covid
Buscar en
Revista Médica Internacional sobre el Síndrome de Down (English Edition)
Toda la web
Inicio Revista Médica Internacional sobre el Síndrome de Down (English Edition) Healthy ageing in people with Down syndrome and dementia: The need to foster edu...
Información de la revista
Vol. 10. Núm. 2.
Páginas 25-29 (julio 2006)
Compartir
Compartir
Descargar PDF
Más opciones de artículo
Vol. 10. Núm. 2.
Páginas 25-29 (julio 2006)
Acceso a texto completo
Healthy ageing in people with Down syndrome and dementia: The need to foster education and support programs for individuals, families and organizations
Visitas
597
Susanna Esteba-Castillo
Autor para correspondencia
sesmdi@ias.scs.es

Correspondence to: Responsable de l’Àrea de DI. Parc Hospitalari Martí i Julià. Institut Assistència Sanitària (IAS). Girona, Spain .
, Nuria Ribas Vidal, Meritxell Baró i Dilmé, Ramón Novell Alsina
Equip Multidisciplinari. Servei Especialitzat en Salut Mental / Trastorn de conducta i Discapacitat Intel·lectual (SESM-DI). Parc Hospitalari Martí i Julià. Institut Assistència Sanitària (IAS)
Este artículo ha recibido
Información del artículo
Resumen
Bibliografía
Descargar PDF
Estadísticas
Abstract

Most individuals with Down syndrome (DS) reach an advanced age which gives rise to specific seniorcitizen needs. These must be considered and addressed, through anticipation and prevention. Difficulties are already emerging in services responsible for this population, as well as for the individuals concerned and their relatives. The inadequacy and unsuitability of policy planning and lack of adequate services are made apparent whenever a person with DS begins to develop cognitive deterioration or dementia.

The World Health Organization (WHO) has drawn up, in conjunction with the International Association for the Scientific Study of Intellectual Disabilities (IASSID) and Inclusion International, a report on the social and health care needs of aging persons with intellectual disabilities, including those with DS. This working document highlights as a priority the need for each country in the European Union to implement “Projects for Healthy Aging” that are naturally conducive to social inclusion while improving support and training for both formal and informal caregivers. The present article provides a rough outline for potential future programs targeting individuals with DS and cognitive deterioration or dementia.

