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[保留瓣膜的主动脉根部置换术治疗马方综合征年轻女性患者]

[Valve-sparing aortic root replacement for young female patients with Marfan syndrome].

作者信息

Nawata Kan, Morota T

机构信息

Department of Cardiothoracic Surgery, Tokyo University, Tokyo, Japan.

出版信息

Kyobu Geka. 2009 Oct;62(11):983-5.

PMID:19827552
Abstract

Annuloaortic ectasia is frequently related with Marfan syndrome, and Bentall procedure or aortic root replacement with valved conduit has been the conventional standard operation for this disease. Recently, some institutes have adopted valve-sparing aortic root replacement (VSARR) instead of Bentall procedure. Young female patients with Marfan syndrome who wishes for childbearing seem to be a group of good candidates of this type of operation, because it let them free from morbidities after artificial valve implantation. Valve-sparing operation should be taken into consideration when the size of Valsalva sinus reaches 45 mm for patients with Marfan syndrome and when it reaches 40 mm for patients with past histories or family histories of aortic dissection or aortic rupture. Since pregnancy is one of the most serious risk factors for aortic events, Valsalva sinus of 40 mm or larger could be the new standard for surgical indication if VSARR is applicable.

摘要

主动脉环扩张常与马凡综合征相关,而Bentall手术或带瓣管道主动脉根部置换术一直是该病的传统标准手术。最近,一些机构采用了保留瓣膜的主动脉根部置换术(VSARR)而非Bentall手术。希望生育的年轻马凡综合征女性患者似乎是这类手术的理想候选人群,因为该手术可使她们免于人工瓣膜植入后的并发症。对于马凡综合征患者,当主动脉窦大小达到45mm时,以及对于有主动脉夹层或主动脉破裂既往史或家族史的患者,当主动脉窦大小达到40mm时,应考虑保留瓣膜手术。由于妊娠是主动脉事件最严重的危险因素之一,如果VSARR适用,40mm或更大的主动脉窦可能成为手术指征的新标准。

相似文献

1
[Valve-sparing aortic root replacement for young female patients with Marfan syndrome].[保留瓣膜的主动脉根部置换术治疗马方综合征年轻女性患者]
Kyobu Geka. 2009 Oct;62(11):983-5.
2
Aortic root replacement in 372 Marfan patients: evolution of operative repair over 30 years.372例马凡综合征患者的主动脉根部置换:30年手术修复的演变
Ann Thorac Surg. 2009 May;87(5):1344-9; discussion 1349-50. doi: 10.1016/j.athoracsur.2009.01.073.
3
Valve-sparing and valve-replacing techniques for aortic root replacement in patients with Marfan syndrome: Analysis of early outcome.马凡综合征患者主动脉根部置换的保留瓣膜和置换瓣膜技术:早期结果分析
J Thorac Cardiovasc Surg. 2009 May;137(5):1124-32. doi: 10.1016/j.jtcvs.2009.03.023.
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Reimplantation valve-sparing aortic root replacement in Marfan syndrome using the Valsalva conduit: an intercontinental multicenter study.使用瓦氏窦导管对马凡综合征患者进行保留瓣膜的主动脉根部再植入置换术:一项跨洲际多中心研究。
Ann Thorac Surg. 2007 Feb;83(2):S769-73; discussion S785-90. doi: 10.1016/j.athoracsur.2006.10.084.
5
[The Tirone Davis operation in a young patient with Marfan syndrome. Description of a clinical case].[蒂罗内·戴维斯手术用于一名患有马凡综合征的年轻患者。临床病例描述]
G Ital Cardiol. 1998 Sep;28(9):1017-20.
6
[Surgical results for aortic involvement in Marfan syndrome].[马凡综合征主动脉受累的手术结果]
Kyobu Geka. 2002 Jul;55(8 Suppl):644-9.
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[The strategy for aortic root reconstruction; Bentall operation or native valve preserving operation?].[主动脉根部重建策略;Bentall手术还是保留自体瓣膜手术?]
Kyobu Geka. 2009 Oct;62(11):952-7.
8
Aortic root replacement in patients with Marfan's syndrome and annulo-aortic ectasia. How and when?
Ann Thorac Cardiovasc Surg. 1998 Aug;4(4):167-70.
9
Cardiovascular surgery in children with Marfan syndrome or Loeys-Dietz syndrome.马凡综合征或洛伊斯-迪茨综合征患儿的心血管手术
J Thorac Cardiovasc Surg. 2009 Jun;137(6):1327-32; discussion 1332-3. doi: 10.1016/j.jtcvs.2009.02.007. Epub 2009 Apr 11.
10
[Successful surgical treatment for severe mitral valve annulus enlargement and mitral regurgitation 5 years after aortic root replacement in Marfan syndrome: a case report].[马凡综合征主动脉根部置换术后5年重度二尖瓣环扩大及二尖瓣反流的成功外科治疗:一例报告]
Kyobu Geka. 1998 Aug;51(9):769-72.