In Sickness and in Health: Couples Coping with Stroke across the Life Span

Health and Social Work

Volumn 40, Issue 3, 2015, Pages e92-e100

  McCarthy, Michael J ^a   Bauer, Elizabeth ^a  

^a UNIVERSITY OF CINCINNATI   (United States)

Author keywords

coping; couples; life span; stroke

Indexed keywords

EID: 84939790662     PISSN: 03607283     EISSN: 15456854     Source Type: Journal    
DOI: 10.1093/hsw/hlv043     Document Type: Article

References (43)

1. ATLAS.ti (Version 5.6) [Computer software]. (2009). Berlin: Scientific Software Development.
2. Banks, P., & Pearson, C. (2004). Parallel lives: Younger stroke survivors and their partners coping with crisis. Sexual and Relationship Therapy, 19, 413-429.
3. Bury, M. (1982). Chronic illness as biographical disruption. Sociology of Health & Illness, 4, 167-182.
4. Buschenfeld, K., Morris, R., & Lockwood, S. (2009). The experience of partners of young stroke survivors. Disability & Rehabilitation, 31, 1643-1651.
5. Chumbler, N. R., Rittman, M., Van Puymbroeck, M., Vogel, W. B., Qin, H., & Qnin, H. (2004). The sense of coherence, burden, and depressive symptoms in informal caregivers during the first month after stroke. International Journal of Geriatric Psychiatry, 19, 944-953.
6. Crane, K., & Mooney, M. (2005). Essential tools: Community resource mapping. Minneapolis: National Center on Secondary Education and Transition.
7. Daniel, K., Wolfe, C.D.A., Busch, M. A., & McKevitt, C. (2009). What are the social consequences of stroke for working-aged adults? A systematic review. Stroke, 40, e431-e440.
8. Elliot, D., & Simmons, T. (2011, August). Marital events of Americans: 2009. Washington, DC: U.S. Census Bureau.
9. Graven, C., Sansonetti, D., Moloczij, N., Cadilhac, D., &Joubert, L. (2013). Stroke survivor and carer perspectives of the concept of recovery: A qualitative study. Disability and Rehabilitation, 35, 578-585.
10. Greenwood, N., & Mackenzie, A. (2010). Informal caring for stroke survivors: Meta-ethnographic review of qualitative literature. Maturitas, 66, 268-276.
11. Gustafsson, L., & Bootle, K. (2013). Client and carer experience of transition home from inpatient stroke rehabilitation. Disability and Rehabilitation, 35, 1380-1386.
12. Hackett, M. L., Yapa, C., Parag, V., & Anderson, C. S. (2005). Frequency of depression after stroke. Stroke, 36, 1330-1340.
13. Haley, W. E., Roth, D. L., Howard, G., & Safford, M. M. (2010). Caregiving strain and estimated risk for stroke and coronary heart disease among spouse caregivers: Differential effects by race and sex. Stroke, 41, 331-336.
14. Johnson, P. D. (1998). Rural stroke caregivers: A qualitative study of the positive and negative response to the caregiver role. Topics in Stroke Rehabilitation, 5, 51-68.
15. Jongbloed, L. (1994). Adaptation to a stroke: The experience of one couple. American Journal of Occupational Therapy, 48, 1006-1013.
16. Kautz, D. D., Van Horn, E. R., & Moore, C. (2009). Sex after stroke: An integrative review and recommendations for clinical practice. Critical Reviews in Physical and Rehabilitation Medicine, 21, 99-115.
17. Kelly-Hayes, M., Beiser, A., Kase, C. S., Scaramucci, A., D'Agostino, R. B., & Wolf, P. A. (2003). The influence of gender and age on disability following ischemic stroke: The Framingham Study. Journal of Stroke and Cerebrovascular Diseases, 12, 119-126.
18. Kissela, B. M., Khoury, J. C., Alwell, K., Moomaw, C. J., Woo, D., Adeoye, O., et al. (2012). Age at stroke: Temporal trends in stroke incidence in a large, biracial population. Neurology, 79, 1781-1787.
19. Lawrence, M. (2010). Young adults' experience of stroke: A qualitative review of the literature. British Journal of Nursing, 19, 241-248.
20. Lawrence, M., & Kinn, S. (2013). Needs, priorities, and desired rehabilitation outcomes of family members of young adults who have had a stroke: Findings from a phenomenological study. Disability and Rehabilitation, 35, 586-595.
