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首页> 外文期刊>The American Journal of Cardiology >Frequency of cardiac death in children with idiopathic dilated cardiomyopathy.
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Frequency of cardiac death in children with idiopathic dilated cardiomyopathy.

机译:特发性扩张型心肌病患儿的心源性死亡频率。

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The prognosis in children with idiopathic dilated cardiomyopathy (IDC) is guarded, with the 5-year mortality rate ranging from 14% to 50%, owing to sudden cardiac death (SCD) or pump failure. The risk factors for SCD in adults with IDC include asymptomatic nonsustained ventricular tachycardia and poor left ventricular function. It is unclear whether these findings can be extrapolated to the pediatric population. A retrospective review of all patients with the diagnosis of IDC seen at a single institution from 1990 to 2004 was performed. A total of 85 patients (46 males), with a median age of 3.8 years (0 days to 17.3 years) were studied. The mean left ventricular ejection fraction was 25 +/- 12% (median 23%, range 45% to 45%) at presentation. The following arrhythmias occurred at presentation or during the initial hospitalization: nonsustained ventricular tachycardia in 6, sustained ventricular tachycardia or fibrillation in 1, supraventricular arrhythmias in 6, and both atrial and ventricular arrhythmias in 1. During a subsequent hospitalization or outpatient follow-up, 7 patients had the following arrhythmias: supraventricular arrhythmias in 2, nonsustained ventricular tachycardia in 4, and both atrial and ventricular arrhythmias in 1. The cumulative survival rate was 40% at a mean follow-up of 6.2 years (95% confidence interval 4.4 to 8.1). One single episode of SCD occurred in 1 patient without a history of sustained arrhythmias. In conclusion, in children with IDC, despite the low left ventricular ejection fraction and presence of ventricular arrhythmias, only one episode of SCD occurred in this group of patients. Given the 1% incidence of SCD in this cohort, the use of implantable cardioverter-defibrillators as primary prevention in children with IDC might not be indicated.
机译:特发性扩张型心肌病(IDC)患儿的预后受到保护,由于心源性猝死(SCD)或泵功能衰竭,其5年死亡率为14%至50%。 IDC成人SCD的危险因素包括无症状的非持续性室性心动过速和左室功能不佳。尚不清楚这些发现是否可以推断到儿科人群。回顾性分析了1990年至2004年在同一家机构就诊的所有IDC诊断患者。共研究了85位患者(46位男性),中位年龄为3.8岁(0天至17.3岁)。呈现时平均左心室射血分数为25 +/- 12%(中位数23%,范围45%至45%)。在就诊时或初次住院期间发生以下心律失常:6例非持续性室性心动过速,1例持续性室性心动过速或纤颤,1例室上性心律不齐,1例发生房性和室性心律失常,在随后的住院或门诊随访中, 7例患者出现以下心律不齐:室上性心律失常2例,非持续性室性心动过速4例,房性和室性心律失常1例。平均随访6.2年,累积生存率为40%(95%置信区间4.4至8.1)。 1例患者发生1次SCD发作,无持续性心律失常史。总之,在IDC患儿中,尽管左室射血分数低且存在室性心律不齐,但在这一组患者中仅发生了一次SCD发作。鉴于该人群中SCD的发生率为1%,可能不建议使用植入式心脏复律除颤器作为IDC儿童的一级预防措施。

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