The burden of caregivers of patients after stroke;Obciażenie osób sprawujacych opieke nad chorymi po przebytym udarze mózgu

Udar Mozgu - Problemy Interdyscyplinarne

Volumn 8, Issue 1, 2006, Pages 42-47

  Grabowska Fudala, Barbara ^a   Jaracz, Krystyna ^a  

^a POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

Author keywords

Burden; Caregivers; Stroke

Indexed keywords

BARTHEL INDEX; CAREGIVER BURDEN; DAILY LIFE ACTIVITY; EMPIRICAL RESEARCH; FRENCHAY ACTIVITIES INDEX; FUNCTIONAL ASSESSMENT; HUMAN; INTERVIEW; MENTAL STRESS; NOTTINGHAM EXTENDED ACTIVITIES OF DAILY LIVING SCALE; PHYSICAL STRESS; PROFESSIONAL COMPETENCE; QUESTIONNAIRE; RANKIN SCALE; RATING SCALE; REVIEW; STROKE;

EID: 33750381254     PISSN: 15056740     EISSN: 16443292     Source Type: Journal    
DOI: None     Document Type: Review

References (42)

1. Czloukowska A., Ryglewicz D., Weissbein T., Baranska-Gieruszczak M., Hier D.B.: A prospective community-based study of stroke in Warsaw, Poland. Stroke 1994, 25, 547-551.
2. Kozubski W.: Choroby naczyniowe układu nerwowego. W: Kozubski W., Liberski P.P. (red.): Choroby układu nerwowego. Wydawnictwo Lekarskie PZWL. Warszawa 2004, 101-145.
3. Sacco R.L., Benjamin E.J., Broderick J.P. i wsp.: Risk factors. Stroke 1997, 28, 1507-1517.
4. Elmståhl S., Malmberg B., Annerstendt L.: Caregiver's burden of patients 3 years after stroke assessed by a novel caregiver burden scale. Arch. Phys. Med. Rehabil. 1996, 77, 177-182.
5. Jönsson A.C., Lindgren L, Hallström B., Norrving B., Lindgren A.: Determinants of quality of life in stroke survivors and their informal caregivers. Stroke 2005, 36, 803-808.
6. Smith L.N., Norrie J., Kerr S.M., Lawrence M., Langhorne P., Lees K.R.: Impact and influences on caregiver outcomes at one year post-stroke. Cerebrovasc. Dis. 2004, 18, 145-153.
7. Evans R.L.: Caregiver compliance and feelings of burden in poststroke home care. Psychol. Rep. 1986, 59, 1013-1014.
8. Pearlin L.I., Mullan J.T., Semple S.J., Skaff M.M.: Caregiving and the stress process: an overview of concepts and their measures. Gerontologist 1990, 30, 583-594.
9. Forsberg-Wärleby G., Möller A., Blomstrand C.: Spouses of first-ever stroke patients psychological well-being in the first phase after stroke. Stroke 2001, 32, 1646-1651.
10. Cantor M.H.: Strain among caregivers: a study of experience in the United States. Gerontologist 1983, 23, 597-604.
11. Sales E.: Family burden and quality of life. Qual. Life Res. 2003, 12, 33-41.
12. Maurin J., Boyd B.: Burden of mental illness on the family: A critical review. Arch. Psychiatr. Nurs. 1990, 4, 99-107.
13. Foster M., Chaboyer W.: Family carers of ICU survivors: A survey of the burden they experience. Scand. J. Caring Sci. 2003, 17, 205-214.
14. van Exel N.J.A., Koopmanschap M.A., van den Berg B., Brouwer W.B.F., van den Bos G.A.M.: Burden of informal caregiving for stroke patients. Cerebrovasc. Dis. 2005, 19, 11-17.
15. van Exel N.J.A., Scholte op Reimer W.J.M., Brouwer W.B.F., van den Berg B., Koopmanschap M.A., van den Bos G.A.M.: Instruments for assessing the burden of informal caregiving for stroke patients in clinical practice: a comparison of CSI, CRA, CSQ and self-rated burden. Clin. Rehabil. 2004, 18, 203-214.
16. Lawton M.P., Kleban M.H., Moss M., Rovine M., Glicksman A.: Measuring caregiver appraisal. J. Gerontol. 1989, 44, 61-67.
17. Anderson C.S., Linto J., Stewart-Wynne E.G.: A population - based assessment of the impact and burden of caregiving for long-term stroke survivors. Stroke 1995, 26, 843-849.
18. Wade D.T., Legh-Smith J., Langton Hewer R.: Effects of living with and looking after survivors of a stroke. BMJ 1986, 16, 418-420.
19. Morimoto T., Schreiner A.S., Asano H.: Caregiver burden and health-related quality of life among Japanese stroke caregivers. Age Ageing 2003, 32, 218-223.
