Sobrecarga y afrontamiento al estrés en el cuidador informales de personas con alguna enfermedad crónica
Overload and coping with stress in the informal caregiver with a chronic disease
Resumen
Abstract
Bibliografía
Aldwin, C. M. (2017). Health, illness, and optimal aging: Biological and psychosocial perspectives (Third Edition ed.). Springer Publishing Company.
Alves, L. C. (2019). Burnout syndrome in informal caregivers of older adults with dementia: A systematic review. Dementia & neuropsychologia, 13(4), 415-421. doi:https://doi.org/10.1590/1980-57642018dn13-040008
Ángel, J. E., (2020). Relación entre sobrecarga y competencias del cuidar en cuidadores informales de personas con enferme-dades crónicas. Recuperado de: http://hdl.handle.net/20.500.12749/9902.
Arabi, M. &. (2019). El cuidador informal en el proceso de rehabilitación de personas con discapacidad física. Mirada desde un abordaje psicosocial. Revista Latinoamericana en Discapacidad, Sociedad y Derechos Humanos, 3(2), 120-138.
Ávila-Toscano, J. H. (2014). Calidad de vida en cuidadores informales de personas con enfermedades crónicas. Aquichan, 14(3), 417-429. doi:http://dx.doi.org/10.5294/aqui.2014.14.3.11
Baharudin, A. D. (2019). The associations between behavioral-psychological symptoms of dementia (BPSD) and coping strategy, burden of care and personality style among low-income caregivers of patients with dementia. BMC Public Health, 19(4), 1-12. doi:https://doi.org/10.1186/s12889-019-6868-0
Barken, R. D. (2017). Family matters: The work and skills of family/friend carers in long-term residential care. Journal of Canadian Studies, 50(2), 321-347. doi:https://doi.org/10.3138/jcs.50.2.321
Bastawrous, M. (2013). Caregiver burden—A critical discussion. International journal of nursing studies, 50(3), 431-441. doi:https://doi.org/10.1016/j.ijnurstu.2012.10.005
Bullock, L. B.‐G. (2019). Pain assessment and pain treatment for community‐dwelling people with dementia: A systematic review and narrative synthesis. International journal of geriatric psychiatry, 34(6), 807-821. doi:https://doi.org/10.1002/gps.5078
Cheng, S. T. (2017). Dementia caregiver burden: a research update and critical analysis. Current psychiatry reports, 19(9), 1-8. doi:https://doi.org/10.1007/s11920-017-0818-2
Chiu, M. W. (2013). Improving caregiving competence, stress coping, and mental well-being in informal dementia carers. World journal of Psychiatry, 3(3), 65-73. doi:https://dx.doi.org/10.5498%2Fwjp.v3.i3.65
Choustikova, J. T.‐S. (2020). raumatic brain injury patients’ family members’ evaluations of the social support provided by healthcare professionals in acute care hospitals. Journal of clinical nursing, 29, 3325-3335. doi: https://doi.org/10.1111/jocn.15359
Contreras, F., D. (2020) Sobrecarga y estilos de humor en padres que migran a Lima junto con el niño con cáncer infantil. (Tesis de Licenciatura) Lima: Pontificia Universidad Católica Boliviana del Perú.
De Valle-Alonso, M. J.-L.-V.-A. (2015). Sobrecarga y Burnout en cuidadores informales del adulto mayor. Enfermería universitaria, 12(1), 19-27.
Feast, A. O.-C. (2016). Behavioural and psychological symptoms in dementia and the challenges for family carers: systematic review. The British Journal of Psychiatry, 208(5), 429-434. doi:doi:10.1192/bjp.bp.114.153684
Ferrell, B. &. (2017). A review of family caregiving intervention trials in oncology. CA: a cancer journal for clinicians, 67(4), 318-325. doi:https://doi.org/10.3322/caac.21396
Flores, E. &. (2016). Functional social support in family caregivers of elderly adults with severe dependence. 34(1), 68-73. doi:http://dx.doi.org/10.17533/udea.iee.v34n1a08
Garzón, N. E. (2021). Rol del cuidador informal novel de adultos en situación de dependencia: Scoping Review. Revista Cuidarte, 12(2). doi:https://doi.org/10.15649/cuidarte.1368
Gilbert, P. &. (2017). Compassion: Fears, blocks, and resistances: An evolutionary investigation.
Gilmour, J. A. (2010). Representations of people with dementia–subaltern, person, citizen. Nursing inquiry, 17(3), 240-247. doi:https://doi.org/10.1111/j.1440-1800.2009.00475.x
Haley, W. E. (2020). Effects of transitions to family caregiving on well‐being: a longitudinal population‐based study. Journal of the American Geriatrics Society, 68(2), 2839-2846. doi:https://doi.org/10.1111/jgs.16778
Jalali, G. T. (2020). Investigation the effect of group hope therapy on quality of life in elderly. Iranian Journal of Psychiatric Nursing, 8(2), 104-115. Obtenido de http://ijpn.ir/article-1-1444-en.html
Lazarus, R. &. (1984). Stress, appraisal, and coping. Springer publishing company.
