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3.
Rev. méd. Chile ; 130(9): 1051-1054, sept. 2002. tab
Artículo en Español | LILACS | ID: lil-323241

RESUMEN

In 1997, the Chilean Government and the International Bank for Development convened on a strategy to improve Chilean university education. It was based on quality improvement, effectiveness, relevancy and innovation on university education programs. A US$ 245 millions fund was afforded, for a five years competitive grants program, among certain traditional Universities and Technical Education Institutes. The authors reviewed the projects that won the contests during the first three years in the health area, to determine their impact, demands supported, difficulties and assets. These projects obtained 13.6 percent of the assigned funds (a total of US$ 16.5 millions). Funds were requested mostly to build spaces, obtain equipment, laboratories and computational support. Funds were also requested to carry out methodological changes and teaching improvements. The importance of teaching health sciences in locations outside the Metropolitan area of Santiago, the modification of undergraduate medical curriculum and the development of post graduate networks are emphasized


Asunto(s)
Humanos , Apoyo a la Formación Profesional/tendencias , Centros Educacionales de Áreas de Salud/economía , Educación Médica/economía
4.
Rev. méd. Chile ; 130(5): 585-589, mayo 2002. tab
Artículo en Español | LILACS, MINSALCHILE | ID: lil-317381

RESUMEN

Sustaining quality control of learning programs for health professions has become a central issue in university systems, under the pressure of an unexpected merging of new medical schools in Chile, during the last decade, and the massive arrival of other Latin American physicians. Accreditation of institutions and programs represents valid safeguards used in most countries where professional training processes take place. Due guarantee of its quality is required to assure proper health care to people. The authors provide specific arguments to support systematic evaluation and accreditation processes, as those introduced in our country to fulfill the requirements of a high level medical practice


Asunto(s)
Humanos , Acreditación/tendencias , Educación Médica/tendencias , Distribución de Médicos , Facultades de Medicina/tendencias
5.
Rev. méd. Chile ; 129(3): 317-23, mar. 2001. tab
Artículo en Español | LILACS | ID: lil-286869

RESUMEN

There is still great collective paucity in our society in appreciating the importance of scientific work for the devolopment of the nation. In this context, relevant clinical research has ben greatly discouraged. The Ministry of Education and the National Comission for Technical and Scientific research (CONICYT) have been committed, with no outstanding results however, to encourage these activities, specially sustaining individual projects originated in the tradicional universities. Precarious conditions persist as manifested by meager budgets for investigation. Public health policies and organization are scarcely endorsed in locally generated clinical or public health knowledge. Postgraduate training programs, specially doctorates, needed to increase the academic human resources with a consistent scientific potential, are very limited. Recent governmental initiatives, altogether with specific proposals waiting for implementation, would certainly contribute to optimize and promote the revival of our impoverished scenarios in clinical research


Asunto(s)
Humanos , Investigación/tendencias , Apoyo a la Investigación como Asunto/tendencias , Educación Médica/tendencias , Investigación/economía , Proyectos de Investigación/tendencias
10.
Rev. chil. pediatr ; 67(3): 112-5, jun. 1996. tab
Artículo en Español | LILACS | ID: lil-185110

RESUMEN

En un estudio colaborativo de 99 niños con síndrome nefrótico en un período de 30 meses, 8 (5 mujeres) eran menores de un año (mediana 7,5 meses) y constituyen el motivo de esta comunicación. Los niños cuyo síndrome nefrótico se expresa antes del cuarto mes de vida tienen mal pronóstico, pues morfológicamente sus lesiones se relacionan con esclerosis mesangial difusa o el tipo finlandés y fallecen precozmente de complicaciones infecciosas severas. Los pacientes menores de 1 año con glomeruloesclerosis focal y segmentaria o cambios mínimos se comportan como los de edades posteriores


Asunto(s)
Humanos , Masculino , Femenino , Recién Nacido , Lactante , Síndrome Nefrótico/diagnóstico , Lesión Renal Aguda/diagnóstico , Albúmina Sérica/análisis , Creatinina/sangre , Glomeruloesclerosis Focal y Segmentaria/diagnóstico , Hematuria/diagnóstico , Hipertensión/diagnóstico , Proteínas Sanguíneas/análisis
11.
Rev. méd. Chile ; 124(5): 567-72, mayo 1996. tab, graf
Artículo en Español | LILACS | ID: lil-174775

RESUMEN

Ninety six patients agred from 6 months to 16 years old were admitted to chilean hospitals with the diagnosis of primary nephrotic syndrome in a period of 30 months. These patients were randomly separated in 2 groups, group A received prednosone for 8 weeks and group B received the same drug during 12 weeks. All patients were evaluated at 6, 12 and 18 months after the end of treatment. The moment and number of relapses per patient, accumulated percentage of relapses, relapse rate per 100 patients, total number of relapses and complications were assessed. Frequent relapsers were subjected to a kidney biopsy, leaving in the protocol only those patients that had minimal changes. Patients resistent or dependant to steroid therapy were discarded. Thus we report the results of 56 treated poatients followed during 18 months. No differences in analyzed parameters were observed between the 2 treatment groups. It is concluded that these preliminary results do not support the prolongation of prednisone treatment in children with primary nephrotic syndrome


Asunto(s)
Humanos , Masculino , Femenino , Lactante , Preescolar , Adolescente , Prednisona/administración & dosificación , Síndrome Nefrótico/tratamiento farmacológico , Recurrencia , Estudios de Seguimiento , Esquema de Medicación
12.
Rev. chil. pediatr ; 64(4): 252-8, jul.-ago. 1993. tab, ilus
Artículo en Español | LILACS | ID: lil-125411

RESUMEN

El raquitismo hipofosfatémico familiar (raquitismo hipofosfémico familiar) se caracteriza por alteración del transporte renal de fosfatos, hipofosfatemia difícil de tratar, raquitismo, normocalcemia y talla baja final. La hipofosfatemia se transmite por herencia dominante ligada al cromosoma X. El calcitriol 1,25 (OH)2 D3 plasmático es inapropiadamente bajo para la magnitud de la hipofosfatemia, por lo que se postula un defecto en su síntesis. El tratamiento incluye dosis orales altas de fosfato y calcitriol, a pesar de lo cual persiste la hipofosfatemia y tallas finales resultan bajas en la mayoría de los pacientes


Asunto(s)
Humanos , Niño , Calcitriol/administración & dosificación , Hipofosfatemia Familiar/tratamiento farmacológico , Fosfatos/administración & dosificación , Raquitismo/tratamiento farmacológico , Trastornos del Crecimiento/etiología , Raquitismo/metabolismo
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