Cited by 119Multiple Sclerosis Research StudiesHealth Systems, Economic Evaluations, Quality of LifeCancer survivorship and care

Quality of life in multiple sclerosis in France, Germany, and the United Kingdom

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Murphy, N, Confavreux, C, Haas, J, Konig, N, Roullet, E, Sailer, M, Swash, M, Young, C +1 more·1998·Journal of Neurology, Neurosurgery & Psychiatry

Abstract

OBJECTIVE: To assess the quality of life (QoL) of patients with multiple sclerosis in France, Germany, and the United Kingdom with a cross sectional study. METHODS: Patients were classified into three severity groups according to the expanded disability severity scale (EDSS); stage I, II, and III, corresponding to mild (EDSS 1.0-3.5), moderate (EDSS 4.0-6.0), or severe (EDSS 6.5-8.0) multiple sclerosis respectively. Ninety patients with multiple sclerosis and 30 control patients without multiple sclerosis were recruited in each country. Control patients were matched to the patients with multiple sclerosis according to age and sex. Quality of life was assessed using the functional status questionnaire (FSQ). RESULTS: The aspects of QoL that were mostly affected in the three countries under study were physical function and general wellbeing. Social role function decreased with increased severity of disease in France and in particular in Germany. Multiple sclerosis did not seem to have an impact on psychological function. The QoL of control patients was systematically higher than that of patients with multiple sclerosis. CONCLUSIONS: Use of such a generic scale showed that progression of multiple sclerosis is accompanied by a decrease in QoL and suggested that this could be a relevant measurement in assessing the effect of treatment and progression of disease. Variation between countries, however, may be important.

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  • HRQOL psychosocial impairment is, to an important degree, independent of extent of disease among patients with multiple sclerosis.

    “HRQOL psychosocial impairment shows great variation among patients with MS and is, to an important degree, independent of extent of disease.6–10”

    From MS quality of life, depression, and fatigue improve after mindfulness training: A randomized trial (2010) · cites this paper as [8]

    The MAIN SCALES and Discussion sections (page unavailable) report that psychological function was lower in patients with MS than in controls but did not correlate with disease severity. The claim is broader than that finding: social role function, another psychosocial measure, was associated with severity in some countries, and the paper does not establish that psychosocial impairment generally varies greatly between patients. (LLM, conf=0.87)

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  • HRQOL psychosocial impairment shows great variation among patients with multiple sclerosis.

    “HRQOL psychosocial impairment shows great variation among patients with MS and is, to an important degree, independent of extent of disease.6–10”

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Research works printed but not linked: 15

  1. Spilker B, ed. Quality of life and pharmacoeconomics in clinical trials. Philadephia: Lippincott-Raven.
  2. Rudick RA, Miller D, Clough JD, et al. Quality of life in multiple sclerosis. Arch Neurol 1992;49:1237-42.
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  4. Jette AM, Davies AR, Cleary PD, et al. The functional status questionnaire: reliability and validity when used in primary care. Gen Intern Med 1986;1:143-9.
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  6. Monteban H, Hardens M, Vera M, et al. Validation of the functional status questionnaire in mental disorders. Qual Life Res 1994;3:87.
  7. Murphy N, Confavreux C, Haas J, et al. Pharmacoeconomics 1998 (in press).
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  12. Slevin ML, Plant H, Lynch D, et al. Who should measure the quality of life, the doctor or the patient? Br J Cancer 1988;57:109-12.
  13. Gerhart KA, Koziol-McLain J, Lowenstein SR, et al. Qual- ity of life following spinal cord injury: knowledge and atti- tudes of emergency care providers. Ann Emerg Med 1994;23:807-12.
  14. Rothwell PM, McDowell Z, Wong CK, et al. Doctors and patients don't agree: cross sectional study of patients' and doctors' perceptions and assessments of disability in multi- ple sclerosis. BMJ 1997;314:1580-3.
  15. Staquet M, Berzon R, Osoba D, et al. Guidelines for report- ing results of quality of life assessments in clinical trials. Qual Life Res 1996;5:496-502.

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Authors
Murphy, N., Confavreux, C., Haas, J., Konig, N., Roullet, E., Sailer, M., Swash, M., Young, C., & J-L, M.
Corresponding author
Murphy, N
Venue
Journal of Neurology, Neurosurgery & Psychiatry
Publisher
BMJ
Published
1998-10-01
Volume
65
Issue
4
Pages
460-466
ISSN
0022-3050 (ISSN-L)
OpenAlex
W2135934250
Cited by
119
References
2
Citations by year
2024: 1 · 2023: 2 · 2022: 4 · 2021: 2 · 2020: 1 · 2019: 3 · 2017: 4 · 2015: 5 · 2013: 5 · 2012: 2
FWCI
2.58
Type
journal article
Language
en
Open access
Locations
  • Journal of Neurology Neurosurgery & Psychiatry (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Multiple Sclerosis Research Studies
  • Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Health Systems, Economic Evaluations, Quality of Life
  • Health Sciences › Medicine › Oncology › Cancer survivorship and care
Keywords
multiple sclerosis, quality of life, disease severity, Expanded Disability Status Scale, functional status, psychological functioning, cross-national comparison, France, Germany, United Kingdom
MeSH terms
Adult, Cross-Sectional Studies, Female, France, Germany, United Kingdom, Humans, Male, Middle Aged, Multiple Sclerosis, Quality of Life, Surveys and Questionnaires, Severity of Illness Index

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