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1.
Int J Cardiol ; 47(1): 5-11, 1994 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-7868285

RESUMO

Chagasic patients with advanced heart disease have fluid retention-dependent symptoms. Since fluid retention is mostly dependent on the renin-angiotensin-aldosterone system, chagasic patients with congestion related symptoms should have activation of the renin-angiotensin-aldosterone system. The purpose of this investigation was to determine the plasma renin activity baseline values of chagasic patients with and without congestive heart failure. Twenty-eight patients with positive serology for Chagas' disease were studied. Nineteen patients were asymptomatic (functional class I New York Heart Association) and nine were symptomatic (functional classes II-IV). Cardiac catheterization and ventricular cineangiography were performed on 20 patients. The symptomatic patients had significantly higher plasma renin activity levels (4.11 +/- 1.03 ng/ml/h) than the asymptomatic patients (1.08 +/- 0.11 ng/ml/h, P < 0.001) and the normal sedentary controls (1.65 +/- 0.22 ng/ml/h, P < 0.05, mean +/- S.E.). The plasma renin activity baseline values of the asymptomatic and symptomatic patients correlated directly with the baseline heart rate (r = 0.77, P < 0.0001). The symptomatic patients had larger ventricular volumes, moderately depressed ejection fractions and increased left ventricular end-diastolic pressures. The plasma renin activity baseline values also correlated directly with the left ventricular diastolic pressures (r = 0.70, P < 0.0006) and with the left ventricular diastolic (r = 0.66, P < 0.001) and systolic volumes (r = 0.67, P < 0.001). These results indicate that chagasic patients with fluid retention-dependent symptoms and hemodynamic evidence of left ventricular systolic dysfunction have activation of the renin-angiotensin-aldosterone system.


Assuntos
Doença de Chagas/sangue , Insuficiência Cardíaca/etiologia , Renina/sangue , Adulto , Análise de Variância , Cateterismo Cardíaco , Cardiomiopatia Chagásica/sangue , Cardiomiopatia Chagásica/fisiopatologia , Doença de Chagas/fisiopatologia , Cineangiografia , Eletrocardiografia , Feminino , Insuficiência Cardíaca/sangue , Hemodinâmica/fisiologia , Humanos , Masculino , Pessoa de Meia-Idade , Renina/biossíntese , Disfunção Ventricular Esquerda/sangue , Disfunção Ventricular Esquerda/etiologia
2.
Int J Cardiol ; 41(2): 141-5, 1993 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-8282437

RESUMO

We studied eight patients to determine whether changes occur in the QRS amplitude when these patients are submitted to hemodialysis. The following variables were assessed before and after each (N = 28) hemodialysis session: (1) plasma sodium and potassium concentrations, (2) QRS amplitude, (3) the heart rate and its variability, (4) ventricular volumes, ventricular mass, ejection fraction and circumferential fiber shortening, (5) arterial pressure and end systolic stress, and (6) body weight. QRS amplitude was computed as the algebraic sum of the positive and negative waves of each QRS complex of the electrocardiogram. QRS amplitude changes were compared to body weight, ventricular volumes, ventricular mass, ejection fraction, circumferential fiber shortening, plasma potassium and sodium concentrations, arterial pressure, end systolic stress, heart rate, and R-R variability. After the hemodialysis sessions we found a significant increase (P = 0.0006) in QRS amplitude and a significant decrease in body weight (P = 0.0001), end diastolic volume (P = 0.043), plasma potassium concentration (P = 0.000001), end systolic stress (P = 0.025) and systolic arterial pressure (P = 0.023). Hemodialysis did not produce significant changes in the other variables. The statistical analyses performed did not show any significant influence of any of the measured variables on the QRS amplitude change. The QRS amplitude increases after hemodialysis but the cause of this increase is still unclear.


Assuntos
Eletrocardiografia , Falência Renal Crônica/fisiopatologia , Diálise Renal , Arritmias Cardíacas/diagnóstico por imagem , Arritmias Cardíacas/fisiopatologia , Arritmias Cardíacas/terapia , Pressão Sanguínea/fisiologia , Peso Corporal/fisiologia , Volume Cardíaco/fisiologia , Ecocardiografia , Sistema de Condução Cardíaco/fisiopatologia , Frequência Cardíaca/fisiologia , Humanos , Falência Renal Crônica/diagnóstico por imagem , Falência Renal Crônica/terapia , Derrame Pericárdico/diagnóstico por imagem , Derrame Pericárdico/fisiopatologia , Derrame Pericárdico/terapia , Potássio/sangue , Sódio/sangue , Volume Sistólico/fisiologia , Sístole/fisiologia
3.
Med Hypotheses ; 40(1): 33-7, 1993 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-8455464

RESUMO

According to the neurogenic theory of Chagas' heart disease, the cardiac parasympathetic abnormalities of chagasic cardiac patients are due to a selective destruction of the cardiac parasympathetic neurons. Trypanosoma cruzi would selectively destroy the cardiac vagal neurons, during the acute stage of the disease. However, these cardiac parasympathetic abnormalities are found mainly in chagasic patients who are in very advanced stages of the disease. Furthermore, the extent of cardiac parasympathetic involvement correlates with the degree of left ventricular dilation. Cardiac parasympathetic abnormalities, and a reciprocal sympathetic hyperactivity are also present in non-chagasic cardiac patients. Modern medical treatment, with sympatholytic drugs, prevents ventricular dilatation and prolongs life in these non-chagasic cardiac patients. Consequently, if chagasic cardiac patients have ventricular dilatation-related parasympathetic abnormalities; it is of the utmost importance to ask: first, do they also have a progressive activation of their neurohumoral systems?; and second, would they benefit from sympatholytic drugs?.


Assuntos
Sistema Nervoso Autônomo/fisiopatologia , Cardiomiopatia Chagásica/fisiopatologia , Cardiomiopatia Chagásica/tratamento farmacológico , Cardiomiopatia Chagásica/etiologia , Cardiopatias/fisiopatologia , Humanos , Modelos Biológicos , Sistema Nervoso Parassimpático/fisiopatologia , Simpatolíticos/uso terapêutico
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