首页> 外文期刊>Journal of the American College of Cardiology >Surgical valvotomy and repair for neonatal and infant congenital aortic stenosis achieves better results than interventional catheterization
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Surgical valvotomy and repair for neonatal and infant congenital aortic stenosis achieves better results than interventional catheterization

机译:外科valvotomy和新生儿和婴儿先天性主动脉狭窄的修复比介入导尿管更好地实现了更好的结果

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Objectives This study sought to compare outcomes after surgical valvuloplasty and balloon dilation of the aortic valve in neonates and infants. Background Surgical techniques of aortic valve repair have improved and there is today controversy on the best approach to treat neonatal congenital aortic valve stenosis. Methods Retrospective review of data and follow-up of 123 consecutive neonates and infants (35 females, 88 males) undergoing intervention for congenital aortic stenosis. Results From 1977 to 2009, 123 consecutive neonates (<30 days) and infants (31 days to 1 year) underwent relief of congenital aortic stenosis. Median age at procedure was 27 days (6 to 76 days). Twenty-year survival was 80 ± 7%. Fifty-four patients required a re-intervention and freedom from re-intervention was 55 ± 6% at 10 years and 40 ± 6% at 20 years. By multivariate analysis, having the relief of stenosis by balloon valvuloplasty and undergoing initial treatment as a neonate were predictive of re-intervention. Freedom from re-intervention at 5 years was 27% after balloon valvuloplasty versus 65% after surgery. At latest follow-up, an additional 16 patients had moderate or severe stenosis and 8 had regurgitation. Freedom from re-intervention or stenosis was 39 ± 5% at 15 years. By multivariate analysis, balloon valvuloplasty (p < 0.001) and treatment as a neonate (p = 0.003) were again predictive of stenosis or re-intervention. Thirty-five patients ultimately needed a valve replacement. Significant predictor of the requirement of valve replacement was unicuspid aortic valve (p < 0.001). Freedom from valve replacement was 55 ± 7% at 20 years. Conclusions Surgical valvuloplasty remains the best approach to treat neonates and infants with congenital aortic stenosis. After surgery, a higher proportion of patients remain free of re-intervention than after interventional catheterization and the relief of their stenosis lasts longer.
机译:目的这项研究寻求在新生儿和婴儿的主动脉瓣膜外科瓣膜成形术和球囊扩张后进行比较。背景技术主动脉瓣修复的手术技术有所改善,目前争论了治疗新生儿先天性主动脉瓣狭窄的最佳方法。方法回顾性审查数据和随访123个连续的新生儿和婴儿(35名女性,88名男性)进行先天性主动脉狭窄的干预。结果1977年至2009年,123名连续新生儿(<30天)和婴儿(31天至1年)接受了先天性主动脉狭窄的缓解。手术中位年龄为27天(6至76天)。二十年生存率为80±7%。五十四名患者需要重新干预,从再生干预的自由为55±6%,10年,20年±6%。通过多变量分析,通过球囊瓣成形术缓解狭窄,并作为新生儿进行初始治疗是预测的重新干预。在手术后,在球囊胰腺成形术和65%后,从5年的重新干预的自由是27%。在最新的随访中,额外的16名患者具有中度或严重的狭窄,8名患者进行了反流性。 15年来,从重新干预或狭窄的自由为39±5%。通过多变量分析,球囊瓣膜成形术(P <0.001)和作为新生儿的治疗(P = 0.003)再次预测狭窄或再干预。三十五名患者最终需要阀门更换。瓣膜置换要求的重要预测因子是Unicuspid主动脉瓣膜(P <0.001)。 20年来瓣膜置换自由度为55±7%。结论外科valvuloplasty仍然是治疗新生儿和先天性主动脉狭窄的最佳方法。手术后,较高比例的患者仍然没有重新干预,而不是在介入导尿管下进行介入后,他们的狭窄的缓解持续更长时间。

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