15-Year Analysis of Surgical Approaches and Outcomes for Coarctation in 132 Neonates and Infants.

IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Pediatric Cardiology Pub Date : 2025-01-01 Epub Date: 2024-04-01 DOI:10.1007/s00246-023-03360-1
Yuriy Stukov, Jeffrey P Jacobs, Omar M Sharaf, Giles J Peek, Andrew D Pitkin, Susana C Cruz Beltrán, Dalia Lopez-Colon, Connie S Nixon, Mark S Bleiweis
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引用次数: 0

Abstract

A variety of surgical approaches exist to treat aortic coarctation in neonates and infants. Our institutional approach is designed to match the surgical approach to the individual anatomy of the patient. The objective of this study is to evaluate operative characteristics and outcomes of all neonates and infants who underwent surgical repair of coarctation of the aorta or hypoplastic aortic arch at University of Florida from 2006 to 2021, inclusive, either in isolation or with concomitant repair of atrial septal defect (ASD) and/or ventricular septal defect (VSD). A retrospective review was performed of 132 patients aged 0-1 year who underwent surgical repair of aortic coarctation or hypoplastic aortic arch between 2006 and 2021, inclusive, either in isolation or with concomitant repair of ASD and/or VSD. Patients were divided into two groups based on the surgical approach: Group 1 = Median Sternotomy and Group 2 = Left Lateral Thoracotomy. Continuous variables are presented as median (minimum-maximum); categorical variables are presented as N (%). The most common operative technique in Group 1 was end-to-side reconstruction with ligation of the aortic isthmus. The most common operative technique in Group 2 was extended end-to-end repair. Operative Mortality was one patient (1/132 = 0.76%). Transcatheter intervention for recurrent coarctation was performed in seven patients (7/132 = 5.3%). Surgical re-intervention for recurrent coarctation was performed in three patients (3/132 = 2.3%). From these data, one can conclude that a strategy of matching the surgical approach to the anatomy of neonates and infants who underwent surgical repair of aortic coarctation or hypoplastic aortic arch, either in isolation or with concomitant repair of ASD and/or VSD, is associated with less than 1% Operative Mortality and less than 3% recurrent coarctation requiring reoperation.

对 132 名新生儿和婴儿冠状动脉畸形手术方法和疗效的 15 年分析。
治疗新生儿和婴儿主动脉闭塞症的手术方法多种多样。我们医院的方法旨在使手术方法与患者的个体解剖结构相匹配。本研究的目的是评估 2006 年至 2021 年(含 2021 年)期间在佛罗里达大学接受主动脉瓣闭锁或主动脉弓发育不良手术修复的所有新生儿和婴儿的手术特点和疗效,包括单独修复或同时修复房间隔缺损 (ASD) 和/或室间隔缺损 (VSD)。该研究对2006年至2021年(含2021年)期间接受主动脉瓣闭锁或主动脉弓发育不良手术修复的132名0-1岁患者进行了回顾性研究,这些患者要么单独接受了修复手术,要么同时接受了ASD和/或VSD修复手术。根据手术方法将患者分为两组:第 1 组 = 中位缝合术,第 2 组 = 左侧胸廓切开术。连续变量以中位数(最小值-最大值)表示;分类变量以N(%)表示。第 1 组最常见的手术技术是结扎主动脉峡部的端侧重建术。第 2 组最常见的手术技术是扩展的端对端修复术。手术死亡率为一名患者(1/132 = 0.76%)。有七名患者(7/132 = 5.3%)因复发性主动脉瓣闭塞而接受了经导管介入治疗。有 3 名患者(3/132 = 2.3%)因复发性冠状动脉畸形而接受了手术再介入治疗。从这些数据中我们可以得出结论:对于接受主动脉闭锁或主动脉弓发育不良手术修复的新生儿和婴儿,无论是单独接受手术还是同时接受 ASD 和/或 VSD 修复,根据其解剖结构选择合适的手术方法都能使手术死亡率低于 1%,需要再次手术的复发性闭锁率低于 3%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Cardiology
Pediatric Cardiology 医学-小儿科
CiteScore
3.30
自引率
6.20%
发文量
258
审稿时长
12 months
期刊介绍: The editor of Pediatric Cardiology welcomes original manuscripts concerning all aspects of heart disease in infants, children, and adolescents, including embryology and anatomy, physiology and pharmacology, biochemistry, pathology, genetics, radiology, clinical aspects, investigative cardiology, electrophysiology and echocardiography, and cardiac surgery. Articles which may include original articles, review articles, letters to the editor etc., must be written in English and must be submitted solely to Pediatric Cardiology.
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