Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador

97 Páginas.

Autores:: Giraldo Rendón, Gabriel Eduardo

Tipo de recurso:

Fecha de publicación:: 2012

Institución:: Universidad de la Sabana

Repositorio:: Repositorio Universidad de la Sabana

Idioma:: spa

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dc.title.es_CO.fl_str_mv	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador
title	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador
spellingShingle	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador Tratamiento paliativo Enfermedad de Parkinson Calidad de vida Enfermedad de Alzheimer
title_short	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador
title_full	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador
title_fullStr	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador
title_full_unstemmed	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador
title_sort	Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador
dc.creator.fl_str_mv	Giraldo Rendón, Gabriel Eduardo
dc.contributor.advisor.none.fl_str_mv	Martín Padilla, Mario Andrés Ernesto
dc.contributor.author.none.fl_str_mv	Giraldo Rendón, Gabriel Eduardo
dc.subject.es_CO.fl_str_mv	Tratamiento paliativo Enfermedad de Parkinson Calidad de vida Enfermedad de Alzheimer
topic	Tratamiento paliativo Enfermedad de Parkinson Calidad de vida Enfermedad de Alzheimer
description	97 Páginas.
publishDate	2012
dc.date.accessioned.none.fl_str_mv	2012-05-25T21:21:38Z
dc.date.available.none.fl_str_mv	2012-05-25T21:21:38Z
dc.date.issued.none.fl_str_mv	2012-05-25
dc.date.created.none.fl_str_mv	2016
dc.type.none.fl_str_mv	bachelorThesis
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dc.identifier.citation.none.fl_str_mv	Burton, C. L, Strauss E, Hultsch D, Moll A, y Hunter A. (2006) Intraindividual Variability as a Marker of Neurological Dysfunction: A Comparison of Alzheimer’s Disease and Parkinson’s Disease. Journal of Clinical and Experimental Neuropsychology, 28:67– 83, Caap-Ahlgren M., Dehlim O. (2002). Factors of importance to the caregiver burden experienced by family caregivers of Parkinson disease patients. Aging Clinic Exp Res. 14:371-377. Cassidy, T. (2000). Stress, healthiness and health behaviours: An exploration of the role of life events, daily hassles, cognitive appraisal and the coping process. Counselling Psychology Quarterly, 13, 293–311. Cox, D. (1987). Anger and Depression management: Psycho-educational skills Training Intervention for Women Caregivers of a relative with dementia. The Gerontologist. 43, 678-689. Davey, C., Wiles, R., A., Murphy, C. (2004). Falling in Parkinson’s disease: The Impact on informal care givers. Disability and Rehabilitation. V. 26 N. 23, 1360-1 Edwards, NE., Sheetz PS. (2002). Predictors of burden for caregivers of patients with Parkinson’s disease. Journals of Neuro Psychology Nurs. 34:184-190 Epstein NB, Ryan, CE, Bishop, DS. (2003). The McMaster model: View of healthy family functioning. In F. Walsh (Ed.) Normal family processes (pp. 138-160). New York. Guilford Press. Farias G. (2004). La subjetividad del paciente terminal y el abordaje de cuidados paliativos. Material de Diplomado Psicología Clínica y de la Salud, Modulo de Bioética 2007. Universidad de la Sabana Feb-May. Fisher L., Lieberman, M.A, (1996). The effects of context on adult offspring of patients with Alzheimer disease. A longitudinal study. Journal of family Psychology, 62, 265- 272 Gage H., Kaye J., Owen Charles, Trend Patrick, Wade D. (2006). Clinical Rehabilitation. 20:232-238. Goode, KT., Haley, WE., Roth, DL. Ford, GR. (1998). Predicting longitudinal changes in caregiver physical and mental health. A stress process model. Health Psychology, 17(2), 190-198 Gilliam, CM., Steffen, AM. (2006). The relationship between caregiving self-efficacy and depressive symptoms in dementia family caregivers. Aging & Mental Health, 10(2): 79–86 Gómez-Batiste J., Roca E, (1990). Palliative Care in Population with cancer. Palliative Medicine. 