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Mohammed T. Abou-Saleh

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760 PRINCIPLES AND PRACTICE OF GERIATRIC PSYCHIATRYWhen caregivers lack the necessary skills to manageproblematic behaviors effectively, care recipient behaviorsoften escalate, leading to increased levels of confusion andagitation 23,103 that have been cited as the primary reasons forinstitutionalizing a family member with dementia 46,119,120 . Consideringthe psychological and financial expense associated withplacing a person with dementia in an institutional setting,interventions which help caregivers in the prevention and/ormanagement of behavioral problems are both timely andsignificant. In support of this position, the 1993 Report of theAdvisory Panel on Alzheimer’s Disease recommends thatemphasis be directed toward health services research thatfocuses on reducing the burdens of care for family membersof persons with dementia.Although our understanding of the dementias and the severenegative consequences of caregiving for this population hasgrown, too little research has focused on the development,implementation and evaluation of interventions, especially forfamily caregivers. The American Association for GeriatricPsychiatry, the Alzheimer’s Association and the AmericanGeriatrics Society, in consensus, state: ‘‘Interventions thatreduce the risk of caregiver depression and improve toleranceand the capacity to care for patients in the home, includingeducational materials, counseling support groups, day care andrespite care, are among the most promising areas for futureresearch’’ 121 .CONCLUSIONCaring for a person with cognitive impairment is chronicallystressful. For persons with dementia, caregiving can last anaverage of 15 years, with the task being a demanding and oftenoverwhelming experience 62 . This chapter has summarized theresearch on family caregiving of persons with dementia in thecommunity setting. Informal caregiving, mostly by familymembers, of elders with chronic illnesses and disabilities hasincreased during the past two decades due to growth in theproportion of elders in the population, shorter hospital stays,advancing technologies that forestall mortality, and continuinghigher costs of health care, with limited reimbursement ofcaregiving by professionals in the home. As a result, the impactof informal caring on family members quickly became a concernof health professionals and social and behavioral researchers,especially in the context of dementia caregiving. After two decadesof extensive attention by the public and researchers, there is someconsensus that, while there are both negative and positive effectsof informal caregiving, outcomes are different depending uponcharacteristics of the caregiver and the care recipient. Moreover,different interventions are effective in ameliorating negativecaregiver outcomes for specific caregiver and care recipientcontingencies.REFERENCES1. Doty P. Family care of the elderly: the role of public policy. MilbankQuarterly 1986; 64: 34–75.2. Daniels M, Irwin M. Caregiver stress and well-being. In Light BDLE,ed., Alzheimer’s Disease Treatment and Family Stress: Directions forResearch. New York: Hemisphere, 1990; 292–309.3. Grant I, Patterson T, Hauger R, Irwin M. Current research ondementia and Alzheimer’s disease. Arch Psychiat 1992; 4(suppl): 77–80.4. Mittelman MS, Ferris SH, Shulman E et al. A family intervention todelay nursing home placement of patients with Alzheimer’s disease. JAm Med Assoc 1996; 276: 1725–31.5. Buckwalter KC. Report of the advisory panel on Alzheimer’s disease.Arch Psychiat Nurs 1989; 3: 358–62.6. MaloneBeach EE, Zarit SH. Current research issues in caregiving tothe elderly. Int J Aging Hum Dev 1991; 32: 103–4.7. Walker AJ, Pratt CC, Eddy L. Informal caregiving to aging familymembers: a critical review. Fam Relat 1995; 44: 