Follow-up by questionnaire?
Early Hum Dev
; 41(2): 87-95, 1995 Apr 14.
Article
en En
| MEDLINE
| ID: mdl-7541336
Recently, proposals have been made to include larger numbers of infants and reduce the cost of obtaining follow-up information pertaining to modern perinatal management. These proposals have been made in response to requests from purchasers and providers of health care as well as the obstetricians and neonatologists actively engaged in delivery of the service. These initiatives are welcome, but care must be taken to provide objective, meaningful data. In addition to standardised recording including by questionnaire, standardised data collection designed to identify relevant impairments must be the primary objective; the nature and extent of disability at particular ages can then be assigned but it is misleading to regard disability as the principle outcome measure.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Cuidado Intensivo Neonatal
/
Discapacidades del Desarrollo
/
Encuestas y Cuestionarios
/
Evaluación de Resultado en la Atención de Salud
Tipo de estudio:
Observational_studies
/
Prognostic_studies
Límite:
Female
/
Humans
/
Male
/
Newborn
Idioma:
En
Revista:
Early Hum Dev
Año:
1995
Tipo del documento:
Article
Pais de publicación:
Irlanda