5, 120-135 Hasselkus BR. (1997). Everyday ethics in dementia care: narratives of crossing the line. Journal of Gerontologist 37: 640–649 Haugarvoll K., Aarsland D., Wentzel-Larzen T., Larsen JP. (2005). The Influence of cerebro vascular risk factors on incident dementia in patients with Parkinson Disease. Acta Neurologica Scandinavica. 112: 386-390 Hudson, P., Toye, C., Kristjanson, L.(2006) Would people with Parkinson's disease benefit from palliative care?. Palliative Medicine 20:87-94 Hughes TA, Ross HF, Mindham RHS, Spokes EGS. (2005), Mortality in Parkinson’s disease. Acta Neurologica Scandinavica 111: 71 Ibáñez, E. y Andreu, Y. (1988). Calidad de vida y Psicología oncológica. Anuario de Psicología. nº 38, 7-21. James A., Wood-Mitchell, A., Waterworth A., Mackenzie y Waterworth Cunningham J. (2006). Lying to people with dementia: developing ethical guidelines for care settings, International Journal of Geriatric Psychiatry. 21: 800–801. Jones, K., Johnston, M. y Speck, P. (1989). Despair felt by the patient and the professional carer: a case study of the use of cognitive behavioral methods. Palliative Medicine, 3, 39-46. Lundh, U. (1999); Family carers 2: Sources of Satisfaction among Swedish carers. British Journal of Nursing 8(10), 647-652 Marinus, J., Leentjens, AFG. Visser, M., Stiggelbout, AM., van Hilten, JJ.(2002). Evaluation of the Hospital Anxiety and Depression Scale in Patiens with Parkinson's disease. Journal of Clinical Neuropharmacologist 25:318-324. Martínez-Martín, P., Benito-León, J., Alonso, F., Catalán, M., Pondal, M., Zamarbide, L,. Tobías, A., Pedro, J. (2005). Quality of life of caregivers in Parkinson Disease. Quality of life Res. 14, 463-472 Maciado, O.L. (2007). Modulo VIH / SIDA. Diplomado en Psicología Clínica y de la Salud. Universidad de la Sabana Neisa C. (2007). Modulo salud y trabajo. Diplomado en Psicología Clínica y de la Salud. Universidad de la Sabana Ortiz LB, Pinto-Afanador N y Sánchez-Herrera B. (2006) Evaluación de un Programa para Fortalecer a los Cuidadores Familiares de Enfermos Crónicos. Bogotá: Universidad nacional de Colombia. Olafsdottir M, Foldevi M, Marcunsson J. (2001). Dementia in Primary care: why the low detection rate?. Scandinavica Journal of Primary Healt Care. 19: 194-198. Perl, Olanow, & Calne, (1998). Relationship between age, gender, and cognitive performance in the very old: The effect of selective survival. Journal of the American Geriatrics Society. 159, 436-442 Pinel JPJ. (2001).Biopsicología. Cuarta edición, Ed Parsons Education S.A. Madrid cap. 6 y 14. Reischies, FM, Roissius, W, Felsenberg. (2001) Brain Atrophy Parameters of very old subjects in a population – Based Sample with and without dementia syndrome. European Archieve Clinical Neuropsichology 251: 99- 104. Russell R. (2007), Men Doing “Women’s Work:” Elderly Men Caregivers and the Gendered Construction of Care Work. The journal of men´s studies, Vol 15 No. 1. Winter 2007. 1-18. Sarmiento P. (2007). Modulo Bioética y Salud. Diplomado en Psicología Clínica y de la Salud.Universidad de la Sabana Saunders, C. M. (1990). El manejo de la enfermedad terminal. Anales de Psicología, 6(2), Enero, 317-320. Schestatsky P., Zanatto VC, R Margis, Chachamovich E, Reche M, Gomes-Batista R, Fricke D, C Rieder. (2006). Quality of life in a Brazilian sample of patients with Parkinson’s disease and their caregivers. Rev Bras Psiquiatr.;28(3):209-11 Schulz RS, Beach SR. (1995) Caregiving as a risk factor of mortality: The caregiver Health Effects Study. Journal of Anging Health 2, 81-102 Sgreccia E. (1996) Manual de Bioética. Instituto de Humanismo en Ciencias de la Salud. Ed Diana. Barcelona, España. Sharma N, Richman E., Waters DB. (2005). Parkinson’s Disease and the