402–11.8. Horowitz A. Family caregiving to the frail elderly. In Eisdorfor, ed.,Annual Review of Gerontology and Geriatrics. New York: Springer,1985; 194–246.9. Kramer BJ, Kipnis S. Eldercare and work-role conflict: toward anunderstanding of gender differences in caregiver burden. Gerontologist1995; 35: 340–8.10. Miller B, Cafasso L. Gender differences in caregiving: fact or artifact?The Gerontologist 1992; 32: 498–507.11. Tennstedt SL, Crawford S, McKinley JB. Determining the pattern ofcommunity care: is coresidence more important than caregiverrelationship? J Gerontol 1993; 48: 574–83.12. Ford GR, Goode KT, Barrett JJ et al. Gender roles and caregivingstress: an examination of subjective appraisals of specific primarystressors in Alzheimer’s caregivers. Aging Ment Health 1997; 1: 158–65.13. Day AT. Who cares? Demographic trends challenge family care forthe elderly. Populat Trends Publ Policy 1985; 9: 1–17.14. United States Administration on Aging (AOA). Aging Research &Training News. Silver Springs: Business Publishers, 1999.15. Baumgarten M, Battista RN, Infante-Rivard C et al. Thepsychological and physical health of family members caring for anelderly person with dementia. J Clin Epidemiol 1992; 45: 61–70.16. Schulz R, Visintainer P, Williamson GM. Psychiatric and physicalmorbidity effects of caregiving. J Gerontol 1990; 45: 181–91.17. Dunkin JJ, Hanley CA. Dementia caregiver burden: a review of theliterature and guidelines for assessment and intervention. Neurology1998; 51(suppl 1): S53–60.18. Montgomery RJV, Gonyea JG, Hooyman NR. Caregiving and theexperience of subject burden. Fam Relat 1985; 34: 19–26.19. George LK, Gwyther LP. Caregiver well-being: a multidimensionalexamination of family caregivers of demented adults. Gerontologist1986; 26: 253–9.20. Kuhlman GJ, Wilson HS, Hutchinson SA, Wallhagen M. Alzheimer’sdisease and family caregiving: critical synthesis of the literature andresearch agenda. Nurs Res 1991; 40; 331–7.21. Pushkar-Gold D, Reis MF, Markiewicz D, Andres D. When homecaregiving ends: a longitudinal study of outcomes for caregivers ofrelatives with dementia. J Am Geriat Soc 1995; 43: 10–16.22. Chick N, Meleisa. Nursing Research Methodology: Issues inImplementation. Rockville: Aspen, 1986.23. Hall GR, Buckwalter KC. Progressively lowered stress threshold: Aconceptual model for care of adults with Alzheimer’s disease. ArchPsychiat Nurs 1987; 1: 399–406.24. Kahana E. A Congruence Model of Person–Environment Interaction.Washington, DC: Gerontological Society, 1975.25. Hardy M, Conway M. Role Therapy: Perspectives for HealthProfessionals. New York: Appleton-Century-Crofts, 1978.26. Lawton M. Competence, Environmental Press, and the Adaptation ofOlder People. Washington, DC: Gerontological Society, 1975.27. Parr J. The interaction of persons and living arrangements. In PoonLW, ed., Aging in the 1980’s: Psychological Issues. Washington, DC,1980.28. Pearlin LI, Mullan JT, Skaff MM. Caregiving and the stress process:an overview of concepts and their measures. Gerontologist 1990; 30:583–94.29. Hadjistavropoulos T, Taylor S, Tuokko H, Beattie BL. Neuropsychologicaldeficits, caregivers’ perceptions of deficits and caregiverburden. J Am Geriat Soc 1994; 42: 308–14.30. Vitaliano PP, Russo J, Young HM et al. Predictors of burden inspouse caregivers of individuals with Alzheimer’s disease. PsycholAging 1991; 6; 392–402.31. Stephens MAP, Kinney JM. Caregiver stress instruments: assessmentof content and measurement quality. Gerontol Rev 1989; 2: 40–54.32. Vitaliano PP, Maiuro RD, Ochs H, Russo J. A Model of Burden inCaregivers of DAT Patients. DHHS Publication No. (ADM)89-1569.Bethesda, MD: National Institutes of Health, 1989.33. Light E, Lebowitz BD. Alzheimer’s Disease Treatment and FamilyStress: Directions for Future Research. Rockville: National Instituteof Mental Health, 1989.

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