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. 2013 Jun 11;8(6):e65640.
doi: 10.1371/journal.pone.0065640. Print 2013.

How people with multiple sclerosis rate their quality of life: an EQ-5D survey via the UK MS register

Kerina H Jones  1 , David V Ford, Philip A Jones, Ann John, Rodden M Middleton, Hazel Lockhart-Jones, Jeffrey Peng, Lisa A Osborne, J Gareth Noble
Affiliations

How people with multiple sclerosis rate their quality of life: an EQ-5D survey via the UK MS register

Kerina H Jones et al. PLoS One. .

Abstract

Introduction: The EQ-5D is a widely-used, standardised, quality of life measure producing health profiles, indices and states. The aims of this study were to assess the role of various factors in how people with Multiple Sclerosis rate their quality of life, based on responses to the EQ-5D received via the web portal of the UK MS Register.

Methods: The 4516 responses to the EQ-5D (between May 2011 and April 2012) were collated with basic demographic and descriptive MS data and the resulting dataset was analysed in SPSS (v.20).

Results: The mean health state for people with MS was 59.73 (SD 22.4, median 61), compared to the UK population mean of 82.48 (which is approximately 1SD above the cohort mean). The characteristics of respondents with high health states (at or above +1SD) were: better health profiles (most predictive dimension: Usual Activities), higher health indices, younger age, shorter durations of MS, female gender, relapsing-remitting MS, higher educational attainment and being in paid employment (all p-values<0.001). Conversely, the characteristics of respondents with low health states (at or below -1SD) were: poorer health profiles (most predictive dimension: Mobility), lower health indices, older age, longer durations of MS, male gender, progressive MS, lower educational attainment and having an employment status of sick/disabled (p = 0.0014 for age, all other p-values<0.001). Particular living arrangements were not associated with either the high or low health status groups.

Conclusions: This large-scale study has enabled in-depth analyses on how people with MS rate their quality of life, and it provides new knowledge on the various factors that contribute to their self-assessed health status. These findings demonstrate the impact of MS on quality of life, and they can be used to inform care provision and further research, to work towards enhancing the quality of life of people with MS.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exis.

Figures

Figure 1
Figure 1. Health profiles of the cohort of people with MS.
The frequencies of people with MS reporting no problems (level 1), some problems (level 2) and severe problems (level 3) on each of the 5 dimensions are indicated to show the health profiles of the cohort.
See this image and copyright information in PMC

References

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    1. Multiple Sclerosis Society of Great Britain and Northern Ireland website. Available: http://www.mssociety.org.uk/. Accessed 2013 February 20.
    1. Ford DV, Jones KH, Middleton RM, Lockhart-Jones H, Maramba IDC, et al.. (2012) The feasibility of collecting information from people with Multiple Sclerosis for the UK MS Register via a web portal: characterising a cohort of people with MS. BMC Medical Informatics and Decision Making, 12(1), 73. - PMC - PubMed

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