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1.
Arch Inst Cardiol Mex ; 56(4): 333-8, 1986.
Artigo em Espanhol | MEDLINE | ID: mdl-2945528

RESUMO

Fifty-six consecutive patients with acute anterior infarction were studied by two-dimensional echocardiography to determine the incidence and complications of left-ventricular thrombosis. Mean follow-up period was 4.4 months. Left-ventricular thrombus was demonstrated in 14 patients (25%) between 25 and 54 days after infarction (group A), in 42 patients (group B) it was not demonstrated. Apical and septal dyskinesis, and Forrester's hemodynamic subset-III were significantly (P less than 0.02) associated with thrombus development. Ten patients of group A received heparin (6.6 days mean); the remaining four patients received aspirin and dipyridamole. Thrombi formation were not significantly prevented with both treatments (chi 2 = 0.635). During follow-up period, thrombus persisted in 6 patients of group A, all of them with apical and septal dyskinesis. Three patients had a cerebrovascular accident (5.3%), one of them of group A; no heparin anticoagulation was administered in two. We conclude that apical and septal dyskinesis during acute anterior infarction is generally associated with mural thrombi development. Due to the embolic risk therapeutic anticoagulation must be considered in these patients.


Assuntos
Anticoagulantes/uso terapêutico , Infarto do Miocárdio/complicações , Trombose/etiologia , Aspirina/uso terapêutico , Ecocardiografia , Ventrículos do Coração , Heparina/uso terapêutico , Humanos , Trombose/tratamento farmacológico , Trombose/prevenção & controle
3.
Rev Gastroenterol Mex ; 45(3): 125-30, 1980.
Artigo em Espanhol | MEDLINE | ID: mdl-7466139

RESUMO

Rotor's syndrome is a rare entity in our Country. We report here a case of this anomaly in a seventeen years old girl with jaundice from birth, normal biliary channels, elevated urinary coproporphyrins and retarded excretion of bromosulphalein with normal histology of the liver. The familiar study showed that the mother, but not the brothers, had a similar defect in excretion of bromosulphalein.


Assuntos
Hiperbilirrubinemia Hereditária/genética , Adolescente , Coproporfirinas/urina , Feminino , Humanos , Hiperbilirrubinemia Hereditária/metabolismo , Hiperbilirrubinemia Hereditária/patologia , Fígado/patologia , Linhagem
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