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单心室心脏主动脉瓣下狭窄的手术治疗

Operations for subaortic stenosis in univentricular hearts.

作者信息

Karl T R, Watterson K G, Sano S, Mee R B

机构信息

Victorian Paediatric Cardiac Surgical Unit, Royal Children's Hospital, Melbourne, Australia.

出版信息

Ann Thorac Surg. 1991 Sep;52(3):420-7; discussion 427-8. doi: 10.1016/0003-4975(91)90901-2.

DOI:10.1016/0003-4975(91)90901-2
PMID:1898129
Abstract

Optimal prevention and treatment of subaortic stenosis (SAS) in the univentricular heart with subaortic outlet chamber and high pulmonary blood flow remains controversial, especially when complicated by aortic arch obstruction. Herein we analyze our surgical results. Group 1 consisted of 11 infants (mean age, 10 days) with univentricular heart and SAS. Ten required repair of interrupted aortic arch (n = 7) or coarctation with hypoplastic arch (n = 7). Four patients had relief of SAS by either Damus-Kaye-Stansel connection (n = 2) or aortopulmonary window (n = 2), with three operative deaths and one late death. Six had one-stage arterial switch and atrial septectomy with arch repair (5/6) with one operative death and one late death. Two survivors have progressed to bidirectional cavopulmonary shunt, a third has had a Fontan operation, and a fourth awaits Fontan. In group 2, 11 children required operation for acquired SAS after pulmonary artery banding. Nine have progressed to Fontan operation with either staged (n = 3) or concurrent (n = 6) relief of SAS by Damus-Kaye-Stansel connection or subaortic resection. Fontan mortality was 11% (70% confidence limits, 2% to 32%). Group 3 consisted of 3 patients without pulmonary artery banding who had SAS diagnosed at Fontan evaluation. All 3 survived Fontan operation and relief of SAS by Damus-Kaye-Stansel connection or subaortic resection. Group 4 consisted of 1 patient with previous pulmonary artery banding (no SAS) who underwent Fontan operation but required Damus-Kaye-Stansel connection 30 months later for SAS.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对于存在主动脉下出口腔且肺血流量高的单心室心脏患者,主动脉下狭窄(SAS)的最佳预防和治疗仍存在争议,尤其是当合并主动脉弓梗阻时。在此我们分析我们的手术结果。第1组由11例患有单心室心脏和SAS的婴儿(平均年龄10天)组成。其中10例需要修复中断的主动脉弓(n = 7)或伴有发育不良主动脉弓的缩窄(n = 7)。4例患者通过Damus-Kaye-Stansel吻合术(n = 2)或主肺动脉窗(n = 2)缓解了SAS,有3例手术死亡和1例晚期死亡。6例患者进行了一期动脉调转术和房间隔切除术并修复主动脉弓(5/6),有1例手术死亡和1例晚期死亡。2例幸存者已进展至双向腔肺分流术,第3例已进行了Fontan手术,第4例等待Fontan手术。在第2组中,11名儿童在肺动脉环扎术后因获得性SAS需要手术。其中9例已进展至Fontan手术,通过Damus-Kaye-Stansel吻合术或主动脉下切除术分期(n = 3)或同期(n = 6)缓解了SAS。Fontan手术死亡率为11%(70%置信区间,2%至32%)。第3组由3例未进行肺动脉环扎的患者组成,他们在Fontan评估时被诊断为SAS。所有3例均在Fontan手术中存活,并通过Damus-Kaye-Stansel吻合术或主动脉下切除术缓解了SAS。第4组由1例先前进行过肺动脉环扎(无SAS)的患者组成,该患者接受了Fontan手术,但30个月后因SAS需要进行Damus-Kaye-Stansel吻合术。(摘要截断于250字)

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