Levenson, R. (2019). Stress and Illness: A role for specific emotions. Psychosomatic medicine, 81(8), 720. doi:https://dx.doi.org/10.1097%2FPSY.0000000000000736
Livingston, G. S. (2017). Dementia prevention, intervention, and care. The Lancet, 390(10113), 2673-2734. doi:https://doi.org/10.1016/S0140-6736(17)31363-6
Mahdavi, B. F.-K. (2017). Effects of spiritual group therapy on caregiver strain in home caregivers of the elderly with Alzheimer's disease. Archives of Psychiatric Nursing, 31(3), 269-273.
Motamedi, A. M. (2018). The Effectiveness of hope group therapy on enhancement of happiness and quality of life in elderly women in tasouj. Aging Psychology, 3(4), 243-252.
Nunes, I. D. C. B. R. (2015). O humor e o luto nos enfermeiros que trabalham em Cuidados Paliativos (Doctoral dissertation). Lisboa: Universidad Católica Portuguesa.
Nemati, S. R. (2018). Perceptions of family caregivers of cancer patients about the challenges of caregiving: a qualitative study. Scandinavian journal of caring sciences, 32(1), 309-316. doi:https://doi.org/10.1111/scs.12463
Perpiñá-Galvañ, J., Orts-Beneito, N., Fernández-Alcántara, M., García-Sanjuán, S., García-Caro, M. P., & Cabañero-Martínez, M. J. (2019). Level of burden and health-related quality of life in caregivers of palliative care patients. International journal of environmental research and public health, 16(23), 4806. doi:https://doi.org/10.3390/ijerph16234806
Phinney, A. K. (2016). Walking in the neighbourhood: Performing social citizenship in dementia. Dementia, 15(3), 381-394. doi:https://doi.org/10.1177%2F1471301216638180
Pitthayapong, S. T. (2017). A community based program for family caregivers for post stroke survivors in Thailand. Asian Nursing Research,, 11(2), 150-157. doi:https://doi.org/10.1016/j.anr.2017.05.009
Ploeg, J., Markle-Reid, M., Valaitis, R., McAiney, C., Duggleby, W., Bartholomew, A., & Sherifali, D. (2017). Web-based interventions to improve mental health, general caregiving outcomes, and general health for informal caregivers of adults with chronic conditions living in the community: rapid evidence review. Journal of medical Internet research, 19(7), e263.
Ruiz-Fernández, M. D., Hernández-Padilla, J. M., Ortiz-Amo, R., Fernández-Sola, C., Fernández-Medina, I. M., & Granero-Molina, J. (2019). Predictor factors of perceived health in family caregivers of people diagnosed with mild or moderate Alzheimer’s disease. International journal of environmental research and public health, 16(19), 3762.
Sakanashi, S. &. (2017). Empowerment of family caregivers of adults and elderly persons: A concept analysis. International journal of nursing practice, 23(5), 112-126. doi:https://doi.org/10.1111/ijn.12573
Sampaio, A. M.-A. (2020). Physical fitness in institutionalized older adults with dementia: association with cognition, functional capacity and quality of life. Aging clinical and experimental research, 32, 2329-2338. doi:https://doi.org/10.1007/s40520-019-01445-7
Sharma, N. C. (2016). Gender differences in caregiving among family-caregivers of people with mental illnesses. World journal of psychiatry, 6(1), 7-17. doi:https://dx.doi.org/10.5498%2Fwjp.v6.i1.7
Van Bruggen, S. G. (2016). Problems experienced by informal caregivers with older care recipients with and without cognitive impairment. Home health care services quarterly, 35(1), 11-24. doi:https://doi.org/10.1080/01621424.2016.1145166
Vargas, L. M. (2018). Caracterización sociodemográfica y principales afecciones físicas y psicológicas del cuidador informal. Pensamiento Americano, 11(22). doi:https://doi.org/10.21803/pensam.v11i21-1.265
Vásquez, M. D. (2007). Sentido de coherencia, afrontamiento y sobrecarga en cuidadores familiares de ancianos con enfer-medad crónica. Avances en psicología latinoamericana, 25(1), 64-71.
Veloso, V. I. (2016). Caregivers burden in palliative care patients: a problem to tackle. Current opinion in supportive and palliative care, 10(4), 330-335. doi:https://doi.org/10.1097/SPC.0000000000000239
Zarit, S. H.-P. (1980). Relatives of the impaired elderly: correlates of feelings of burden. The gerontologist, 20(6), 649-655. doi:https://doi.org/10.1093/geront/20.6.649
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