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儿童瓣环上二尖瓣置换术。

Supra-annular mitral valve replacement in children.

机构信息

Division of Cardiothoracic Surgery, Department of Surgery, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

出版信息

Ann Thorac Surg. 2011 Dec;92(6):2221-7; discussion 2227-9. doi: 10.1016/j.athoracsur.2011.06.023. Epub 2011 Oct 1.

Abstract

BACKGROUND

Despite improved mitral repair techniques, some children need mitral valve replacement (MVR). Due to small annulus size, supra-annular MVR is useful.

METHODS

From 2003 to 2010, 15 children had 23 supra-annular MVRs. At first supra-annular MVR, median age was 6.5 months (28 days to 47 months); median weight was 5.4 kg (3.3-11.8 kg). Twelve (80%) had prior operations, 8 (53%) had previous mitral repair. Eight had congenital mitral anomalies (4 with Shone's), 5 had atrioventricular septal defects, 1 had endocarditis, and 1 had a repaired anomalous left coronary artery. All primary MVRs used mechanical valves (≤ 17 mm in 9 patients).

RESULTS

There was one early death (93% survival) in an 11-month-old with congenital pulmonary vein stenosis. One intraoperative conversion from annular to supra-annular MVR developed heart block. Three pacemakers were implanted for supraventricular rhythm disturbances. Three children had valve thrombosis early postoperatively treated medically. On follow-up of 4.3 ± 2.8 years, 8 had reoperation including redo MVR in 6 for pannus formation or thrombus (1 had three redo MVRs). At redo, a larger valve was used in 5 and a bioprosthetic valve in 4 patients. There was one late death after third redo MVR with pulmonary vein stenosis relief (overall survival 87%).

CONCLUSIONS

Supra-annular MVR is useful for children with a small annulus. Operative survival is good with infrequent heart block. Complications are common, including redo MVR and need for left ventricular outflow tract obstruction relief. Pulmonary vein stenosis is a marker for poor outcome; all patients without pulmonary vein stenosis survive long term.

摘要

背景

尽管二尖瓣修复技术有所提高,但仍有一些儿童需要二尖瓣置换术(MVR)。由于瓣环较小,因此使用瓣上 MVR 很有用。

方法

从 2003 年到 2010 年,15 名儿童接受了 23 次瓣上 MVR。首次瓣上 MVR 时,中位年龄为 6.5 个月(28 天至 47 个月);体重中位数为 5.4 公斤(3.3-11.8 公斤)。12 例(80%)有先前的手术,8 例(53%)有先前的二尖瓣修复。8 例有先天性二尖瓣畸形(4 例有 Shone 畸形),5 例有房室间隔缺损,1 例有感染性心内膜炎,1 例有修复的左冠状动脉异常。所有原发性 MVR 均使用机械瓣膜(9 例患者的瓣膜直径≤17mm)。

结果

在一名患有先天性肺静脉狭窄的 11 个月大的婴儿中,早期死亡 1 例(存活率 93%)。1 例术中从环形转为瓣上 MVR 时发生了心脏传导阻滞。3 例因室上性心律紊乱而植入起搏器。3 例儿童术后早期发生瓣膜血栓形成,经药物治疗。随访 4.3±2.8 年后,8 例需要再次手术,其中 6 例因肉芽组织形成或血栓形成而再次进行二尖瓣置换术(1 例进行了 3 次二尖瓣置换术)。在再次手术中,5 例使用了更大的瓣膜,4 例使用了生物瓣。在第三次二尖瓣置换术缓解肺静脉狭窄后,1 例患者晚期死亡(总生存率为 87%)。

结论

瓣上 MVR 对瓣环较小的儿童很有用。手术存活率较高,心脏传导阻滞罕见。常见并发症包括再次二尖瓣置换术和需要解除左心室流出道梗阻。肺静脉狭窄是预后不良的标志物;所有无肺静脉狭窄的患者均长期存活。

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