20. Kotila M., Numminen H., Waltimo O., Kaste M.: Depression after stroke results of the finnstroke study. Stroke 1998, 29, 368-372.
21. Berg A., Palomaki H., Lonnqvist J., Lehtihalmes M., Kaste M.: Depression among caregivers of stroke survivors. Stroke 2005, 36, 639-643.
22. Han B., Haley W.E.: Family caregiving for patients with stroke. Review and analysis. Stroke 1999, 30, 1478-1485.
23. Adams C.: Quality of Life for caregivers and stroke survivors in the immediate discharge period. Appl. Nurs. Res. 2003, 16, 126-130.
24. McCullagh E., Brigstocke G., Donaldson N., Karla L.: Determinants of caregiving burden and quality of life in caregivers of stroke patients. Stroke 2005, 36, 2181-2186.
25. Visser-Meily J.M.A., Post M.W.M., Lindeman E., Riphagen I.I.: Measures used to assess burden among caregivers of stroke patients: a review. Clin. Rehabil. 2004, 18, 601-623.
26. Zarit S.H., Todd P.A., Zarit J.M.: Subjective burden of husbands and wives as caregivers: a longitudinal study. Gerontologist 1986, 26, 260-206.
27. Vernooij-Dassen M.J.F.J., Persoon J.M.G., Felling A.J.A.: Predictors of sense of competence in caregivers of demented persons. Soc. Sci. Med. 1996, 43, 41-49.
28. Scholte op Reimer W.J.M., de Haan R.J., Pijnenborg J.M.A., Limburg M., van den Bos G.A.M.: Assessment of burden in partners of stroke patients with the sense of competence questionnaire. Stroke 1998, 29, 373-379.
29. Robinson B.C.: Validation of a caregiver strain index. J. Gerontol. 1983, 38, 144-148.
30. Given C.W., Given B., Stommel M., Collins C., King S., Franklin S.: The caregiver reaction assessment (CRA) for caregivers to persons with chronic physical and mental impairment. Res. Nurs. Health 1992, 15, 271-283.
31. Larson J., Franzén-Dahlin A., Billing E., Murray V., Wredling R.: Spouse's life situation after partner's stroke event: psychometric testing of a questionnaire. J. Adv. Nurs. 2005, 52, 300-306.
32. Mahoney F.I., Barthel D.W.: Functional evaluation: The Barthel Index. Md. State Med. J. 1965, 14, 61-65.
33. Bamford J.M., Sandercock P.A.G., Warlow C.P., Slattery J.: Interobserver agreement for the assessment of handicap in stroke patients. Stroke 1989, 20, 828.
34. Katz S., Ford A.B., Mostkowitz R.W., Jackson B.A., Jaffe M.W.: Studies of illness in the aged: The index of ADL - a standardized measure of biological and psychosocial function. JAMA 1963, 185, 914-919.
35. Nouri F., Lincoln N.B.: An extended activities of daily living scale for stroke patients. Clin. Rehabil. 1987, 1, 301-305.
36. Holbrook M., Skilbeck C.E.: An activities index for use with stroke patients. Age Ageing 1983, 12, 166-170.
37. Blake H., Lincoln N.B.: Factors associated with strain in co-resident spouses of patients following stroke. Clin. Rehabil. 2000, 14, 307-314.
38. Scholte op Reimer W.J.M., de Haan R.J., Rijnders P.T., Limburg M., van den Bos G.A.M.: The burden of caregiving in partners of long-term stroke survivors. Stroke 1998, 29, 1605-1611.
39. Chumbler N.R., Rittman M., Van Puymbroeck M., Vogel W.B., Quin H.: The sense of coherence, burden, and depressive symptoms in informal caregivers during the first month after stroke. Int. J. Geriatr. Psychiatry 2004, 19, 944-953.
40. Visser-Meily A., van Heugten C., Post M., Schepers V., Lindeman E.: Intervention studies for caregivers of stroke survivors: a critical review. Patient Educ. Couns. 2005, 56, 257-267.
41. Stoltz P., Udén G., Willman A. Support for family carers who care an elderly person at home - a systematic literature review. Scand. J. Caring Sci. 2004, 18, 111-119.
42. van den Heuvel E.T.P., de Witte L.P., Schure L.M., Sanderman R., Meyboom-de Jong B.: Risk factors for burn-out in caregivers of stroke patients, and possibilities for intervention. Clin. Rehabil. 2001, 15, 669-677.