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[儿童孤立性房室传导阻滞的预后。135例单中心研究]

[Prognosis of isolated atrioventricular block in children. Single center study of 135 cases].

作者信息

Marijon E, Costedoat-Chalumeau N, Georgin-Lavialle S, Fermont L, Bonnet D, Villain E

机构信息

Service de cardiologie pédiatrique, hôpital Necker-Enfants malades, Paris.

出版信息

Arch Mal Coeur Vaiss. 2007 Nov;100(11):909, 912-16.

Abstract

INTRODUCTION

Isolated complete atrio-ventricular (AV) block in children occurs in anatomically normal hearts in the absence of any known predisposing factor likely to have caused the block. This study aimed to define the current prognosis of these conduction disorders.

METHODS

135 patients with isolated complete AV block, diagnosed before the age of 15 years, were included in this monocentric, retrospective study.

RESULTS

52.6% of the cases were diagnosed in the antenatal or neonatal period, demonstrating their congenital nature. The disease was heralded by symptoms in only 6.7% of cases. A search for maternal anti-Ro/La antibodies was performed in 111 of the patients. It was positive in 56 cases, and was associated with an early diagnosis, a short delay in cardiac pacemaker implantation, and the occurrence of cardiomyopathy (16 cases), the latter representing a critical point in the progression of the disease (37.5% mortality at 6 years). Among the 55 cases not associated with antibodies, 2 cases were familial and no etiology was discovered in the others. The diagnosis was therefore made later, and no progression to cardiomyopathy was noted. A cardiac pacemaker was implanted in 122 patients (66 epicardial, 56 endocardial).

CONCLUSIONS

Isolated complete AV block in children is not a homogenous entity: 'immunological' blocks are genuinely congenital and their prognosis remains grave, owing to the risk of cardiomyopathy, which is sometimes diagnosed late. The other types of block are diagnosed much later in childhood, and their mechanism is still unknown. They have a good prognosis as long as the indications for pacing the child are respected.

摘要

引言

儿童孤立性完全房室传导阻滞发生于解剖结构正常的心脏,且不存在任何已知的可能导致该阻滞的易感因素。本研究旨在明确这些传导障碍的当前预后情况。

方法

本单中心回顾性研究纳入了135例15岁前诊断为孤立性完全房室传导阻滞的患者。

结果

52.6%的病例在产前或新生儿期被诊断,显示出其先天性。仅6.7%的病例有症状预示该病。对111例患者进行了母体抗Ro/La抗体检测。56例呈阳性,与早期诊断、心脏起搏器植入延迟短以及心肌病的发生相关(16例),后者是疾病进展中的关键点(6年时死亡率为37.5%)。在55例与抗体无关的病例中,2例为家族性,其他病例未发现病因。因此诊断较晚,且未观察到进展为心肌病的情况。122例患者植入了心脏起搏器(66例为心外膜起搏,56例为心内膜起搏)。

结论

儿童孤立性完全房室传导阻滞并非同质疾病:“免疫性”阻滞确实是先天性的,其预后仍然严重,因为存在心肌病风险,有时诊断较晚。其他类型的阻滞在儿童期诊断要晚得多,其机制仍不清楚。只要遵循儿童起搏的指征,它们的预后良好。

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