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氟卡尼:一种新型抗心律失常药物。

Flecainide: a new antiarrhythmic agent.

作者信息

Somberg J C, Tepper D

出版信息

Am Heart J. 1986 Oct;112(4):808-13. doi: 10.1016/0002-8703(86)90478-3.

DOI:10.1016/0002-8703(86)90478-3
PMID:3094352
Abstract

PVCs (trigger mechanisms) and the vulnerability of the myocardium to sustain a life-threatening ventricular tachycardia (substrate) are two variables in the sudden death equation. Physicians treating patients at risk for sudden death should consider PVC frequency and vulnerability as interrelated variables. Risk assessment must take into consideration both variables. Antiarrhythmic drug efficacy can be assessed in terms of a reduction in trigger mechanisms (PVCs) as well as decreasing myocardial vulnerability (induction of VT at PES). Flecainide acetate, at a reduced dosage of 100 mg twice daily, is effective in both aspects, markedly decreasing PVC frequency and preventing VT induction at PES testing. Holter monitoring and electrophysiologic testing evaluate different aspects of the problem. With the addition of an agent as potent as flecainide, which is devoid of many of the bothersome side effects previously limiting antiarrhythmic therapy, an agent is now available that may be useful to treat both the trigger mechanism and the substrate in sudden death. We must be careful not to worsen the situation through the profound effects of flecainide on depolarization and refractoriness that in some patients cause life-threatening arrhythmias to be more frequent.

摘要

室性早搏(触发机制)以及心肌维持危及生命的室性心动过速的易损性(基质)是心源性猝死等式中的两个变量。治疗有猝死风险患者的医生应将室性早搏频率和易损性视为相互关联的变量。风险评估必须考虑这两个变量。抗心律失常药物的疗效可以通过减少触发机制(室性早搏)以及降低心肌易损性(程序电刺激诱发室性心动过速)来评估。醋酸氟卡尼,每日两次,剂量减至100毫克,在这两方面均有效,可显著降低室性早搏频率并在程序电刺激测试时预防室性心动过速的诱发。动态心电图监测和电生理检查评估该问题的不同方面。随着像氟卡尼这样强效药物的加入,它没有许多以前限制抗心律失常治疗的令人烦恼的副作用,现在有一种药物可用于治疗心源性猝死中的触发机制和基质。我们必须小心,以免因氟卡尼对去极化和不应期的深远影响而使情况恶化,这种影响在一些患者中会导致危及生命的心律失常更频繁发生。

相似文献

1
Flecainide: a new antiarrhythmic agent.氟卡尼:一种新型抗心律失常药物。
Am Heart J. 1986 Oct;112(4):808-13. doi: 10.1016/0002-8703(86)90478-3.
2
Antiarrhythmic drug efficacy at electrophysiology testing: predictive effectiveness of procainamide and flecainide.抗心律失常药物在电生理检查中的疗效:普鲁卡因胺和氟卡尼的预测有效性
Am Heart J. 1986 Apr;111(4):632-8. doi: 10.1016/0002-8703(86)90090-6.
3
[Propafenone and flecainide in the therapy of ventricular arrhythmias].[普罗帕酮和氟卡尼在室性心律失常治疗中的应用]
Minerva Cardioangiol. 1995 Oct;43(10):449-57.
4
Flecainide: a new antiarrhythmic agent.
Am Fam Physician. 1986 Nov;34(5):197-200.
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Use of flecainide acetate in the treatment of premature ventricular contractions.醋酸氟卡尼在室性早搏治疗中的应用。
Am Heart J. 1983 Feb;105(2):227-30. doi: 10.1016/0002-8703(83)90518-5.
6
[Flecainide: a new antiarrhythmic agent].氟卡尼:一种新型抗心律失常药物
Arch Mal Coeur Vaiss. 1983 Oct;76(10):1218-30.
7
Oral flecainide acetate for the treatment of ventricular arrhythmias.口服醋酸氟卡尼治疗室性心律失常。
N Engl J Med. 1981 Aug 27;305(9):473-7. doi: 10.1056/NEJM198108273050901.
8
Short- and long-term experience with flecainide acetate in the management of refractory life-threatening ventricular arrhythmias.醋酸氟卡尼治疗难治性危及生命的室性心律失常的短期和长期经验。
J Am Coll Cardiol. 1985 Oct;6(4):772-9. doi: 10.1016/s0735-1097(85)80481-2.
9
[Effects of oral flecainide treatment of refractory tachyarrhythmias].口服氟卡尼治疗难治性快速性心律失常的疗效
Kokyu To Junkan. 1990 May;38(5):471-6.
10
[Antiarrhythmic therapy with flecainide in acute experimental myocardial infarction (author's transl)].急性实验性心肌梗死中氟卡尼的抗心律失常治疗(作者译)
Z Kardiol. 1981 Feb;70(2):124-30.

引用本文的文献

1
Multiple targets for flecainide action: implications for cardiac arrhythmogenesis.氟卡尼的多种作用靶点:对心脏心律失常发生机制的影响。
Br J Pharmacol. 2018 Apr;175(8):1260-1278. doi: 10.1111/bph.13807. Epub 2017 May 12.
2
Flecainide is effective against premature supraventricular and ventricular contractions during general anesthesia.氟卡尼可有效对抗全身麻醉期间的过早室上性和室性收缩。
J Anesth. 1994 Sep;8(3):284-7. doi: 10.1007/BF02514651.
3
Drug effects on the electrocardiogram. A review of their clinical importance.药物对心电图的影响。对其临床重要性的综述。
Drugs. 1993 Aug;46(2):219-48. doi: 10.2165/00003495-199346020-00002.
4
Sodium channel-blocking properties of flecainide, a class IC antiarrhythmic drug, in guinea-pig papillary muscles. An open channel blocker or an inactivated channel blocker.ⅠC类抗心律失常药物氟卡尼在豚鼠乳头肌中的钠通道阻滞特性。一种开放通道阻滞剂还是失活通道阻滞剂。
Naunyn Schmiedebergs Arch Pharmacol. 1989 Apr;339(4):441-7. doi: 10.1007/BF00736059.
5
Antiarrhythmic effects of a benzothiazine derivative (SD-3211) and its stereoisomer (SA3212) in anaesthetized rats and isolated perfused rat hearts compared with bepridil.与苄普地尔相比,一种苯并噻嗪衍生物(SD - 3211)及其立体异构体(SA3212)对麻醉大鼠和离体灌流大鼠心脏的抗心律失常作用。
Naunyn Schmiedebergs Arch Pharmacol. 1990 Jun;341(6):557-64. doi: 10.1007/BF00171737.
6
Electrophysiological effects of the combination of mexiletine and flecainide in guinea-pig ventricular fibres.美西律与氟卡尼联合应用对豚鼠心室肌纤维的电生理效应
Br J Pharmacol. 1991 Jun;103(2):1411-6. doi: 10.1111/j.1476-5381.1991.tb09803.x.
7
Effects of flecainide on isolated vascular smooth muscles of rat.氟卡尼对大鼠离体血管平滑肌的作用。
Br J Pharmacol. 1991 Nov;104(3):726-30. doi: 10.1111/j.1476-5381.1991.tb12495.x.