Wu Qing-Yu, Li Dong-Hai, Li Hong-Yin, Zhang Ming-Kui, Xu Zhong-Hua, Xue Hui
Department of Cardiology, The First Hospital of Tsinghua University, Medical Center, Tsinghua University, Beijing 100016, China.
Chin Med J (Engl). 2017 Feb 20;130(4):409-413. doi: 10.4103/0366-6999.199827.
Double outlet right ventricle (DORV) is a group of complex congenital heart abnormalities. Preoperative pulmonary hypertension (PH) is considered an important risk factor for early death during the surgical treatment of DORV. The aim of this study was to report our experience on surgical treatment of DORV complicated by PH.
From June 2004 to November 2016, 61 patients (36 males and 25 females) aged 2 weeks to 26 years (median: 0.67 years and interquartile range: 0.42-1.67 years) with DORV (two great arteries overriding at least 50%) complicated by PH underwent surgical treatment in our center. All patients were categorized according to surgical age and lesion type, respectively. Pulmonary artery systolic pressure (PASP), pulmonary artery diastolic pressure (PADP), and mean pulmonary artery pressure (mPAP) were measured directly before cardiopulmonary bypass (CPB) was established and after CPB was removed. An intracardiac channel procedure was performed in 37 patients, arterial switch procedure in 19 patients, Rastelli procedure in three patient, Senning procedure in one patients, and Mustard procedure in one patient. The Student's t-test and Chi-squared test were performed to evaluate clinical outcomes of the surgical timing and operation choice.
Fifty-five patients had uneventful recovery. PASP fell from 55.3 ± 11.2 mmHg to 34.7 ± 11.6 mmHg (t = 14.05, P < 0.001), PADP fell from 29.7 ± 12.5 mmHg to 18.6 ± 7.9 mmHg (t = 7.39, P < 0.001), and mPAP fell from 40.3 ± 10.6 mmHg to 25.7 ± 8.3 mmHg (t = 11.85, P < 0.001). Six (9.8%) patients died owing to complications including low cardiac output syndrome in two patients, respiratory failure in two, pulmonary hemorrhage in one, and sudden death in one patient. Pulmonary artery pressure (PAP) dropped significantly in infant and child patients. Mortality of both infants (13.9%) and adults (33.3%) was high.
PAP of patients with DORV complicated by PH can be expected to fall significantly after surgery. An arterial switch procedure can achieve excellent results in patients with transposition of the great arteries type. Higher incidence of complications may occur in patients with ventricular septal defect (VSD) type before 1 year of age. For those with remote VSD type, VSD enlargement and right ventricle outflow tract reconstruction are usually required with acceptable results. The degree of aortic overriding does not influence surgical outcome.
右心室双出口(DORV)是一组复杂的先天性心脏畸形。术前肺动脉高压(PH)被认为是DORV手术治疗期间早期死亡的重要危险因素。本研究的目的是报告我们对合并PH的DORV手术治疗的经验。
2004年6月至2016年11月,61例年龄2周至26岁(中位数:0.67岁,四分位间距:0.42 - 1.67岁)的DORV(两大动脉骑跨至少50%)合并PH患者在我院接受手术治疗。所有患者分别根据手术年龄和病变类型进行分类。在建立体外循环(CPB)前和撤除CPB后直接测量肺动脉收缩压(PASP)、肺动脉舒张压(PADP)和平均肺动脉压(mPAP)。37例患者行心内通道手术,19例患者行动脉调转术,3例患者行Rastelli手术,1例患者行Senning手术,1例患者行Mustard手术。采用Student t检验和卡方检验评估手术时机和手术选择的临床结果。
55例患者恢复顺利。PASP从55.3±11.2 mmHg降至34.7±11.6 mmHg(t = 14.05,P < 0.001),PADP从29.7±12.5 mmHg降至18.6±7.9 mmHg(t = 7.39,P < 0.001),mPAP从40.3±10.6 mmHg降至25.7±8.3 mmHg(t = 11.85,P < 0.001)。6例(9.8%)患者因并发症死亡,其中2例死于低心排综合征,2例死于呼吸衰竭,1例死于肺出血,1例猝死。婴幼儿患者肺动脉压(PAP)显著下降。婴儿(13.9%)和成人(33.3%)的死亡率均较高。
合并PH的DORV患者术后PAP有望显著下降。动脉调转术对大动脉转位型患者可取得良好效果。1岁前室间隔缺损(VSD)型患者并发症发生率较高。对于远距离VSD型患者,通常需要扩大VSD并重建右心室流出道,效果尚可。主动脉骑跨程度不影响手术结果。