Management of the aortic arch in patients with syndromic heritable thoracic aortic disease.

0 CARDIAC & CARDIOVASCULAR SYSTEMS
Maria Nucera, Murat Yildiz, Selim Mosbahi, Marina Rieder, Silvan Jungi, Vladimir Makaloski, Matthias Siepe, Florian S Schoenhoff
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Abstract

Objectives: The aim of this study was to examine the evolution of the aortic arch over time in patients with HTAD.

Methods: We screened all patients with Marfan syndrome (MFS) or Loeys-Dietz syndrome (LDS) who were seen at our HTAD clinic since 1995. Patients who had undergone aortic surgery were included in the present study. Patients were analysed based on (1) extent of aortic arch replacement, (2) history of aortic dissection and (3) outcome after secondary total aortic arch replacement (TAR).

Results: A cohort of 260 patients was identified of whom 165 patients with MFS (n = 138) and LDS (n = 27) had already undergone aortic surgery and were included in this study. LDS: initial presentation was acute aortic dissection (AAD) in five (19%) patients, while 22 (81%) patients presented with aneurysmal disease. Only two patients required secondary TAR during follow-up. MFS: initial presentation was AAD in 41 (30%) patients, while 97 (70%) presented with aneurysmal disease. Only 3% (n = 3) of the MFS patients without primary aortic arch replacement required a secondary TAR. There was significantly more secondary TAR in MFS patients with history of aortic dissection compared to those without (P = 0.019). However, there was no significant differences in rate of downstream aortic events in MFS patients with secondary TAR compared to those without (P = 0.089). There was no significant difference in mortality in MFS patients with secondary TAR compared to those without (P = 0.366).

Conclusions: Concomitant prophylactic TAR in MFS patients undergoing elective root repair is not justified. One out of four MFS patients with history of AAD will have to undergo secondary TAR during follow-up. MFS patients undergoing secondary TAR do not have worse survival compared to those without. Current data do not provide enough evidence for strong recommendations regarding the need for prophylactic aortic arch replacement in LDS patients.

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综合征遗传性胸主动脉疾病患者主动脉弓的处理。
目的:本研究的目的是研究HTAD患者主动脉弓随时间的演变。方法:我们筛选自1995年以来在我们HTAD诊所就诊的所有马凡综合征(MFS)或Loeys-Dietz综合征(LDS)患者。接受过主动脉手术的患者被纳入本研究。根据(1)主动脉弓置换术的范围,(2)主动脉夹层史,(3)二次全主动脉弓置换术(TAR)的结果对患者进行分析。结果:确定了260例患者的队列,其中165例MFS (n = 138)和LDS (n = 27)已接受主动脉手术并纳入本研究。LDS: 5例(19%)患者最初表现为急性主动脉夹层(AAD),而22例(81%)患者表现为动脉瘤性疾病。随访期间,仅有2例患者需要二次TAR治疗。MFS: 41例(30%)患者最初表现为AAD,而97例(70%)患者表现为动脉瘤性疾病。没有主动脉弓置换术的MFS患者中,只有3% (n = 3)需要二次TAR。有主动脉夹层病史的MFS患者继发TAR明显高于无主动脉夹层病史的MFS患者(P = 0.019)。然而,与没有继发性TAR的MFS患者相比,继发性TAR患者的下游主动脉事件发生率没有显著差异(P = 0.089)。伴有继发性TAR的MFS患者与未伴有继发性TAR的MFS患者的死亡率无显著差异(P = 0.366)。结论:选择性牙根修复的MFS患者同时使用预防性TAR是不合理的。在随访期间,有AAD病史的MFS患者中有1 / 4必须接受二次TAR治疗。与未接受二次TAR治疗的MFS患者相比,接受二次TAR治疗的MFS患者的生存率并不差。目前的数据没有提供足够的证据来强烈建议LDS患者需要预防性主动脉弓置换术。
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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