Syed Shahabuddin ( Division of Congenital Cardiac Surgery, Department of Surgery, The Aga Khan University Hospital, Karachi. )
Saulat Fatimi ( Division of Congenital Cardiac Surgery, Department of Surgery, The Aga Khan University Hospital, Karachi. )
Mehnaz Atiq ( Division of Congenital Cardiac Surgery, Department of Surgery, The Aga Khan University Hospital, Karachi. )
Muneer Amanullah ( Division of Congenital Cardiac Surgery, Department of Surgery, The Aga Khan University Hospital, Karachi. )
January 2009, Volume 59, Issue 1
Case Reports
Abstract
A seven years old girl was admitted via emergency with severe cyanosis. She had tricuspid atresia, azygos continuation of IVC with single ventricle physiology. She had a complicated postoperative course with prolonged hospital stay after bilateral bidirectional Glen shunt (Kawashima operation). She successfully has completed Fontan after 5 years. The second case of a 7 year old girl had elective surgery for DORV (double outlet right ventricle), pulmonary atresia and azygos continuation of IVC and persistent left SVC. She had an uneventful postoperative course.
The Kawashima operation is an established surgical procedure to deal with bilateral SVCs. The procedure is safe; outcome is favourable and prepares the patient for total cavo-pulmonary shunt.
Introduction
The role of Bidirectional Glen (superior vena cava to pulmonary artery) shunt has been well established as an intermediate palliation in patients with single ventricular physiology.1 We have already established the safety of bidirectional Glen shunt in a single ventricle.2 The management of such patients is even more challenging for congenital cardiac surgeons in presence of bilateral SVC's. Two children underwent bilateral bidirectional cavo pulmonary shunt operation for tricuspid atresia and a variant of double outlet right ventricle. The first child underwent salvage bilateral bidirectional Glen shunt with expected stormy postoperative course. The second child had an elective uneventful surgery. These children had bilateral superior vena cavae, interrupted inferior vena cava with Azygos continuation of IVC. This modified bilateral bidirectional Glen shunt is also known as the Kawashima operation.3 We describe our surgical strategy in two cases with presence of left superior vena cava and azygos continuation of the IVC in patients with a single ventricular morphology.
Case-1
A seven year old girl was diagnosed to have Tricuspid Atresia with Ventricular Septal Defect (VSD), pulmonary stenosis, Azygos continuation of IVC, and a single ventricle physiology. She had a modified Blalock Taussig (BT) shunt, that is, subclavian artery to pulmonary artery in infancy. She presented with progressively increasing cyanosis and failure to thrive. She was advised surgical intervention abroad. On her way to the airport she became unwell and was brought to the emergency, room of Aga Khan Hospital with severe cyanosis. While she was being wheeled to the operating room for a BT shunt operation, she had a cardiopulmonary arrest necessitating cardiopulmonary resuscitation (CPR). While CPR was being performed, cardiopulmonary bypass (CPB) was established. This was done with aortic and right atrial venous cannulae after full systemic heparinization (300U/Kg). Instead of a BT shunt a bilateral Glen shunt (BDG) was thought to be more beneficial. In the presence of bilateral SVC's three venous cannulae were used. The right and left SVC's were divided at their junction with atria and anastomosed to right and left pulmonary artery respectively Fig-1a & 1b. She was weaned off cardiopulmonary support [(Fig1)], [(Fig2)] with heavy doses of inotropic support. She had re-exploration of the mediastinum for bleeding and was extubated on first post-operative day. She had a prolonged stay in the Intensive Care Unit (ICU) to optimize cardiac function, and was discharged on the 17th post-operative day. She did well at follow up and subsequently underwent completion of Fontan operation after 5 years.
Case-2
Another seven years old girl was diagnosed to have DORV, Pulmonary atresia and azygos continuation of IVC into a persistent left SVC. She had presented at birth with cyanosis and underwent construction of a modified BT shunt at four days of age. As she grew older her cyanosis worsened. She was evaluated regarding further surgical intervention and her anatomical lesions were found unsuitable for biventricular repair. It was planned to treat her in line of single ventricle. A decision was made to perform Bidirectional Glenn shunt to improve pulmonary blood flow and prepare her for future Fontan circulation. She underwent elective bilateral bidirectional Glen shunt on cardiopulmonary bypass. She came off CPB on small dose of inotropes. Her postoperative course was uneventful. She was extubated on first postoperative day and was discharged on 6th post-op day. She has been asymptomatic on follow up. She will be requiring completion of Fontan operation in the future.
Discussion
In the Indian Sub-continent, severe complex congenital cardiac problems are considered uncorrectable and hence several children are deprived of surgical correction or palliation. Our report of two cases is an effort to provide palliation to such children and make them participate in the society at a better functional level.
To conclude, in patients with this unusual anatomy, the Kawashima operation is safe and associated with good outcome. It also prepares the patient for future Fontan circulation by establishing a near total cavo-pulmonary shunt.
Acknowledgement
Footnotes
References
2. Khan G, Ali SS, Fatimi SH. Bidirectional cavopulmonary shunt for cyanotic heart diseases: surgical experience from a developing country. J Pak Med Assoc 2003 ; 53:506-9.
3. Kawashima Y, Kitamura S, Matsuda H, Shimazaki Y, Nakano S, Hirose H. Total cavopulmonary shunt operation in complex cardiac anomalies: A new operation. J Thorac Cardiovasc Surg 1984; 87: 74-81.
4. Annecchino FP, Fontan F, Chauve A, Quaegebeur J. Palliative reconstruction of the right ventricular outflow tract in tricuspid atresia: a report of 5 patients. Ann Thorac Surg 1980; 29:317-21
5. Bartram U, Wirbelauer J, Speer CP. Heterotaxy Syndrome - asplenia and polysplenia as indicators of visceral malposition and complex congenital heart disease. Biol Neonate 2005; 88:278-90.
6. McElhinney DB, Kreutzer J, Lang P, Mayer JE Jr, del Nido PJ, Lock JE. Incorporation of the hepatic veins into the cavopulmonary circulation in patients with heterotaxy and pulmonary arteriovenous malformations after a Kawashima procedure. Ann Thorac Surg 2005; 80: 1597 - 603.
Journal of the Pakistan Medical Association has agreed to receive and publish manuscripts in accordance with the principles of the following committees:




