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a Department of Congenital Heart Disease, Albert-Ludwigs University of Freiburg, Freiburg, Germany
b Department of Cardiovascular Surgery, Albert-Ludwigs University of Freiburg, Freiburg, Germany
Accepted for publication August 6, 2007.
* Address correspondence to Dr Dittrich, Department of Pediatric Cardiology, University of Erlangen, Loschgestrasse 15, Erlangen, D-91054, Germany (Email: sven.dittrich{at}kinder.imed.uni-erlangen.de).
| Abstract |
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| Introduction |
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First corrective surgery on TOF was performed in this patient at the age of 15 months using a polytetrafluoroethylene patch to reconstruct an 8-mm right ventricular outflow tract (RVOT) to the diameter of 14 mm. Primary surgical outcome was good with no residual RVOT obstruction, no residual shunts, and an uneventful clinical course. On regular echocardiography follow-ups a continuous enlargement of the RVOT and the right ventricle was noticed. At the age of 5 years, right heart catheterization showed high-graded pulmonary regurgitation. Right ventricular pressure was 27/0 to 3 mm Hg, and diameter of the pulmonary valve annulus was 25 mm. Three years later at the age of 8 years (35 kg), an echocardiography showed further enlargement of the pulmonary valve annulus to 28 mm (Fig 1) and further enlargement of the right ventricle and tricuspid valve annulus with the development of tricuspid valve regurgitation on echocardiography, thus giving us indication for pulmonary valve replacement. To spare reopening of the median thoracotomy, the new technique was applied as follows: after exposure of the main pulmonary artery through the third intercostals space a pursestring suture was put on the upper side of the pulmonary artery bifurcation. After full heparinization (300 IE/kg/kg), the femoral artery and vein was cannulated and connected to the cardiopulmonary bypass. Off pump, the pulmonary artery was incised within the pursestring suture, and the introducer system with the stented valve was placed under transesophageal guidance into the RVOT (Figs 2, 3).
During a brief episode of rapid ventricular pacing, plus additional unloading of the right ventricle using the cardiopulmonary bypass, the valve was implanted. Thereafter, the introducer system was withdrawn and the pursestring suture was tightened. To avoid migration of the valve, the metal stent was anchored with three additional Prolene sutures (Ethicon Inc, Somerville, NJ) to the free wall of the pulmonary artery. Postoperative echocardiography demonstrated perfect valve function with no residual regurgitation (Fig 4). The patient recovered uneventfully and he was discharged on day 4 after surgery.
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We believe this is the first report of a transpulmonal implantation of a 29-mm stented tissue valve (Shelhigh injectable porcine pulmonic valve; Shelhigh Inc, Fumedica Medizintechnik, Herne, Germany) through a transverse mini-thoracotomy in the third intercostals space in an 8-year-old boy (35 kg) after transannular repair of TOF. Our new technique allows the implantation of large stented tissue valves through a small mini-thoracotomy. Migration of the valve can be avoided after fixing the stent of the valve to the pulmonary artery wall with additional sutures, which might be important in patients with enlarged flexible RVOTs. The transpulmonary approach avoids ventriculotomy and myocardial damage. Although the procedure can theoretically be done without the use of cardiopulmonary bypass we recommend preparing the femoral vessels for cannulation to implant the stented valve safely during ventricular unloading and to be able to control unexpected events such as bleeding from the pulmonary artery or repositioning of the device.
In conclusion, hybrid implantation of large pulmonary valves can be safely performed without a full sternotomy. The available introducer system (stiff and straight) was developed for transventricular valve application and has to be modified for routine valve implantation through a mini-thoracotomy in a wide spectrum of different RVOT anatomies.
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