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J Thorac Cardiovasc Surg 1997;113:607-608
© 1997 Mosby, Inc.
BRIEF COMMUNICATIONS |
New Haven, Conn.
Received for publication August 2, 1996 accepted for publication Sept. 17, 1996. Address for reprints: Elchanan Bruckheimer, MB, BS, Section of Pediatric Cardiology, Yale University School of Medicine, 333 Cedar St., New Haven, CT 06520.
J Thorac Cardiovasc Surg 1997;113:607-8
The Glenn shunt, direct end-to-end anastomosis of the superior vena cava (SVC) to the right pulmonary artery (RPA), when first described in 1958,
1 provided a method of augmenting effective pulmonary blood flow in congenital heart disease. However, palliation by a Glenn shunt diminishes with time and often an additional shunt or definitive correction of the heart defect is required.
2-5 Glenn shunt takedown during a corrective procedure has been reported rarely and mainly in children.
3-5 We report herein successful takedown of a Glenn shunt in four adults, three during corrective procedures. In two patients reconstitution of pulmonary arterial continuity was done primarily for relief of severe unilateral left pulmonary hypertension.
Patients.
Four patients who had undergone Glenn shunt takedown were identified in the database of patients who had undergone operation for congenital heart disease. The data and indications for Glenn shunt takedown are summarized in
Table I. The Glenn shunt operation had been done for palliation of cyanosis at a mean age of 5 years. In patients 1 and 2 left pulmonary artery (LPA) hypertension developed as a result of a Blalock-Taussig shunt and a patent ductus arteriosus supplying the LPA, respectively. Glenn shunt takedown was done at a mean age of 29.5 years. All patients underwent cardiac catheterization before the operation.
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Results and follow-up.
All patients were alive at a mean follow-up of 7.7 years (range 3.7 to 16.3 years) and were free of cyanosis with a maintained or improved level of function. Two patients with LPA hypertension showed a marked decrease in pulmonary vascular resistance at follow-up cardiac catheterization from preoperative levels
(Table II). The PTFE grafts were patent with no pressure gradients at the anastomoses. Patient 3 underwent cardiac catheterization 15 years after operation for assessment of subaortic obstruction with normal pulmonary hemodynamic findings and no pressure gradients at the anastomoses. Patient 4 had patent PTFE grafts on repeated color Doppler echocardiographic studies.
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Cardiopulmonary bypass was effective with venous cannulation of the inferior vena cava and innominate vein and allowed unobstructed access to the right atrium. Because of extensive scarring, operation involved prolonged and difficult dissection, particularly of the SVC-RPA anastomosis, which led to inclusion of the SVC in the pulmonary arterial confluence in one case. In previous reports, restoration of pulmonary arterial and caval-atrial continuity was achieved with Dacron grafts or direct anastomoses.
3-5 Synthetic grafts were required in our adult patients to bridge the large distances caused by significant growth since the creation of the Glenn shunt. Prosthetic material in the venous system can predispose to thrombosis; however, this was not observed. All patients received anticoagulation therapy after operation.
Glenn shunt takedown has not been recommended during a corrective procedure, because it may add risk and complexity.
2 This has been our practice with uncomplicated Glenn shunt when the anteroposterior displacement of the pulmonary arteries was considerable or the right ventricle was of inadequate size. In selected adult patients, however, Glenn shunt takedown is feasible and obviates the long-term complications of the shunt, and the restoration of pulmonary arterial continuity can provide relief of unilateral LPA hypertension.
Footnotes
From the Sections of Pediatric Cardiologya and Pediatric Cardiothoracic Surgery,b Yale University School of Medicine and Children's Hospital at YaleNew Haven, New Haven, Conn. ![]()
References
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