ATRESIA PULMONAR CIV PDF

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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Morphometric characteristics of the pulmonary arteries and major aortopulmonary collateral arteries surgical procedures and treatment stages in relation to the age and the body surface area in Group B.

Medline, Lilacs and SciELO databases were searched from to using specific descrip-tors as “22q11”, “DiGeorge syndrome”, “velocardiofacial syndrome”, “congenital heart defects” and “cardiovascular malformations”. Morphometric characteristics of the pulmonary arteries, surgical procedures and stages of treatment in relation to the age and the body surface area in Group A.

In subgroup A2 there was a greater number of patients who required two procedures than in subgroup A1. Br Heart J ; 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 pulmlnar between the ventricles and the central pulmonary arteries CPA.

Chromosome abnormalities in congenital heart disease. The fate of children with microdeletion 22q Cardiac defects and results of cardiac surgery in 22q Kapil D, Bagga A. Similarly, there was no statistical agresia between group Atrsia and C2 in relation to the procedures performed.

6to. Congreso Virtual de Cardiología

We reviewed a retrospective case series of patients with this complex lesion. Deletion 22q11 and isolated congenital heart disease.

In conclusion, pklmonar morphological knowledge of this severe congenital heart disease is more important than morphometric measurements which can be obtained, as diverse factors should be considered for guidance in the surgical treatment and evaluation of risk of mortality. Chromosome 22q11 deletions in patients with conotruncal heart defects.

Morphometric characteristics of the major aortopulmonary collateral arteries, surgical procedures and treatment stages in relation to the age and the body surface area in Cic C. The only patients who underwent DPT were from subgroup B1.

Rev Assoc Med Bras ; Congenital cardiac defects with 22q11 deletion. Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies.

22q deletion syndrome and congenital heart defects

Phenotype of adults with the 22q11 deletion syndrome: Hoffman JI, Kaplan S. J Thorac Cardiovasc Surg ; In this study, a greater mortality rate was registered in group C than in group B, different to the result in our study.

The system was calibrated based on the diameter of the distal portion of the catheter.

A population study of chromosome 22q11 deletions in infancy. Analysis of Group A The cardiac cineangiographic studies of all the patients of this group were submitted to morphometric analysis as can be seen in Table 1.

Am J Cardiol ; In addition, the majority of the patients present a microdeletion identified mainly by molecular cytogenetic techniques as fluorescent in situ hybridization, which are rarely available in Brazil. In a puljonar heart this presents with an orifice in the interventricular septum [1]. The majority of the patients with DT were submitted to two procedures.

Atresia pulmonar

A1 with 5 patients The other achieved PT, independently of their indices, showing that the morphologic characteristics are more important than the morphometric aspects in this subgroup. Staged repair of pulmonary atresia with ventricular septal defect and major aortopulmonary collateral arteries: The other lobes were irrigated by major aortopulmonary collateral arteries.

The lack of confluence of the CPA was not a relevant factor for DT and survival, however it should be noted div this only included two patients and both of whom presented with mean PAI Thus, the A1 subgroup was schematically represented by the patients who presented with normal-sized or hypoplastic confluent CPA without stenosis. 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 right-to-left ventricle pressure ratio after complete repair.

Subjects with atresa syndrome very often present abnormalities of mul-tiple pul,onar, that could result in difficulties and complica-tions pupmonar their clinical and surgical course. Arch Mal Coeur ; Genetic syndromes and congenital heart defects: Chromosome 22 microdeletion by F.

Results Of the total of 63 patients, 15 Congenital heart disease and genetic syndromes: Heart malformations are the most fre-quent congenital defects at birth and represent an important Public Health problem.