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酮色林引起的QT间期延长和尖端扭转型室性心动过速。

QT prolongation and torsade de pointes ventricular tachycardia produced by Ketanserin.

作者信息

Aldariz A E, Romero H, Baroni M, Baglivo H, Esper R J

出版信息

Pacing Clin Electrophysiol. 1986 Nov;9(6):836-41. doi: 10.1111/j.1540-8159.1986.tb06633.x.

DOI:10.1111/j.1540-8159.1986.tb06633.x
PMID:2432486
Abstract

A 65-year-old man with arterial hypertension received oral treatment with Ketanserin, a new drug, during a period of five months. He developed marked QT interval prolongation and have several Stokes-Adams attacks. A Holter recording obtained during one of these episodes showed torsade de pointes ventricular tachycardia. The arrhythmias occurred during maximum QT interval prolongation. The correlation between Ketanserin and QT interval prolongation was evaluated by using several Holter studies during administration and withdrawal of the drug. The effect of Ketanserin on the QTc interval was analyzed retrospectively in six patients who had been taking the drug orally. Following a period of four to eight months, the QTc interval was prolonged by the drug (5 to 31%, mean 17%) in five patients. We conclude that torsade de pointes is a potential hazard of long-term treatment with Ketanserin.

摘要

一名65岁的动脉高血压男性在五个月的时间里接受了新型药物酮色林的口服治疗。他出现了明显的QT间期延长,并发生了几次斯托克斯-亚当斯发作。在其中一次发作期间进行的动态心电图记录显示为尖端扭转型室性心动过速。心律失常发生在QT间期延长的最大值时。通过在给药和停药期间进行多次动态心电图研究,评估了酮色林与QT间期延长之间的相关性。对六名口服该药物的患者的QTc间期受酮色林影响的情况进行了回顾性分析。在四至八个月的时间后,五名患者的QTc间期被该药物延长了(5%至31%,平均17%)。我们得出结论,尖端扭转型室性心动过速是长期使用酮色林治疗的潜在风险。

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QT prolongation and torsade de pointes ventricular tachycardia produced by Ketanserin.酮色林引起的QT间期延长和尖端扭转型室性心动过速。
Pacing Clin Electrophysiol. 1986 Nov;9(6):836-41. doi: 10.1111/j.1540-8159.1986.tb06633.x.
2
[Prolongation of the QT interval and torsade de pointes caused by ketanserin].[酮色林引起的QT间期延长和尖端扭转型室性心动过速]
G Ital Cardiol. 1990 Sep;20(9):869-72.
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Ventricular arrhythmias and QT-prolongation during therapy with ketanserin: report of a case.酮色林治疗期间的室性心律失常和QT间期延长:一例报告。
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引用本文的文献

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The past, present and perhaps future of pharmacovigilance: homage to Folke Sjoqvist.药物警戒的过去、现在和未来:向 Folke Sjoqvist 致敬。
Eur J Clin Pharmacol. 2013 May;69 Suppl 1:33-41. doi: 10.1007/s00228-013-1486-8. Epub 2013 May 3.
2
The 5-HT2 antagonist ketanserin is an open channel blocker of human cardiac ether-à-go-go-related gene (hERG) potassium channels.5-羟色胺2(5-HT2)拮抗剂酮色林是人类心脏去甲肾上腺素能相关基因(hERG)钾通道的一种开放通道阻滞剂。
Br J Pharmacol. 2008 Oct;155(3):365-73. doi: 10.1038/bjp.2008.261. Epub 2008 Jun 23.
3
A prolonged QTc interval. Is it an important effect of antiarrhythmic drugs?
QTc间期延长。这是抗心律失常药物的一个重要效应吗?
Med Toxicol Adverse Drug Exp. 1989 Nov-Dec;4(6):400-11. doi: 10.1007/BF03259922.
4
Acute electrophysiologic effects of an HT2-serotonin antagonist, ketanserin, in humans.5-羟色胺2(HT2)受体拮抗剂酮色林对人体的急性电生理效应。
Cardiovasc Drugs Ther. 1990 Aug;4(4):1157-60. doi: 10.1007/BF01856513.
5
Clinical pharmacokinetics of ketanserin.酮色林的临床药代动力学
Clin Pharmacokinet. 1991 Apr;20(4):263-79. doi: 10.2165/00003088-199120040-00002.