Efficacy of Propafenone for Treating Idiopathic Premature Ventricular Contractions in Children

K. Alekseeva, T. Kruchina, Mohiniso Sh. Maljarova, G. A. Novik
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Abstract

Background. Premature ventricular contractions (PVCs) are a common heart rhythm disorder in children, often following a benign course. However, in rare cases, antiarrhythmic therapy is required for managing this arrhythmia. Limited data is available regarding the effectiveness of such therapy specifically in children. Objective. To evaluate the efficacy and safety of propafenone administration in children with idiopathic PVCs. Methods. The study enrolled 33 children aged 11.1 ± 4.8 years (29 days — 17 years) with idiopathic PVCs. Propafenone dose was titrated from initial (5–7 mg/kg/day) to effective (no more than 15 mg/kg/day) dose under clinical and electrocardiographic control to monitor for proarrhythmias and other side effects. An increase in PQ interval duration and a widening of the QRS complex no more than 25% compared to baseline was considered acceptable. Results. The incidence of PVCs before propafenone administration was 36.3 ± 10.1 (22.0–60.6) thousands/day or 33.2 ± 8.4% (20.5–50.0). Complex forms of PVCs were observed in 25 (75.8%) children: 25 (75.8%) had frequent paired PVCs, 6 (18.2%) had polymorphic PVCs, 20 (60.6%) had short runs of ventricular tachycardia (VT), and 19 (27.6%) had a combination of various forms of PVCs. The starting dose of propafenone was 5.6 ± 2.2 mg/kg/day with subsequent increases to 10 ± 0.8 mg/kg/day. Propafenone was employed as the initial therapy in 23 (69.7%) children and as a second line therapy in 10 (30.3%) children, following the ineffectiveness or adverse effects of beta-adrenoblockers. The duration of propafenone therapy was 95.8 ± 62.8 days. Propafenone was effective in 25 (75.8%) children. The average reduction in the number of PVCs during therapy was 71.7 ± 32.6% (13.0–100.0) during therapy. One (3%) child developed proarrhythmia — sustained VT and 1 (3%) child had gastrointestinal side effects. Conclusion. Propafenone is an effective antiarrhythmic drug in children with idiopathic PVCs, including patients with poor response to beta-adrenoblockers. Arrhythmogenic and extracardiac side effects are possible during propafenone therapy, which require clinical and electrocardiographic observation in the process of selecting an effective dose of the drug.
普罗帕酮治疗儿童特发性室性早搏的疗效
背景。室性早搏(PVC)是儿童常见的心律失常,通常是良性的。但在极少数情况下,需要使用抗心律失常治疗来控制这种心律失常。有关儿童接受此类治疗的效果的数据十分有限。目的评估对特发性 PVC 儿童使用普罗帕酮的有效性和安全性。方法。研究共招募了 33 名特发性 PVCs 患儿,年龄为 11.1 ± 4.8 岁(29 天 - 17 岁)。在临床和心电图控制下,普罗帕酮剂量从初始剂量(5-7 毫克/千克/天)滴定到有效剂量(不超过 15 毫克/千克/天),以监测原发性心律失常和其他副作用。与基线相比,PQ 间期持续时间延长和 QRS 波群增宽不超过 25% 即可接受。结果服用普罗帕酮前,PVC 的发生率为 36.3 ± 10.1 (22.0-60.6) 千次/天或 33.2 ± 8.4% (20.5-50.0)。25名(75.8%)患儿出现了复杂形式的PVC:25名(75.8%)患儿频繁出现成对PVC,6名(18.2%)患儿出现多形性PVC,20名(60.6%)患儿出现短程室性心动过速(VT),19名(27.6%)患儿同时出现多种形式的PVC。普罗帕酮的起始剂量为 5.6 ± 2.2 毫克/千克/天,随后增至 10 ± 0.8 毫克/千克/天。23名(69.7%)患儿将普罗帕酮作为初始疗法,10名(30.3%)患儿在使用β-肾上腺素受体阻滞剂无效或出现不良反应后将普罗帕酮作为二线疗法。普罗帕酮的疗程为(95.8 ± 62.8)天。普罗帕酮对 25 名儿童(75.8%)有效。治疗期间,PVC次数平均减少了71.7 ± 32.6% (13.0-100.0)。1名儿童(3%)出现了前心律失常--持续VT,1名儿童(3%)出现了胃肠道副作用。结论:普罗帕酮是一种有效的抗心律失常药物。普罗帕酮是一种有效的抗心律失常药物,适用于特发性PVC儿童,包括对β-肾上腺素受体阻滞剂反应不佳的患者。普罗帕酮治疗期间可能会出现致心律失常和心外副作用,在选择有效药物剂量的过程中需要对临床和心电图进行观察。
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