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Acute Efficacy of a Traditional Chinese Medicine for Treatment of Frequent Premature Ventricular Contractions in Patients with Concomitant Sinus Bradycardia: Results from a Double-Blind Placebo-Controlled Multicentre Randomized Clinical Trial

机译:中药治疗伴发窦性心动过缓患者频繁室性早搏的急性疗效:双盲安慰剂对照多中心随机临床试验的结果

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摘要

Pharmacological antiarrhythmic therapy such as beta-blockers in patients with frequent premature ventricular contractions (PVCs) and concomitant bradycardia is challenging. A traditional Chinese medicine, Shensong Yangxin (SSYX), has been effective in treatment of frequent PVCs and sinus bradycardia (SB) in separate patient cohorts. This double-blind, placebo-controlled, multicentre, randomized clinical trial investigates the acute efficacy of SSYX in reducing PVCs burden in patients with concomitant SB. Patients with symptomatic, frequent PVCs, and SB, defined as mean heart rate (MHR) of 45 to 59 beats per min (bpm), were recruited at 33 medical centres in mainland China and randomly assigned by computer to either SSYX or matching placebo for eight weeks. Patients, investigators, and trial personnel were masked to treatment allocation. Primary endpoints were changes in PVCs burden and MHR as assessed by 24-hour Holter monitoring relative to baseline. Secondary efficacy endpoints were subjective symptom score, ECG, and biochemical parameters. Analysis was based on intention-to-treat principles. 333 patients were randomized, of which 166 received SSYX and 167 placebo. Baseline characteristics did not differ. SSYX reduced PVCs burden by 68.2% (p < 0.001) and increased MHR by 10.9% (p < 0.001) compared to 32.2% and 4.7%, respectively, in the placebo group. SSYX group experienced greater symptomatic improvement (p < 0.001). No differences in reported adverse events were seen (20 versus 23). SSYX is an effective antiarrhythmic therapy for symptomatic, frequent PVCs uniquely suited patients with concomitant SB. Clinical trial number was .
机译:对于频繁发生过早的心室收缩(PVC)和伴随的心动过缓的患者,药理学抗心律不齐疗法(例如β受体阻滞剂)具有挑战性。神松养心(SSYX)是一种传统中药,可有效治疗不同患者群中的频繁的PVC和窦性心动过缓(SB)。这项双盲,安慰剂对照,多中心,随机临床试验研究了SSYX减轻伴发SB患者PVC负担的急性疗效。在中国大陆的33个医疗中心招募有症状,频繁的PVC和SB(定义为平均心率(MHR)每分钟45至59次心跳(bpm))的患者,并通过计算机将其随机分配给SSYX或匹配的安慰剂八个星期。患者,研究人员和试验人员被掩盖了治疗分配。主要终点是通过24小时动态心电图监测相对于基线评估的PVC负荷和MHR的变化。次要疗效终点是主观症状评分,ECG和生化参数。分析基于意向性治疗原则。 333名患者被随机分组​​,其中166名接受SSYX和167名安慰剂。基线特征没有差异。与安慰剂组相比,SSYX减少了68.2%(p <0.001)的PVC负担,并使MHR增加了10.9%(p <0.001),而安慰剂组分别为32.2%和4.7%。 SSYX组症状改善更大(p <0.001)。报道的不良事件未见差异(20比23)。 SSYX是一种有效的抗心律不齐疗法,适用于有症状,频发的PVC,特别适合伴发SB的患者。临床试验编号为。

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