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对Fontan手术风险因素的重新审视。

A reconsideration of risk factors for the Fontan operation.

作者信息

Myers J L, Waldhausen J A, Weber H S, Arenas J D, Cyran S E, Gleason M M, Baylen B G

机构信息

Department of Surgery, Milton S. Hershey Medical Center, Pennsylvania State University, Hershey 17033.

出版信息

Ann Surg. 1990 Jun;211(6):738-43; discussion 744. doi: 10.1097/00000658-199006000-00013.

Abstract

We reviewed our experience in 38 patients who underwent a Fontan operation. In the first five patients ages 7.5 to 23 years (mean, 15 years), a conduit was placed from the right atrium to the small right ventricle or the pulmonary artery (PA). The remaining 33 patients, ages 7 months to 14 years (mean, 4.8 years), had a modified Fontan operation with direct systemic venous or right atrial to PA anastomosis. The diagnoses were tricuspid atresia (n = 14), single ventricle (n = 10), hypoplastic right or left ventricle (n = 9), double-outlet right ventricle with inlet ventricular septal defect and pulmonary atresia or stenosis (n = 3), criss-cross ventricles and transposition of the great arteries (n = 1), and atrioventricular canal and anomalous pulmonary venous connection (n = 1). Thirty-two patients had previous surgery. Other procedures included PA banding (n = 7), systemic to PA shunts (n = 25), Norwood operation (n = 3), and a Damus-Kaye-Stansel anastomosis (n = 1), repair of total anomolous pulmonary venous connection (n = 1), a Blalock-Hanlon atrial septectomy (n = 1), and enlargement of a restrictive ventricular septal defect (n = 1). There were four operative deaths (10.5%), three from low cardiac output and one from subaortic obstruction. There were no deaths in patients younger than 3 years of age (n = 13). Subaortic obstruction developed in six of the seven patients who had pulmonary artery banding and resulted in three deaths. In our experience, diagnosis, previous surgery, type of previous operation, PA pressure, and younger age are not risk factors for early or late death. Subaortic obstruction is a major risk factor for late death. Accordingly we now perform a Damus-Kaye-Stansel anastomosis combined with a systemic to PA shunt in those children with excessive pulmonary blood flow who anatomically are likely to develop subaortic obstruction. A modified Fontan operation can be performed any time after 1 year of age and in some patients after 6 months of age, providing the anatomy and physiology of the patient are acceptable.

摘要

我们回顾了38例接受Fontan手术患者的经验。在前5例年龄为7.5至23岁(平均15岁)的患者中,将一根导管从右心房置入小的右心室或肺动脉(PA)。其余33例患者年龄为7个月至14岁(平均4.8岁),接受了改良Fontan手术,即直接进行体静脉或右心房与PA吻合。诊断包括三尖瓣闭锁(n = 14)、单心室(n = 10)、右或左心室发育不良(n = 9)、右心室双出口合并室间隔入口部缺损及肺动脉闭锁或狭窄(n = 3)、交叉心室及大动脉转位(n = 1)、房室管畸形及肺静脉异位连接(n = 1)。32例患者曾接受过手术。其他手术包括肺动脉环缩术(n = 7)、体-肺动脉分流术(n = 25)、Norwood手术(n = 3)、Damus-Kaye-Stansel吻合术(n = 1)、完全性肺静脉异位连接修复术(n = 1)、Blalock-Hanlon房间隔切除术(n = 1)以及限制性室间隔缺损扩大术(n = 1)。有4例手术死亡(10.5%),3例死于低心排血量,1例死于主动脉下梗阻。3岁以下患者(n = 13)无死亡病例。7例接受肺动脉环缩术的患者中有6例发生主动脉下梗阻,导致3例死亡。根据我们的经验,诊断、既往手术、既往手术类型、PA压力及年龄较小并非早期或晚期死亡的危险因素。主动脉下梗阻是晚期死亡的主要危险因素。因此,对于那些肺血流过多且解剖结构上可能发生主动脉下梗阻的儿童,我们现在进行Damus-Kaye-Stansel吻合术并联合体-肺动脉分流术。改良Fontan手术可在1岁以后的任何时间进行,部分患者在6个月以后进行,前提是患者的解剖结构和生理状况可接受。

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