| 195 7 References 1. Potkin SG. The ABC of Alzheimer’s Disease: ADL and Improving Day-to-Day Functioning of Patients. International Psychogeriatrics. 2002;14(S1):7-26. 2. Abreu W, Tolson D, Jackson GA, Costa N. A cross-sectional study of family caregiver burden and psychological distress linked to frailty and functional dependency of a relative with advanced dementia. Dementia. 2020;19(2):301-18. 3. Gauthier L, Gauthier S. Assessment of Functional Changes in Alzheimer’s Disease. Neuroepidemiology. 1990;9(4):183-8. 4. Wimo A, Gauthier S, Prince M. Global estimates of informal care. London: Alzheimer’s Disease International (ADI),; 2018 July 2018. 5. Brimblecombe N, Pickard L, King D, Knapp M. Perceptions of unmet needs for community social care services in England. A comparison of working carers and the people they care for. Health Soc Care Community. 2017;25(2):435-46. 6. Collins RN, Kishita N. Prevalence of depression and burden among informal care-givers of people with dementia: a meta-analysis. Ageing and Society. 2020;40(11):2355-92. 7. Srivastava G, Tripathi RK, Tiwari SC, Singh B, Tripathi SM. Caregiver Burden and Quality of Life of Key Caregivers of Patients with Dementia. Indian Journal of Psychological Medicine. 2016;38(2):133-6. 8. Di Lorito C, Bosco A, Godfrey M, Dunlop M, Lock J, Pollock K, et al. Mixed-Methods Study on Caregiver Strain, Quality of Life, and Perceived Health. Journal of Alzheimer’s Disease. 2021;80:799-811. 9. Miyamoto Y, Tachimori H, Ito H. Formal Caregiver Burden in Dementia: Impact of Behavioral and Psychological Symptoms of Dementia and Activities of Daily Living. Geriatric Nursing. 2010;31(4):246-53. 10. Liu Z, Heffernan C, Tan J. Caregiver burden: A concept analysis. International Journal of Nursing Sciences. 2020;7(4):438-45. 11. Etters L, Goodall D, Harrison BE. Caregiver burden among dementia patient caregivers: A review of the literature. Journal of the American Academy of Nurse Practitioners. 2008;20(8):423-8. 12. Tokovska M, Nour MM, Sørensen A, Småland Goth U. Informal Caregivers and Psychosocial Support: Analysis of European Dementia Policy documents. Journal of Public Health Research. 2022;11(1):jphr.2021.416. 13. Wiegelmann H, Speller S, Verhaert L-M, Schirra-Weirich L, Wolf-Ostermann K. Psychosocial interventions to support the mental health of informal caregivers of persons living with dementia – a systematic literature review. BMC Geriatrics. 2021;21(1):94. 14. Egan KJ, Pinto-Bruno ÁC, Bighelli I, Berg-Weger M, van Straten A, Albanese E, et al. Online Training and Support Programs Designed to Improve Mental Health and Reduce Burden Among Caregivers of People With Dementia: A Systematic Review. Journal of the American Medical Directors Association. 2018;19(3):200-6.e1. 15. Poon E. A Systematic Review and Meta-Analysis of Dyadic Psychological Interventions for BPSD, Quality of Life and/or Caregiver Burden in Dementia or MCI. Clinical Gerontologist. 2022;45(4):77797. 16. Sun Y, Ji M, Leng M, Li X, Zhang X, Wang Z. Comparative efficacy of 11 non-pharmacological interventions on depression, anxiety, quality of life, and caregiver burden for informal caregivers of people with dementia: A systematic review and network meta-analysis. International Journal of Nursing Studies. 2022;129:104204. 17. Christie HL, Bartels SL, Boots LMM, Tange HJ, Verhey FRJ, de Vugt ME. A systematic review on the implementation of eHealth interventions for informal caregivers of people with dementia. Internet Interventions. 2018;13:51-9. 18. Lethin C, Hallberg IR, Karlsson S, Janlöv A-C. Family caregivers experiences of formal care when caring for persons with dementia through the process of the disease. Scandinavian Journal of Caring Sciences. 2016;30(3):526-34.
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