Cavigelli-Brunner Anna, Bauersfeld Urs, Prêtre René, Kretschmar Oliver, Oxenius Angela, Valsangiacomo Buechel Emanuela R
Division of Pediatric Cardiology, University Children's Hospital, Steinwiesstrasse 75, CH 8032 Zurich, Switzerland.
Pediatr Cardiol. 2012 Apr;33(4):506-12. doi: 10.1007/s00246-011-0142-2. Epub 2011 Dec 11.
The decision to perform biventricular repair for infants with multiple obstructive or hypoplastic left heart lesions (LHL) and borderline left ventricle (LV) may be controversial. This study sought to assess the mortality and morbidity of patients with LHL after biventricular repair and to determine the growth of the left-sided cardiac structures. Retrospective analysis of 39 consecutive infants with LHL who underwent biventricular repair was performed. The median age at surgery was 7 days (range 1-225 days), and the median follow-up period was 34 months (range 1-177 months). Between diagnosis and the end of the follow-up period, the size of the aortic annulus (z-score -4.1 ± 2.8 vs. -0.1 ± 2.7) and the LV (LV end-diastolic diameter z-score -1.7 ± 2.8 vs. 0.21 ± 1.7) normalized. During the follow-up period, 23 patients required 39 reinterventions (62%) consisting of redo surgery for 21 patients (57%) and catheter-guided reinterventions for 8 patients (22%). At the end of the follow-up period, 25 of 34 patients were doing subjectively well; 10 children (29%) received cardiac medication; 12 (35%) presented with failure to thrive (weight ≤ P3) and 5 (15%) with pulmonary hypertension. The overall mortality rate was 13%. Biventricular repair for patients with multiple LHL results in sufficient growth of the left-sided cardiac structures. Nevertheless, residual or newly developing obstructive lesions and pulmonary hypertension are frequent, causing significant morbidity that requires reintervention.
对于患有多种梗阻性或左心发育不良病变(LHL)且左心室(LV)临界的婴儿,决定进行双心室修复可能存在争议。本研究旨在评估双心室修复术后LHL患者的死亡率和发病率,并确定左侧心脏结构的生长情况。对39例连续接受双心室修复的LHL婴儿进行了回顾性分析。手术时的中位年龄为7天(范围1 - 225天),中位随访期为34个月(范围1 - 177个月)。在诊断至随访期末,主动脉瓣环大小(z评分 -4.1 ± 2.8对比 -0.1 ± 2.7)和左心室(左心室舒张末期直径z评分 -1.7 ± 2.8对比0.21 ± 1.7)恢复正常。在随访期间,23例患者需要进行39次再次干预(62%),其中21例患者(57%)进行了再次手术,8例患者(22%)进行了导管引导下的再次干预。在随访期末,34例患者中有25例主观状况良好;10名儿童(29%)接受心脏药物治疗;12例(35%)出现生长发育迟缓(体重≤第3百分位数),5例(15%)出现肺动脉高压。总死亡率为13%。对患有多种LHL的患者进行双心室修复可使左侧心脏结构充分生长。然而,残余或新出现的梗阻性病变和肺动脉高压很常见,会导致严重的发病率,需要再次干预。