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新生儿重度主动脉瓣狭窄的经皮球囊瓣膜成形术

Percutaneous balloon valvuloplasty in neonates with critical aortic stenosis.

作者信息

Kasten-Sportes C H, Piechaud J F, Sidi D, Kachaner J

机构信息

Département de Pédiatrie, Hôpital des Enfants-Malades, Paris, France.

出版信息

J Am Coll Cardiol. 1989 Apr;13(5):1101-5. doi: 10.1016/0735-1097(89)90268-4.

Abstract

Percutaneous balloon valvuloplasty was attempted in 10 newborn infants with critical aortic valve stenosis and severe congestive heart failure. Three had a very small left ventricle and aortic anulus. In one infant, the aortic valve could not be passed, and in another infant, a technical error resulted in severe valvular damage, aortic insufficiency and death. Among the eight patients who had effective dilation, the stenosis was relieved in seven as assessed by a significant decrease in transvalvular pressure gradient, improvement of left ventricular contraction and eventual inversion of the ductal shunting. The procedure failed in the only patient whose dilation was performed with an undersized balloon. Aortic insufficiency occurred in three infants and was severe (perforated cusp) in one, moderate in one whose valve was dilated with an excessively large balloon and mild and transient in one. None of the three infants with a very small left ventricle recovered (two died and one underwent cardiac transplantation). Among the seven infants with a left ventricle of acceptable size, three underwent subsequent aortic valvotomy; one of these died and two bad good results. The remaining four are doing well 16 +/- 5 months later (mean +/- SD) with mild to moderate residual aortic stenosis and normal left ventricular function. In conclusion, percutaneous balloon valvuloplasty is an acceptable alternative to surgery in neonates with critical aortic valve stenosis. Incidence of complications and good relief of the obstruction depend on a careful technique. Immediate results are similar to those of surgery. Late prognosis depends on the quality of the left heart structures.

摘要

对10例患有严重主动脉瓣狭窄和严重充血性心力衰竭的新生儿尝试进行经皮球囊瓣膜成形术。其中3例左心室和主动脉瓣环非常小。1例婴儿的主动脉瓣无法通过,另1例婴儿因技术失误导致严重瓣膜损伤、主动脉瓣关闭不全和死亡。在8例扩张有效的患者中,7例狭窄得到缓解,表现为跨瓣膜压力梯度显著降低、左心室收缩改善以及动脉导管分流最终逆转。仅1例使用过小气囊进行扩张的患者手术失败。3例婴儿出现主动脉瓣关闭不全,其中1例严重(瓣膜穿孔),1例因使用过大气囊扩张瓣膜导致中度关闭不全,1例轻度且为短暂性关闭不全。3例左心室非常小的婴儿均未康复(2例死亡,1例接受心脏移植)。在7例左心室大小可接受的婴儿中,3例随后接受了主动脉瓣膜切开术;其中1例死亡,2例效果良好。其余4例在16±5个月后(平均±标准差)情况良好,有轻度至中度残余主动脉瓣狭窄,左心室功能正常。总之,经皮球囊瓣膜成形术是患有严重主动脉瓣狭窄新生儿手术的可接受替代方法。并发症的发生率和梗阻的良好缓解取决于仔细的操作技术。即时结果与手术相似。远期预后取决于左心结构的质量。

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