Elige el tipo de letra:
 Arimo
 Merriweather
 Mukta Malar
 Open Sans Condensed
 Rokkitt
 Source Sans Pro
 Login


 Español 
 Français 
 English 
 Português 

[Valid RSS] RSS
bar

Base de datos - (CIANE)

Presentación de esta base de datos documental (Sitio web de CIANE)
Actualmente 3109 registros
Canal de YouTube (tutorial)

https://ciane.net/id=1060

Creado el : 23 Nov 2004
Alterado em : 02 Dec 2007

 Editar este registro
¡Sólo siga este enlace si tiene una contraseña de editor!


Compartir : Facebook logo   Tweeter logo   Especializado

Ficha bibliográfica (sin autores) :

Levels of evidence: universal newborn hearing screening (UNHS) and early hearing detection and intervention systems (EHDI) JOURNAL OF COMMUNICATION DISORDERS 37 (5): 451-465 SEP-OCT 2004

Autores :

Yoshinaga-Itano C

Año de publicación :

2004

URL(s) :

Résumé (français)  :

Abstract (English)  :

Levels of evidence differ according to the audience addressed. Implementation of universal newborn hearing screening requires responses to a complex myriad of diverse groups: the general public, families with children who are deaf or hard of hearing, the deaf and hard of healing communities, hospital administrators, physicians (pediatricians, general practitioners, ear nose and throat physicians, geneticists), managed care, Medicaid, insurance agencies, and politicians. The level of evidence required by medical/health agencies and task forces may differ from the levels of evidence available in education and intervention. Issues related to the low incidence of the disability, the lack of a normal distribution within the disability study, the obstacles to random assignment to treatment, and designs that include a control group with "no treatment" have implications legally and ethically for the professional providing services to families and children who are deaf or hard of hearing. This session will discuss issues related to "convenience samples," number of subjects included in research studies, and the population required to obtain a large enough sample of children with low-incidence disabilities. The level of evidence required to demonstrate sensitive periods of development, which are a critical element for justification of implementing a universal newborn hearing screening includes both behavioral and neurological information. Sensitive periods may have different duration for different aspects of development, such as social-emotional development, auditory and speech development, or language development. Further complicating the question of sensitive periods of development are the distinct possibility that different sensitive periods exist for development of age-level vocabulary, for establishing English phonology, or for mastering English syntax. Research outcomes provide evidence that age of identification of hearing loss is reduced, that age of intervention initiation is lowered, and that the outcomes of intervention are better because of the establishment of a screening program. Most professionals in communication disorders believe that screening is not the actual cause of better developmental outcomes but that the age when children begin to have access to language and communication and the characteristics of the intervention are the primary cause of better outcomes. Screening is the avenue through which access to quality intervention is made available. The research still remains at an infant level of development such that there is very little evidence for the efficacy of specific characteristics of the intervention provided.

Learning outcomes: (1) The learner will be able to identify the obstacles in conducting research on the effectiveness of intervention of children identified through universal newborn hearing screening programs. (2) The learner will be able to identify the type of research on developmental outcomes of children with early-identified hearing loss.

Sumário (português)  :

Resumen (español)  :

Comentarios :

Argument (français) :

Argument (English):

Argumento (português):

Argumento (español):

Palabras claves :

➡ patologías del recién nacido

Autor de este registro :

Sandrine Péneau — 23 Nov 2004

Debate (mostrar sólo español)
 
➡ Sólo para usuarios identificados



 He leído la política de debate y acepto las condiciones (ver la constitución)

barre

Realizar otra consulta de expertos --- Realice otra consulta sencilla

Creación de un registro --- Importación de registros

Gestión de usuarios --- Salvaguardar la base de datos --- Contacto

bar

Esta base de datos creada por la Alliance francophone pour l'accouchement respecté (AFAR) está gestionada
por el Collectif interassociatif autour de la naissance (CIANE, https://ciane.net).
Se nutre de las contribuciones de voluntarios interesados en compartir información científica.
Si está de acuerdo con este proyecto, puede ayudarnos de varias maneras:
(1) convertirse en colaborador de esta base de datos, si tiene alguna experiencia en documentación
(2) ou apoio financeiro CIANE (veja abaixo)
(3) o hacerse miembro de otra asociación afiliada al CIANE.
Inicie sesión o cree una cuenta para seguir los cambios o convertirse en editor.
Contacta con bibli(arobase)ciane.net para más información.

Valid CSS! Valid HTML!
Donar a CIANE (haga clic en 'Faire un don') nos ayudará a mantener y desarrollar
sitios y bases de datos públicas para apoyar las decisiones informadas de los progenitores
y profesionales de la salud con respecto al parto