Hani K Najm, Munir Ahmad, Tara Karamlou, Malek El-Yaman, Nicholas A Oh
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引用次数: 0
Abstract
Objectives: Complex congenital hearts could be deemed 'unseptatable' or unsuitable for biventricular circulation. We described our novel approach to utilize the left ventricle (LV) as the sub-pulmonary ventricle, termed 'ventricular switch'. We report our updated experience and highlight lessons learned.
Methods: This is a retrospective cohort study (2016-2023) of patients who underwent ventricular switch, which utilizes series of surgical techniques resulting in a biventricular circulation with a sub-systemic right ventricle (RV). These patients were selected when LV-based biventricular repair was not feasible, or with a failing single-ventricle physiology. The majority of these cases are complex heterotaxy with complex systemic and pulmonary connections. Pre- and postoperative data were analysed, focusing on modifications from iterative experience.
Results: Seventeen patients underwent ventricular switch. Median conversion age was 5.2 years (4 months-47 years). Three (17%) had an operative mortality. Systemic saturation significantly improved postoperatively (79 ± 6 vs 94 ± 4, P = 0.008). Elevated central venous pressure (CVP) decreased by 13 mmHg ± 5 postoperatively. Eleven out of 17 (65%) patients underwent preemptive atrioventricular valve (AVV) repair as part of the procedure, and all maintained or improved AVV function postoperatively. One-year and 5-year survival was 79% and 72%, respectively. Patients demonstrated stable biventricular function, well-functioning AVV and improved symptoms.
Conclusions: Ventricular switch can be an option in complex lesions that are not amenable to LV based biventricular circulation. Our results demonstrate improvement in oxygen saturation, CVP and stable ventricular function at follow-up. Our experience suggests that systemic AVV competency is critical for satisfactory postoperative haemodynamics and outcomes. Successful surgery requires normal preoperative RV function and end-diastolic volumes.
复杂的先天性心脏可能被认为是“不可分割的”或不适合双心室循环。我们描述了利用左心室(LV)作为肺下心室的新方法,称为“心室开关”。我们报告最新的经验,并强调吸取的教训。方法:这是一项回顾性队列研究(2016-2023),患者接受了心室开关手术,该手术利用一系列手术技术导致双心室循环与亚系统右心室(RV),这些患者是在基于左心室的双心室修复不可行的情况下选择的,或者单心室生理学失败。这些病例大多数是复杂的异位,有复杂的全身和肺部连接。对术前和术后数据进行分析,重点关注迭代经验的改进。结果:17例患者行心室开关术。中位转化年龄为5.2岁(4个月-47岁)。3例(17%)手术死亡。术后全身饱和度显著提高(79±6 vs 94±4,P = 0.008)。术后CVP升高降低13mmHg±5。11/17(65%)的患者作为手术的一部分接受了先行性房室瓣膜(AVV)修复,所有患者术后均维持或改善了AVV功能。1年和5年生存率分别为79%和72%。患者表现出稳定的双心室功能,功能良好的AVV和改善的症状。结论:对于不能适应左室双心室循环的复杂病变,心室开关可以作为一种选择。我们的结果表明,在随访中,氧饱和度、CVP和稳定的心室功能得到改善。我们的经验表明,系统的AVV能力对于满意的术后血流动力学和结果至关重要。成功的手术需要正常的术前右心室功能和舒张末期容积。
期刊介绍:
The primary aim of the European Journal of Cardio-Thoracic Surgery is to provide a medium for the publication of high-quality original scientific reports documenting progress in cardiac and thoracic surgery. The journal publishes reports of significant clinical and experimental advances related to surgery of the heart, the great vessels and the chest. The European Journal of Cardio-Thoracic Surgery is an international journal and accepts submissions from all regions. The journal is supported by a number of leading European societies.