A frequência da Anomalia de Ebstein encontrada foi semelhante a de outros Centros. A técnica de Cone foi viável na maior parte dos pacientes. A mortalidade. Ebstein’s anomaly is a malformation of the tricuspid valve. In this defect, there is a downward displacement of the tricuspid valve (located between the upper and. Antecedentes: en la actualidad, con la ecocardiografía fetal, es pos ble confirmar el diagnóstico in utero de la anomalía de Ebstein y determinar, con certeza.
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Prognosis Asymptomatic patients, and patients with mild ebstdin of the disease, have a normal life expectancy.
What Is Ebstein’s Anomaly? Surgical decision making in neonatal Ebstein’s anomaly an algorithmic approach based on 48 consecutive neonates. A descriptive statistical analysis was performed absolute and relative frequencies, mean and standard deviation.
Several techniques have been described to avoid this complication.
Orphanet: Anomalia de Ebstein
Cardiol Young, 16pp. Ventricular septal defect in children and adolescents in Angola: The complexity of the anatomical and functional changes in EA and the possibility of association ebstekn other CHDs mean that the surgical approach should be individualized. Rev Port Cardiol, 33pp. Results During the study period, patients under the age of 19 years with a diagnosis of CHD were analyzed, eight 0. Receba a nossa Newsletter.
All patients amomalia operated: For all other comments, please send your remarks via contact us. Finally, it is noteworthy that one patient in our series had an extremely rare association ostium primum ASD, pulmonary atresia and PDA. Teratology, 50pp. The documents contained in this web site are presented for information purposes only. The patient who underwent cone reconstruction and a Glenn procedure was in functional class I. Data on X-ray, echocardiography, indications for surgery, type of surgical techniques and complications are presented in Table This result is similar to that reported in a study conducted in Sudan, in which the authors found that half of the patients were symptomatic.
Emmanuilides A, Riemenschneider G.
The low in-hospital mortality and long-term clinical improvement reported by da Silva et al. The material is in no way intended esbtein replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Cardiothoracic index, echocardiographic findings, surgical indications, surgery performed and early post-operative evaluation. Diagnostic methods Diagnosis is based on cross-sectional or 3D echocardiography, which reveals the rotational displacement of the leaflets, the extent of abnormal tethering of the antero-superior leaflet, the extent of thinning of the atrialized inlet component of the right ventricle, and the degree of regurgitation or stenosis of the abnormal valve.
To improve our services and products, we use ebsteni own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. This result contrasts with those of Anderson 9 and Da Silva, 15 who report a slight predominance of anomaliq, and with other studies that described no predominance of either gender.
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Uber einen sehr seltenen fall von insufficienz der valvula tricuspidalis, bedingt durch eine angeborene hochgradige missbikdung derselben. J Am Coll Cardiol ; Medical treatment relies on inotropic agents in case of cardiac failure and antiarrhythmic drugs in case of anomapia.
Valdano Manuel a. The authors have no conflicts of interest to declare. New York Heart Association.
This, as can Ebstein’s malformation if associated with pulmonary atresia, can lead to gross thinning of the walls of the right ventricle which should not be confused with Uhl’s anomaly see this term. CTI decreased in all patients, by a mean of 0.
Artigo anterior Artigo seguinte. At discharge, in this group two patients had no TR and three had mild TR. Under a Creative Commons license. Ebstein’s Anomaly congenital heart defect ebsteins-anomaly.
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Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. In one of these cases an extremely aomalia association was found ostium primum ASD, pulmonary atresia and patent ductus arteriosus [PDA]. Continuing navigation will be considered as acceptance of this use. CR was performed in the majority of patients with excellent immediate and short-term results.
Foram analisados ecocardiogramas sequenciais.
Data on X-ray, echocardiography, indications for surgery, type of surgical techniques and complications are presented in Table 2. An international co-operative study of cases. Ebstein’s anomaly is a rare complex congenital heart defect of the tricuspid valve. Br Heart J ; A retrospective cross-sectional study was conducted over a period of 37 months.
Both sexes are equally affected.