Reinhartz Olaf, Reddy V Mohan, Petrossian Edwin, Suleman Sam, Mainwaring Richard D, Rosenthal David N, Feinstein Jeffrey A, Gulati Raj, Hanley Frank L
Department of Cardiothoracic Surgery, Division of Pediatric Cardiac Surgery, Stanford University, Stanford, California 94305, USA.
Ann Thorac Surg. 2006 Sep;82(3):934-8; discussion 938-9. doi: 10.1016/j.athoracsur.2006.03.063.
Unifocalization of major aortopulmonary collateral arteries (MAPCAs) in pulmonary atresia with ventricular septal defect and intracardiac repair has become the standard of care. However, there are no reports addressing unifocalization of MAPCAs in single-ventricle patients. It is unknown whether their pulmonary vascular bed can be reconstructed and low enough pulmonary vascular resistance achieved to allow for superior or total cavopulmonary connections.
We reviewed data on all patients with functional single ventricles and unifocalization procedures of MAPCAs. From 1997 to 2005, 14 consecutive children with various single-ventricle anatomies were operated on.
Patients had a median of three surgical procedures (range, 1 to 5). Two patients had absent, all others diminutive central pulmonary arteries, with an average of 3.5 +/- 1.2 MAPCAs. Seven patients (50%) had bidirectional Glenn procedures, and 3 of these had Fontan procedures. Median postoperative pulmonary artery pressures measured 12.5 mm Hg (Glenn) and 14 mm Hg (Fontan), respectively. Six patients are alive today (46%), with 1 patient lost to follow-up. Three patients died early and 3 late after initial unifocalization to shunts. One other patient survived unifocalization, but was not considered a candidate for a Glenn procedure and died after high-risk two-ventricle repair. Another patient with right-ventricle-dependent coronary circulation died of sepsis late after Glenn.
In selected patients with functional single ventricles and MAPCAs, the pulmonary vascular bed can be reconstructed sufficiently to allow for cavopulmonary connections. Venous flow to the pulmonary vasculature decreases cardiac volume load and is likely to increase life expectancy and quality of life for these patients.
在室间隔缺损合并肺动脉闭锁且行心内修复的患者中,将主要体肺侧支动脉(MAPCAs)单支化已成为标准治疗方法。然而,尚无关于单心室患者MAPCAs单支化的报道。目前尚不清楚其肺血管床能否重建,以及能否将肺血管阻力降低到足以进行上腔静脉-肺动脉吻合术或全腔静脉-肺动脉吻合术的程度。
我们回顾了所有功能性单心室患者及MAPCAs单支化手术的数据。1997年至2005年,连续对14例具有不同单心室解剖结构的儿童进行了手术。
患者平均接受了3次手术(范围为1至5次)。2例患者中央肺动脉缺如,其他患者中央肺动脉细小,平均有3.5±1.2支MAPCAs。7例患者(50%)接受了双向格林手术,其中3例接受了Fontan手术。术后肺动脉压中位数分别为12.5 mmHg(格林手术)和14 mmHg(Fontan手术)。6例患者至今存活(46%),1例失访。3例患者在首次单支化分流术后早期死亡,3例晚期死亡。另1例患者单支化术后存活,但不被认为适合行格林手术,在进行高风险双心室修复后死亡。另1例右心室依赖型冠状动脉循环的患者在格林手术后晚期死于败血症。
对于部分功能性单心室合并MAPCAs的患者,肺血管床可充分重建以进行腔肺连接。肺血管系统的静脉血流可减少心脏容量负荷,可能会提高这些患者的预期寿命和生活质量。