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婴幼儿主动脉瓣球囊成形术后升主动脉扩张。

Dilation of the ascending aorta after balloon valvuloplasty for aortic stenosis during infancy and childhood.

机构信息

Department of Cardiology, Children's Hospital Boston, Boston, Massachusetts, USA.

出版信息

Am J Cardiol. 2012 Sep 1;110(5):702-8. doi: 10.1016/j.amjcard.2012.04.053. Epub 2012 May 19.

DOI:10.1016/j.amjcard.2012.04.053
PMID:22608951
Abstract

Dilation of the ascending aorta (AA) is common in patients with a bicuspid aortic valve. The natural history of the aortic root and AA and the risk factors for dilation have not been characterized in patients with congenital aortic stenosis (AS) treated with balloon valvuloplasty during childhood. The present study was performed to determine the prevalence of aortic dilation in patients with congenital AS before and up to 20 years after balloon valvuloplasty performed during childhood. In patients who underwent balloon valvuloplasty for AS at age ≤ 18 years from 1984 to 2005, the aortic diameter measurements before intervention and at 5-year intervals afterward were recorded and the Z scores calculated. Among 156 patients (median age 1.5 years at valvuloplasty), the AA Z scores were significantly larger than normal before intervention (median Z score 1.5) and at all follow-up points (all p <0.001). Using mixed modeling, with time as a categorical variable (before intervention, 5-year window, 10-year window, and so forth), the mean AA Z score was greater at all postvalvuloplasty points than before the intervention, with mean Z score increases of 1.20 at 5 years and 2.11 at 20 years (p <0.001). Moderate or greater aortic regurgitation early after valvuloplasty was associated with greater AA Z scores than mild or less aortic regurgitation, with a progressive difference over time. More significant residual AS after valvuloplasty was associated with lower AA Z scores over time. In conclusion, AA dilation is common in children with congenital AS and continues to progress over many years after balloon valvuloplasty.

摘要

升主动脉扩张(AA)在二叶式主动脉瓣患者中很常见。在儿童期接受球囊瓣膜成形术治疗的先天性主动脉瓣狭窄(AS)患者中,尚未对主动脉根部和 AA 的自然史以及扩张的危险因素进行描述。本研究旨在确定儿童期接受球囊瓣膜成形术治疗的先天性 AS 患者在接受治疗前和接受治疗后 20 年内主动脉扩张的发生率。在 1984 年至 2005 年间因 AS 接受球囊瓣膜成形术的患者中,记录了介入治疗前和之后每 5 年的主动脉直径测量值,并计算了 Z 评分。在 156 例患者(球囊瓣膜成形术时的中位年龄为 1.5 岁)中,AA 的 Z 评分在介入治疗前显著大于正常值(中位 Z 评分 1.5),且在所有随访点均如此(均 P <0.001)。使用混合模型,将时间作为分类变量(介入治疗前、5 年窗、10 年窗等),所有球囊瓣膜成形术后时间点的平均 AA Z 评分均大于介入治疗前,术后 5 年平均 Z 评分增加 1.20,20 年增加 2.11(P <0.001)。瓣膜成形术后早期出现中度或重度主动脉瓣反流与 AA Z 评分较高相关,且随时间推移差异逐渐增大。瓣膜成形术后残余 AS 更为严重与 AA Z 评分随时间降低相关。总之,先天性 AS 患儿的 AA 扩张很常见,且在球囊瓣膜成形术后多年仍持续进展。

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