Wu M H, Wang J K, Lin J L, Lai L P, Lue H C, Hsieh F J
Department of Pediatrics, National Taiwan University, Taipei.
Pacing Clin Electrophysiol. 2001 Nov;24(11):1631-8. doi: 10.1046/j.1460-9592.2001.01631.x.
This long-term study sought to determine the clinical implication of defective sinus node and AV conduction tissue in patients with left atrial isomerism (LAI). From 1984 to 1998, a total of 22 patients were identified as LAI. Patient age at the last follow-up ranged from 2 to 276 months (90+/-70 months). Associated cardiac anomalies were interruption of the inferior vena cava (n = 18, 82%), common atrium (n = 9, 41%), AV canal (n = 14, 64%), double-outlet right ventricle (n = 8, 36%), and pulmonary stenosis (n = 15, 68%). Palliative interventions were performed in 16 patients (Fontan-type operation in 4 patients, shunt followed by Fontan-type operation in 2, repair of septal defect in 4, and extracardiac intervention in 6). During the follow-up, over half of the patients (n = 14, 64%) developed bradyarrhythmia (onset age: from 1 to 264 months; median 78 months): junctional rhythm (n = 11), sinus bradycardia (n = 8) (5 patients also had junctional rhythm), and AV block (n = 2, both also had junctional rhythm). The probability free from bradyarrhythmia was 80% and 46% at the age of 2 and 6 years, respectively. None of the bradyarrhythmias were directly related to open-heart surgery. Besides, junctional ectopic tachycardia occurred after Fontan-type operation in three of six patients. In two patients, a Mahaim-like pathway was identified during the electrophysiological study. The patients with LAI had a high probability of developing bradyarrhythmias due to abnormal sinus node function. Varied AV conduction abnormalities may include compromised AV conduction, junctional ectopic tachycardia after Fontan-type operation, and an association of Mahaim-like pathway.
这项长期研究旨在确定左心房异构(LAI)患者窦房结和房室传导组织缺陷的临床意义。1984年至1998年期间,共识别出22例LAI患者。最后一次随访时患者年龄为2至276个月(90±70个月)。相关心脏异常包括下腔静脉中断(n = 18,82%)、共同心房(n = 9,41%)、房室通道(n = 14,64%)、右心室双出口(n = 8,36%)和肺动脉狭窄(n = 15,68%)。16例患者接受了姑息性干预(4例患者接受Fontan类手术,2例患者先行分流术再行Fontan类手术,4例患者行房间隔缺损修补术,6例患者行心外干预)。随访期间,超过半数患者(n = 14,64%)出现缓慢性心律失常(发病年龄:1至264个月;中位数78个月):交界性心律(n = 11)、窦性心动过缓(n = 8)(5例患者同时有交界性心律)和房室传导阻滞(n = 2,均同时有交界性心律)。2岁和6岁时无缓慢性心律失常的概率分别为80%和46%。所有缓慢性心律失常均与心脏直视手术无直接关联。此外,6例患者中有3例在Fontan类手术后出现交界性异位性心动过速。2例患者在电生理研究中发现类似Mahaim通道的旁路。LAI患者因窦房结功能异常发生缓慢性心律失常的概率较高。各种房室传导异常可能包括房室传导受损、Fontan类手术后交界性异位性心动过速以及类似Mahaim通道的旁路关联。