Family: A New Guide. Harvard University Press Cambridge, MA. Simmons AD. Tarsy D (2005). Chronic Conditions in Later Life Parkinson's Disease in Later Life. Scandinavica Journal of Primary Healt Care. 22: 104-139 Stone, Cafferta, & Sangl, (1987). Chronic pain in the setting of the Parkinson's disease and depression. Clinical Neuroscience Journal 14, 255-268. Suárez, A. (2007). Modulo Psicooncología. Diplomado en Psicología Clínica y de la Salud. Feb-Mar. Universidad de la Sabana World Health Organization (WHO). (2002) National Cancer control programmes: policies and managerial guidelines, second edition. Acevedo, G. R., Santos, V. L. (2006) Handicapped Caregiver: The social representations of family members about the care giving process. Revista Latinoamericana de Enfermería. 14(5), 770-780. Adler, E. (2005). Profiles in caregiving. The unexpected career. San Diego. Academic Press. Inc American Psychiatric Association, (2000), DSM IV-TR, Washington D.C. Alison, M., Heru, MD., Ryan, C. (2006). Family Functioning in the caregivers of Patients with Dementia: One-Year Follow–up. Bulletin of the Menninger Clinic. Vol. 70, No. 3 (Summer 2006), 222 – 31. Asociación Latinoamericana de Psicología- ALAPSA. (1999). Seccional Colombia Australian Government Department of health and ageing (2004). Guidelines for a palliative approach in residential aged care. Australian Government Department of health and aging. Barreto P, (1990). El psicólogo ante el enfermo en situación terminal. Anales de Psicología, 6 (2), 169-180 Ba¨ckman, L., Jones, S., Small, B.J., Agu¨ero-Tortres, H., & Fratiglioni, L. (2003). Cognitive Functioning in Aging and Dementia: The Kungsholmen Project. Aging Neuropsichology and Cognition. 6 (2-3) p. 212-244 Bejano O. (2007). Extracto de la carta contra la Eutanasia, 1995. Material del Seminario Clínica y Salud. Universidad la Sabana Feb-May Billings, J.A. (1989). Specialized care of the terminally ill patient. En V.E. DeVita, S. Hellmann y S.A. Rosenberg (Eds.), Cancer, principles and practice of oncology (pp. 2237-2244). Filadelfia: Lippincott. Boeve, (2005). While you were sleeping. News Feature Nature. Vol. 437, 27 Braak, E., Griffin, K, Arai, Bohl J, Bratzke, H, & Braak, H. (1999). Neurophatology of Alzheimer´s disease: What is new since A. Alzheimer? . European Archives of Psychiatry and Clinical Neuroscience, 249, 14-20 Bronnick K, Aarsland D, Larsen JP. (2005). Neuropsychiatric disturbances in Parkinson’s disease clusters in five groups with different prevalence of dementia. Acta Psychiatrica Scandinavica: 112: 201–207 Burch, D., Sheering F. (2005). Parkinson’s disease. Lancet. 365, 22-27. Burns, A. (2000) The Burden of Alzheimer’s Disease. International Journal of Neuropsychotherapy. 3(7), 31-38
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identifier_str_mv	Burton, C. L, Strauss E, Hultsch D, Moll A, y Hunter A. (2006) Intraindividual Variability as a Marker of Neurological Dysfunction: A Comparison of Alzheimer’s Disease and Parkinson’s Disease. Journal of Clinical and Experimental Neuropsychology, 28:67– 83, Caap-Ahlgren M., Dehlim O. (2002). Factors of importance to the caregiver burden experienced by family caregivers of Parkinson disease patients. Aging Clinic Exp Res. 14:371-377. Cassidy, T. (2000). Stress, healthiness and health behaviours: An exploration of the role of life events, daily hassles, cognitive appraisal and the coping process. Counselling Psychology Quarterly, 13, 293–311. Cox, D. (1987). Anger and Depression management: Psycho-educational skills Training Intervention for Women Caregivers of a relative with dementia. The Gerontologist. 