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一项关于埃布斯坦畸形患儿心律失常的多中心长期研究。

A multicenter, long-term study on arrhythmias in children with Ebstein anomaly.

作者信息

Delhaas Tammo, Sarvaas Gideon J du Marchie, Rijlaarsdam Marry E, Strengers Jan L, Eveleigh Rhona M, Poulino Sumayah E, de Korte Chris L, Kapusta Livia

机构信息

Department of Pediatrics, Maastricht University Medical Center, Maastricht, The Netherlands.

出版信息

Pediatr Cardiol. 2010 Feb;31(2):229-33. doi: 10.1007/s00246-009-9590-3.

Abstract

To assess the prevalence, history, and treatment of arrhythmias, in particular preexcitation and Wolff-Parkinson-White (WPW) syndrome, in patients with Ebstein anomaly (EA) during childhood and adolescence, we performed a multicenter retrospective study of all consecutive live-born patients with EA, diagnosed, and followed by pediatric cardiologists between 1980 and 2005 in The Netherlands. During a follow-up after EA diagnosis of 13 years 3 months (range: 6 days to 28 years 2 months), 16 (17%) of the 93 pediatric EA patients exhibited rhythm disturbances. Nine patients showed arrhythmic events starting as of the neonatal period. Supraventricular tachycardia was noted in 11 patients. One patient died in the neonatal period due to intractable supraventricular tachycardia resulting in heart failure and one patient died at 5 weeks of age most probably due to an arrhythmic event. The 14 surviving patients all show preexcitation, albeit 4 of them intermittently, and all have a right-sided accessory pathway location. Nine patients underwent catheter ablation of an accessory pathway. Only four patients are currently on antiarrhythmic drugs. The 17% prevalence of rhythm disturbances in pediatric EA patients, most commonly supraventricular arrhythmias, is significantly lower than in adult EA patients. Life-threatening rhythm disturbances are not frequent early in life. Symptomatic patients are well treated with radiofrequency catheter ablation.

摘要

为评估儿童和青少年期埃布斯坦畸形(EA)患者心律失常的患病率、病史及治疗情况,尤其是预激和 Wolff-Parkinson-White(WPW)综合征,我们对1980年至2005年期间在荷兰由儿科心脏病专家诊断并随访的所有连续存活的EA患者进行了一项多中心回顾性研究。在EA诊断后的13年3个月(范围:6天至28年2个月)随访期间,93例儿科EA患者中有16例(17%)出现节律紊乱。9例患者自新生儿期起即出现心律失常事件。11例患者记录到室上性心动过速。1例患者在新生儿期因难治性室上性心动过速导致心力衰竭死亡,1例患者在5周龄时死亡,很可能是由于心律失常事件。14例存活患者均显示预激,尽管其中4例为间歇性预激,且所有患者的旁路均位于右侧。9例患者接受了旁路导管消融术。目前只有4例患者服用抗心律失常药物。儿科EA患者节律紊乱的患病率为17%,最常见的是室上性心律失常,显著低于成年EA患者。危及生命的节律紊乱在生命早期并不常见。有症状的患者通过射频导管消融术治疗效果良好。

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