Silver Eric S, Pass Robert H, Hordof Allan J, Liberman Leonardo
Division of Pediatric Cardiology, Morgan Stanley Children's Hospital, Columbia University, New York, New York 10032, USA.
Pacing Clin Electrophysiol. 2008 Mar;31(3):322-6. doi: 10.1111/j.1540-8159.2008.00992.x.
Syncope due to episodes of paroxysmal atrioventricular (AV) block, defined as transient advanced second or third-degree block, is rarely reported in pediatric patients without congenital heart disease.
We reviewed our institutional arrhythmia database from January 1988 to January 2007 to identify all patients less than 18 years of age with normal cardiac anatomy and episodes of syncope associated with paroxysmal AV block. Demographic and clinical information was collected.
Six patients were identified (Table I). Five of the six patients were female, with an average age of 9.3 +/- 4.4 years. Patients had episodes of syncope for an average of 5.6 +/- 3.3 years prior to diagnosis. All patients had normal physical examinations, electrocardiograms, and echocardiograms. None were on medications known to interfere with AV nodal function, and laboratory evaluation including Lyme titers were negative. Five of the six patients' episodes were atypical for vasovagal syncope (except patient 6). All patients had documented paroxysmal AV block on either inpatient cardiac monitor, Holter monitor, or event recorder at the time of syncope. There was maintenance or acceleration of the sinus rate during episodes of syncope in all patients (mean atrial rate 107 +/- 37 bpm). All six patients had permanent transvenous pacemakers implanted with resolution of symptoms over a mean follow-up of 5.2 +/- 6.3 years.
Paroxysmal AV nodal block is a rare finding in pediatric patients, but should be considered as a possible etiology in patients presenting with episodes atypical for vasovagal syncope. Pacemaker therapy prevented future episodes in all six of our patients.
阵发性房室(AV)阻滞发作导致的晕厥,定义为短暂的高度二度或三度阻滞,在无先天性心脏病的儿科患者中鲜有报道。
我们回顾了1988年1月至2007年1月我院的心律失常数据库,以确定所有年龄小于18岁、心脏解剖结构正常且有与阵发性AV阻滞相关晕厥发作的患者。收集了人口统计学和临床信息。
共确定6例患者(表I)。6例患者中有5例为女性,平均年龄为9.3±4.4岁。患者在诊断前平均有5.6±3.3年的晕厥发作史。所有患者的体格检查、心电图和超声心动图均正常。无人服用已知会干扰房室结功能的药物,包括莱姆病滴度在内的实验室检查均为阴性。6例患者中有5例的发作不符合血管迷走性晕厥的典型表现(患者6除外)。所有患者在晕厥发作时,住院心脏监护仪、动态心电图监测仪或事件记录仪均记录到阵发性AV阻滞。所有患者在晕厥发作期间窦性心律均维持或加快(平均心房率107±37次/分)。所有6例患者均植入了永久性经静脉起搏器,平均随访5.2±6.3年症状消失。
阵发性房室结阻滞在儿科患者中罕见,但对于有不符合血管迷走性晕厥典型表现发作的患者,应考虑其为可能病因。起搏器治疗预防了我们所有6例患者的未来发作。