43, 678-689. Davey, C., Wiles, R., A., Murphy, C. (2004). Falling in Parkinson’s disease: The Impact on informal care givers. Disability and Rehabilitation. V. 26 N. 23, 1360-1 Edwards, NE., Sheetz PS. (2002). Predictors of burden for caregivers of patients with Parkinson’s disease. Journals of Neuro Psychology Nurs. 34:184-190 Epstein NB, Ryan, CE, Bishop, DS. (2003). The McMaster model: View of healthy family functioning. In F. Walsh (Ed.) Normal family processes (pp. 138-160). New York. Guilford Press. Farias G. (2004). La subjetividad del paciente terminal y el abordaje de cuidados paliativos. Material de Diplomado Psicología Clínica y de la Salud, Modulo de Bioética 2007. Universidad de la Sabana Feb-May. Fisher L., Lieberman, M.A, (1996). The effects of context on adult offspring of patients with Alzheimer disease. A longitudinal study. Journal of family Psychology, 62, 265- 272 Gage H., Kaye J., Owen Charles, Trend Patrick, Wade D. (2006). Clinical Rehabilitation. 20:232-238. Goode, KT., Haley, WE., Roth, DL. Ford, GR. (1998). Predicting longitudinal changes in caregiver physical and mental health. A stress process model. Health Psychology, 17(2), 190-198 Gilliam, CM., Steffen, AM. (2006). The relationship between caregiving self-efficacy and depressive symptoms in dementia family caregivers. Aging & Mental Health, 10(2): 79–86 Gómez-Batiste J., Roca E, (1990). Palliative Care in Population with cancer. Palliative Medicine. 5, 120-135 Hasselkus BR. (1997). Everyday ethics in dementia care: narratives of crossing the line. Journal of Gerontologist 37: 640–649 Haugarvoll K., Aarsland D., Wentzel-Larzen T., Larsen JP. (2005). The Influence of cerebro vascular risk factors on incident dementia in patients with Parkinson Disease. Acta Neurologica Scandinavica. 112: 386-390 Hudson, P., Toye, C., Kristjanson, L.(2006) Would people with Parkinson's disease benefit from palliative care?. Palliative Medicine 20:87-94 Hughes TA, Ross HF, Mindham RHS, Spokes EGS. (2005), Mortality in Parkinson’s disease. Acta Neurologica Scandinavica 111: 71 Ibáñez, E. y Andreu, Y. (1988). Calidad de vida y Psicología oncológica. Anuario de Psicología. nº 38, 7-21. James A., Wood-Mitchell, A., Waterworth A., Mackenzie y Waterworth Cunningham J. (2006). Lying to people with dementia: developing ethical guidelines for care settings, International Journal of Geriatric Psychiatry. 21: 800–801. Jones, K., Johnston, M. y Speck, P. (1989). Despair felt by the patient and the professional carer: a case study of the use of cognitive behavioral methods. Palliative Medicine, 3, 39-46. Lundh, U. (1999); Family carers 2: Sources of Satisfaction among Swedish carers. British Journal of Nursing 8(10), 647-652 Marinus, J., Leentjens, AFG. Visser, M., Stiggelbout, AM., van Hilten, JJ.(2002). Evaluation of the Hospital Anxiety and Depression Scale in Patiens with Parkinson's disease. Journal of Clinical Neuropharmacologist 25:318-324. Martínez-Martín, P., Benito-León, J., Alonso, F., Catalán, M., Pondal, M., Zamarbide, L,. Tobías, A., Pedro, J. (2005). Quality of life of caregivers in Parkinson Disease. Quality of life Res. 14, 463-472 Maciado, O.L. (2007). Modulo VIH / SIDA. Diplomado en Psicología Clínica y de la Salud. Universidad de la Sabana Neisa C. (2007). Modulo salud y trabajo. Diplomado en Psicología Clínica y de la Salud. Universidad de la Sabana Ortiz LB, Pinto-Afanador N y Sánchez-Herrera B. (2006) Evaluación de un Programa para Fortalecer a los Cuidadores Familiares de Enfermos Crónicos. Bogotá: Universidad nacional de Colombia. Olafsdottir M, Foldevi M, Marcunsson J. (2001). Dementia in Primary care: why the low detection rate?. Scandinavica Journal of Primary Healt Care. 19: 194-198. Perl, Olanow, & Calne, (1998). Relationship between age, gender, and cognitive performance in the very old: The effect of selective survival. Journal of the American Geriatrics Society. 