Deal B J, Mavroudis C, Backer C L
Department of Pediatrics, Northwestern University, Feinberg School of Medicine, Children's Memorial Hospital, 2300 Children's Plaza, Chicago, IL 60614, USA.
Pediatr Cardiol. 2007 Nov-Dec;28(6):448-56. doi: 10.1007/s00246-007-9005-2.
With longer duration of follow-up, as many as 50% of Fontan patients will develop atrial tachycardia, usually in association with significant hemodynamic abnormalities. Arrhythmia management in the Fontan patient is reviewed. The incidence and type of arrhythmia occurrence are examined, including macro-reentrant rhythm which involves the right atrium, reentrant rhythm localized to the pulmonary venous atrium (seen in patients with lateral tunnel procedures), and atrial fibrillation. Risk factors for development of these arrhythmias are considered, and short- and long-term therapeutic options for medical and surgical treatment are discussed. Surgical results are presented for 117 patients undergoing Fontan conversion and arrhythmia surgery (isthmus ablation (9), modified right atrial maze (38) or Cox-maze III (70)). Operative mortality is low (1/117, 0.8%). Seven late deaths occurred, and include two patients who died shortly following cardiac transplantation (2/6, 33%) after Fontan conversion and arrhythmia surgery. Overall arrhythmia recurrence is 12.8% during a mean follow-up of 56 months. Fontan conversion with arrhythmia surgery can be performed with low operative mortality, low risk of recurrent tachycardia, and marked improvement in functional status in most patients. Because the development of tachycardia is usually an electromechanical problem, attention to only the arrhythmia with medications or ablation may allow progression of hemodynamic abnormalities to either a life-threatening outcome or a point at which transplantation is the only potential option. Because cardiac transplantation in Fontan patients is associated with high early mortality, earlier consideration for surgical intervention is warranted.
随着随访时间的延长,多达50%的Fontan手术患者会发生房性心动过速,通常伴有明显的血流动力学异常。本文对Fontan手术患者的心律失常管理进行了综述。研究了心律失常的发生率和类型,包括涉及右心房的大折返性心律、局限于肺静脉心房的折返性心律(见于采用侧隧道手术的患者)以及心房颤动。分析了这些心律失常发生的危险因素,并讨论了药物和手术治疗的短期和长期治疗选择。报告了117例行Fontan转换术和心律失常手术(峡部消融术(9例)、改良右心房迷宫术(38例)或Cox迷宫III型手术(70例))患者的手术结果。手术死亡率较低(1/117,0.8%)。发生了7例晚期死亡,其中包括2例在Fontan转换术和心律失常手术后不久接受心脏移植后死亡的患者(2/6,33%)。在平均56个月的随访期间,总体心律失常复发率为12.8%。Fontan转换术联合心律失常手术可在低手术死亡率、低心动过速复发风险的情况下进行,且大多数患者的功能状态有显著改善。由于心动过速的发生通常是一个电机械问题,仅用药物或消融术关注心律失常可能会使血流动力学异常进展至危及生命的结局或达到仅能选择移植的阶段。由于Fontan手术患者的心脏移植与高早期死亡率相关,因此有必要更早地考虑手术干预。