Radiological and Surgical Anatomy in Tetralogy of Fallot and the Effect on Surgical Prognosis.
نویسندگان
چکیده
The tetralogy of Fallot constitutes the commonest variety of cyanotic congenital heart disease found in patients surviving infancy (Wood, 1956; Keith, Rowe, and Vlad, 1958). Following the pioneer work of Lillehei and his associates (1955), the complete surgical correction of this lesion has become a standard procedure in most centres. Although Malm et al. (1963) have reported 41 consecutive patients undergoing surgery with no immediate operative mortality, other series indicate that an appreciable hazard remains when attempting complete correction (Table I). Although the
منابع مشابه
Early post operative mortality of Total Correction of Tetralogy of Fallot
Introduction: Since 1954, after the first surgical repair of tetralogy of Fallot (TOF), several innovations have occurred in cardiac surgery, especially in children. One stage complete repair of TOF is currently possible even in infancy; however, complications such as hypoxemia, arrhythmia, cardiac dysfunction, sudden death, and valvular disorders may happen. In this study, we evaluated the res...
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Background: Tetralogy of Fallot is the most common cyanotic congenital heart disease. The systolic and diastolic function in both ventricles is altered even after successful corrective surgery for this defect with a transannular patch. Pulmonary regurgitation, a common complication after this treatment, is usually well tolerated in childhood. The aim of this study was to assess the combined dia...
متن کاملMain indications and long-term outcomes of reoperation after initial repair of tetralogy of Fallot
Background and Objective: The aim of this study was to analyze our indications, surgical procedures, and clinical outcomes of patients undergoing reoperation after surgical correction of tetralogy of Fallot (TOF). Methods: Thirty seven consecutive patients who underwent reoperation late after intra-cardiac repair of TOF within a period of 10 years were assessed. Results: The most co...
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Congenital aortocaval fistula in association with complex congenital heart disease has never been described before. We represent an adult with tetralogy of fallot and an undiagnosed subclavian artery to superior vena cava fistula in previous catheterisms. He underwent surgical correction, successfully. After 8 months post operation he was doing well with improved functional capacity and no ...
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عنوان ژورنال:
- British heart journal
دوره 27 شماره
صفحات -
تاریخ انتشار 1965