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[儿童先天性主动脉瓣狭窄的球囊瓣膜成形术]

[Balloon valvuloplasty for congenital aortic valve stenosis in children].

作者信息

Wu Lin, Qi Chunhua, He Lan, Liu Fang, Lu Ying, Huang Guoying

机构信息

Cardiovascular Center, Children's Hospital of Fudan University, Shanghai 201102, China.

出版信息

Zhonghua Er Ke Za Zhi. 2014 Sep;52(9):699-702.

Abstract

OBJECTIVE

To evaluate the efficacy and safety of percutaneous balloon aortic valvuloplasty (PBAV) for congenital aortic valve stenosis in children.

METHOD

This is a retrospective clinical study including 14 children treated with PBAV for congenital aortic valve stenosis from October 2006 to December 2012 in our institute. During clinical follow-up, aortic residual stenosis and restenosis, left ventricular function and the procedure-related complications, including the approach artery injury, and aortic regurgitation were particularly assessed.

RESULT

A total of 14 patients consisting of 12 boys and 2 girls underwent the procedure, with mean age (17.1 ± 10.5) months (range from 8 days to 6 years) and the mean body weight (8.9 ± 5.5) kg (range from 1.9 kg to 23.0 kg). The indication for PBAV was a Doppler-derived peak instaneous gradient of ≥ 75 mmHg(1 mmHg = 0.133 kPa) or a smaller gradient with signs of severe left ventricular dysfunction or left ventricular strain on the ECG. The mean ratio of balloon-annulus was 0.92 ± 0.09 (range from 0.75 to 1.09). The catheter-measured peak systolic valve gradient was successfully relieved in all the patients, decreasing from (69 ± 26) mmHg to (29 ± 13) mmHg immediately after balloon valvuloplasty (t = 7.628, P = 0.000). The Doppler-derived peak and mean gradient decreased from (95 ± 21) mmHg and (50 ± 7) mmHg to (49 ± 16) mmHg and (24 ± 11) mmHg, respectively (t = 7.630, 10.401; P = 0.000, 0.000) . The mean follow-up period was 1 day to 61 months. At follow-up, 2 patients (2/14, 14%) underwent the second balloon valvuloplasty for the significant restenosis, and both showed successful relief of restenosis, however 1 patient required surgical Ross procedure due to significant recurrent systolic pressure gradient and moderate aortic regurgitation 4 years after the second balloon valvuloplasty. Among the 3 young infants who presented with congestive heart failure before intervention, 1 died 1 day after the procedure, the other 2 patients had improved left ventricular systolic function significantly during post-procedural follow-up. Only 1 patient (1/14, 7%) developed moderate aortic regurgitation. There was no other procedure-related complication.

CONCLUSION

PBAV for congenital aortic valve stenosis is effective and safe in children. It is a very feasible palliative intervention for children with severe aortic valve stenosis to postpone the aortic valve surgery.

摘要

目的

评估经皮球囊主动脉瓣成形术(PBAV)治疗儿童先天性主动脉瓣狭窄的有效性和安全性。

方法

这是一项回顾性临床研究,纳入了2006年10月至2012年12月在我院接受PBAV治疗先天性主动脉瓣狭窄的14例儿童。在临床随访期间,特别评估了主动脉残余狭窄和再狭窄、左心室功能以及与手术相关的并发症,包括入路动脉损伤和主动脉瓣反流。

结果

共有14例患者接受了该手术,其中男12例,女2例,平均年龄(17.1±10.5)个月(范围为8天至6岁),平均体重(8.9±5.5)kg(范围为1.9 kg至23.0 kg)。PBAV的指征为经多普勒测量的瞬时峰值梯度≥75 mmHg(1 mmHg = 0.133 kPa),或梯度较小但伴有严重左心室功能障碍或心电图显示左心室劳损的体征。球囊-瓣环平均比例为0.92±0.09(范围为0.75至1.09)。所有患者导管测量的收缩期峰值瓣膜梯度均成功缓解,球囊瓣膜成形术后立即从(69±26)mmHg降至(29±13)mmHg(t = 7.628,P = 0.000)。经多普勒测量的峰值和平均梯度分别从(95±21)mmHg和(50±7)mmHg降至(49±16)mmHg和(24±11)mmHg(t = 7.630,10.401;P = 0.000,0.000)。平均随访期为1天至61个月。随访时,但2例患者(2/14,14%)因严重再狭窄接受了第二次球囊瓣膜成形术,二者再狭窄均成功缓解,然而,1例患者在第二次球囊瓣膜成形术后4年因显著反复出现的收缩压梯度和中度主动脉瓣反流而需要接受Ross手术。在3例干预前出现充血性心力衰竭的幼儿中,1例在术后1天死亡,另外2例患者在术后随访期间左心室收缩功能显著改善。仅1例患者(1/14,7%)出现中度主动脉瓣反流。未发生其他与手术相关的并发症。

结论

PBAV治疗儿童先天性主动脉瓣狭窄是有效且安全的。对于患有严重主动脉瓣狭窄的儿童,这是一种非常可行的姑息性干预措施,可推迟主动脉瓣手术。

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