159, 436-442 Pinel JPJ. (2001).Biopsicología. Cuarta edición, Ed Parsons Education S.A. Madrid cap. 6 y 14. Reischies, FM, Roissius, W, Felsenberg. (2001) Brain Atrophy Parameters of very old subjects in a population – Based Sample with and without dementia syndrome. European Archieve Clinical Neuropsichology 251: 99- 104. Russell R. (2007), Men Doing “Women’s Work:” Elderly Men Caregivers and the Gendered Construction of Care Work. The journal of men´s studies, Vol 15 No. 1. Winter 2007. 1-18. Sarmiento P. (2007). Modulo Bioética y Salud. Diplomado en Psicología Clínica y de la Salud.Universidad de la Sabana Saunders, C. M. (1990). El manejo de la enfermedad terminal. Anales de Psicología, 6(2), Enero, 317-320. Schestatsky P., Zanatto VC, R Margis, Chachamovich E, Reche M, Gomes-Batista R, Fricke D, C Rieder. (2006). Quality of life in a Brazilian sample of patients with Parkinson’s disease and their caregivers. Rev Bras Psiquiatr.;28(3):209-11 Schulz RS, Beach SR. (1995) Caregiving as a risk factor of mortality: The caregiver Health Effects Study. Journal of Anging Health 2, 81-102 Sgreccia E. (1996) Manual de Bioética. Instituto de Humanismo en Ciencias de la Salud. Ed Diana. Barcelona, España. Sharma N, Richman E., Waters DB. (2005). Parkinson’s Disease and the Family: A New Guide. Harvard University Press Cambridge, MA. Simmons AD. Tarsy D (2005). Chronic Conditions in Later Life Parkinson's Disease in Later Life. Scandinavica Journal of Primary Healt Care. 22: 104-139 Stone, Cafferta, & Sangl, (1987). Chronic pain in the setting of the Parkinson's disease and depression. Clinical Neuroscience Journal 14, 255-268. Suárez, A. (2007). Modulo Psicooncología. Diplomado en Psicología Clínica y de la Salud. Feb-Mar. Universidad de la Sabana World Health Organization (WHO). (2002) National Cancer control programmes: policies and managerial guidelines, second edition. Acevedo, G. R., Santos, V. L. (2006) Handicapped Caregiver: The social representations of family members about the care giving process. Revista Latinoamericana de Enfermería. 14(5), 770-780. Adler, E. (2005). Profiles in caregiving. The unexpected career. San Diego. Academic Press. Inc American Psychiatric Association, (2000), DSM IV-TR, Washington D.C. Alison, M., Heru, MD., Ryan, C. (2006). Family Functioning in the caregivers of Patients with Dementia: One-Year Follow–up. Bulletin of the Menninger Clinic. Vol. 70, No. 3 (Summer 2006), 222 – 31. Asociación Latinoamericana de Psicología- ALAPSA. (1999). Seccional Colombia Australian Government Department of health and ageing (2004). Guidelines for a palliative approach in residential aged care. Australian Government Department of health and aging. Barreto P, (1990). El psicólogo ante el enfermo en situación terminal. Anales de Psicología, 6 (2), 169-180 Ba¨ckman, L., Jones, S., Small, B.J., Agu¨ero-Tortres, H., & Fratiglioni, L. (2003). Cognitive Functioning in Aging and Dementia: The Kungsholmen Project. Aging Neuropsichology and Cognition. 6 (2-3) p. 212-244 Bejano O. (2007). Extracto de la carta contra la Eutanasia, 1995. Material del Seminario Clínica y Salud. Universidad la Sabana Feb-May Billings, J.A. (1989). Specialized care of the terminally ill patient. En V.E. DeVita, S. Hellmann y S.A. Rosenberg (Eds.), Cancer, principles and practice of oncology (pp. 2237-2244). Filadelfia: Lippincott. Boeve, (2005). While you were sleeping. News Feature Nature. Vol. 437, 27 Braak, E., Griffin, K, Arai, Bohl J, Bratzke, H, & Braak, H. (1999). Neurophatology of Alzheimer´s disease: What is new since A. Alzheimer? . European Archives of Psychiatry and Clinical Neuroscience, 249, 14-20 Bronnick K, Aarsland D, Larsen JP. (2005). Neuropsychiatric disturbances in Parkinson’s disease clusters in five groups with different prevalence of dementia. Acta Psychiatrica Scandinavica: 112: 201–207 Burch, D., Sheering F. (2005). Parkinson’s disease. Lancet. 365, 22-27. Burns, A. (2000) The Burden of Alzheimer’s Disease. International Journal of Neuropsychotherapy. 3(7), 31-38 88559 TE04657
