The impact of disability, fatigue and sleep quality on the quality of life in multiple sclerosis

Annals of Indian Academy of Neurology

Volumn 11, Issue 4, 2008, Pages 236-241

  Ghaem, Haleh ^a,c   Haghighi, Afshin ^b  

^a SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

Disability; Fatigue; Multiple sclerosis; Quality of life; Sleep quality

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CONTROLLED STUDY; DISABILITY; DISEASE SEVERITY; FATIGUE; FEMALE; HUMAN; MAJOR CLINICAL STUDY; MALE; MENTAL HEALTH; MULTIPLE SCLEROSIS; QUALITY OF LIFE; SLEEP DISORDER;

EID: 58149154357     PISSN: 09722327     EISSN: 19983549     Source Type: Journal    
DOI: 10.4103/0972-2327.44559     Document Type: Article

References (41)

1. Nortvedt MW, Riise T, Myhr KM, Nyland HI. Quality of life in multiple sclerosis: Measuring the disease effects more broadly. Neurology 1999;53:1098-103.
2. Murphy N, Confavreux C, Haas J, Konig N, Roullet E, Sailer M, et al. Quality of life in multiple sclerosis in France, Germany, and the United Kingdom: Cost of Multiple Sclerosis Study Group. J Neurol Neurosurg Psychiatry 1998;65:460-6.
3. The Canadian Burden of Illness Study Group. Burden of illness of multiple sclerosis: Part II: Quality of life. Can J Neurol Sci 1998;25:31-8.
4. Rothwell PM, MC Dowell Z, Wong CK, Dorman PJ. Doctors and patients don.t agree: Cross sectional study of patients and doctors perceptions and assessments of disability in multiple sclerosis. BMJ 1997;314:1580-3.
5. Brunet DG, Hopman WM, Singer MA, Edgar CM, MacKenzie TA. Measurement of health-related quality of life in multiple sclerosis patients. Can J Neurol Sci 1996;23:99-103.
6. Kroencke DC, Denney DR, Lynch SG. Depression during exacerbations in multiple sclerosis: The importance of uncertainty. Mult Scler 2001;7:237-42.
7. Hakim EA, Bakheit AM, Bryant TN, Roberts MW, McIntosh-Michaelis SA, Spackman AJ, et al. The social Impact of multiple sclerosis: A study of 305 patients and their relatives. Disabil Rehabil 2000;22:288-93.
8. Solari A, Filippini G, Mendozzi, Ghezzi A, Cifani S, Barbieri E, et al. Validation of Italian multiple sclerosis quality of life 54 questionnaire. J Neurol Neurosurg Psychiatry 1999;67:158-62.
9. Provinciali L, Ceravolo MG, Bartolini M, Logullo F, Danni M. A multidimensional assessment of multiple sclerosis: Relationships between disability domains. Acta Neurol Scand 1999;100:156-62.
10. Jonsson A, Dock J, Ravnborg MH. Quality of life as a measure of rehabilitation outcome in patients with multiple sclerosis. Acta Neurol Scand 1996;93:229-35.
11. Fruewald S, Loeer-Stastka H, Eher R, Saletu B, Baumahackl U. Depression and quality of life in multiple sclerosis patients. Acta Neurol Scand 2001;104:257-61.
12. Lobentanz IS, Asendbaum S, Vass K, Sauter C, Klosch G, Kollegger H, et al. Factors influencing quality of life in Multiple Sclerosis patients: Disability depressive mode, fatigue and sleep quality. Acta Neurol Scand 2004;110:6-13.
13. Modrego PJ, Pina MA, Simon A, Azuara MC. The interrelations between disability and quality of life in patients with multiple sclerosis in the area of Bajo Aragon, Spain: A geographically based survey. Neurorehabil Neural Repair 2001;15:69-73.
14. Casanova B, Coret F, Landete L. A study of various scales of fatigue and impact on the quality of life among patients with multiple sclerosis. Rev Neurol 2000;30:1235-41.
15. Amato MP, Ponziani G, Rossi F, Leidi CL, Stefanile C, Rossi L. Quality of life in multiple sclerosis: The impact of depression, fatigue and disability. Mult Scler 2001;7:340-4.
16. Pittion-Vouyovitch S, Debouverie M, Guillemin F, Vandenberghe N, Anxionnat R, Vespignani H. Fatigue in multiple sclerosis is related to disability, depression and quality of life. J Neurol Sci 2006;243:39-45.
17. Benedict RH, Wahlig E, Bakshi R, Fishman I, Munschauer F, Zivadinov R, et al. Predicting quality of life in multiple sclerosis: Accounting for physical disability, fatigue, cognition, mood disorder, personality and behavior change. J Neurol Sci 2005;231:29-34.
