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J Thorac Cardiovasc Surg 2007;134:543-544
© 2007 The American Association for Thoracic Surgery
Brief Communication |
Department of Thoracic and Cardiovascular Surgery, Hannover Medical School, Hannover, Germany.
Received for publication January 12, 2007; accepted for publication January 23, 2007. * Address for reprints: Klaus Kallenbach, MD, University Hospital Heidelberg, Department of Cardiac Surgery, INF 110, D-69120 Heidelberg, Germany. (Email: klaus.kallenbach{at}med.uni-heidelberg.de).
For combined heart–lung transplantation, median sternotomy represents the standard approach, allowing exposure of the ascending aorta, both caval veins, and the distal trachea.1
However, aortopulmonary collaterals at the dorsal aspect of pulmonary vessels cannot be reached. Here we report of an innovative approach combined with atypical cannulation for cardiopulmonary bypass (CPB) to control severe aortopulmonary collaterals in a patient requiring combined heart–lung transplantation after multiple congenital heart operations.
A 25-year-old female patient presented with congestive heart failure of New York Heart Association class IV, vertigo, and central cyanosis. She was born with atresia of the pulmonary artery, a high ventricle septal defect, and multiple aortopulmonary collaterals, and she was operated on several times for re-establishment of pulmonary circulation: placement of a right-sited modified Blalock–Taussig shunt and unifocal attachment of a bronchial collateral vessel, resection of the infundibulum, and connection of the right ventricle to the pulmonary artery combined with closure of a ventricular septal defect and placement of a Blalock–Taussig shunt. Postoperative arterial pulmonary hypertension required reopening of the ventricular septal defect and banding of the homograft. However, arterial pulmonary hypertension persisted and finally led to Eisenmengers reaction combined with persistent aortopulmonary collaterals perfusing both the left and right pulmonary arteries (Figure 1). Because of rapid clinical deterioration but absence of alternate therapeutic options, the young patient was listed for high-urgency combined heart–lung transplantation.
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Postoperatively, 2 rethoracotomies were required because of bleeding. Otherwise, the postoperative course was uneventful. Today, the patient is doing well and runs a business on an island. The incisions healed without complications but with excessive scar tissue, and the thorax is stabile (Figure 2).
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Median sternotomy represents the standard approach for combined heart–lung transplantation, allowing excellent access to the upper and anterior mediastinum.1
However, a clamshell incision allows more extensive access to lung hili and dorsal mediastinum.2,3
Marta and colleagues4
reported an inverse T incision, combining a clamshell incision with a partial proximal median sternotomy for access to anterior, supra-aortic, and lateral mediastinal structures. However, the remaining caudal sternum makes access to the posterior and caudal aspects of the heart difficult. To allow mobilization and luxation of the severely adhered heart, we added a partial distal median sternotomy to the clamshell incision.
The combination of both incisions has not been reported previously. It allows excellent exposure to all relevant structures that must be dissected for heart–lung transplantation as a redo case but leaves the upper sternum intact. Possible injury of mediastinal structures during resternotomy can be avoided, and postoperative stability of the thorax with intact upper mediastinum will quicken recovery.
In anticipation of aortopulmonary collaterals, we chose the clamshell incision initially. With use of double cannulation for exclusion of the descending aorta from perfusion and establishment of hypothermia, we safely controlled the collaterals. This cannulation technique has not been described yet for controlling severe aortopulmonary collaterals during heart–lung transplantation but was the pivotal strategy to conduct the operation successfully. With increasing numbers of adults requiring heart–lung transplantation after correction of congenital heart disease but eventually development of Eisenmengers reaction,5
our approach might help to reduce the operative risk.
References
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K. Januszewska, E. Malec, G. Juchem, I. Kaczmarek, R. Sodian, P. Uberfuhr, and B. Reichart Heart-lung transplantation in patients with pulmonary atresia and ventricular septal defect J. Thorac. Cardiovasc. Surg., September 1, 2009; 138(3): 738 - 743. [Abstract] [Full Text] [PDF] |
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