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spelling	Martín Padilla, Mario Andrés ErnestoGiraldo Rendón, Gabriel EduardoPsicólogo2012-05-25T21:21:38Z2012-05-25T21:21:38Z20162012-05-25Burton, C. L, Strauss E, Hultsch D, Moll A, y Hunter A. (2006) Intraindividual Variability as a Marker of Neurological Dysfunction: A Comparison of Alzheimer’s Disease and Parkinson’s Disease. Journal of Clinical and Experimental Neuropsychology, 28:67– 83,Caap-Ahlgren M., Dehlim O. (2002). Factors of importance to the caregiver burden experienced by family caregivers of Parkinson disease patients. Aging Clinic Exp Res. 14:371-377.Cassidy, T. (2000). Stress, healthiness and health behaviours: An exploration of the role of life events, daily hassles, cognitive appraisal and the coping process. Counselling Psychology Quarterly, 13, 293–311.Cox, D. (1987). Anger and Depression management: Psycho-educational skills Training Intervention for Women Caregivers of a relative with dementia. The Gerontologist. 43, 678-689.Davey, C., Wiles, R., A., Murphy, C. (2004). Falling in Parkinson’s disease: The Impact on informal care givers. Disability and Rehabilitation. V. 26 N. 23, 1360-1Edwards, NE., Sheetz PS. (2002). Predictors of burden for caregivers of patients with Parkinson’s disease. Journals of Neuro Psychology Nurs. 34:184-190Epstein NB, Ryan, CE, Bishop, DS. (2003). The McMaster model: View of healthy family functioning. In F. Walsh (Ed.) Normal family processes (pp. 138-160). New York. Guilford Press.Farias G. (2004). La subjetividad del paciente terminal y el abordaje de cuidados paliativos. Material de Diplomado Psicología Clínica y de la Salud, Modulo de Bioética 2007. Universidad de la Sabana Feb-May.Fisher L., Lieberman, M.A, (1996). The effects of context on adult offspring of patients with Alzheimer disease. A longitudinal study. Journal of family Psychology, 62, 265- 272Gage H., Kaye J., Owen Charles, Trend Patrick, Wade D. (2006). Clinical Rehabilitation. 20:232-238.Goode, KT., Haley, WE., Roth, DL. Ford, GR. (1998). Predicting longitudinal changes in caregiver physical and mental health. A stress process model. Health Psychology, 17(2), 190-198Gilliam, CM., Steffen, AM. (2006). The relationship between caregiving self-efficacy and depressive symptoms in dementia family caregivers. Aging & Mental Health, 10(2): 79–86Gómez-Batiste J., Roca E, (1990). Palliative Care in Population with cancer. Palliative Medicine. 5, 120-135Hasselkus BR. (1997). Everyday ethics in dementia care: narratives of crossing the line. Journal of Gerontologist 37: 640–649Haugarvoll K., Aarsland D., Wentzel-Larzen T., Larsen JP. (2005). The Influence of cerebro vascular risk factors on incident dementia in patients with Parkinson Disease. Acta Neurologica Scandinavica. 112: 386-390Hudson, P., Toye, C., Kristjanson, L.(2006) Would people with Parkinson's disease benefit from palliative care?. Palliative Medicine 20:87-94Hughes TA, Ross HF, Mindham RHS, Spokes EGS. (2005), Mortality in Parkinson’s disease. Acta Neurologica Scandinavica 111: 71Ibáñez, E. y Andreu, Y. (1988). Calidad de vida y Psicología oncológica. Anuario de Psicología. nº 38, 7-21.James A., Wood-Mitchell, A., Waterworth A., Mackenzie y Waterworth Cunningham J. (2006). Lying to people with dementia: developing ethical guidelines for care settings, International Journal of Geriatric Psychiatry. 21: 800–801.Jones, K., Johnston, M. y Speck, P. (1989). Despair felt by the patient and the professional carer: a case study of the use of cognitive behavioral methods. Palliative Medicine, 3, 39-46.Lundh, U. (1999); Family carers 2: Sources of Satisfaction among Swedish carers. British Journal of Nursing 8(10), 647-652Marinus, J., Leentjens, AFG. Visser, M., Stiggelbout, AM., van Hilten, JJ.