Impact of Noncaregiving-Related Stressors on Informal Caregiver Outcomes

dc.contributor.authorAustrom, Mary Guerriero
dc.contributor.authorLu, Yvonne Yueh-Feng
dc.contributor.authorPerkins, Anthony J.
dc.contributor.authorBoustani, Malaz
dc.contributor.authorCallahan, Christopher M.
dc.contributor.authorHendrie, Hugh C.
dc.contributor.departmentDepartment of Psychiatry, IU School of Medicineen_US
dc.date.accessioned2016-05-10T16:55:30Z
dc.date.available2016-05-10T16:55:30Z
dc.date.issued2014-08
dc.description.abstractBACKGROUND: Caregivers of persons with dementia are stressed. Stressors not related to care recipients' needs impact caregiver outcomes, yet are seldom reported. The purpose of this study was to report the most stressful events experienced by spouse caregivers of older adults with Alzheimer s disease during a 6-month period. METHODS: 31 caregivers completed the Most Stressful Event form, Patient Health Questionnaire (PHQ-9) and the Revised Memory Behavioral Problem Checklist (R-MBPC). Fisher's exact test and two-sample t-test were used to compare Most Stressful Events between caregivers. ANOVA model tested whether the PHQ-9 and R-MBPC subscales differed by stressor. RESULTS: Caregivers reported no stressors 21.5% of the time, 1-2 stressors 25% of the time, and 3 stressors 53% of the time with 318 stressors reported in total. Care recipient needs (30.2%), caregiver needs (26.7%), and decision-making (16.7%) were the most frequently reported stressors. Using a mixed effects model, there were associations between the Most Stressful Events and depression (p = 0.016), mobility (p = 0.024) and caregiver issues (p = 0.009) subscales of R-MBPC. CONCLUSION: Results can be used to develop targeted intervention and support strategies for spouse caregivers experiencing non-caregiving related stressorsas well as the traditional challenges with caregiving related issues.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationAustrom, M. G., Lu, Y. Y.-F., Perkins, A. J., Boustani, M., Callahan, C. M., & Hendrie, H. C. (2014). Impact of Non-caregiving Related Stressors on Informal Caregiver Outcomes. American Journal of Alzheimer’s Disease and Other Dementias, 29(5), 426–432. http://doi.org/10.1177/1533317513518652en_US
dc.identifier.issn1938-2731en_US
dc.identifier.urihttps://hdl.handle.net/1805/9562
dc.language.isoen_USen_US
dc.publisherSage Publicationsen_US
dc.relation.isversionof10.1177/1533317513518652en_US
dc.relation.journalAmerican Journal of Alzheimer's Disease and Other Dementiasen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectcaregiversen_US
dc.subjectdementiaen_US
dc.subjectDepressionen_US
dc.subjectnoncaregiving-related stressorsen_US
dc.subjectAlzheimer Diseaseen_US
dc.titleImpact of Noncaregiving-Related Stressors on Informal Caregiver Outcomesen_US
dc.typeArticleen_US
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