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部分肺静脉异常连接至心脏右侧。

Partial anomalous pulmonary venous connection to the right side of the heart.

作者信息

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

机构信息

Department of Surgery, West Virginia University School of Medicine, Morgantown 26506.

出版信息

J Thorac Cardiovasc Surg. 1989 Nov;98(5 Pt 2):861-8.

PMID:2682021
Abstract

Partial anomalous pulmonary venous connection to the right side of the heart often complicates surgery for atrial septal defects. Between 1964 and 1987, 39 patients, ranging from 2 to 52 years old, underwent repair of partial anomalous pulmonary venous connection. At least one anomalous pulmonary vein arose from the right upper lobe in 38 patients and right middle lobe in 30 patients and connected to the superior vena cava in 28 patients and the right atrium only in 11 patients. An atrial septal defect was present in 32 patients (82%). Patients who had partial anomalous pulmonary venous connection to the superior vena cava-right atrium junction, the right atrium or both were treated by septal translocation (two patients) or patch redirection of the anomalous pulmonary venous flow to the left atrium through a native atrial septal defect (eight patients) or a surgically created atrial septal defect in two patients with intact atrial septum. For partial anomalous pulmonary venous connection to the high superior vena cava (27 patients), the superior vena cava was transected and oversewn above the anomalous veins. The anomalous pulmonary venous flow was redirected through the proximal superior vena cava into the left atrium across a sinus venous atrial septum defect (22 patients) or a surgically created atrial septal defect in five patients with intact atrial septum. The atrial septal defect was coapted to the intracardiac orifice of the superior vena cava, and the distal superior vena cava was anastomosed to the right atrial appendage. One 31-year-old woman with severe pulmonary hypertension died early and was the only death in the series. A technical error early in the series resulted in one symptomatic superior vena cava obstruction. Only one patient remains in sick sinus syndrome late. All patients remain well over long follow-up (1 to 24 years). Postoperative catheterization or echocardiography has revealed no intracardiac defects, pulmonary venous obstruction, or superior vena cava obstruction (except the one technical error). Correction of partial anomalous pulmonary venous connection should be individualized according to the site of connection of the anomalous pulmonary veins and the location of the atrial defect to minimize undesirable postoperative sequelae often associated with other methods of repair.

摘要

部分性肺静脉异位连接至心脏右侧常使房间隔缺损手术复杂化。1964年至1987年间,39例年龄在2至52岁的患者接受了部分性肺静脉异位连接修复术。38例患者至少有1条异常肺静脉起自右上叶,30例起自右中叶;28例连接至上腔静脉,仅11例连接至右心房。32例患者(82%)存在房间隔缺损。部分性肺静脉异位连接至上腔静脉-右心房交界处、右心房或两者的患者,采用房间隔移位术(2例)或通过天然房间隔缺损(8例)或在2例房间隔完整的患者中通过手术制造的房间隔缺损将异常肺静脉血流补片重定向至左心房进行治疗。对于部分性肺静脉异位连接至高上腔静脉(27例),在上腔静脉异常静脉上方横断并缝合。异常肺静脉血流通过近端上腔静脉经静脉窦房间隔缺损(22例)或在5例房间隔完整的患者中通过手术制造的房间隔缺损重定向至左心房。将房间隔缺损与上腔静脉的心内开口对合,远端上腔静脉与右心耳吻合。1例31岁重度肺动脉高压女性患者早期死亡,是该系列中唯一的死亡病例。该系列早期的1例技术失误导致1例有症状性上腔静脉梗阻。仅有1例患者后期出现病态窦房结综合征。所有患者经长期随访(1至24年)情况良好。术后心导管检查或超声心动图未发现心内缺损、肺静脉梗阻或上腔静脉梗阻(除1例技术失误外)。部分性肺静脉异位连接的矫正应根据异常肺静脉的连接部位和心房缺损的位置个体化进行,以尽量减少常与其他修复方法相关的不良术后后遗症。

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