(2002). Evaluation of the Hospital Anxiety and Depression Scale in Patiens with Parkinson's disease. Journal of Clinical Neuropharmacologist 25:318-324.Martínez-Martín, P., Benito-León, J., Alonso, F., Catalán, M., Pondal, M., Zamarbide, L,. Tobías, A., Pedro, J. (2005). Quality of life of caregivers in Parkinson Disease. Quality of life Res. 14, 463-472Maciado, O.L. (2007). Modulo VIH / SIDA. Diplomado en Psicología Clínica y de la Salud. Universidad de la SabanaNeisa C. (2007). Modulo salud y trabajo. Diplomado en Psicología Clínica y de la Salud. Universidad de la SabanaOrtiz LB, Pinto-Afanador N y Sánchez-Herrera B. (2006) Evaluación de un Programa para Fortalecer a los Cuidadores Familiares de Enfermos Crónicos. Bogotá: Universidad nacional de Colombia.Olafsdottir M, Foldevi M, Marcunsson J. (2001). Dementia in Primary care: why the low detection rate?. Scandinavica Journal of Primary Healt Care. 19: 194-198.Perl, Olanow, & Calne, (1998). Relationship between age, gender, and cognitive performance in the very old: The effect of selective survival. Journal of the American Geriatrics Society. 159, 436-442Pinel JPJ. (2001).Biopsicología. Cuarta edición, Ed Parsons Education S.A. Madrid cap. 6 y 14.Reischies, FM, Roissius, W, Felsenberg. (2001) Brain Atrophy Parameters of very old subjects in a population – Based Sample with and without dementia syndrome. European Archieve Clinical Neuropsichology 251: 99- 104.Russell R. (2007), Men Doing “Women’s Work:” Elderly Men Caregivers and the Gendered Construction of Care Work. The journal of men´s studies, Vol 15 No. 1. Winter 2007. 1-18.Sarmiento P. (2007). Modulo Bioética y Salud. Diplomado en Psicología Clínica y de la Salud.Universidad de la SabanaSaunders, C. M. (1990). El manejo de la enfermedad terminal. Anales de Psicología, 6(2), Enero, 317-320.Schestatsky P., Zanatto VC, R Margis, Chachamovich E, Reche M, Gomes-Batista R, Fricke D, C Rieder. (2006). Quality of life in a Brazilian sample of patients with Parkinson’s disease and their caregivers. Rev Bras Psiquiatr.;28(3):209-11Schulz RS, Beach SR. (1995) Caregiving as a risk factor of mortality: The caregiver Health Effects Study. Journal of Anging Health 2, 81-102Sgreccia E. (1996) Manual de Bioética. Instituto de Humanismo en Ciencias de la Salud. Ed Diana. Barcelona, España.Sharma N, Richman E., Waters DB. (2005). Parkinson’s Disease and the Family: A New Guide. Harvard University Press Cambridge, MA.Simmons AD. Tarsy D (2005). Chronic Conditions in Later Life Parkinson's Disease in Later Life. Scandinavica Journal of Primary Healt Care. 22: 104-139Stone, Cafferta, & Sangl, (1987). Chronic pain in the setting of the Parkinson's disease and depression. Clinical Neuroscience Journal 14, 255-268.Suárez, A. (2007). Modulo Psicooncología. Diplomado en Psicología Clínica y de la Salud. Feb-Mar. Universidad de la SabanaWorld Health Organization (WHO). (2002) National Cancer control programmes: policies and managerial guidelines, second edition.Acevedo, G. R., Santos, V. L. (2006) Handicapped Caregiver: The social representations of family members about the care giving process. Revista Latinoamericana de Enfermería. 14(5), 770-780.Adler, E. (2005). Profiles in caregiving. The unexpected career. San Diego. Academic Press. IncAmerican Psychiatric Association, (2000), DSM IV-TR, Washington D.C.Alison, M., Heru, MD., Ryan, C. (2006). Family Functioning in the caregivers of Patients with Dementia: One-Year Follow–up. Bulletin of the Menninger Clinic. Vol. 70, No. 3 (Summer 2006), 222 – 31.Asociación Latinoamericana de Psicología- ALAPSA. (1999). Seccional ColombiaAustralian Government Department of health and ageing (2004). Guidelines for a palliative approach in residential aged care. Australian Government Department of health and aging.Barreto P, (1990). El psicólogo ante el enfermo en situación terminal. Anales de Psicología, 6 (2), 169-180Ba¨ckman, L., Jones, S., Small, B.J., Agu¨ero-Tortres, H., & Fratiglioni, L. (2003). Cognitive Functioning in Aging and Dementia: The Kungsholmen Project. Aging Neuropsichology and Cognition. 