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Differential effects of patient symptom subtypes on informal hospice caregiver depression

Published online by Cambridge University Press:  31 January 2017

Chelsey M. Wilkes
Affiliation:
Rosalind Franklin University of Medicine and Science, North Chicago, Illinois
Karla T. Washington*
Affiliation:
University of Missouri, Columbia, Missouri
William M. Palmer
Affiliation:
Harry S. Truman Memorial Veterans Hospital, Columbia, Missouri
Debra Parker Oliver
Affiliation:
University of Missouri, Columbia, Missouri
George Demiris
Affiliation:
University of Washington, Seattle, Washington
Kevin Craig
Affiliation:
University of Missouri, Columbia, Missouri
*
Address correspondence and reprint requests to: Karla T. Washington, Department of Family and Community Medicine, University of Missouri, MA306 Medical Sciences Building, DC032.00 Columbia, Missouri, 65212. E-mail: WashingtonKar@health.missouri.edu.

Abstract

Objective:

Researchers sought to determine the extent to which burden related to patients' symptom subtypes could predict informal hospice caregiver depression, and to illustrate the differences between caregivers who experience suicidal ideation and those who do not.

Method:

Informal caregivers recruited from a not-for-profit community-based hospice agency participated in a cross-sectional survey. Self-report questionnaires assessed caregiver burden associated with patient symptomatology (via a modified version of the Memorial Symptom Assessment Scale–Short Form) and caregiver depressive symptoms, including suicidal ideation (measured by the Patient Health Questionnaire–9). Multiple regressions evaluated the unique predictability of patients' symptom subtypes on caregiver depression. Exploratory analyses examined mean differences of study variables between participants who did and did not endorse suicidal ideation.

Results:

Caregiver burden related to patients' psychological symptoms accounted for significant variance in caregiver depression scores when controlling for burden related to physical symptoms. Among 229 caregivers (M age = 61.4 years), 12 reported suicidal ideation, where 6 of the 12 were male, despite male caregivers comprising less than 20% of the total sample.

Significance of results:

Burden associated with patients' psychological symptoms uniquely contributed to caregiver depression, further highlighting the clinical utility and necessity for hospice providers to address the emotional needs of patients and their caregivers alike. Developing clinical procedures to identify and respond to such needs would not only behoove hospice agencies, but it would likely enhance the caregiving experience holistically, which might be particularly imperative for male caregivers.

