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Ann Thorac Surg 2000;70:277-278
© 2000 The Society of Thoracic Surgeons
a Department of Thoracic, Cardiac, and Vascular Surgery, Eberhard-Karls-University, Tübingen, Germany
Address reprint requests to Dr Albes, Division of Cardiac Surgery, University Hospital Jena, Bachstr 18, 07743 Jena, Germany
e-mail: johannes.albes{at}med.uni-jena.de
| Abstract |
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| Introduction |
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A 23-year-old male patient suffered from end-stage cardiomyopathy due to cardiac sarcoidosis. Right heart catheterization performed 1 week prior to transplantation revealed a pulmonary vascular resistance of 232 dynes · sec · cm-5. When an excellent matching male donor heart of the same size, blood type, and age was available, the patient underwent transplantation. The total ischemic time of the organ was 115 minutes. One thousand milligrams methylprednisolone were administered before release of the cross-clamp. During reperfusion, the transplanted heart gained initial sinus rhythm and appeared to be functionally unaltered while supported by cardiopulmonary bypass. However, in three consecutive weaning efforts from cardiopulmonary bypass, the right ventricle was unable to overcome a mean pulmonary pressure of 50 mm Hg. After the third attempt, the left ventricular function began to deteriorate as well with left atrial pressure rising from 8 mm Hg to 18 mm Hg. All pharmacological efforts to decrease the pulmonary vascular resistance with nitrates, prostacyclin, and nitric oxide, as well as all efforts to improve the inotropic support by means of catecholamines and phosphodiesterase-inhibitors failed. At that time, it was decided to implant a biventricular pulsatile assist device to save the life of the patient. A Berlin Heart (right chamber 60 cc; left chamber 80 cc) was implanted and adjusted to an output of 6.5 l/min. The chest was closed and the patient was transferred to the intensive care unit with intact pulmonary as well as renal function. Heparinization was adjusted to an activated clotting time of 150 seconds. Mediastinal reexploration was necessary 8 hours later because of bleeding from the pulmonary arterial cannulation site. Triple drug immunosuppression with antithymocyte globulin induction was initiated according to a standard protocol. Additionally, the patient was kept on a calculated antibiotic regimen throughout the period of ventricular assist device-support. The mean pulmonary artery pressure did not decrease substantially during the next few days, although nitric oxide and prostacyclin were continuously administered. Because of the fixed pulmonary vascular resistance, an acute retransplantation was not considered to be an option. Daily esophageal echocardiographies were performed showing a constant improvement of the biventricular function. The patient was therefore gradually weaned from the Berlin Heart over postoperative days 6 and 7. Pump output was eventually reduced from 6.5 to 1.5 l/min. Successful explantation of the assist device under extracorporeal circulation was performed at postoperative day 7, while the pulmonary vascular resistance was still substantially elevated (170 dynes · sec · cm-5). During the following course, the patient developed a septic problem with consecutive renal failure requiring hemofiltration. Severe periods of atrial and ventricular arrhythmias were effectively treated either pharmacologically or with electrical cardioversions. Two weeks postoperatively, renal function had recovered. Four weeks postoperatively, a pacemaker was implanted due to intermittent atrioventricular dissociation. Twelve weeks postoperatively, the patient was discharged in good condition with excellent cardiac and sufficient renal function. Echocardiography showed a marked right ventricular hypertrophy accompanied by a mild tricuspid insufficiency, but excellent right and left ventricular function. Five months postoperatively, the patient is in good condition and followed as an outpatient. His explanted heart showed cardiomyopathy as a sequela of generalized cardiac sarcoidosis.
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Cardiomyopathy due to sarcoidosis is rare. In the review of the literature, not much is known about the outcome of these patients and potential contraindications for transplantation. Indications for transplantation in these patients have been made only on a very individual basis. Since the therapy of sarcoidosis requires steroids, a cardiac transplantation and consecutive immunosuppression was thought to be a reasonable therapeutic strategy [9].
We conclude from this case that in situations with fixed and untractable pulmonary vascular resistance after cardiac transplantation, the implantation of a pulsatile BIVAD offers a safe time frame for complete recovery of the right ventricle and weaning from the supporting device. We believe that the additional support of the already impaired left ventricle by means of the BIVAD played an important role in the successful outcome of the patient.
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