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J Thorac Cardiovasc Surg 2005;129:451-452
© 2005 The American Association for Thoracic Surgery
Brief Communications |
a Division of Cardiac Surgery, Congenital Cardiac and Transplantation Unit, American Cardiac Center, American Hospital, Montevideo, Uruguay
b Department of Cardiology, Congenital Cardiac and Transplantation Unit, American Cardiac Center, American Hospital, Montevideo, Uruguay
c Intensive Care Unit, Congenital Cardiac and Transplantation Unit, American Cardiac Center, American Hospital, Montevideo, Uruguay
Received for publication June 7, 2004; accepted for publication June 10, 2004. * Address for reprints: Dante Picarelli, MD, Unidad de Cardiopatías Congénitas y Trasplante, Centro Cardiológico Americano, Sanatorio AmericanoIsabelino Bosch 2469, Montevideo 11600 Uruguay (E-mail: picarelli54@hotmail.com).
| The first 20% of the full text of this article appears below. |
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Cases involving small infants undergoing the Kawashima operation for left atrial isomerism, single ventricle, and azygos continuation of the inferior vena cava are rare and challenging because of the risk associated with this particular circulation, which is similar to a total cavopulmonary shunt, except for the hepatic flow.1
Taking into account the recent encouraging report from Hannan and associates,2 we decided to perform a modified fenestrated Kawashima operation, preserving a limited antegrade flow, in a 5
-month-old infant with severe cyanosis caused by progressive pulmonary stenosis.
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After 5 months, cyanosis progressively increased (oxygen
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