Type
Original Article
Copyright
Copyright © Cambridge University Press 2017 

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References

REFERENCES

Abbott, C.H., Prigerson, H.G. & Maciejewski, P.K. (2014). The influence of patients' quality of life at the end of life on bereaved caregivers' suicidal ideation. Journal of Pain and Symptom Management, 48(3), 459464. Epub ahead of print Dec 8, 2013. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048331/pdf/nihms537890.pdf.Google Scholar
Beck, A.T., Weissman, A., Lester, D., et al. (1974). The measurement of pessimism: The hopelessness scale. Journal of Consulting and Clinical Psychology, 42(6), 861865.CrossRefGoogle ScholarPubMed
Bevans, M. & Sternberg, E.M. (2012). Caregiving burden, stress, and health effects among family caregivers of adult cancer patients. The Journal of the American Medical Association, 307(4), 398403. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3304539/pdf/nihms-355747.pdf.CrossRefGoogle ScholarPubMed
Chang, V.T., Hwang, S.S., Feuerman, M., et al. (2000). The Memorial Symptom Assessment Scale–Short Form (MSAS–SF). Cancer, 89(5), 11621171.3.0.CO;2-Y>CrossRefGoogle ScholarPubMed
Chentsova-Dutton, Y., Shucter, S., Hutchin, S., et al. (2000). The psychological and physical health of hospice caregivers. Annals of Clinical Psychiatry, 12(1), 1927.Google Scholar
Clark, P.C. & King, K.B. (2003). Comparison of family caregivers: Stroke survivors vs. persons with Alzheimer's disease. Journal of Gerontological Nursing, 29(2), 4553.CrossRefGoogle ScholarPubMed
Cohen, C.A., Colantonio, A. & Vernich, L. (2002). Positive aspects of caregiving: Rounding out the caregiver experience. International Journal of Geriatric Psychiatry, 17(2), 184188.Google Scholar
Fassberg, M.M., Cheung, G., Canetto, S.S., et al. (2016). A systematic review of physical illness, functional disability, and suicidal behaviour among older adults. Aging & Mental Health, 20(2), 166194. Epub ahead of print Sep 18, 2015. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720055/pdf/camh-20-166.pdf.Google Scholar
Fiske, A., Smith, M. & Price, E. (2015). Suicidal behavior in older adults. In APA handbook of clinical geropsychology, Vol. 2: Assessment, treatment, and issues of later life. Lichtenberg, P.A. et al. (eds.), pp. 145172. Washington, DC: American Psychological Association.CrossRefGoogle Scholar
Garlo, K., O'Leary, J.R., Van Ness, P.H., et al. (2010). Burden in caregivers of older adults with advanced illness. Journal of the American Geriatrics Society, 58(12), 23152322. Epub ahead of print Nov 18. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058825/pdf/nihms240985.pdf.CrossRefGoogle ScholarPubMed
George, L.K. & Gwyther, L.P. (1986). Caregiver well-being: A multidimensional examination of family caregivers of demented adults. The Gerontologist, 26(3), 253259.Google Scholar
Given, B., Wyatt, G., Given, C., et al. (2004). Burden and depression among caregivers of patients with cancer at the end of life. Oncology Nursing Forum, 31(6), 11051117. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1315286/pdf/nihms4363.pdf.CrossRefGoogle ScholarPubMed
Grov, E.K. & Valeberg, B.T. (2012). Does the cancer patient's disease stage matter? A comparative study of caregivers' mental health and health related quality of life. Palliative & Supportive Care, 10(03), 189196. Epub ahead of print Mar 22.Google Scholar
Hudson, P.L., Aranda, S. & Kristjanson, L.J. (2004). Meeting the supportive needs of family caregivers in palliative care: Challenges for health professionals. Journal of Palliative Medicine, 7(1), 1925.Google Scholar
Kim, Y. & Schulz, R. (2008). Family caregivers' strains: Comparative analysis of cancer caregiving with dementia, diabetes, and frail elderly caregiving. Journal of Aging and Health, 20(5), 483503. Epub ahead of print Apr 17. Available from http://journals.sagepub.com/doi/pdf/10.1177/0898264308317533.Google Scholar
Kroenke, K., Spitzer, R.L. & Williams, J.B. (2001). The PHQ–9: Validity of a brief depression severity measure. Journal of General Internal Medicine, 16, 606613. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1495268/pdf/jgi_01114.pdf.CrossRefGoogle ScholarPubMed
Kroenke, K., Spitzer, R.L., Williams, J.B., et al. (2010). The Patient Health Questionnaire Somatic, Anxiety, and Depressive Symptom Scales: A systematic review. General Hospital Psychiatry, 32(4), 345359. Epub ahead of print May 7.Google Scholar
Lindenbaum, K., Stroka, M.A. & Linder, R. (2014). Informal caregiving for elderly people with mental illnesses and the mental health of the informal caregivers. Journal of Mental Health Policy and Economics, 17(3), 99105.Google ScholarPubMed
Lobchuk, M.M. & Vorauer, J.D. (2003). Family caregiver perspective-taking and accuracy in estimating cancer patient symptom experiences. Social Science & Medicine, 57(12), 23792384.Google Scholar
Malouff, J.M., Thorsteinsson, E.B. & Schutte, N.S. (2007). The efficacy of problem solving therapy in reducing mental and physical health problems: A meta-analysis. Clinical Psychology Review, 27(1), 4657. Epub ahead of print Feb 9, 2006. Available from https://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0024910/.Google Scholar
