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法洛四联症和肺动脉闭锁/室间隔缺损。

Tetralogy of Fallot and pulmonary atresia/ventricular septal defect.

作者信息

Warnes C A

机构信息

Department of Medicine, Mayo Medical School, Rochester, Minnesota.

出版信息

Cardiol Clin. 1993 Nov;11(4):643-50.

PMID:8252564
Abstract

Surgical repair of tetralogy of Fallot is associated with excellent results. Long-term complications include arrhythmias, sudden death, and right ventricular aneurysm formation. Reoperation is necessary in approximately 5% of patients for residual ventricular septal defect, pulmonary regurgitation, or pulmonary stenosis. Pulmonary atresia/ventricular septal defect is a more complex situation, and the anatomy needs careful delineation by cardiac catheterization prior to any surgical intervention. Palliation with a shunt or first-stage repair may be effective, or radical repair may be considered in those with adequate pulmonary distribution.

摘要

法洛四联症的外科修复效果良好。长期并发症包括心律失常、猝死和右心室动脉瘤形成。约5%的患者因残余室间隔缺损、肺动脉反流或肺动脉狭窄需要再次手术。肺动脉闭锁/室间隔缺损情况更为复杂,在进行任何外科干预之前,需要通过心导管检查仔细描绘解剖结构。分流姑息术或一期修复可能有效,对于肺血分布充足的患者可考虑根治性修复。

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