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[Percutaneous implantation of a pulmonary valve in 3 children with surgically corrected cardiac anomalies].

作者信息

Bökenkamp R, Hazekamp M G, Schalij M J, Clur S A B, Ottenkamp J, Blom N A

机构信息

Centrum voor Aangeboren Hartafwijkingen Amsterdam-Leiden, p/a Leids Universitair Medisch Centrum, Postbus 9600, 2300 RC Leiden.

出版信息

Ned Tijdschr Geneeskd. 2007 Nov 17;151(46):2580-5.

Abstract

An 11-year-old girl, a 15-year-old boy and a 12-year-old girl all underwent percutaneous implantation of a Melody pulmonary valve prosthesis to replace a stenotic and insufficient homograft in the pulmonary artery. Preoperatively, 2 of the children suffered from fatigue and dyspnoea on exertion The homografts had been implanted between the ages of 1-2, to establish surgical continuity between the right ventricle and the pulmonary artery. The anomalies were tetralogy of Fallot, pulmonary atresia with intact ventricular septum and pulmonary atresia with a ventricular septum defect. Percutaneous pulmonary valve replacement was successful in all 3 patients. After implantation, right ventricular pressure decreased to 30% of systemic pressure and regurgitation was not observed. All patients were discharged in a good condition on the day after the implantation. Percutaneous pulmonary valve replacement is a promising technique with good short-term results. In selected patients this percutaneous technique can substitute or postpone the surgical replacement ofa stenotic or insufficient homograft.

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