Loomba Rohit S, Willes Richard J, Kovach Joshua R, Anderson Robert H
Division of Cardiology, Children's Hospital of Wisconsin/Medical College of Wisconsin, Milwaukee, Wis, USA.
Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom.
Congenit Heart Dis. 2016 Jan-Feb;11(1):7-18. doi: 10.1111/chd.12288. Epub 2015 Jul 29.
So-called heterotaxy affects lateralization of the thoracic and abdominal organs. Congenital malformations may be present in one of several organ systems. Cardiac involvement includes both structural and conduction abnormalities. Data regarding arrhythmias in heterotaxy come from case reports and small case series. We pooled available data to further characterize arrhythmias in heterotaxy. A systematic review of the literature for manuscripts describing arrhythmias in heterotaxy patients was conducted. Databases including PubMed, EMBASE, and Ovid were searched. Studies describing arrhythmias in patients with heterotaxy were included if they were in English and presented characteristics of the arrhythmias. Arrhythmia characteristics were abstracted and are presented as pooled data. Freedom from arrhythmia by age was then analyzed using Kaplan-Meier analysis. A total of 19 studies with 121 patients were included in the pooled analysis. Those with right isomerism were found to be more likely to have atrial flutter, atrial tachycardia, junctional tachycardia, and ventricular tachycardia. Those with left isomerism were more likely to have atrioventricular block, intraventricular conduction delay, sick sinus syndrome, and atrioventricular nodal reentry tachycardia. Median age of onset for all arrhythmias was 4 years with no difference by specific arrhythmia or isomerism. Those with right and left isomerism are at risk for different arrhythmias but are likely to develop arrhythmias at the same age. Those with left isomerism are more likely to require pacemaker placement due to atrioventricular block. Understanding these differences allows for focused surveillance of development of these arrhythmias.
所谓的内脏异位会影响胸腹部器官的定位。先天性畸形可能存在于多个器官系统中的一个。心脏受累包括结构和传导异常。关于内脏异位中心律失常的数据来自病例报告和小型病例系列。我们汇总现有数据以进一步描述内脏异位中的心律失常。对描述内脏异位患者心律失常的文献进行了系统综述。检索了包括PubMed、EMBASE和Ovid在内的数据库。如果描述内脏异位患者心律失常的研究为英文且呈现了心律失常的特征,则将其纳入。提取心律失常特征并作为汇总数据呈现。然后使用Kaplan-Meier分析按年龄分析无心律失常情况。汇总分析共纳入19项研究中的121例患者。发现右位异构的患者更易发生心房扑动、房性心动过速、交界性心动过速和室性心动过速。左位异构的患者更易发生房室传导阻滞、室内传导延迟、病态窦房结综合征和房室结折返性心动过速。所有心律失常的中位发病年龄为4岁,特定心律失常或异构情况之间无差异。右位和左位异构的患者有发生不同心律失常的风险,但可能在相同年龄发生心律失常。左位异构的患者因房室传导阻滞更可能需要植入起搏器。了解这些差异有助于对这些心律失常的发生进行重点监测。