Outcomes among family caregivers of aphasic versus nonaphasic stroke survivors

Rehabilitation Nursing

Volumn 31, Issue 1, 2006, Pages 33-42

  Bakas, Tamilyn ^c   Kroenke, Kurt ^c   Plue, Laurie D ^c   Perkins, Susan M ^a   Williams, Linda S ^a,b  

^a INDIANA UNIVERSITY   (United States)

^b Veterans Administration   (United States)

^c NONE

Author keywords

Aphasia; Caregiver; Depression; Outcome; Stroke

Indexed keywords

ADAPTIVE BEHAVIOR; ADULT; AGED; ANALYSIS OF VARIANCE; APHASIA; ARTICLE; CAREGIVER; CEREBROVASCULAR ACCIDENT; COMPARATIVE STUDY; DEPRESSION; FEMALE; FOLLOW UP; HUMAN; MALE; MIDDLE AGED; PSYCHOLOGICAL ASPECT; QUALITY OF LIFE; UNITED STATES; WORKLOAD;

ADAPTATION, PSYCHOLOGICAL; ADULT; AGED; AGED, 80 AND OVER; ANALYSIS OF VARIANCE; APHASIA; CAREGIVERS; CEREBROVASCULAR ACCIDENT; DEPRESSIVE DISORDER; FEMALE; FOLLOW-UP STUDIES; HUMANS; INDIANA; MALE; MIDDLE AGED; QUALITY OF LIFE; WORKLOAD;

EID: 33644859285     PISSN: 02784807     EISSN: None     Source Type: Journal    
DOI: 10.1002/j.2048-7940.2006.tb00008.x     Document Type: Article

References (30)

1. American Heart Association. (2003). 2004 Heart and Stroke Statistical Update. Dallas: Author.
2. Anderson, C. S., Linto, J., & Stewart-Wynne, E. G. (1995). A population-based assessment of the impact and burden of caregiving for long-term stroke survivors. Stroke, 26 (5), 843-849.
3. Bakas, T., Austin, J. K., Jessup, S. L., Williams, L. S., & Oberst, M. T. (2004). Time and difficulty of tasks provided by family caregivers of stroke survivors. Journal of Neuroscience Nursing, 36 (2), 95-106.
4. Bakas, T., Austin, J. K., Okonkwo, K. F., Lewis, R. R., & Chadwick, L. (2002). Needs, concerns, strategies, and advice of stroke caregivers the first 6 months after discharge. Journal of Neuroscience Nursing, 34 (5), 242-251.
5. Bakas, T., & Burgener, S. C. (2002). Predictors of emotional distress, general health, and caregiving outcomes in family caregivers of stroke survivors. Topics in Stroke Rehabilitation, 9 (1), 34-45.
6. Bakas, T., & Champion, V. (1999). Development and psychometric testing of the Bakas Caregiving Outcomes Scale. Nursing Research, 48 (5), 250-259.
7. Booth, S., & Swabey, D. (1999). Group training in communication skills for carers of adults with aphasia. International Journal of Language and Communication Disorders, 34 (3), 291-309.
8. Carey, P. J., Oberst, M. T., McCubbin, M. A., & Hughes, S. H. (1991). Appraisal and caregiving burden in family members caring for patients receiving chemotherapy. Oncology Nursing Forum, 18 (8), 1341-1348.
9. Dewey, H. M., Thrift, A. G., Mihalopoulos, C., Carter, R., Macdonell, R. A., McNeil, J. J., et al. (2002). Informal care for stroke survivors: Results from the North East Melbourne Stroke Incidence Study (NEMESIS). Stroke, 33 (4), 1028-1033.
10. Dorsey, M. K., & Vaca, K. J. (1998). The stroke patient and assessment of caregiver needs. Journal of Vascular Nursing, 16 (3), 62-67.
11. Han, B., & Haley, W. E. (1999). Family caregiving for patients with stroke. Review and analysis. Stroke, 30 (7), 1478-1485.
12. Hartke, R. J., & King, R. B. (2002). Analysis of problem types and difficulty among older stroke caregivers. Topics in Stroke Rehabilitation, 9 (1), 16-33.
13. Kagan, A., Winckel, J., Black, S., Duchan, J. F., Simmons-Mackie, N., & Square, P. (2004). A set of observational measures for rating support and participation in conversation between adults with aphasia and their conversation partners. Topics in Stroke Rehabilitation, 11 (1), 67-83.
14. Kelly-Hayes, M., Robertson, J. T., Broderick, J. P., Duncan, P. W., Hershey, L. A., Roth, E. J., et al. (1998). The American Heart Association Stroke Outcome Classification. Stroke, 29 (6), 1274-1280.
15. Knapp, P., & Hewison, J. (1999). Disagreement in patient and care assessment of functional abilities after stroke. Stroke, 30 (5), 934-938.
16. 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 (9), 606-613.
17. McClenahan, R., & Weinman, J. (1998). Determinants of carer distress in non-acute stroke. International Journal of Language and Communication Disorders, 33 (Suppl.), 138-143.
18. Munro, B. H. (2001). Statistical Methods for Health Care Research (4th ed.). Philadelphia: Lippencott.
19. Oberst, M. T. (1990). Unpublished data.
20. Schulz, R., & Beach, S. R. (1999). Caregiving as a risk factor for mortality: The Caregiver Health Effects Study. Journal of the American Medical Association, 282 (23), 2215-2219.
21. Silliman, R. A., Fletcher, R. H., Earp, J. L., & Wagner, E. H. (1986). Families of elderly stroke patients. Effects of home care. Journal of American Geriatrics Society, 34 (9), 643-648.
22. Spitzer, R. L., Kroenke, K., & Williams, J. B. (1999). Validation and utility of a self-report version of PRIME-MD: The PHQ primary care study. Primary Care Evaluation of Mental Disorders. Patient Health Questionnaire. Journal of the American Medical Association, 282 (18), 1737-1744.
23. Spitzer, R. L., Williams, J. B., Kroenke, K., Hornyak, R., & McMurray, J. (2000). Validity and utility of the PRIME-MD patient health questionnaire in assessment of 3000 obstetric-gynecologic patients: The PRIME-MD Patient Health Questionnaire Obstetrics-Gynecology Study. American Journal of Obstetrics and Gynecology, 183 (3), 759-769.
24. Tabachnick, B. G., & Fidell, L. S. (1996). Using Multivariate Statistics (3rd ed.). New York: HarperCollins.
25. Teri, L., Truax, P., Logsdon, R., Uomoto, J., Zarit, S., & Vitaliano, P. P. (1992). Assessment of behavioral problems in dementia: The revised memory and behavior problems checklist. Psychology and Aging, 7 (4), 622-631.
26. Williams, A. (1994). What bothers caregivers of stroke victims? Journal of Neuroscience Nursing, 26 (3), 155-161.
27. Williams, A. M. (1993). Caregivers of persons with stroke: Their physical and emotional wellbeing. Quality of Life Research, 2 (3), 213-220.
28. Williams, A. M., & Dahl, C. W. (2002). Patient and caregiver perceptions of stroke survivor behavior: A comparison. Rehabilitation Nursing, 27, 19-24.
29. Williams, L. S., Redmon, G., Martinez, B., & Weinberger, M. (2000). Proxy ratings of Stroke-Specific Quality of Life (SS-QOL) scores. Oral abstracts of the 25th International Stroke Conference. Stroke, 31, 301.
30. Williams, L. S., Weinberger, M., Harris, L. E., Clark, D. O., & Biller, J. (1999). Development of a stroke-specific quality of life scale. Stroke, 30 (7), 1362-1369.