![]() Sete doentes (87,5%) tinham regurgitação tricúspide grave e 5 (62,5%) tinham outra cardiopatia congénita associada. A média do índice cardiotorácico foi de 0,72. Cinco estavam em classe funcional III ou IV da NYHA. As idades variaram entre 4 a 168 meses, a média foi de 69 ± 59 meses. Oito doentes (0,6%) tinham anomalia de Ebstein, destes 6 (75%) eram do género feminino. Resultadosįoram analisados 1362 ecocardiogramas sequenciais. Os ecocardiogramas foram realizados pelos Cardiologistas Pediátricos numa máquina Vivid 7 G.E. O diagnóstico foi feito com base no exame clínico e dados da ecocardiografia transtorácica e Doppler. Foram analisados todos os doentes com diagnóstico de cardiopatia congénita. ![]() MétodosĮstudo transversal retrospetivo no único centro com tratamento integrado em cardiopatias congénitas em recém nascidos, crianças e adolescentes (<18 anos de idade) em Angola, num período de 37 meses. Descrever a frequência, o perfil clínico e os resultados pós operatórios imediatos desta anomalia em crianças e adolescentes. Cone reconstruction was viable in the majority of patients, with good early and short-term results.Ī anomalia de Ebstein é uma cardiopatia congénita complexa e rara da válvula tricúspide. The frequency of Ebstein's anomaly was similar to that in other centers. The patient who underwent cone reconstruction and a Glenn procedure was in functional class I. Three patients had mild and two had moderate tricuspid regurgitation. Mean cardiothoracic index decreased to 0.64. At the end of the study, of the five patients in whom cone reconstruction was performed, four (80%) were in functional class I. The mean follow-up time was 1.22☐.6 years, and mortality during follow-up was 12.5% (n=1). All patients were operated: two had complications and one (12.5%) died in the early post-operative period. Seven patients (87.5%) had severe tricuspid regurgitation and five (62.5%) had another associated congenital heart defect. Five patients were in NYHA functional class III or IV. Of the 1362 patients studied, eight (0.6%) had Ebstein's anomaly six patients (75%) were female. We analyzed all patients diagnosed with congenital heart defects. MethodsĪ retrospective cross-sectional study was conducted over a period of 37 months. 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. Ebstein's anomaly is a rare complex congenital heart defect of the tricuspid valve.
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