首页> 外文期刊>Journal of the American College of Cardiology >Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia.
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Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia.

机译:氟卡尼治疗可降低儿茶酚胺能性多形性室性心动过速患者运动引起的室性心律失常。

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OBJECTIVES: This study evaluated the efficacy and safety of flecainide in addition to conventional drug therapy in patients with catecholaminergic polymorphic ventricular tachycardia (CPVT). BACKGROUND: CPVT is an inherited arrhythmia syndrome caused by gene mutations that destabilize cardiac ryanodine receptor Ca(2+) release channels. Sudden cardiac death is incompletely prevented by conventional drug therapy with beta-blockers with or without Ca(2+) channel blockers. The antiarrhythmic agent flecainide directly targets the molecular defect in CPVT by inhibiting premature Ca(2+) release and triggered beats in vitro. METHODS: We collected data from every consecutive genotype-positive CPVT patient started on flecainide at 8 international centers before December 2009. The primary outcome measure was the reduction of ventricular arrhythmias during exercise testing. RESULTS: Thirty-three patients received flecainide because of exercise-induced ventricular arrhythmias despite conventional (for different reasons, not always optimal) therapy (median age 25 years; range 7 to 68 years; 73% female). Exercise tests comparing flecainide in addition to conventional therapy with conventional therapy alone were available for 29 patients. Twenty-two patients (76%) had either partial (n = 8) or complete (n = 14) suppression of exercise-induced ventricular arrhythmias with flecainide (p < 0.001). No patient experienced worsening of exercise-induced ventricular arrhythmias. The median daily flecainide dose in responders was 150 mg (range 100 to 300 mg). During a median follow-up of 20 months (range 12 to 40 months), 1 patient experienced implantable cardioverter-defibrillator shocks for polymorphic ventricular arrhythmias, which were associated with a low serum flecainide level. In 1 patient, flecainide successfully suppressed exercise-induced ventricular arrhythmias for 29 years. CONCLUSIONS: Flecainide reduced exercise-induced ventricular arrhythmias in patients with CPVT not controlled by conventional drug therapy.
机译:目的:本研究评估了氟卡尼和传统药物治疗儿茶酚胺能性多形性室性心动过速(CPVT)患者的疗效和安全性。背景:CPVT是一种遗传性心律失常综合症,由基因突变引起,该基因突变使心脏瑞丹碱受体Ca(2+)释放通道不稳定。常规的药物治疗可使用带有或不带有Ca(2+)通道阻滞剂的β受体阻滞剂来预防猝死。抗心律不齐药flecainide通过抑制过早的Ca(2+)释放并触发体外搏动直接靶向CPVT中的分子缺陷。方法:我们收集了2009年12月之前在8个国际中心开始使用氟卡尼治疗的每位连续基因型阳性CPVT患者的数据。主要结果指标是运动测试期间室性心律失常的减少。结果:33例患者因运动引起的室性心律失常而接受了氟卡尼治疗,尽管采用了常规治疗(由于各种原因,并不总是最佳的)(中位年龄25岁;范围7至68岁;女性73%)。对29名患者进行的运动测试将氟卡尼除常规治疗外与仅常规治疗进行了比较。 22例患者(76%)接受了氟卡尼对运动性室性心律失常的部分抑制(n = 8)或完全抑制(n = 14)(p <0.001)。没有患者经历运动引起的室性心律失常恶化。响应者中氟卡尼的每日平均剂量为150 mg(范围为100至300 mg)。在20个月的中位随访期间(12到40个月),有1例患者因多形性室性心律失常而发生了植入式心脏复律除颤器电击,这与低血浆氟卡尼特水平有关。在1例患者中,氟卡尼胺成功抑制了运动引起的室性心律失常长达29年。结论:非常规药物治疗无法控制的CPVT患者中,氟卡尼减少了运动引起的室性心律失常。

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