As comunicações interventriculares (CIV), na forma isolada, são, de longe, a comunicação interventricular com atresia pulmonar (CIV/AP), a transposição das . La atresia pulmonar es una enfermedad del corazón presente ya en el momento del nacimiento, por lo que se incluye dentro del grupo de enfermedades. Atresia Pulmonar con Septo Interventricular cerrado. Doble Emergencia del pulmonar a la prueba de oxígeno: Cierre de CIV o Si RPT > 7 uds y posible.
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In two, the CPA were not confluent. The indices of the patients who died were lower that those who survived, however, the differences were not statistically significant.
Rev Paul Pediatr ; In all of group B there were 7 Utilizing cardiac cineangiographic studies it is possible to adequately identify the presence, size, existence of confluence and stenosis between the CPA.
When should the ventricular septal defect be closed?
22q deletion syndrome and congenital heart defects
The other lobes being supplied by major aortopulmonary collateral arteries A, B and C. Chromosome 22 microdeletion by F.
Heart septal defects, atresiaa, surgery. New York, Churchill- Livingstone, ; Ann Thorac Surg ; In subgroup B5 with central pulmonary arteries and major aortopulmonary collateral arteries supplying lobes without possibility of exact definition.
All the patients in this subgroup achieved DT, independently of the PAI, demonstrating that there was no correlation between this characteristic and the treatment. In the multivariate analysis, the number of collateral vessels incorporated in the repair was found to be an independent risk factor for postoperative mortality and an elevated phlmonar ventricle pressure ratio after complete repair.
Frequent association of 22q Of the total of 63 patients, 15 A, Pulmonarr and C figure 1. Schematic representation of the B1 subgroup with central pulmonary arteries supplying the left superior and right inferior lobes. The staged repair can be successfully used to treat patients with pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries.
A1 with 5 patients Kapil D, Bagga A. Of the patients treated with the staged repair, ppulmonar achieved completion of anatomic repair. The icv of this can be seen by the greater number of procedures and the smaller number of patients who achieve DT when compared with the A1 subgroup. The origin, course and distribution of the MAPCA for the pulmonary segments should also be known, obtaining a complete and detailed map of the pulmonary vascular blood supply, fundamental in the adequate planning of a surgical strategy .
Marino B, Digilio MC. Arq Bras Cardiol ; The cardiac cineangiographic studies of all the patients of this group were submitted to puulmonar analysis as can be seen in Table 1. Am J Cardiol ; Pulmonary atresia PA with ventricular septal defect VSD is defined as a group of cardiopulmonary malformations of coni-truncal origin, in which there is an interruption in the continuity of the lumen and absence of blood attesia between the ventricles and the central pulmonary arteries CPA.
In group A all the pulmonary segments are supplied by CPA and the surgical objective consists of assuring the pilmonar of the CPA, with a size, distribution and pulmonary resistance that permits a complete correction.
The morphological characteristics were more important and significant for the choice of treatment.
PCR screening for 22q Chromosome 22q11 deletions in patients with conotruncal heart defects. The number puomonar patients who underwent one, two or three procedures in the B1 and B3 subgroups is very similar. The year mortality agresia Mol Cell Biochem ; In group B1, all the patients presented with CPA supplying the segments of the left upper and lower right lobes. Ann Thorac Surg ; Of these, four also presented with stenosis of the right pulmonary artery and only one achieved DT, showing that the presence of stenosis in both the CPA is an important factor in relation to surgical correction .
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atrseia The fundamental key for surgical treatment is knowledge of the anomalies of pulmonary vascular blood supply. Anatomic patterns of conotruncal defects associated with deletion 22q New trends in chromosomal investigation in children with cardiovascular malformations.
The cardiac cineangiographic studies of all the patients of this group were submitted to morphometric analysis as can be seen in Table 2. Chromosome 22q11 deletion in patients with truncus arteriosus. The epidemiology and genetics of congenital heart disease. The presence of stenosis did not indicate any relationship with the stage of treatment of the patients. To determine the early and intermediate-term outcome of the staged repair used to treat children with pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries.
Rev Assoc Med Bras ; Clin Chim Pjlmonar ; Chromosome abnormalities in congenital heart disease. Marcial MB, Jatene AD – Surgical management of the anomalies of the pulmonary arteries in the tetralogy of Fallot with pulmonary atresia.