Keywords:
Care programs
Dementia
Down syndrome
Main caregiver overload
El Texto completo está disponible en PDF
References
[1.]
D. Strauss, R.K. Eyman.
Mortality of people with mental retardation in California with and without Down Syndrome, 1986–1991.
Am J Mental Retard, 100 (1996), pp. 643-653
[2.]
M.A. Maaskant, A.G.H. Akker, M.J. Kessels, H.M. Haveman, Schrojenstein Lantman-de Valk, H.F.J. Urligs.
Care dependence and activities daily living in relationa to ageing Results of a longitudinal study.
J Intellect Disab Res, 40 (1996), pp. 535-543
[3.]
D.A. Devenny, W.P. Silverman, A.L. Hilla, E. Jenkins, E.A. Seren, K.E. Wisniewski.
Normal aging in adults with Down's Syndrome: A longitudinal study.
J Intellect Disab Res, 40 (1996), pp. 209-221
[4.]
J. Tyrrekk, M. Cosgrave, M. McCarron, J. McPher son, J. Calvert, A. Kelly, M. McLaughlin, M. Gill, B.A. Laelor.
Dementia in peolple with Down's syndrome.
Int J Geriatr Psychiatry, 16 (2001), pp. 1168-1174
[5.]
L.I. Pearlin, J.T. Mullan, S.J. Semple, M.M. Skaff.
Caregiving and stress process: an overview of concepts and their measures.
Gerontologist, 30 (1990), pp. 583-594
[6.]
D.P. Gold, C. Cohen, K. Shulman, C. Zucchero, D. Andrés, J. Etezadi.
Caregiving and dementia: predicting negative and positive outcomes for caregivers.
Int J Aging Hum Develop, 41 (1995), pp. 183-201
[7.]
M. Gallant, C. Connell.
The stress process among dementia spouse caregivers.
Research on aging, 20 (1998), pp. 267-297
[8.]
J.A. Muela, C.J. Torres, E.M. Peláez.
La evaluación de la asertividad como predictor de carga en cuidadores de enfermos de Alzheimer.
Rev Esp Geriatr Gerontol, 36 (2001), pp. 41-45
[9.]
M.V. Roig, M.C. Abengózar, E. Serra.
La sobrecarga en los cuidadores principales de enfermos de Alzheimer.
An Psicol, 14 (1998), pp. 215-227
[10.]
Torres CJ, Muela Jam Peláez EM, Huertas J, Leal A. Parentesco, estrutura familiar y carga percibida en cuidadores de enfermos de Alzheimer. Comunicación presentada en el II Congreso Virtual de Psiquiatría, Internet, Marzo 2001.
[11.]
S. Teunisse, M. Derix, H. van Crevel.
Assessing the severity of dementia. Patient and caregiver.
Arch Neurol, 48 (1991), pp. 274-277
[12.]
D. Stull, K. Koloski, K. Kercher.
Caregiver burden and generic web-being: opposite sides of the same coin?.
Gerontologist, 34 (1994), pp. 88-94
[13.]
S. Harper, D. Lund.
Wives, husbands and daughters caring for institutionalized and non institutionalised dementia patients: towards a model of caregiver burden.
Int J Aging Human Development, 30 (1990), pp. 241-262
[14.]
C. Graham, C. Ballard, P. Sham.
Caregiver's knowledege of dementia, their coping stratgeies and morbidity.
Int Geriatr Psychiatry, 12 (1997), pp. 931-936
[15.]
L.D. Clyburn, M.J. Stones, T. Hadjistavropoulos, et al.
Prediciting caregiver burden and depression in Alzheimer's disease.
J Gerontol B Psychol Sci So Sci, 55 (2000), pp. S2-S13
[16.]
Eloniemi-Sulkava, et al.
Effects of Supporting Community-Living Demented Patients and Their Caregivers: A Randomized Trial.
JAGS, 49 (2001), pp. 1282-1287
[17.]
M. Burgeois, R. Schulz, L. Burgio.
Interventions for caregivers of patients with Alzheimer's disease: a review and análisis of content, process amd outcomes.
Int J Aging Human Develop, 43 (1996), pp. 35-92
[18.]
A. Babarro, A. Garrido Barral, A. Díaz Ponce, R. Casquero Ruiz, M. Riera Pastor.
Perfil y sobrecarga de los cuidadores de pacientes con demencia incluidos en el programa ALOIS.
Aten Primaria, 33 (2004), pp. 61-68
[19.]
M. Mittelman, S. Ferris, E. Shulman, G. Steinberg, L. Bruce.
A family Intervention to Delay Nursing Home Placement of Patients with Alzheimer Disease: A randomized controlled trial.
JAMA, 276 (1996), pp. 1725-1731
[20.]
B.G. Kinght, S.M. Lutzki, F. Macofsky-Urban.
A meta-analytic review of interventions for caregiver distress: recommendations for futures research..
Gerontologist, 33 (1993), pp. 240-248
[21.]
E. Gräsel.
Temporary institutional restite in dementia cases: who utilizaes this from respite care and what effect does it have?.
Int Psychogeriatr, 9 (1997), pp. 437-438
[22.]
J. Hogg, R. Lucchino, K. Wang, M. Janicki.
y grupo de trabajo. Healthy Ageing – Adults with Intellectual Disabilities: Aging and Social Policy.
OMS, (2000),
[23.]
M.P. Janicki, L.A. Knox, J.W. Jacobson.
Planning for an older developmentally disabled population.
Aging and development disabilities: Issues and approaches, pp. 143-159
[24.]
Necessitats de salut mental en persones amb discapacitat intel·lectual (SM-DI) 2002. Barcelona: Servei Català de la Salut; 2003.
Copyright © 2006. Fundació Catalana Síndrome Down
Descargar PDF
Opciones de artículo