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马方综合征患者的主动脉根部再次手术

Redo Aortic Root Operations in Patients with Marfan Syndrome.

作者信息

Orozco-Sevilla Vicente, Whitlock Richard, Preventza Ourania, de la Cruz Kim I, Coselli Joseph S

机构信息

Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas.

Section of Adult Cardiac Surgery, Department of Cardiovascular Surgery, Texas Heart Institute, Houston, Texas.

出版信息

Int J Angiol. 2018 Jun;27(2):92-97. doi: 10.1055/s-0038-1649485. Epub 2018 May 17.

DOI:10.1055/s-0038-1649485
PMID:29896041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5995685/
Abstract

Aortic root aneurysm is the most common cardiovascular manifestation requiring surgical intervention in patients with Marfan syndrome (MFS), a heritable thoracic aortic disease. Elective replacement of the aortic root is the treatment of choice for patients with aneurysmal complications of the aortic root and ascending aorta. There are two basic approaches to aortic root replacement: valve-sparing (VS) and valve-replacing (VR) techniques. After successful aortic root replacement surgery, several patients with MFS may develop a late complication related to their aortic disease process, such as developing a pseudoaneurysm of the coronary artery reattachment buttons, aneurysmal expansion, or aortic dissection in the remaining native aorta. These patients may also develop other late complications that are not specifically related to the heritable thoracic aortic disease, such as infections that can lead to dehiscence of some or all of the distal or proximal anastomosis. Because these complications are rare, the clinical volume of reoperations of the aortic root in patients with MFS is low, making it difficult to assess contemporary experiences with these procedures. Only a few published reports have examined reoperative aortic root surgery in patients with MFS, each of which had only a small series of patients. Herein, we describe our contemporary experience with reoperative aortic root replacement in patients with MFS and provide our operative approach for these uncommon procedures.

摘要

主动脉根部瘤是马凡综合征(MFS)患者最常见的需要手术干预的心血管表现,马凡综合征是一种遗传性胸主动脉疾病。对于主动脉根部和升主动脉出现动脉瘤并发症的患者,选择性主动脉根部置换是首选治疗方法。主动脉根部置换有两种基本方法:保留瓣膜(VS)和置换瓣膜(VR)技术。在成功进行主动脉根部置换手术后,一些马凡综合征患者可能会出现与主动脉疾病进程相关的晚期并发症,例如冠状动脉重新附着纽扣处形成假性动脉瘤、动脉瘤扩张或剩余主动脉发生主动脉夹层。这些患者还可能出现其他与遗传性胸主动脉疾病无特定关联的晚期并发症,如感染,可导致部分或全部远端或近端吻合口裂开。由于这些并发症罕见,马凡综合征患者主动脉根部再次手术的临床病例数较少,因此难以评估这些手术的当代经验。仅有少数已发表的报告研究了马凡综合征患者的再次手术主动脉根部手术,每份报告的患者系列都很小。在此,我们描述我们在马凡综合征患者再次手术主动脉根部置换方面的当代经验,并提供我们针对这些不常见手术的手术方法。

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本文引用的文献

1
Long-Term Results of Aortic Root Surgery in Marfan Syndrome Patients: A Single-Center Experience.马凡综合征患者主动脉根部手术的长期结果:单中心经验
J Heart Valve Dis. 2017 Jul;26(4):397-404.
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Systematic review and meta-analysis of surgical outcomes in Marfan patients undergoing aortic root surgery by composite-valve graft or valve sparing root replacement.对接受复合瓣膜移植或保留瓣膜根部置换术的马凡氏综合征患者主动脉根部手术的手术结果进行系统评价和荟萃分析。
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J Heart Valve Dis. 2017 Jan;26(1):45-53.
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Reimplantation of the aortic valve at 20 years.20 年后再次行主动脉瓣置换术。
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Aortic Valve Repair.主动脉瓣修复术
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It's time to get to the root of things.是时候探究事情的根源了。
J Thorac Cardiovasc Surg. 2016 Feb;151(2):291-3. doi: 10.1016/j.jtcvs.2015.09.054. Epub 2015 Sep 24.