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氟卡尼联合β受体阻滞剂在致心律失常性右室心肌病中的安全性和疗效。

Safety and efficacy of flecainide associated with beta-blockers in arrhythmogenic right ventricular cardiomyopathy.

机构信息

Sorbonne Universités, UPMC Univ Paris 06, Paris, France.

APHP, Pitié-Salpêtriére University Hospital, Institute of Cardiology, Paris, France.

出版信息

Europace. 2022 Feb 2;24(2):278-284. doi: 10.1093/europace/euab182.

Abstract

AIMS

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited cardiomyopathy associated with a high risk of ventricular arrhythmia (VA). Current guidelines recommend beta-blockers as first-line medical therapy and if ineffective, sotalol or amiodarone. We describe our experience, as a tertiary centre for ARVC, with the effectiveness and tolerance of flecainide in addition to beta-blockers to prevent VA in ARVC.

METHODS AND RESULTS

We retrospectively included 100 consecutive ARVC patients who received flecainide with beta-blockers between May 1999 and November 2017. Treatment persistence and related side effects were assessed, as was VA-free survival on treatment, 24-h Holter monitoring and programmed ventricular stimulation (PVS) off- and on-treatment. Tolerance was good, with 10% flecainide discontinuations (lack of efficacy in six, atrial fibrillation in one, and side effects in three). No Brugada-induced electrocardiography pattern on flecainide or haemodynamic impairment was reported. Premature ventricular contraction burden at 24-h Holter monitoring was significantly decreased under treatment [median 415 (interquartile range, IQR 97-730) vs. 2370 (1572-3400) at baseline, P < 0.0001, n = 46]. Among the 33 patients with PVS under treatment, PVS was positive in 40% on-treatment vs. 94% off-treatment (P < 0.001). During a median follow-up of 47 months (IQR 23-73), 22 patients presented sustained VA on treatment, corresponding to an event rate of 5% [95% confidence interval (CI) (0.6-9)] at 1 year and 25% [95% CI (14-35)] at 5 years under treatment. No patient died.

CONCLUSION

This study suggests that flecainide and beta-blockers association is complementary to implantable cardioverter-defibrillator and catheter ablation and is safe for treating persistent symptomatic VA in patients with ARVC.

摘要

目的

致心律失常性右室心肌病(ARVC)是一种遗传性心肌病,与室性心律失常(VA)的高风险相关。目前的指南建议将β受体阻滞剂作为一线医学治疗,如果无效,则使用索他洛尔或胺碘酮。我们描述了我们作为 ARVC 三级中心的经验,即在 ARVC 患者中,除了β受体阻滞剂之外,还使用氟卡尼来预防 VA 的有效性和耐受性。

方法和结果

我们回顾性纳入了 1999 年 5 月至 2017 年 11 月期间接受氟卡尼联合β受体阻滞剂治疗的 100 例连续 ARVC 患者。评估了治疗的持续性和相关副作用,以及治疗、24 小时 Holter 监测和程控心室刺激(PVS)的 VA 无复发生存率。耐受性良好,氟卡尼的停药率为 10%(无效 6 例,房颤 1 例,副作用 3 例)。未报告氟卡尼引起的 Brugada 心电图模式或血液动力学损害。治疗后 24 小时 Holter 监测的室性早搏负荷显著降低[中位数 415(四分位距 IQR 97-730)vs. 基线时 2370(1572-3400),P<0.0001,n=46]。在 33 例接受治疗的 PVS 患者中,治疗时 PVS 阳性率为 40%,而停药时阳性率为 94%(P<0.001)。在中位数为 47 个月(IQR 23-73)的随访期间,22 例患者在治疗期间出现持续性 VA,治疗 1 年时的事件发生率为 5%[95%置信区间(CI)(0.6-9)],治疗 5 年时为 25%[95% CI(14-35)]。无患者死亡。

结论

这项研究表明,氟卡尼联合β受体阻滞剂与植入式心脏复律除颤器和导管消融相辅相成,对于治疗 ARVC 患者持续性有症状的 VA 是安全的。

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