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1.
J & G rev. epidemiol. comunitária ; 3(2): 5-15, abr.-jun. 1992. tab
Artigo em Espanhol | LILACS | ID: lil-312032

RESUMO

El presente trabajo se de sarrolló en dos fases: en la primera los pdiatras respondieron a preguntas de un cuestionario, para poner en evidencia los tratamientos personales practicados en caso de Otitis Media Aguda (OMA) así como otitis media concaracter recurrente (ver cuadro 1). La segunda fase del trabajo consiste en evaluar críticamente cada uno de los estudios clínicos publicados sobre prevención farmacológica de OMAR y discutirlos en encuentros formales, de caracter colegial


Assuntos
Humanos , Otite Média , Farmacologia , Itália
2.
Pediatr Med Chir ; 8(1): 9-13, 1986.
Artigo em Italiano | MEDLINE | ID: mdl-3725619

RESUMO

The aim of the paper is to assess the value of a series of clinical and laboratory indices used in determining the degree of iron overload in homozygous beta-thalassaemic patients. 155 thalassaemic patients of different age in chelation with subcutaneous infusions of desferrioxamine for a period of 2-7 years have been studied. Calculation of the total iron accumulated and the iron load per kg of body weight in patients undergoing chelation requires an exact knowledge of their compliance and faecal and urinary iron elimination, and is clearly open to many errors. Despite this, usefull information can be derived from its determination. We have found, for example, that serious organ damage tends to appear when iron accumulation exceeds 1 g/kg. In addition, the serum ferritin and the evaluation of the growth have been proved to be the most important and helpful indices for checking the effectiveness of the chelation therapy and forecasting the appearance of the serious complications as diabetes or hypothyroidism.


Assuntos
Ferro/sangue , Talassemia/sangue , Adolescente , Adulto , Peso Corporal , Criança , Pré-Escolar , Desferroxamina/uso terapêutico , Ferritinas/sangue , Crescimento , Humanos , Lactente , Talassemia/tratamento farmacológico
3.
Pediatr Med Chir ; 8(1): 27-31, 1986.
Artigo em Italiano | MEDLINE | ID: mdl-3725610

RESUMO

An account is given of the model employed for the provision of psychological care over the last 9 years at the Microcythemia Centre, Department of Paediatrics, University of Turin, by a team composed of paediatricians and child neuropsychiatrists. Reference is made to a series of 280 patients aged 0-25 years. The psychodynamic is adopted and provision is made for individual and group meetings with young and adolescent patients and their parents that are held as part of the Centre's ordinary activities. This procedure has made it possible to understand and face up to the psychological implications of thalassaemia and its treatment and has considerably improved both compliance and the quality of life. Stress is laid on the importance of a good rapport between patients and the Centre. This can be obtained through continuous collaboration between physicians and psychiatrists and or psychologists with a psychodynamic background.


Assuntos
Talassemia/psicologia , Adolescente , Adulto , Atitude Frente a Morte , Transfusão de Sangue , Criança , Pré-Escolar , Humanos , Lactente , Relações Interpessoais , Ferro/metabolismo , Relações Pais-Filho , Prognóstico , Qualidade de Vida , Autoimagem , Papel do Doente , Talassemia/metabolismo , Talassemia/terapia
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