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在儿童主动脉瓣狭窄的治疗中,开放性外科瓣膜切开术是否仍有一席之地?来自南安普敦的观点。

Is there still a place for open surgical valvotomy in the management of aortic stenosis in children? The view from Southampton.

作者信息

Alexiou C, Chen Q, Langley S M, Salmon A P, Keeton B R, Haw M P, Monro J L

机构信息

Department of Cardiac Surgery, The General Hospital, Tremona Road, Southhampton SO16 6YD, UK.

出版信息

Eur J Cardiothorac Surg. 2001 Aug;20(2):239-46. doi: 10.1016/s1010-7940(01)00813-2.

Abstract

OBJECTIVE

The most appropriate management of aortic stenosis (AS) in children remains controversial. The purpose of this study was to determine the outcome following open valvotomy for AS in children.

METHODS

Ninety-seven consecutive, unselected, children (mean age 3.2 +/- 3.6 years, 1 day--15 years) underwent an open valvotomy for critical (n=36) or severe (n=61) AS between 1979 and 2000 in Southampton. Twenty-six were neonates (1--31 days), 27 were infants (1--12 months) and 44 were older children (1--15 years). Mean follow-up was 10 +/- 5.4 years, 1 month--21.9 years.

RESULTS

Two neonates died early giving an overall operative mortality of 2.1% (7.7% for the neonates and 0% for infants and older children). The mean aortic gradient was reduced from 76 to 24.5 mmHg (P < 0.0001). Residual or recurrent AS occurred in 17 patients and severe aortic regurgitation in eight patients. Kaplan--Meier 10-year freedom from residual or recurrent AS was 83.1 +/- 4.7% and from severe aortic regurgitation was 95.3 +/- 2.7%. Twenty-five patients required an aortic re-operation or re-intervention, 18 of whom had an aortic valve replacement (AVR) (mean valve size 21.8 +/- 0.9 mm, range 21--25 mm). Ten-year freedom from any aortic re-operation or re-intervention was 78.4 +/- 5.2% and from AVR was 85.1 +/- 4.6%. There were ten late deaths. Overall 10-year survival, including hospital mortality, was 90.2 +/- 3.1% (69.7 +/- 9.7% for the neonates, 92 +/- 5.4% for the infants and 100% for older children, (P < 0.0001). Ten-year survival for children with isolated AS (n = 69) was 100% and for those with associated cardiovascular problems (n = 28) was 67.3 +/- 8.9% (P < 0.0001). All survivors are in New York Heart Association functional class I.

CONCLUSIONS

Open valvotomy remains the gold standard in the management of AS in neonates, infants and older children. It is associated with low operative mortality and provides lengthy freedom from recurrent AS and regurgitation. Re-operations are common but if AVR is required, implantation of an adult-sized prosthesis is usually possible. There is a late death-hazard for those with severe associated lesions, but the survival prospects for the patients with isolated AS are excellent.

摘要

目的

儿童主动脉瓣狭窄(AS)的最佳治疗方案仍存在争议。本研究旨在确定儿童AS行直视瓣膜切开术后的结局。

方法

1979年至2000年期间,在南安普敦,97例连续入选的儿童(平均年龄3.2±3.6岁,1天至15岁)因重度(n = 36)或严重(n = 61)AS接受了直视瓣膜切开术。其中26例为新生儿(1至31天),27例为婴儿(1至12个月),44例为大龄儿童(1至15岁)。平均随访时间为10±5.4年,1个月至21.9年。

结果

2例新生儿早期死亡,总体手术死亡率为2.1%(新生儿为7.7%,婴儿和大龄儿童为0%)。平均主动脉压差从76 mmHg降至24.5 mmHg(P < 0.0001)。17例患者出现残余或复发性AS,8例患者出现严重主动脉瓣反流。Kaplan-Meier法计算的10年无残余或复发性AS生存率为83.1±4.7%,无严重主动脉瓣反流生存率为95.3±2.7%。25例患者需要再次进行主动脉手术或干预,其中18例行主动脉瓣置换术(AVR)(平均瓣膜尺寸21.8±0.9 mm,范围21至25 mm)。10年无任何主动脉再次手术或干预生存率为78.4±5.2%,无AVR生存率为85.1±4.6%。有10例晚期死亡。总体10年生存率,包括住院死亡率,为90.2±3.1%(新生儿为69.7±9.7%,婴儿为92±5.4%,大龄儿童为100%,P < 0.0001)。孤立性AS患儿(n = 69)的10年生存率为100%,合并心血管问题患儿(n = 28)的10年生存率为67.3±8.9%(P <

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