18. Bakshi R. Fatigue associated with multiple sclerosis: Diagnosis, impact and management. Mult Scler 2003;9:219-27.
19. Merkelbach S, Sittinger H, Koenig J. Is there a differential impact of fatigue and physical disability on quality of life in multiple sclerosis? J Nerv Ment Dis 2002;190:388-93.
20. Murray TJ. Amantadine therapy for fatigue in multiple sclerosis. Can J Neurol Sci 1985;12:251-4.
21. Freal JE, Kraft GH, Coryell SK. Symptomatic fatigue in multiple sclerosis. Arch Phy Med Rehabil 1984;65:135-8.
22. Krupp L, La Rocca NG, Muir-Nash J, Steinberg AD. Fatigue severity scale. Neurology 1988;38:99-100.
23. Clark CM, Fleming JA, Li D, Oger, Klonoff H, Paty D. Sleep disturbances, depression, and lesion site in patients with multiple sclerosis. Arch Neurol 1992;49;641-3.
24. McHorney CA, Ware JE Jr, Lu JF, Sherbourne CD. The MOS 36-item short form health survey(SF-36) III: Tests of data quality, scaling assumptions, reliability across diverse patient groups. Med Care 1994;32:40-66.
25. Vickrey BG, Hays RD, Harooni NI R, Myers LW, Ellison GW. A health- related quality of life measure for multiple sclerosis. Qual Life Res 1995;4:187-206
26. Buysse DJ, Reynolds CF 3rd, Monk TH, Berman SR, Kupfer DJ. The Pittsburgh Sleep Quality Index: A new instrument for psychiatric practice and research. Psychiatry Res 1989;28:193-213.
27. Krupp LB, LaRocca NG, Muir-Nash J, Steinberg AD. The Fatigue Severity Scale: Application to patients with multiple sclerosis and systemic lupus erythematosus. Arch Neurol 1989;46:1121-23.
28. th ed. London: Black Well Science Ltd; 2002. p. 189.
29. Miller A, Dishon S. Health-related quality of life in multiple sclerosis: The impact of disability, gender and employment status. Qual Life Res 2006;15:259-71.
30. McHorney CA, Ware JE Jr, Raczek AE. the MOS 36-item shortform health survey (SF-36) II: Psychometric and clinical tests of validity in measuring physical and mental health constructs. Med Care 1993;31:247-63.
31. Leplege A, Ecosse E, Verdier A, Perneger T: The French SF-36 health survey: Translation, cultural adaptation and preliminary psychometric evaluation. J Clin Epidemiol 1998;51:1013-23.
32. Vernay D, Gerbaud L, Biolay S, Coste J, Debourse J, Aufauvre D, et al. Quality of life and multiple sclerosis: Validation of the French version of the self-questionnaire (SEP-59). Rev Neurol 2000;156:247-63.
33. Idiman E, Uzunel F, Ozakbas S, Yozbatiran N, Oguz M, Callioglu B, et al. Cross-cultural adaptation and validation of multiple sclerosis quality of life questionnaire(MSQoL-54) in a Turkish multiple sclerosis sample. J Neurol Sci 2006;240:77-80.
34. Ghaem H, Borhani Haghighi A, Jafari P, Nikseresth AR .Validity and reliability of the Persian version of the multiple sclerosis quality of life questionnaire. Neurol India 2007;55:369-75.
35. Albrecht GL, Fitzpatrick R. A social perspective on health related quality of life research. In: Albrecht GL, Fitzpatrick R, editors. Advances in medical sociology, quality of life in health care, Vol 5. Greenwich CT, London, UK: Jai Press; 1994. p. 1-21.
36. Ware JE, Snow KK, Kosinski M, Gandek B. SF-36 health survey: Manual and interpretion guide, Boston: Nimrod Press; 1993.
37. Ware JE Jr, Sherdbourne CD. The MOS 36-item short-form health survey (SF-36): I, Conceptual framework and item selection. Med Care 1992,30:473-83.
38. McHorney CA, Ware JE Jr, Raczek AE. The MOS 36-item short-form health survey (SF-36) II: Psychometric and clinical tests of validity in measuring physical and mental health constructs. Med Care 1993,31:247-63.
39. Hunt SM, McEwen J, McKenna SP. Measuring health status: A new tool for clinicians and epidemiologists. J Royal Coll Gen Pract 1985;35:185-8.
40. Nicholl CR, Lincoln NB, Francis VM, Stephan TF. Assessing quality of life in people with multiple sclerosis. Disabil Rehabil 2001;23:597-603.
41. Janssens AC, Van Doorn PA, de Boer JB, Vander Meche FG, Passchier J, Hintzen RQ. Impact of recently diagnosed multiple Sclerosis on quality of life, anxiety, depression and distress of patients and partners. Acta Neurol Scand 2003;108:389-95.