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患有复杂先天性心脏病的婴儿的诺伍德手术及后续的Fontan手术。

The Norwood operation and subsequent Fontan operation in infants with complex congenital heart disease.

作者信息

Weldner P W, Myers J L, Gleason M M, Cyran S E, Weber H S, White M G, Baylen B G

机构信息

Division of Cardiothoracic Surgery, Pennsylvania State University, University Hospital, Milton S. Hershey Medical Center, Hershey, USA.

出版信息

J Thorac Cardiovasc Surg. 1995 Apr;109(4):654-62. doi: 10.1016/S0022-5223(95)70346-2.

Abstract

From April 1987 to September 1993, 60 infants underwent a Norwood operation for complex congenital heart disease including hypoplastic left heart syndrome (n = 41), ventricular septal defect and subaortic stenosis with aortic arch interruption/severe coarctation (n = 7), complex single right ventricle with subaortic stenosis (n = 8), critical aortic stenosis with endocardial fibroelastosis (n = 2), and malaligned primum atrial septal defect with coarctation (n = 2). Age at operation ranged from 1 day to 3.9 months (mean 9 days, median 3.5 days). The operative mortality (< 30 days) was 33% (20 patients). Late mortality was 17% (10 patients). Nine of the 20 (45%) operative deaths occurred during the first 2 days after the operation as a result of sudden hemodynamic instability. All four infants with premature closure of the foramen ovale had pulmonary lymphangiectasia and died of pulmonary failure. Seven operative deaths have occurred in 36 patients since 1990 (19%); in the past 2 years, no operative deaths have occurred in 22 patients. Overall, there are 30 long-term survivors (50%). Twenty-one of these 30 infants have undergone a two-stage repair with a modified Fontan operation at 7.3 to 27.6 months of age (mean 18.1 months) with no mortality. Six patients have entered a three-stage repair strategy by undergoing a hemi-Fontan procedure at 6.8 to 23.0 months (mean 8.8 months) with no mortality, and two of these patients have now had their modified Fontan operation at 23.0 to 46.7 months of age with no mortality (four are still awaiting surgery). Two patients have undergone a two-ventricle repair with a Rastelli procedure, with no mortality at 7.4 and 14.1 months of age. Early in our experience, infants undergoing the Norwood operation had a high early mortality most often related to sudden hemodynamic instability. After we instituted a protocol that adds carbon dioxide to the inspired gas during postoperative mechanical ventilation, the postoperative course became more stable and there have been no operative deaths. In summary, the operative mortality for the Norwood operation continues to improve. A subsequent Fontan operation can be performed with excellent clinical results.

摘要

1987年4月至1993年9月,60例婴儿因复杂先天性心脏病接受了诺伍德手术,其中包括左心发育不全综合征(n = 41)、室间隔缺损合并主动脉下狭窄伴主动脉弓中断/严重缩窄(n = 7)、复杂单心室合并主动脉下狭窄(n = 8)、重度主动脉狭窄合并心内膜弹力纤维增生症(n = 2)以及原发孔房间隔缺损合并缩窄(n = 2)。手术时年龄从1天至3.9个月不等(平均9天,中位数3.5天)。手术死亡率(< 30天)为33%(20例患者)。晚期死亡率为17%(10例患者)。20例手术死亡患者中有9例(45%)在术后头2天因突然的血流动力学不稳定而死亡。所有4例卵圆孔过早闭合的婴儿均患有肺淋巴管扩张症,并死于呼吸衰竭。自1990年以来,36例患者中有7例手术死亡(19%);在过去2年中,22例患者未发生手术死亡。总体而言,有30例长期存活者(50%)。这30例婴儿中有21例在7.3至27.6个月龄(平均18.1个月)时接受了改良Fontan手术的两期修复,无死亡病例。6例患者通过在6.8至23.0个月龄(平均8.8个月)时接受半Fontan手术进入了三期修复策略,无死亡病例,其中2例患者现已在23.0至46.7个月龄时接受了改良Fontan手术,无死亡病例(4例仍在等待手术)。2例患者接受了Rastelli手术的双心室修复,在7.4和14.1个月龄时无死亡病例。在我们的经验早期,接受诺伍德手术的婴儿早期死亡率很高,最常见的原因是突然的血流动力学不稳定。在我们制定了一项在术后机械通气期间向吸入气体中添加二氧化碳的方案后,术后过程变得更加稳定,且未发生手术死亡。总之,诺伍德手术的手术死亡率持续改善。随后进行的Fontan手术可取得优异的临床效果。

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