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[先天性心脏缺陷既往修复术后青少年及成人的右心室流出道重建]

[Right ventricular outflow tract reconstruction in adolescents and adults after previous repair of congenital heart defects].

作者信息

Hartyánszky István, Székely László, Szudi László, Mihályi Sándor, Kádár Krisztina, Temesvári András, Bálint Hajnalka, Szatmári András, Tóth Attila

机构信息

Gottsegen György Országos Kardiológiai Intézet Budapest. 1096.

出版信息

Orv Hetil. 2012 Aug 5;153(31):1219-24. doi: 10.1556/OH.2012.29428.

Abstract

UNLABELLED

Due to successful surgical treatment of congenital heart defects in infants and children, the number of patients who reach the adolescent/adult age is continuously increasing.

AIMS

The authors sought to identify the short- and medium-term outcomes of reconstruction of right ventricular outflow tract in adolescents and adults who underwent surgical intervention for congenital heart defect in infancy or early childhood.

METHODS

Between 2001 and 2012, 48 patients (age: 15-39, mean 21 years) (30 tetralogy of Fallot, 11 pulmonary atresia + ventricular septal defect, 6 transposition of great arteries + ventricular septal defect + left ventricular outflow tract obstruction, and 1 truncus arteriosus) had repeat operation because of right ventricular dysfunction. All patients previously underwent right ventricular outflow tract procedures in early childhood.

RESULTS

In 31 patients, the small homograft, and in 9 patients the transannular-paths were replaced for "adult-size" homograft. Bioprosthetic pulmonary valve replacement was performed in pulmonary (6 patients) and homograft annuli (2 patients). In 14 patients, resection of the right ventricular outflow tract aneurism was also necessary to be performed. There was no early and mid-time (10 years) mortality. In 97.5% of patients with homograft-re-implantation, there was no need for repeat intervention for 5 years.

CONCLUSIONS

The right ventricular outflow tract restoration in adolescents and adults is an effective procedure. The reconstruction should be performed in early adolescent period to prevent right ventricular dysfunction. The authors prefer using bioprosthetic pulmonary valve replacement in patients with adult-size pulmonary or homograft annulus.

摘要

未标注

由于婴儿和儿童先天性心脏缺陷的手术治疗取得成功,活到青少年/成年期的患者数量持续增加。

目的

作者试图确定在婴儿期或幼儿期接受先天性心脏缺陷手术干预的青少年和成年人右心室流出道重建的短期和中期结果。

方法

2001年至2012年期间,48例患者(年龄15 - 39岁,平均21岁)(法洛四联症30例,肺动脉闭锁 + 室间隔缺损11例,大动脉转位 + 室间隔缺损 + 左心室流出道梗阻6例,永存动脉干1例)因右心室功能障碍接受再次手术。所有患者早年均接受过右心室流出道手术。

结果

31例患者使用小同种异体移植物,9例患者将跨环路径替换为“成人尺寸”同种异体移植物。6例患者进行了生物人工肺瓣膜置换术,2例患者在同种异体移植物瓣环进行了置换。14例患者还需要切除右心室流出道动脉瘤。无早期和中期(10年)死亡病例。97.5%接受同种异体移植物再植入的患者5年内无需再次干预。

结论

青少年和成年人右心室流出道修复是一种有效的手术。应在青少年早期进行重建以预防右心室功能障碍。作者倾向于在有成人尺寸肺动脉或同种异体移植物瓣环的患者中使用生物人工肺瓣膜置换术。

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