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Ann Thorac Surg 2004;78:1883-1884
© 2004 The Society of Thoracic Surgeons
Department of Pediatric Cardiac Surgery, G. Pasquinucci Hospital, CREAS-IFC-CNR, Via Aurelia Sud, 54100, Massa, Italy
Cardiothoracic Department, St. James's Hospital, Dublin, Ireland
edvinprifti{at}hotmail.com
To the Editor:
We read with interest the report by McMurtry and co-workers [1] regarding surgical correction of anomalous origin of the right pulmonary artery (RPA) from the ascending aorta. When the RPA arises from the ascending aorta, direct implantation is difficult because of the distance between the anomalous RPA and the main pulmonary artery (MPA). Consequently, a synthetic graft, a homograft, or a pericardial patch must be used. Direct implantation of the anomalous RPA does not seem to be the best procedure for several reasons: tension at the anastomosis, stretching of the RPA, stricture at the anastomosis itself, and reduced growth at the anastomotic site [2]. To reduce these potential complications, McMurtry and colleagues suggested use of an aortic cuff and construction of two trapdoors at the MPA with connection to aortic flaps surrounding the RPA. Van Son and Hanley [3] first reported placement of an aortic cuff and creation of a small anterior pulmonary flap to reach the posterior aortic flap for relocation of the RPA using autologous tissue, a method similar to the technique of McMurtry and associates.
In our opinion, the modification suggested by McMurtry and coauthors might enlarge the anastomotic area but would not adequately increase tissue length compared with the technique of Van Son and Hanley. The technique reported by McMurtry and co-workers seems inadequate to provide enough tissue length to permit placement of the newly created RPA anterior to the ascending aorta. An end-to-end anastomosis of the ascending aorta will cause it to retract more posteriorly, and the resulting aortic compression could cause later obstruction of the newly created RPA placed posterior to the aorta [2]. Therefore, reconstruction of the RPA using the "single aortic flap technique" [4] (Fig 1) and the "double-flap technique" proposed by our team [5] (Fig 2) may be advantageous in allowing extra tissue length. This new communication between the MPA and RPA is autologous, viable tissue, which will grow in neonates. The double-flap technique we propose offers the possibility of less tension at the anastomotic site, placement of the newly created RPA anterior to the ascending aorta, and reduced risk of kinking or stenosis of either branch of the pulmonary artery.
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