Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Department of Cardiovascular Therapeutics, Okayama University Graduate School of Medicine Dentistry and Pharmaceutical Sciences, Okayama, Japan
J Am Heart Assoc. 2018 May 10;7(10):e008617. doi: 10.1161/JAHA.118.008617.
A drug provocation test using a sodium channel blocker (SCB) can unmask a type 1 ECG pattern in patients with Brugada syndrome. However, the prognostic value of the results of an SCB challenge is limited in patients with non-type 1 ECG. We investigated the associations of future risk for ventricular fibrillation with SCB-induced ECG changes and ventricular tachyarrhythmias (VTAs).
We administered intravenous pilsicainide to 245 consecutive patients with Brugada syndrome (181 patients with spontaneous type 1 ECG, 64 patients with non-type 1 ECG). ECG parameters before and after the test and occurrence of drug-induced VTAs were evaluated. During a mean follow-up period of 113±57 months, fatal VTA events occurred in 31 patients (sudden death: n=3, ventricular tachycardia/ventricular fibrillation: n=28). Symptomatic patients and spontaneous type 1 ECG were associated with future fatal arrhythmic events. Univariable analysis of ECG parameters after the test showed that long PQ and QRS intervals, high ST level, and SCB-induced VTAs were associated with later VTA events during follow-up. Multivariable analysis showed that symptomatic patients, high ST level (V1) ≥0.3 mV after the test, and SCB-induced VTAs were independent predictors for future fatal arrhythmic events (hazard ratios: 3.28, 2.80, and 3.62, 95% confidence intervals: 1.54-7.47, 1.32-6.35, and 1.64-7.75, respectively; <0.05).
SCB-induced VTAs and ST-segment augmentation are associated with an increased risk of the development of ventricular tachycardia/ventricular fibrillation events during follow-up in patients with Brugada syndrome.
使用钠离子通道阻滞剂(SCB)进行药物激发试验可揭示 Brugada 综合征患者 1 型心电图模式。然而,在非 1 型心电图患者中,SCB 挑战结果的预后价值有限。我们研究了 SCB 诱导的心电图变化和室性心动过速/心室颤动(VTAs)与未来发生室颤风险的相关性。
我们给 245 例 Brugada 综合征患者(181 例自发 1 型心电图,64 例非 1 型心电图)静脉注射匹司卡尼。评估了试验前后的心电图参数和药物诱导 VTAs 的发生情况。在平均 113±57 个月的随访期间,31 例患者发生了致命性 VTAs 事件(猝死:n=3,室性心动过速/心室颤动:n=28)。有症状的患者和自发 1 型心电图与未来致命性心律失常事件相关。试验后心电图参数的单变量分析显示,长 PQ 和 QRS 间期、高 ST 水平和 SCB 诱导的 VTAs 与随访期间的后期 VTA 事件相关。多变量分析显示,有症状的患者、高 ST 水平(V1)≥0.3mV 试验后和 SCB 诱导的 VTAs 是未来致命性心律失常事件的独立预测因子(危险比:3.28、2.80 和 3.62,95%置信区间:1.54-7.47、1.32-6.35 和 1.64-7.75;均<0.05)。
在 Brugada 综合征患者中,SCB 诱导的 VTAs 和 ST 段抬高与随访期间室性心动过速/心室颤动事件发生风险增加相关。