers of cardiomyopathy.心肌病的前沿领域。
Br Heart J. 1982 Jul;48(1):1-18. doi: 10.1136/hrt.48.1.1.

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