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小儿先天性二尖瓣狭窄的二尖瓣修复术。

Mitral valve repair for congenital mitral valve stenosis in the pediatric population.

机构信息

Division of Pediatric Cardiovascular Surgery, Section of Cardiac Surgery, University of Michigan Medical School, Ann Arbor, Michigan 48109-5864, USA.

出版信息

Ann Thorac Surg. 2010 Jul;90(1):36-41. doi: 10.1016/j.athoracsur.2010.03.099.

DOI:10.1016/j.athoracsur.2010.03.099
PMID:20609744
Abstract

BACKGROUND

Mitral valve repair is the preferred approach for congenital mitral valve stenosis in children. However, repairs in this population remain challenging.

METHODS

From 2001 to 2009, mitral valve repair was attempted in 20 consecutive congenital mitral valve stenosis patients. The median age and body weight at operation were 1.4 +/- 1.9 years and 7.4 +/- 4.1 kg, respectively. Multiple level left-side heart obstruction was present in 14 patients (70%). Moderate or more mitral insufficiency was present in 5 patients.

RESULTS

The main etiology of the stenosis was valvular in 5 patients, supravalvular mitral ring in 4, single or predominant papillary muscle in 9, and hammock mitral valve in 2. Freedom from hospital death or transplantation was 85% (17 of 20). Two patients required replacement before discharge. In the 15 successfully repaired patients, mean mitral valve inflow pressure gradient improved from 13.9 +/- 2.7 mm Hg to 5.5 +/- 1.6 mm Hg (p < 0.0001). There were no late deaths at a mean follow-up of 46 +/- 31 months (range, 6.3 to 98.5). One patient required a second repair, and no patient has required replacement. At the last follow-up, mean mitral valve inflow pressure gradient was 7.5 +/- 4.1 mm Hg, and moderate or more mitral insufficiency was detected in 2 patients.

CONCLUSIONS

Mitral valve repair for congenital mitral valve stenosis can be performed in this challenging population of patients with good early survival and freedom from transplantation. Conditional follow-up for successfully repaired patients demonstrates preserved mitral valve function without need for replacement.

摘要

背景

二尖瓣修复是儿童先天性二尖瓣狭窄的首选方法。然而,在该人群中,修复仍然具有挑战性。

方法

2001 年至 2009 年,对 20 例连续先天性二尖瓣狭窄患者尝试了二尖瓣修复。手术时的中位年龄和体重分别为 1.4±1.9 岁和 7.4±4.1kg。14 例患者(70%)存在多水平左侧心脏梗阻。5 例患者存在中度或更严重的二尖瓣关闭不全。

结果

狭窄的主要病因在 5 例患者中为瓣叶,4 例为瓣上二尖瓣环,9 例为单一或主要乳头肌,2 例为吊床二尖瓣。20 例患者中,无院内死亡或移植的生存率为 85%(17/20)。2 例患者在出院前需要更换。在 15 例成功修复的患者中,平均二尖瓣流入压梯度从 13.9±2.7mmHg 改善至 5.5±1.6mmHg(p<0.0001)。平均随访 46±31 个月(范围 6.3 至 98.5)后无晚期死亡。1 例患者需要再次修复,无患者需要更换。最后一次随访时,平均二尖瓣流入压梯度为 7.5±4.1mmHg,2 例患者检测到中度或更严重的二尖瓣关闭不全。

结论

对于先天性二尖瓣狭窄的患者,在具有良好早期生存率和免于移植的情况下,可以对这一具有挑战性的患者群体进行二尖瓣修复。成功修复患者的条件性随访显示,二尖瓣功能得到保留,无需更换。

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