Literature DB >> 8288146

Hispanic culture and family care of Alzheimer's patients.

C Cox1, A Monk.   

Abstract

Caring for Alzheimer's patients places tremendous burdens and strain on families. This study examined the ways cultural values and norms influence the experiences of Hispanic caregivers. The results revealed relationships between attitudes toward caregiving and a sense of burden and depression among the caregivers, with depression being related to stronger adherence to norms of filial support. Factors associated with increased burden include lack of time for oneself, dependency needs of the patient, and belief that one could be doing a better job as caregiver. Problems common to other groups of caregivers--feelings of anger, relationship and financial strain, and isolation--were not apparent. Although relatives provide affective support, the burden of instrumental assistance rests on the primary caregiver. These findings, as well as a reluctance to discuss problems outside of the family, call for active social work interventions.

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Mesh:

Year:  1993        PMID: 8288146     DOI: 10.1093/hsw/18.2.92

Source DB:  PubMed          Journal:  Health Soc Work        ISSN: 0360-7283


  15 in total

Review 1.  Ethnicity and dementia.

Authors:  D G Harwood; R L Ownby
Journal:  Curr Psychiatry Rep       Date:  2000-02       Impact factor: 5.285

2.  Obtaining family consent for participation in Alzheimer's research in a Cuban-American population: strategies to overcome the barriers.

Authors:  C L Williams; R Tappen; C Buscemi; R Rivera; J Lezcano
Journal:  Am J Alzheimers Dis Other Demen       Date:  2001 May-Jun       Impact factor: 2.035

3.  Adult caregiving among American Indians: the role of cultural factors.

Authors:  R Turner Goins; S Melinda Spencer; Lisa C McGuire; Jack Goldberg; Yang Wen; Jeffrey A Henderson
Journal:  Gerontologist       Date:  2010-12-09

Review 4.  Reviews: developing culturally sensitive dementia caregiver interventions: are we there yet?

Authors:  Anna M Napoles; Letha Chadiha; Rani Eversley; Gina Moreno-John
Journal:  Am J Alzheimers Dis Other Demen       Date:  2010-05-27       Impact factor: 2.035

5.  Emotional and physical health of informal caregivers of residents at the end of life: the role of social support.

Authors:  Sharon Wallace Williams; Christianna S Williams; Sheryl Zimmerman; Jean Munn; Debra Dobbs; Philip D Sloane
Journal:  J Gerontol B Psychol Sci Soc Sci       Date:  2008-05       Impact factor: 4.077

6.  Characteristics and mental health of Hispanic dementia caregivers in New York City.

Authors:  José A Luchsinger; Dante Tipiani; Gabriela Torres-Patiño; Stephanie Silver; Joseph P Eimicke; Mildred Ramirez; Jeanne Teresi; Mary Mittelman
Journal:  Am J Alzheimers Dis Other Demen       Date:  2015-01-29       Impact factor: 2.035

7.  Caregiving in Dementia and its Impact on Psychological Functioning and Health-Related Quality of Life: Findings from a Colombian Sample.

Authors:  Jhon Alexander Moreno; Elizabeth Nicholls; Natalia Ojeda; Carlos José De los Reyes-Aragón; Diego Rivera; Juan Carlos Arango-Lasprilla
Journal:  J Cross Cult Gerontol       Date:  2015-12

8.  Predictors of institutionalization in Latinos with dementia.

Authors:  Joseph E Gaugler; Robert L Kane; Rosalie A Kane; Robert Newcomer
Journal:  J Cross Cult Gerontol       Date:  2006 Sep-Dec

9.  Transfers of informal care time in the United States: the role of demographic differentials in intergenerational flows by age, sex, and racial and national background.

Authors:  Denys Dukhovnov; Emilio Zagheni
Journal:  Vienna Yearb Popul Res       Date:  2019-12-03

10.  Activities of daily living in Mexican American caregivers: the key to continuing informal care.

Authors:  Bronwynne C Evans; Michael J Belyea; David W Coon; Ebere Ume
Journal:  J Fam Nurs       Date:  2012-06-26       Impact factor: 3.818

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