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Ann Thorac Surg 1998;66:253-254
© 1998 The Society of Thoracic Surgeons
a Department of Pediatrics, Hôpital des Enfants, University Hospital of Geneva, Geneva, Switzerland
b Department of Cardiovascular Surgery, Hôpital des Enfants, University Hospital of Geneva, Geneva, Switzerland
Accepted for publication January 31, 1998.
Address reprint requests to Dr Rimensberger, Critical Care, Department of Pediatrics, Hôpital des Enfants, University Hospital of Geneva, 6, Rue Willy-Donzé, CH-1211 Geneva 14, Switzerland
e-mail: (rimensberger-peter{at}hcuge.ch)
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A 4-month-old boy (weight, 5 kg) underwent the atrial switch procedure for correction of D-transposition of the great vessels. The early postoperative course was uneventful with normal hemodynamic measurements. However, on day 2 postoperatively hemodynamics became unstable with increasing central venous and left atrial pressure, lower mean arterial pressures, and decreasing diuresis. Chest radiography revealed bilateral pleural effusions, despite chest and pericardial drains in place. Echocardiography showed an important pericardial effusion, a mildly decreased systemic ventricular function, and a gradient of 5 mm Hg at the junction of the superior vena cava with the systemic atrium. Chest and pericardial drains were replaced surgically. Analysis of drainage fluid showed increased cellularity with a predominance of lymphocytic cells (>70%); Sudan III staining was positive. The diagnosis of a bilateral chylothorax and chylopericardium was confirmed.
Total parenteral nutrition was started. Drainage decreased over the first few days (minimum, 500 mL/24 h) but increased again to reach a maximum of 1,150 mL/24 h (230 mL · kg-1 · 24 h-1) on day 17 (Fig 1). Volume and electrolyte homeostasis was maintained and losses of proteins, coagulation factors, and immunoglobulins were replaced regularly. On day 17 echocardiography showed absence of superior vena cava or innominate vein thrombosis and absence of stenosis of superior vena cavasystemic atrium junction.
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