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儿童心脏钠离子通道病功能丧失的诊断和治疗。

The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in children.

机构信息

Department of Pediatric Cardiology, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Heart Rhythm. 2012 Dec;9(12):1986-92. doi: 10.1016/j.hrthm.2012.08.011. Epub 2012 Aug 8.

Abstract

BACKGROUND

Loss-of-function sodium channelopathies manifest as a spectrum of diseases including Brugada syndrome (BrS) and cardiac conduction disease.

OBJECTIVE

To analyze the diagnostic and therapeutic aspects of these disorders in children.

METHODS

Patients aged ≤ 16 years with genetically confirmed loss-of-function sodium channelopathies (SCN5A mutation), presenting with cardiac symptoms, positive family history, and/or abnormal electrocardiogram (ECG), were included. Abnormal ECG consisted of type 1 BrS ECG and/or prolonged conduction intervals (PR interval/QRS duration > 98th percentile for age).

RESULTS

Among the cohort (n = 33, age 6 ± 5 years, 58% male subjects, 30% probands), 14 (42%) patients were symptomatic, presenting with syncope (n = 5), palpitations (n = 1), supraventricular arrhythmias (n = 3), aborted cardiac arrest (n = 3), and sudden cardiac death (n = 2). Heart rate was 91 ± 26 beats/min, PR interval 168 ± 35 ms, QRS duration 112 ± 20 ms, and heart-rate corrected QT interval 409 ± 26 ms. Conduction intervals were prolonged in 28 (85%) patients; 6 of these patients also had spontaneous type 1 BrS ECG. Eight fever-associated events occurred in 6 patients; 2 of these were vaccination-related fever episodes. Treatment included aggressive antipyretics during fever in all patients; antiarrhythmic treatment included implantable cardioverter-defibrillator (n = 4), pacemaker (n = 2), and beta-blockers, either alone (n = 3) or in combination with device (n = 2). During follow-up (4 ± 4 years), 2 previously symptomatic patients had monomorphic ventricular tachycardia; there were no deaths.

CONCLUSIONS

Diagnosis of loss-of-function sodium channelopathies in children relies on cardiac symptoms, family history, and ECG. Fever and vaccination are potential arrhythmia triggers; conduction delay is the commonest finding on ECG. Beta-blockers have a role in preventing tachycardia-induced arrhythmias; implantable cardioverter-defibrillator should probably be reserved for severe cases.

摘要

背景

功能丧失型钠离子通道病表现为一系列疾病,包括 Brugada 综合征(BrS)和心脏传导疾病。

目的

分析儿童中这些疾病的诊断和治疗方面。

方法

纳入年龄≤16 岁、基因确诊为功能丧失型钠离子通道病(SCN5A 突变)、有心脏症状、阳性家族史和/或异常心电图(ECG)的患者。异常 ECG 包括 1 型 BrS ECG 和/或传导间期延长(PR 间期/QRS 时限>年龄第 98 百分位数)。

结果

在该队列(n=33,年龄 6±5 岁,58%为男性,30%为先证者)中,14(42%)例患者有症状,表现为晕厥(n=5)、心悸(n=1)、室上性心律失常(n=3)、心脏骤停中止(n=3)和心源性猝死(n=2)。心率为 91±26 次/分,PR 间期 168±35 ms,QRS 时限 112±20 ms,心率校正 QT 间期 409±26 ms。28 例(85%)患者传导间期延长;其中 6 例患者还有自发性 1 型 BrS ECG。6 例患者发生 8 次发热相关事件,其中 2 例与疫苗接种相关。治疗包括所有患者发热时积极退热;抗心律失常治疗包括植入式心脏复律除颤器(n=4)、起搏器(n=2)和β受体阻滞剂,单独使用(n=3)或与装置联合使用(n=2)。随访(4±4 年)期间,2 例以前有症状的患者出现单形性室性心动过速;无死亡。

结论

儿童功能丧失型钠离子通道病的诊断依赖于心脏症状、家族史和 ECG。发热和疫苗接种可能是心律失常的触发因素;ECG 上最常见的发现是传导延迟。β受体阻滞剂在预防心动过速引起的心律失常方面有作用;植入式心脏复律除颤器可能应保留给严重病例。

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