Hypertrophy Left Ventricular
Mostrando 1-12 de 392 artigos, teses e dissertações.
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1. Common Arterial Trunk with Interrupted Aortic Arch
Abstract Clinical data: Patient diagnosed with common arterial trunk, submitted to pulmonary artery banding in another center and lost to clinical follow-up. Referred to our center at four years old, extremely cyanotic. Chest radiography: Cardiomegaly; attenuated peripheral vascular markings. Electrocardiography: Right ventricular hypertrophy. Echocardiograp
Brazilian Journal of Cardiovascular Surgery. Publicado em: 2022
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2. Importance of epicardial adipose tissue as a predictor of heart failure with preserved ejection fraction
SUMMARY OBJECTIVE: Epicardial adipose tissue is a special form of visceral fat surrounding the heart. It is associated with cardiac and metabolic diseases. Epicardial adipose tissue is associated with risk factors for heart failure with preserved ejection fraction, such as obesity, metabolic syndrome, hypertension, and diabetes. In this study, we examined t
Revista da Associação Médica Brasileira. Publicado em: 2022
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3. Iatrogenic Complications During the Diagnostic Work-Up of an Inflammatory Cardiomyopathy
Abstract A 72-year-old woman was admitted for acute heart failure. The echocardiography revealed moderate depression of the left ventricular ejection fraction. Coronary disease was excluded by coronarography. Cardiac magnetic resonance showed predominantly left ventricular septal hypertrophy and severe depression of the left ventricular systolic function. Th
Int. J. Cardiovasc. Sci.. Publicado em: 2020-12
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4. Coarctation of The Aorta: A Case-Series from a Tertiary Care Hospital
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 2020-02
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5. Coarctation of the Aorta: Its Importance for Pediatricians and Cardiologists
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 2020-02
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6. Fabry disease: genetics, pathology, and treatment
SUMMARY Fabry disease (FD) is a recessive monogenic inheritance disease linked to chromosome X, secondary to mutations in the GLA gene. Its prevalence is estimated between 1:8,454 and 1:117,000 among males and is probably underdiagnosed. Mutations in the GLA gene lead to the progressive accumulation of globotriaosylceramide (Gb3). Gb3 accumulates in lysosome
Rev. Assoc. Med. Bras.. Publicado em: 13/01/2020
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7. Deposit Diseases as Differential Diagnosis of Left Ventricular Hypertrophy in Patients with Heart Failure and Preserved Systolic Function
Arq. Bras. Cardiol.. Publicado em: 02/12/2019
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8. Correlação entre a deflexão intrinsecoide, classificação clínica e parâmetros ecocardiográficos em cães com degeneração mixomatosa valvar mitral
RESUMO A degeneração mixomatosa valvar mitral (DMVM) costuma ser diagnosticada pelo ecocardiograma, porém o eletrocardiograma (ECG) pode sugerir alterações específicas e auxiliar no diagnóstico e no tratamento. A deflexão intrinsecóide (DI) é uma medida simples do ECG, que representa o início da despolarização ventricular e pode indicar a presen
Arq. Bras. Med. Vet. Zootec.. Publicado em: 28/10/2019
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9. Antecedentes de insuficiência cardíaca se associam a tratamento com menor volume de fluidos em pacientes sépticos
RESUMO Objetivo: Identificar os fatores de base que afetam a ressuscitação com fluidos em pacientes sépticos. Métodos: Estudo de caso-controle com 181 pacientes consecutivos admitidos a uma unidade de terapia intensiva clínica entre 2012 e 2016 com diagnóstico de sepse. Analisaram-se os dados demográficos, clínicos, radiológicos e laboratoriais.
Rev. bras. ter. intensiva. Publicado em: 14/10/2019
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10. Left ventricular assessment in patients with mucopolysaccharidosis using conventional echocardiography and myocardial deformation by two-dimensional speckle-tracking method,
Resumo Objetivo: A mucopolissacaridose é uma doença genética rara, caracterizada por depósito intralisossômico de glicosaminoglicanos. O comprometimento cardiovascular é frequente. Sinais e sintomas cardíacos são subestimados pelo envolvimento da doença em outros órgãos. A terapia de reposição enzimática pode ser usada em mucopolissacaridose I
J. Pediatr. (Rio J.). Publicado em: 12/09/2019
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11. Coarctation of The Aorta: A Case-Series from a Tertiary Care Hospital
Abstract Background: Coarctation of the aorta is a congenital segmental narrowing of the aortic arch with severe hemodynamic repercussions and increased cardiovascular mortality. Early surgical correction and life-time echocardiographic follow-up must be performed to improve prognosis. However, this goal has been challenged by high rates of underdiagnosis,
Int. J. Cardiovasc. Sci.. Publicado em: 08/08/2019
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12. Rare Association Between Atrioventricular Septal Defect and Partial Anomalous Pulmonary Venous Connection
Abstract Clinical data: Infant, 7 months, female, referred to our department at one month of age, suspecting of congenital heart disease for further investigation. Chest radiography: Demonstrates cardiomegaly and prominent pulmonary vascular markings. Electrocardiography: Shows right ventricular hypertrophy and left anterior fascicular block. Echocardiog
Braz. J. Cardiovasc. Surg.. Publicado em: 15/07/2019