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[一例曾接受传统格林手术的成年“共同心室”及心房附件异构病例的成功双心室修复]

[A successful biventricular repair in an adult case with "common ventricle" and isomeric atrial appendages previously undergoing the conventional Glenn procedure].

作者信息

Yoshida M, Yagihara T, Uemura H, Yamashita K, Kawahira Y, Yoshizumi K

机构信息

Department of Cardiovascular Surgery, National Cardiovascular Center, Osaka, Japan.

出版信息

Jpn J Thorac Cardiovasc Surg. 1998 Nov;46(11):1177-81. doi: 10.1007/BF03217897.

DOI:10.1007/BF03217897
PMID:9884573
Abstract

We describe herein a successful biventricular repair in a 21-year-old male who had severe hypoplasia of isomeric right appendages. He had previously undergone the conventional Glenn procedure at the age of one and a half years. Although he had grown uneventfully until adolescence, cyanosis as well as fatigue than gradually became worse. When referred to us for further treatment, we deemed a Fontan type procedure to be contraindicated, because of the hypoplastic nature of the right pulmonary artery, and the presence of abundant collateral arteries supplying the right lung. In terms of ventricular morphology, however, because both apical components were present, separated by the hypoplastic septum, biventricular repair seemed feasible. Initially, the Glenn anastomosis was taken down, and systemic-to-pulmonary shunts were constructed via a median sternotomy to both the right and left pulmonary arteries. This was followed by surgical division of the developed collaterals to the right lung via the right thoracotomy. Definitive biventricular repair was then carried out by reconstructing the pulmonary arteries and right ventricular outflow tact, separating and rerouting within the ventricles using a EPTFE patch, and achieving redirection of blood within the atriums using bovine pericardium. Such staged surgical approaches, although extensive, can provide useful options when seeking definitive repair in grown-up patients with complicated malformations.

摘要

我们在此描述了一例对一名患有右心耳异构严重发育不全的21岁男性患者成功实施的双心室修复手术。他在一岁半时曾接受过传统的格林手术。尽管他在青春期前生长过程顺利,但紫绀和疲劳症状逐渐加重。当他前来我们这里寻求进一步治疗时,由于右肺动脉发育不全以及存在大量供应右肺的侧支动脉,我们认为Fontan类手术是禁忌的。然而,就心室形态而言,由于两个心尖部分均存在,被发育不全的室间隔分隔开,双心室修复似乎是可行的。最初,拆除格林吻合口,并通过正中胸骨切开术在左右肺动脉上构建体肺分流。随后,通过右胸切开术对发育的右肺侧支进行手术切断。然后通过重建肺动脉和右心室流出道、使用聚四氟乙烯补片在心室内进行分隔和改道,以及使用牛心包实现心房内血液改道,进行最终的双心室修复。这种分期手术方法虽然复杂,但在为患有复杂畸形的成年患者寻求最终修复时可提供有用的选择。

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本文引用的文献

1
Pulmonary circulation after biventricular repair in patients with major systemic-to-pulmonary collateral arteries.
Eur J Cardiothorac Surg. 1997 Oct;12(4):581-6. doi: 10.1016/s1010-7940(97)00229-7.
2
Factors influencing perioperative morbidity during palliation of the univentricular heart.影响单心室心脏姑息治疗围手术期发病率的因素。
Ann Thorac Surg. 1995 Dec;60(6 Suppl):S550-3. doi: 10.1016/0003-4975(95)00769-5.
3
Prevalence and risk factors for aortopulmonary collateral vessels after Fontan and bidirectional Glenn procedures.Fontan手术和双向格林手术后主肺侧支血管的患病率及危险因素。
J Am Coll Cardiol. 1993 Jul;22(1):207-15. doi: 10.1016/0735-1097(93)90836-p.
4
Extent of aortopulmonary collateral blood flow as a risk factor for Fontan operations.
Ann Thorac Surg. 1995 Feb;59(2):433-7. doi: 10.1016/0003-4975(94)00120-v.
5
What factors affect ventricular performance after a Fontan-type operation?在Fontan类手术后,哪些因素会影响心室功能?
J Thorac Cardiovasc Surg. 1995 Aug;110(2):405-15. doi: 10.1016/S0022-5223(95)70237-7.