21. Lee, S., Colditz, G. A., Berkman, L. F., & Kawachi, I. (2003). Caregiving and risk of coronary heart disease in U.S. women. American Journal of Preventive Medicine, 24, 113-119.
22. Lutz, B. J., Young, M. E., Cox, K. J., Martz, C., & Creasy, K. R. (2011). The crisis of stroke: Experiences of patients and their family caregivers. Topics in Stroke Rehabilitation, 18, 786-797.
23. Mailick, M., & Vigilante, F. (1997). The family assessment wheel: A social constructionist perspective. Families in Society, 78, 361-369.
24. McCarthy, M. J., Lyons, K. S., Powers, L. E., & Bauer, E. A. (2013). Gender, health ambiguity, and depression among survivors of first stroke: A pilot study. Archives of Physical Medicine and Rehabilitation, 94, 193-195.
25. McCarthy, M. J., Powers, L. E., & Lyons, K. S. (2011). Poststroke depression: Social workers' role in addressing an underrecognized psychological problem for couples who have experienced stroke. Health &Social Work, 36, 139-148.
26. rd ed., pp. 375-398). New York: Guilford Press.
27. Moon, H., & Adams, K. B. (2012). The effectiveness of dyadic interventions for people with dementia and their caregivers. Dementia, 12, 821-839.
28. Moore, L. W., Maiocco, G., Schmidt, S. M., Guo, L., &Estes, J. (2002). Perspectives of caregivers of stroke survivors: Implications for nursing. Medsurg Nursing, 11, 289-295.
29. National Stroke Association. (2003). National Stroke Association's complete guide to stroke. Retrieved from https://www.academia.edu/6010090/National-Stroke-Associations-Complete-Guide-to-Stroke
30. Patton, M. Q. (1999). Enhancing the quality and credibility of qualitative analysis. Health Services Research, 34(5, Pt. 2), 1189-1208.
31. th ed., pp. 351-385). New York: Springer.
32. Price, B. (2011). How to map a patient's social support network. Nursing Older People, 23(2), 28-35.
33. Reed, M. C., Wood, V., Harrington, R., & Paterson, J. (2012). Developing stroke rehabilitation and community services: A meta-synthesis of qualitative literature. Disability and Rehabilitation, 34, 553-563.
34. Regan, T. W., Lambert, S. D., Girgis, A., Kelly, B., Kayser, K., & Turner, J. (2012). Do couple-based interventionsmake a difference for couples affected by cancer? A systematic review. BMC Cancer, 12, 279.
35. Roding, J., Lindstrom, B., Malm, J., & Ohman, A. (2003). Frustrated and invisible - Younger stroke patients experiences of the rehabilitation process. Disability and Rehabilitation, 25, 867-874.
36. Roger, V. L., Go, A. S., Lloyd-Jones, D. M., Adams, R. J., Berry, J. D., Brown, T. M., et al. (2012). Heart disease and stroke statistics - 2011 update: A report from the American Heart Association. Circulation, 123, e18-e209.
37. Saban, K. L., & Hogan, N. S. (2012). Female caregivers of stroke survivors: Coping and adapting to a life that once was. Journal of Neuroscience Nursing, 44, 2-14.
38. Schulz, R., & Beach, S. R. (1999). Caregiving as a risk factor for mortality: The caregiver health effects study. JAMA, 282, 2215-2219.
39. Strauss, A., & Corbin, J. (1990). Basics of qualitative research: Grounded theory procedures and techniques. Newbury Park: Sage Publications.
40. Teasell, R. W., McRae, M. P., & Finestone, H. M. (2000). Social issues in the rehabilitation of younger stroke patients. Archives of Physical Medicine and Rehabilitation, 81, 205-209.
41. Thorne, S., Kirkham, S. R., & MacDonald-Emes, J. (1997). Interpretive description: A noncategorical qualitative alternative for developing nursing knowledge. Research in Nursing & Health, 20, 169-177.
42. U.S. Census Bureau. (2013, August). Frequently asked questions about same-sex couple households: Fertility and family statistics branch. Retrieved from http://www.census.gov/hhes/samesex/
43. Wang, W. (2012, February 16). The rise of intermarriage: Rates, characteristics vary by race and gender. Washington, DC: Pew Research Center.