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二叶式主动脉瓣的手术策略:瓣叶延长三尖瓣化与肺动脉自体移植术

Surgical strategy for the bicuspid aortic valve: tricuspidization with cusp extension versus pulmonary autograft.

作者信息

McMullan David Michael, Oppido Guido, Davies Ben, Kawahira Yoichi, Cochrane Andrew Donald, d'Udekem d'Acoz Yves, Penny Daniel J, Brizard Christian P

机构信息

Cardiovascular Surgery, Children's National Medical Center, Washington, DC, USA.

出版信息

J Thorac Cardiovasc Surg. 2007 Jul;134(1):90-8. doi: 10.1016/j.jtcvs.2007.01.054.

Abstract

OBJECTIVE

The congenitally bicuspid aortic valve is the most common etiologic factor associated with clinically significant aortic stenosis and/or regurgitation in pediatric patients. Beyond infancy, surgical intervention typically involves valve repair with cusp thinning and commissurotomy or valve replacement, primarily with pulmonary autograft in the current era. An aortic valve repair technique using tricuspidization with cusp extension was introduced in 1999. This study compares the midterm clinical outcome in patients undergoing valve repair by tricuspidization with cusp extension with those receiving a pulmonary autograft (Ross).

METHODS

A retrospective study was performed on all consecutive patients with symptomatic bicuspid aortic valve disease who underwent tricuspidization with cusp extension or a Ross procedure between 1999 and 2005. In both groups, all patients were at least 1 year of age at time of the operation.

RESULTS

During this period, 21 children (median age 12.6 years, range 2.6-18 years) underwent tricuspidization with cusp extension (TCE group) and 25 children (median age 10.2 years, range 11.5 months-20.1 years) underwent the Ross procedure. Prior balloon valvuloplasty was performed in 5 (24%) of the children in the TCE group and 16 (64%) of the children in the Ross group. Prior surgical commissurotomy was performed in 4 (19%) TCE patients and in 9 (36%) Ross patients. During a median follow-up period of 36.4 months (range 2.5 months-7.4 years), 2 (10%) patients in the TCE group required valve-preserving early revision of the repair, 2 (10%) TCE patients required subsequent aortic valve replacement at 16 and 33 months, 1 (4%) Ross patient required subsequent valve repair at 5 years, and 1 (4%) Ross patient underwent cardiac transplantation at 46 months. At 36 months, the actuarial freedom from reintervention on the aortic valve or autograft was 90% in the TCE group, with 11 patients at risk, and 100% in Ross patients, with 13 patients at risk (P = .39); the freedom from moderate valve dysfunction or reintervention was 66% for TCE patients and 95% for Ross patients (P = .07). There were no deaths, and all but 1 Ross patient remain in New York Heart Association class I.

CONCLUSIONS

Reintervention rates in patients undergoing tricuspidization with cusp extension or a primary Ross procedure are similar. Valve performance in the TCE group is satisfactory at midterm follow-up, but the Ross repair appears to provide greater stability of valve function. These results suggest that repair with valve tricuspidization and cusp extension provides reliable palliation of the symptomatic bicuspid aortic valve.

摘要

目的

先天性二叶式主动脉瓣是小儿患者临床上显著主动脉瓣狭窄和/或反流最常见的病因。婴儿期之后,手术干预通常包括瓣叶变薄和交界切开的瓣膜修复或瓣膜置换,在当前时代主要是采用自体肺动脉瓣移植。1999年引入了一种通过瓣叶延长进行三尖瓣化的主动脉瓣修复技术。本研究比较了接受瓣叶延长三尖瓣化瓣膜修复的患者与接受自体肺动脉瓣移植(Ross手术)的患者的中期临床结局。

方法

对1999年至2005年间所有连续接受瓣叶延长三尖瓣化或Ross手术的有症状二叶式主动脉瓣疾病患者进行回顾性研究。两组患者在手术时均至少1岁。

结果

在此期间,21例儿童(中位年龄12.6岁,范围2.6 - 18岁)接受了瓣叶延长三尖瓣化(TCE组),25例儿童(中位年龄10.2岁,范围11.5个月 - 20.1岁)接受了Ross手术。TCE组5例(24%)儿童和Ross组16例(64%)儿童曾接受球囊瓣膜成形术。4例(19%)TCE患者和9例(36%)Ross患者曾接受外科交界切开术。在中位随访期36.4个月(范围2.5个月 - 7.4年)内,TCE组2例(10%)患者需要进行保留瓣膜的早期修复翻修,2例(10%)TCE患者分别在16个月和33个月时需要进行后续主动脉瓣置换,1例(4%)Ross患者在5岁时需要进行后续瓣膜修复,1例(4%)Ross患者在46个月时接受了心脏移植。在36个月时,TCE组11例有风险患者中主动脉瓣或自体肺动脉瓣无需再次干预的精算生存率为90%,Ross组13例有风险患者中为100%(P = 0.39);TCE组患者无中度瓣膜功能障碍或无需再次干预的生存率为66%,Ross组患者为95%(P = 0.07)。无死亡病例,除1例Ross患者外,所有患者仍处于纽约心脏协会I级。

结论

接受瓣叶延长三尖瓣化或初次Ross手术的患者再次干预率相似。TCE组在中期随访时瓣膜性能令人满意,但Ross修复似乎能提供更稳定的瓣膜功能。这些结果表明,通过瓣叶延长进行三尖瓣化修复可为有症状的二叶式主动脉瓣提供可靠的姑息治疗。

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