Abstract

easier. The aorta was crossclamped and blood cardioplegic solution was administered antegradely. The optimal positioning of the HeartMate vented electric device was back-tofront, with the inflow directed toward the diaphragmatic wall of the right ventricle and the outflow toward the apex region. Two incisions were made in the diaphragm corresponding to the inflow and outflow tracts. To avoid damage to the liver, from the front of the pump, we made a “pillow” from polytetrafluoroethylene (Preclude pericardial membrane*) stuffed with Dacron felt. When the device was in place, the inflow was on the right side and the outflow on the left side (Fig 2). An expected pulmonary hypertension was prevented with inhaled aerosolized epoprostenol (prostacyclin).4 The early postoperative course in the intensive care unit was uneventful, and after 2 weeks the patient was transferred to the ward. Five weeks after the operation the patient was discharged from the hospital to his home, located 1500 km from our hospital, to await a donor heart. Comment. The need for assist devices in patients with complex congenital heart conditions, as after atrial correction for transposition of the great arteries, could be a surgical technical challenge. Because the right ventricle is the systemic ventricle in transposition, several points must be considered. To place the device on the right side in the abdomen Implantation of mechanical assist devices has saved the lives of patients awaiting heart transplantation.1 The HeartMate left ventricular assist device (Thermo Cardiosystems, Inc, Woburn, Mass) is made to connect the inflow cannula to the apex of the left ventricle.2 We describe a successful case in which the device was placed back-to-front with the inflow cannula inserted into the diaphragmatic wall of the right ventricle and the outflow graft through the left side of the diaphragm and in the left pleura to the ascending aorta (Fig 1). Medical history. A 15-year-old boy who was born with transposition of the great arteries underwent several balloon septostomies at birth because of desaturation. Despite this treatment, the desaturation was persistent. He therefore underwent an operation on an emergency basis at 3 months of age with an atrial switch as described by Mustard (pericardial baffle). At 4 years of age he required a reoperation because of residual atrial shunt and stenosis of the superior vena cava. Ten days after this operation a VVI pacemaker system was implanted because of atrioventricular dissociation. He then had an active life for almost 9 years, after which he gradually noted progressive fatigue and dyspnea. He had a cough, nausea, and cyanosis. Cardiac assessment revealed severe biventricular failure, gross atrioventricular valve regurgitation, and pulmonary hypertension (although reversible), and he was listed for heart transplantation. Despite “optimal” inotropic support, his condition continued to deteriorate with signs of multiorgan failure. Because no donor was available, we decided to implant a HeartMate left ventricular assist system, even though we expected major technical difficulties since the right ventricle, where the inflow cannula had to be placed, was the systemic ventricle. Surgical procedure. A median sternotomy was performed, and the heart, which was heavily adherent, was carefully dissected. Because the patient was thin, we decided to place the pump intraperitoneally.3 The aorta was cannulated. The systemic atrium was cannulated, and a left-sided bypass was instituted. This made the subsequent cannulation of the cavae

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