Abstract
We report long-term outcome after one-stage, surgical repair, in a two months-old girl with persistent truncus arteriosus type I, II. The operation was carried out with the remodeling of the right ventricle, using a swine bicuspid pulmonary prosthesis. Twenty-six years later, the patient is in excellent clinical condition, CF I (NYHA), with normal peripheral oxygen saturation. Recent invasive and not invasive imaging show: absence of intracardiac shunt and growing of the right ventricle outlet tract and discrete double lesion of the pulmonary valve. The pulmonary flow directed uniformly for both lungs. In selected cases, the long-term prognosis of patients with persistent truncus arteriosus, undergoing early surgical repair, avoiding the use of valved conduit, makes for an excellent evolution, without new interventions. Endovascular procedures, now well standardized, for the implantation of a pulmonary valve stent, through a catheter, will allow an effective approach, in the presence of late obstructions, in patients who have undergone right ventricular remodeling, without the use of valved conduits.
Highlights
Persistent truncus arteriosus represents less than 3% of all congenital heart defects.Rapid evolution of pulmonary hypertension and congestive heart failure, is the main reason for indication, for surgical correction, in the neonatal or lactating phase
[1] This model of prostheses, will require its early replacement, in growing patients, to avoid the mismatch and mineralization process, that occurs in practically all pediatric patients The remodeling of the right ventricular outflow tract, eliminating the use of valved conduits, was described by the author [2], using a monocuspid biological prosthesis
In persistent Truncus Arteriosus, pulmonary circulation is under the systemic pressure regime, due to the fact that pulmonary arteries originate from the ascending aorta and absent pulmonary valve
Summary
Persistent truncus arteriosus represents less than 3% of all congenital heart defects.Rapid evolution of pulmonary hypertension and congestive heart failure, is the main reason for indication, for surgical correction, in the neonatal or lactating phase. [1] This model of prostheses, will require its early replacement, in growing patients, to avoid the mismatch and mineralization process, that occurs in practically all pediatric patients The remodeling of the right ventricular outflow tract, eliminating the use of valved conduits, was described by the author [2], using a monocuspid biological prosthesis.
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