ANOMALIA DE EBSTEIN PRENATAL PDF

Fetal cardiology. Fetal Echocardiography Prenatal Diagnostic anomalía de Ebstein fetal cardiología fetal diagnóstico prenatal ecocardiografía fetal; Language of. A case of prenatal diagnosis of Ebstein’s anomaly in a Anomalia de Ebstein detectada in utero e síndrome de Down: diagnóstico pré-natal. PDF | Ebstein’s anomaly is an uncommon congenital heart defect, with a Anomalia de Ebstein Com Valva Tricúspide Imperfurada.

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Ventricular septal defect in children and adolescents in A new reconstructive operation for Ebstein’s anomaly of the tricuspid valve. Se continuar a navegar, consideramos que aceita o seu uso.

However, the technique could not be applied in two patients for the reasons described above. Female gender was predominant, with a female: During the study period, patients under the age of 19 years with a diagnosis of CHD were analyzed, eight 0.

Mean hospital stay was Circulation, prenaatl, pp. In a study of 44 consecutive patients with Ebstein anomaly, Digilio et al. Transthoracic echocardiography is the most important diagnostic test for EA, to determine TV morphology and physiology and to assess the cardiac chambers and the presence of other CHD.

Anomalía de Ebstein en niños | HCA Healthcare

We analysed echocardiographic parameters and its correlation with the perinatal development of 16 cases diagnosed with Ebstein’s anomaly. The third patient showed the greatest improvement Figure 3. Various techniques for tricuspid valve reconstruction have been developed in the last 35 years, with different results. We analyzed all patients diagnosed with congenital heart defects.

The low in-hospital mortality and long-term clinical improvement reported by da Silva et al. Results During the study period, patients under the age of 19 years with a diagnosis of CHD were analyzed, eight 0. The severity of this defect includes a spectrum ranging from severe disturbance in fetal and neonatal life to virtually asymptomatic survival to adult life. In one of these cases an extremely rare association was found ostium primum ASD, pulmonary atresia and patent ductus arteriosus [PDA].

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Secondary repair of Ebstein’s anomaly with atrioventricular septal defect using the cone technique. Three patients had mild and two had moderate tricuspid regurgitation. Data on X-ray, echocardiography, indications for surgery, type of surgical techniques and complications are presented in Table 2.

Clinical Synopsis Toggle Dropdown. Users should refer to the original published version of the material for the full abstract.

Anomalía de Ebstein en niños

Ebsfein A, Riemenschneider G. The cone reconstruction of the tricuspid valve in Ebstein’s anomaly. Demographic data, clinical presentations, and NYHA functional class of the study population are shown in Table 1.

Cavopulmonary shunt is reserved for patients with severe RV dysfunction. Arch Anat Physiol ; Prog Pediatr Cardiol, 2pp. Infective endocarditis in an HIV-infected intravenous drug Distribution of demographic data, year of diagnosis, clinical presentation and NYHA functional class. The mean follow-up was 1. Ginecologia y Obstetricia de Mexico.

Br Heart J ; Introduction and Objective Ebstein’s anomaly is a rare complex congenital heart defect of the tricuspid valve. Access to health care services are still a serious problem in our continent, from the prenatal period to old age, which is why we have a small sample without neonates with severe forms of EA and older patients with good functional status.

Ventricular septal defect in children and adolescents in Angola: Foram analisados ecocardiogramas sequenciais. Data on X-ray, echocardiography, indications for surgery, type of surgical techniques and complications are presented in Table Cavopulmonary shunt was reserved for patients less than six months old and for those with significant RV dysfunction.

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Diagnóstico y pronóstico fetales de la anomalía de Ebstein.

Familial Ebstein anomaly, left ventricular hypertrabeculation, prneatal ventricular septal defect associated with a MYH7 mutation. Evolution of functional class in the five patients undergoing cone reconstruction.

In 2 unrelated patients with Ebstein anomaly and other malformations, de Lonlay-Debeney et al. The indications for surgery were: Syndromes and congenital heart defects.

Evolution of cardiothoracic index in the five patients undergoing cone reconstruction. We are determined to keep this website freely accessible.

No patients with a genetic syndrome or WPW syndrome were found. Pedigree analysis indicated that CTVM segregated as an autosomal dominant trait with reduced penetrance. The 2 additional kindreds showed a conserved disease haplotype, indicating a founder effect in apparently unrelated Labrador retriever kindreds. We aimed to describe the frequency, clinical profile, and early and short-term post-operative results in patients under the age of 18 years operated for this anomaly in a tertiary center in Angola.

The patient who underwent cone reconstruction and a Glenn procedure was in functional class I. CC ]. J Am Coll Cardiol ; Of the patients studied, eight 0. We aimed to describe the frequency, clinical profile, and early and short-term post-operative results in patients under the age of 18 years operated for this anomaly in a tertiary center in Angola.

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