McMillan, S.C., Small, B.J., Weitzner, M., et al. (2006). Impact of coping skills intervention with family caregivers of hospice patients with cancer. Cancer, 106(1), 214222.Google Scholar
Nielsen, M., Hansen, J., Ritz, B., et al. (2014). Cause-specific mortality among spouses of Parkinson disease patients. Epidemiology, 25(2), 225232.Google Scholar
O'Dwyer, S.T., Moyle, W., Pachana, N.A., et al. (2014). Feeling that life is not worth living (death thoughts) among middle-aged, Australian women providing unpaid care. Maturitas, 77(4), 375379. Available from http://www.maturitas.org/article/S0378-5122(14)00048-6/pdf.Google Scholar
O'Riley, A.A. & Fiske, A. (2012). Emphasis on autonomy and propensity for suicidal behavior in younger and older adults. Suicide & Life-Threatening Behavior, 42(4), 394404. Epub ahead of print May 14. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134248/pdf/nihms-812861.pdf.Google Scholar
Parker Oliver, D., Washington, K., Smith, J., et al. (2016). The prevalence and risks for depression and anxiety in hospice caregivers. Journal of Palliative Medicine, Epub ahead of print Dec 2.Google ScholarPubMed
Pinquart, M. & Sörensen, S. (2006). Gender differences in caregiver stressors, social resources, and health: An updated meta-analysis. The Journals of Gerontology. Series B, Psychological Sciences and Social Sciences, 61(1), P33P45. Available from http://psychsocgerontology.oxfordjournals.org/content/61/1/P33.full.pdf+html.Google Scholar
Portenoy, R.K., Thaler, H.T., Kornblith, A.B., et al. (1994). The Memorial Symptom Assessment Scale: An instrument for the evaluation of symptom prevalence, characteristics and distress. European Journal of Cancer, 30(9), 13261336. Available from http://home.uchicago.edu/~tmurray1/research/articles/printed%20and%20read/the%20Memorial%20Symptom%20Assessment%20Scale_an%20instrument%20for%20the%20evaluation%20of%20symptom%20prevalence,%20characteristics%20and%20distress.pdf.Google Scholar
Ratkowski, K.L., Washington, K.T., Craig, K.W., et al. (2015). The stress of sadness: The most stressful symptoms for hospice family caregivers. The American Journal of Hospice & Palliative Care, 32(7), 745749. Epub ahead of print Jun 30, 2014. Available from http://journals.sagepub.com/doi/pdf/10.1177/1049909114540034.Google Scholar
Sarna, L. & Brecht, M.L. (1997). Dimensions of symptom distress in women with advanced lung cancer: A factor analysis. Heart & Lung: The Journal of Critical Care, 26(1), 2330.Google Scholar
Sautter, J.M., Tulsky, J.A., Johnson, K.S., et al. (2014). Caregiver experience during advanced chronic illness and last year of life. Journal of the American Geriatrics Society, 62(6), 10821090. Epub ahead of print May 6. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4070184/pdf/nihms574832.pdf.Google Scholar
Schulz, R., Hebert, R.S., Dew, M.A., et al. (2007). Patient suffering and caregiver compassion: New opportunities for research, practice, and policy. The Gerontologist, 47(1), 413. Available from http://gerontologist.oxfordjournals.org/content/47/1/4.long.CrossRefGoogle ScholarPubMed
Spitzer, R.L., Williams, J.B., Kroenke, K., et al. (1994). Utility of a new procedure for diagnosing mental disorders in primary care: The PRIME–MD 1000 study. The Journal of the American Medical Association, 272(22), 17491756.Google Scholar
Stajduhar, K., Funk, L., Toye, C., et al. (2010). Part 1: Home-based family caregiving at the end of life: A comprehensive review of published quantitative research (1998–2008). Palliative Medicine, 24(6), 573593. Epub ahead of print Jun 18. Available from http://journals.sagepub.com/doi/pdf/10.1177/0269216310371412.Google Scholar
Stansfeld, S., Smuk, M., Onwumere, J., et al. (2014). Stressors and common mental disorder in informal carers: An analysis of the English Adult Psychiatric Morbidity Survey 2007. Social Science & Medicine, 120, 190198. Epub ahead of print Sep 16. Available from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4224501/.CrossRefGoogle ScholarPubMed
Tarlow, B.J., Wisniewski, S.R., Belle, S.H., et al. (2004). Positive aspects of caregiving: Contributions of the REACH Project to the development of new measures for Alzheimer's caregiving. Research on Aging, 26(4), 429453. Available from https://www.researchgate.net/publication/249630647_Positive_Aspects_of_Caregiving_Contributions_of_the_REACH_Project_to_the_Development_of_New_Measures_for_Alzheimer's_Caregiving.Google Scholar
Washington, K.T., Albright, D.L., Parker Oliver, D., et al. (2016). Hospice and palliative social workers' experiences with clients at risk of suicide. Palliative & Supportive Care, 14(6), 664671. Epub ahead of print May 23.Google Scholar
Weitzner, M.A., McMillan, S.C. & Jacobsen, P.B. (1999). Family caregiver quality of life: Differences between curative and palliative cancer treatment settings. Journal of Pain and Symptom Management, 17(6), 418428. Available from http://www.jpsmjournal.com/article/S0885-3924(99)00014-7/pdf.Google Scholar
Wilkinson, A.M. & Lynn, J. (2005). Caregiving for advanced chronic illness patients. Techniques in Regional Anesthesia & Pain Management, 9(3), 122132.Google Scholar