Fontan procedure for tricuspid atresia.
نویسندگان
چکیده
A Fontan procedure has been performed on 29 patients for tricuspid valvular atresia. The age range was 8 months to 33 years (median 10 years), the pulmonary vascular resistance ranged from 1.8-6.1 units . m2 (mean 3.3 units . m2), and the mean pulmonary arterial pressure ranged from 13-45 mm Hg (mean 21 mm Hg). Twenty-nine previous operations had been performed in 23 patients. Fourteen other associated cardiopulmonary anomalies were present in 12 patients. There were four hospital deaths (13.8%), all in patients with complicating features. Among the last 22 consecutive patients who have undergone operation, one died (4.5%). Complete atrioventricular block necessitated pacemaker implantation in one patient. No late deaths occurred. Of the 19 patients followed 3 months or more from the time of operation, eight have no restriction of exercise capacity, nine have only mild restriction, and two have a poor result. The Fontan approach to tricuspid atresia has several theoretical advantages over previously used shunts or pulmonary artery banding, the operative mortality in patients who have suitable anatomy and hemodynamics is low, and the results have been good.
منابع مشابه
Tricuspid atresia with I-transposition.
Sir, In their recent article (1987;57:543-7) on tricuspid atresia with transposition of the great arteries Warnes and Somerville emphasised the inportance of subaortic stenosis in these patients, especially those with coarctation. They suggested that the Fontan procedure was the procedure of choice in these patients but remarked that in patients with subaortic stenosis the prognosis after Fonta...
متن کاملThe Fontan procedure for tricuspid atresia: early and late results of a 25-year experience with 216 patients.
OBJECTIVES We assessed the operative and late mortality and the present clinical status of 216 patients with tricuspid atresia who had a nonfenestrated Fontan procedure performed at the Mayo Clinic in the 25-year period 1973 to 1998. BACKGROUND The Fontan operation eliminates the systemic hypoxemia and ventricular volume overload characteristic of prior forms of palliation. However, it origin...
متن کاملTricuspid Atresia Presenting in Infancy
Background. The Fontan operation is the usual goal of therapy for children with tricuspid atresia. The influences of morphology and different management strategies on survival and subsequent suitability for this procedure are crucial but unstudied in an unselected population during the Fontan era. Methods and Results. The fates of 237 consecutive infants with tricuspid atresia were reviewed (19...
متن کاملRespiratory exacerbation in a young adult with cystic fibrosis and tricuspid atresia
Tricuspid atresia (TAt) is a complex congenital heart defect (CHD) characterized by the absence of the tricuspid valve and right ventricular hypoplasia requiring surgery in childhood, the Fontan procedure. We present a case of a 21-year-old male with TAt and cystic fibrosis (CF), who underwent a Fontan procedure in childhood, presenting to an adult CF clinic with severe deterioration in his res...
متن کاملTricuspid atresia. Clinical course in 62 cases (1967--1974).
Sixty-two patients with tricuspid atresia admitted for cardiac catheterisation between 1967 and 1974 have been classified according to the anatomical and radiological findings into those with normally related great arteries (type I: 39 cases) and those with transposition of the great arteries (type II: 23 cases). These types were further subdivided into group A (reduced lung vascularity),groupB...
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ورودعنوان ژورنال:
- Circulation
دوره 62 1 شماره
صفحات -
تاریخ انتشار 1980