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法洛四联症的早期一期修复术。

Early primary repair of tetralogy of Fallot.

作者信息

Gustafson R A, Murray G F, Warden H E, Hill R C, Rozar G E

机构信息

Department of Surgery, West Virginia University Medical Center, Morgantown 26505.

出版信息

Ann Thorac Surg. 1988 Mar;45(3):235-41. doi: 10.1016/s0003-4975(10)62455-1.

Abstract

Young age, low weight, and the requirement for transannular patch reconstruction of the right ventricular outflow tract (RVOT) are thought to adversely affect intracardiac repair of tetralogy of Fallot. Forty patients underwent complete repair between January, 1984, and January, 1987. Only infants with pulmonary atresia, complete atrioventricular canal, or coronary artery anomalies were shunted initially. The malalignment ventricular septal defect was closed with a Dacron patch. Infundibular resection was minimized. All atrial communications were left open. Thirty-four patients (85%) had a transannular RVOT patch, and 2 patients (5%) had a nontransannular patch. All 10 infants weighing 3.4 to 9.6 kg had a transannular RVOT patch at 7 weeks to 12 months of age. An RVOT patch was used in 26 of 30 children operated on between 1 and 6 years of age (median age, 24 months). No patient undergoing intracardiac repair died. Postoperative RVOT pullback gradients were between 0 and 35 mm Hg (mean, 18.5 mm Hg). Postoperative pulmonary artery saturation (mean, 73%) did not reveal any residual ventricular septal defect. The right ventricular/arterial pressure ratio was always less than 0.6 (mean, 0.4). All children are doing well at follow-up from two to 37 months. Serial echocardiograms reveal no residual ventricular septal defect and only 1 moderate RVOT gradient. Follow-up cardiac catheterization in 15 patients revealed no residual ventricular septal defect and RVOT gradients between 5 and 35 mm Hg. The right ventricular/left ventricular pressure ratio was always less than 0.6 (mean, 0.48). The early and late results justify continued primary repair of tetralogy of Fallot in symptomatic children, regardless of age or weight.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

年轻、低体重以及右心室流出道(RVOT)跨环补片重建的需求被认为会对法洛四联症的心内修复产生不利影响。1984年1月至1987年1月期间,40例患者接受了完全修复。仅患有肺动脉闭锁、完全性房室通道或冠状动脉异常的婴儿最初进行了分流。采用涤纶补片闭合对位不良的室间隔缺损。漏斗部切除术尽量减少。所有心房交通均保持开放。34例患者(85%)有跨环RVOT补片,2例患者(5%)有非跨环补片。所有10例体重3.4至9.6千克的婴儿在7周龄至12月龄时有跨环RVOT补片。30例1至6岁接受手术的儿童中,26例(中位年龄24个月)使用了RVOT补片。没有患者在心内修复后死亡。术后RVOT回撤梯度在0至35毫米汞柱之间(平均18.5毫米汞柱)。术后肺动脉饱和度(平均73%)未显示任何残余室间隔缺损。右心室/动脉压比值始终小于0.6(平均0.4)。所有儿童在2至37个月的随访中情况良好。系列超声心动图显示无残余室间隔缺损,仅有1例中度RVOT梯度。15例患者的随访心导管检查显示无残余室间隔缺损,RVOT梯度在5至35毫米汞柱之间。右心室/左心室压比值始终小于0.6(平均0.48)。早期和晚期结果证明,对于有症状的儿童,无论年龄或体重如何,继续进行法洛四联症的一期修复是合理的。(摘要截短于250字)

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