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孤立性单纯性主动脉瓣下狭窄的长期儿科转归。

Long-term pediatric outcome of isolated discrete subaortic stenosis.

机构信息

Montréal Children's Hospital, McGill University Health Centre, Montréal, Québec, Canada.

出版信息

Can J Cardiol. 2011 May-Jun;27(3):389.e19-24. doi: 10.1016/j.cjca.2010.12.051. Epub 2011 Apr 19.

Abstract

BACKGROUND

The management of pediatric discrete subaortic stenosis remains controversial.

OBJECTIVES

Document the natural history and surgical outcomes for discrete subaortic stenosis to adolescence.

METHODS

Retrospective review of clinical and echocardiographic findings in 74 patients diagnosed in childhood between 1985 and 1998.

RESULTS

Twenty-five patients were followed only medically for 9.4 ± 0.9 years to 15.9 ± 0.6 years of age. Their echocardiographic left ventricular outflow peak gradient did not progress, 19 ± 1.4 (SEM) vs 20 ± 2.3 mm Hg. The proportion with aortic insufficiency (AI) increased (4% to 52%). Forty-nine patients were operated for discrete subaortic stenosis at 7.8 ± 0.6 years. Their peak gradient at diagnosis was 36 ± 3 mm Hg with AI in 33%. Preoperatively their peak gradient progressed to 60 ± 5 mm Hg with AI in 82%. Assessment 6.2 ± 0.5 years postoperativly showed a peak gradient of 14 ± 2 mm Hg with AI in 88%. Ten patients required reoperation for recurrent discrete subaortic stenosis, 3 acquired complete heart block, and 1 developed endocarditis. There was no mortality. At diagnosis, surgical patients were younger, had greater peak gradients, and greater incidence of AI, than those followed only medically. The progression of discrete subaortic stenosis was positively associated with severity of obstruction and negatively associated with older age at diagnosis. The risk of having surgery over time was associated with greater preoperative obstruction and presence of AI.

CONCLUSIONS

Many pediatric patients with mild discrete subaortic stenosis exhibit little progression of obstruction and need not undergo immediate surgery. Others with more severe stenosis may progress precipitously and will benefit from early resection.

摘要

背景

小儿局限性主动脉瓣下狭窄的治疗仍存在争议。

目的

记录小儿局限性主动脉瓣下狭窄至青春期的自然病史和手术结果。

方法

回顾性分析 1985 年至 1998 年间诊断为局限性主动脉瓣下狭窄的 74 例患儿的临床和超声心动图资料。

结果

25 例患儿仅接受药物治疗,随访时间为 9.4 ± 0.9 年至 15.9 ± 0.6 岁。其左心室流出道峰值梯度无进展,分别为 19 ± 1.4(SEM)和 20 ± 2.3mmHg。主动脉瓣关闭不全(AI)的比例增加(4%至 52%)。49 例患儿因局限性主动脉瓣下狭窄于 7.8 ± 0.6 岁时接受手术治疗。其诊断时的峰值梯度为 36 ± 3mmHg,伴 AI 者占 33%。术前,其峰值梯度进展至 60 ± 5mmHg,伴 AI 者占 82%。术后 6.2 ± 0.5 年评估显示,峰值梯度为 14 ± 2mmHg,伴 AI 者占 88%。10 例患儿因复发性局限性主动脉瓣下狭窄需要再次手术,3 例患儿发生完全性心脏传导阻滞,1 例患儿发生心内膜炎。无死亡病例。诊断时,手术组患儿较仅接受药物治疗组患儿年龄更小,峰值梯度更高,且 AI 发生率更高。局限性主动脉瓣下狭窄的进展与梗阻严重程度呈正相关,与诊断时年龄呈负相关。随着时间的推移,行手术治疗的风险与术前梗阻程度和 AI 的存在有关。

结论

许多小儿局限性主动脉瓣下狭窄患者的梗阻程度进展较小,不需要立即手术。其他梗阻程度较重的患者可能会急剧进展,从早期切除中获益。

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