6 (2-3) p. 212-244Bejano O. (2007). Extracto de la carta contra la Eutanasia, 1995. Material del Seminario Clínica y Salud. Universidad la Sabana Feb-MayBillings, J.A. (1989). Specialized care of the terminally ill patient. En V.E. DeVita, S. Hellmann y S.A. Rosenberg (Eds.), Cancer, principles and practice of oncology (pp. 2237-2244). Filadelfia: Lippincott.Boeve, (2005). While you were sleeping. News Feature Nature. Vol. 437, 27Braak, E., Griffin, K, Arai, Bohl J, Bratzke, H, & Braak, H. (1999). Neurophatology of Alzheimer´s disease: What is new since A. Alzheimer? . European Archives of Psychiatry and Clinical Neuroscience, 249, 14-20Bronnick K, Aarsland D, Larsen JP. (2005). Neuropsychiatric disturbances in Parkinson’s disease clusters in five groups with different prevalence of dementia. Acta Psychiatrica Scandinavica: 112: 201–207Burch, D., Sheering F. (2005). Parkinson’s disease. Lancet. 365, 22-27.Burns, A. (2000) The Burden of Alzheimer’s Disease. International Journal of Neuropsychotherapy. 3(7), 31-38http://hdl.handle.net/10818/230388559TE0465797 Páginas.Realizar un aporte sobre el tema de la prestación de cuidados paliativos, como práctica del discurso del mejoramiento del nivel de calidad de vida de personas que se contempla como un factor importante dentro de la definición salud (WHO, 2002). El objetivo es identificar los factores que desempeñan un papel importante en la calidad de vida de pacientes característicos de esta población y ofrecerlos como material de información sobre le manejo y los aspectos éticos y prácticos de interés para la familia de cuidadores, los servicios de atención social y todo el equipo profesional relacionado con su manejo. Pretende contribuir a resaltar la importancia que tienen los cuidados paliativos en el mantenimiento de la dignidad humana en pacientes terminales.Universidad de la SabanaPsicologíaFacultad de PsicologíaUniversidad de la SabanaIntellectum Repositorio Universidad de la SabanaTratamiento paliativoEnfermedad de ParkinsonCalidad de vidaEnfermedad de AlzheimerCuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidadorbachelorThesisTesis de pregradopublishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_7a1fspahttp://purl.org/coar/access_right/c_abf2ORIGINAL131492.pdf131492.pdfVer documento en PDFapplication/pdf241632https://intellectum.unisabana.edu.co/bitstream/10818/2303/1/131492.pdf164a05b036589b8c3da6d942e9e4573eMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-8498https://intellectum.unisabana.edu.co/bitstream/10818/2303/2/license.txtf52a2cfd4df262e08e9b300d62c85cabMD52TEXT131492.pdf.txt131492.pdf.txtExtracted texttext/plain177708https://intellectum.unisabana.edu.co/bitstream/10818/2303/3/131492.pdf.txted84bc18bce2c6d3fb4d006d8d316259MD5310818/2303oai:intellectum.unisabana.edu.co:10818/23032019-06-07 12:41:36.869Intellectum Universidad de la Sabanacontactointellectum@unisabana.edu.coPGEgcmVsPSJsaWNlbnNlIiBocmVmPSJodHRwOi8vY3JlYXRpdmVjb21tb25zLm9yZy9saWNlbnNlcy9ieS1uYy1uZC8zLjAvIj48aW1nIGFsdD0iTGljZW5jaWEgQ3JlYXRpdmUgQ29tbW9ucyIgc3R5bGU9ImJvcmRlci13aWR0aDowIiBzcmM9Imh0dHA6Ly9pLmNyZWF0aXZlY29tbW9ucy5vcmcvbC9ieS1uYy1uZC8zLjAvODh4MzEucG5nIiAvPjwvYT48YnIgLz5Fc3RlIDxzcGFuIHhtbG5zOmRjdD0iaHR0cDovL3B1cmwub3JnL2RjL3Rlcm1zLyIgaHJlZj0iaHR0cDovL3B1cmwub3JnL2RjL2RjbWl0eXBlL1RleHQiIHJlbD0iZGN0OnR5cGUiPm9icmE8L3NwYW4+IGVzdMOhIGJham8gdW5hIDxhIHJlbD0ibGljZW5zZSIgaHJlZj0iaHR0cDovL2NyZWF0aXZlY29tbW9ucy5vcmcvbGljZW5zZXMvYnktbmMtbmQvMy4wLyI+bGljZW5jaWEgQ3JlYXRpdmUgQ29tbW9ucyBSZWNvbm9jaW1pZW50by1Ob0NvbWVyY2lhbC1TaW5PYnJhRGVyaXZhZGEgMy4wIFVucG9ydGVkPC9hPi4K

Cuidados paliativos en enfermedades neuro-degeneraticas generalidades, aspectos del cuidado e implicaciones en la calidad de vida del paciente y del cuidador

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