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先天性心脏缺陷中的心律失常。

Arrhythmias in congenital heart defects.

作者信息

Kaldararova M, Balazova E, Bordacova L, Lakomy M, Hraska V, Nosal M, Sojak V, Valentik P, Masura J, Milovsky V, Vrsanska V

机构信息

Children's Cardiac Center of Slovak Republic, Bratislava, Slovakia.

出版信息

Bratisl Lek Listy. 2007;108(1):14-9.

Abstract

AIM OF THE STUDY

Evaluation of the incidence and severity of late arrhythmias in patients with predisposing congenital heart defects--either due to the anatomy of the defect itself or as a result of a particular type of surgical intervention.

PATIENTS AND METHODS

In a retrospective long-term study authors analyzed 158 patients (divided into 5 groups) with congenital heart defects after surgical correction. Evaluated were: the incidence of rhythm disturbances, the type of arrhythmia and the need for medication or intervention.

RESULTS

The most rhythm disturbances occurred in patients after physiological correction of D-transposition of the great arteries (68.5%) and these patients also mostly needed medication or pacemaker implantation; followed were by patients with hypoplastic left heart syndrome after Fontan procedure (40%), then were patients after long-term correction of tetralogy of Fallot (31.1%), atrial septal defect sinus venosus type with partial anomalous pulmonary venous return after Warden correction (25.7%) and congenitally corrected L-transposition of the great arteries (25 %). Most of these arrhythmias were asymptomatic and there was no need to treat them. There was an increased incidence of arrhythmias with time (p < 0.05).

DISCUSSION

During childhood in patients after surgical correction late arrhythmias mostly do not represent a severe problem, but with time, when reaching adulthood, this may be an issue. It is therefore very important to understand the anatomy, physiology and the arrhythmogenic substrate of every high risk congenital heart defect (Tab. 2, Fig. 6, Ref. 10).

摘要

研究目的

评估患有先天性心脏缺陷的患者发生晚期心律失常的发生率和严重程度,这些先天性心脏缺陷要么是由于缺陷本身的解剖结构,要么是特定类型手术干预的结果。

患者与方法

在一项回顾性长期研究中,作者分析了158例接受手术矫正后患有先天性心脏缺陷的患者(分为5组)。评估内容包括:心律失常的发生率、心律失常的类型以及药物治疗或干预的必要性。

结果

大动脉转位(D-TGA)生理性矫正术后的患者发生心律失常的情况最为常见(68.5%),这些患者大多也需要药物治疗或植入起搏器;其次是接受Fontan手术的左心发育不全综合征患者(40%),然后是法洛四联症长期矫正术后的患者(31.1%)、Warden矫正术后的静脉窦型房间隔缺损伴部分肺静脉异位引流患者(25.7%)以及先天性矫正型大动脉转位(L-TGA)患者(25%)。这些心律失常大多无症状,无需治疗。心律失常的发生率随时间增加(p<0.05)。

讨论

在儿童期,手术矫正后的患者晚期心律失常大多不构成严重问题,但随着时间推移,成年后可能会成为一个问题。因此,了解每一种高危先天性心脏缺陷的解剖结构、生理机制和致心律失常基质非常重要(表2、图6、参考文献10)。

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