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在马凡综合征和洛伊茨-迪茨综合征中,可预期再植入保留瓣膜的主动脉根部置换术具有长期耐久性。

Long-term durability of a reimplantation valve-sparing aortic root replacement can be expected in both Marfan syndrome and Loeys-Dietz syndrome.

机构信息

National Cerebral and Cardiovascular Center, Department of Cardiovascular Surgery, Osaka, Japan.

Sakakibara Heart Institute, Department of Medical Genetics, Tokyo, Japan.

出版信息

Eur J Cardiothorac Surg. 2022 May 27;61(6):1318-1325. doi: 10.1093/ejcts/ezac050.

Abstract

OBJECTIVES

The goal of this study was to evaluate the surgical outcomes of a valve-sparing root replacement using the reimplantation technique for annuloaortic ectasia in patients with Marfan syndrome (MFS) and in those with Loeys-Dietz syndrome (LDS).

METHODS

We reviewed 103 patients with MSF with mutations in the fibrillin-1 gene and 28 patients with LDS with mutations in the transforming growth factor-beta receptor and 2, SMAD3 and transforming growth factor beta-2 from 1988 to 2020.

RESULTS

Forty-four (42.7%) patients with MFS [26 men, 31 (7.6) years] and 10 (35.7%) patients with Loeys-Dietz syndrome (LDS) [7 men, 22 (standard deviation: 8.6) years] who had no aortic dissection and underwent valve-sparing root replacement were included. The preoperative sinus diameter [46 (45-50.5) mm in those with MFS vs 48 (47-50) mm in those with LDS, p = 0.420] and the percentage of aortic insufficiency > grade 2+ [31.8% (10/44) in patients with MFS vs 10.0% (1/10) in those with LDS, p = 0.667] revealed no significant differences between the 2 groups. The cumulative incidences of aortic insufficiency greater than grade 1 (p = 0.588) and aortic valve reoperation (p = 0.310) were comparable between the 2 groups. Patients with LDS had a higher tendency towards aortic dissection after the initial operation (p = 0.061) and a significantly higher cumulative incidence of aortic reoperation (p = 0.003) versus those with MFS.

CONCLUSIONS

Patients with MFS and those with LDS showed similar cumulative incidences of recurrent aortic valve insufficiency and aortic valve reoperation. Those with LDS revealed a higher cumulative incidence of aortic reoperation and a greater tendency towards aortic dissection after the initial operation compared with those with MFS.

摘要

目的

本研究旨在评估使用再植入技术对马凡综合征(MFS)和洛伊茨-迪茨综合征(LDS)患者行保留瓣膜主动脉根部替换术的手术效果。

方法

我们回顾了 1988 年至 2020 年间 103 例携带纤维连接蛋白 1 基因突变的 MFS 患者和 28 例携带转化生长因子-β受体、2、SMAD3 和转化生长因子β-2 基因突变的 LDS 患者。

结果

共纳入 44 例 MFS [26 例男性,31(7.6)岁]和 10 例 LDS 患者(7 例男性,22(标准差:8.6)岁),这两组患者均未发生主动脉夹层且均接受了保留瓣膜主动脉根部替换术。MFS 组术前窦部直径[46(45-50.5)mm 比 LDS 组 48(47-50)mm,p=0.420]和主动脉瓣关闭不全程度>2+的百分比[31.8%(10/44)比 LDS 组 10.0%(1/10),p=0.667]无显著差异。两组主动脉瓣关闭不全程度>1 级的累积发生率(p=0.588)和主动脉瓣再次手术的发生率(p=0.310)相当。初始手术后 LDS 患者发生主动脉夹层的倾向更高(p=0.061),主动脉再次手术的累积发生率也显著更高(p=0.003)。

结论

MFS 患者和 LDS 患者的主动脉瓣再次关闭不全和主动脉瓣再次手术的累积发生率相似。与 MFS 患者相比,LDS 患者的主动脉再次手术累积发生率更高,初始手术后发生主动脉夹层的倾向更大。

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