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J Thorac Cardiovasc Surg 2005;130:1717-1718
© 2005 The American Association for Thoracic Surgery
Brief Communications |
a Departments of Cardiovascular Surgery
b Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University, Tokyo, Japan
c Divisions of Cardiovascular Surgery
d Neonatology, Matsudo Municipal Hospital, Chiba, Japan
Received for publication July 2, 2005; accepted for publication August 3, 2005. * Address for reprints: Takahiko Sakamoto, MD, Division of Cardiovascular Surgery, Kanagawa Children's Medical Center, 2-138-4, Mutsukawa,Minami-ku, Yokohama-city, Kanagawa 232-8555, Japan (Email: takasakamoto@yahoo.co.jp).
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Clinical Summary
The patient was noted to be cyanotic immediately after birth. Echocardiography revealed tetralogy of Fallot with an absent pulmonary valve. He showed severe respiratory dysfunction 1 month later and was intubated because of the appearance of apnea. Cardiac catheterization showed left ventricular end-diastolic volume of 88% of normal, left ventricular ejection fraction of 58%, right ventricular end-diastolic volume of 188% of normal, right ventricular ejection fraction of 53%, pulmonary/systemic flow ratio of 2.7, and pulmonary artery (PA) index of 1290 mm2/m2. Repeated inadequate ventilation required a careful examination, and bronchoscopy elucidated a narrowing of the trachea and a flat shape of the right bronchus with granulations. High positive end-expiratory pressure ventilation therapy for 2 weeks under deep sedation was scheduled to cure the granulations, and definitive surgical intervention was performed at the age of 3 months.
Through a median sternotomy, the trachea and right bronchus were dissected carefully. Ringed expanded polytetrafluoroethylene (ePTFE) grafts (
14 mm) were trimmed to a circumference of 12 mm. They
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