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Criteria and uses of the Minimal Record of Disability in multiple sclerosis

R J Slater

    Acta Neurologica Scandinavica. Supplementum
    |January 1, 1984
    PubMed

    Insights

    A new Minimal Record of Disability (MRD) for Multiple Sclerosis (MS) was developed across twelve countries. This tool aids in personal disability assessment and resource allocation planning for individuals with MS.

    Area of Science:

    • Neurology
    • Rehabilitation Medicine
    • Public Health

    Background:

    • Multiple Sclerosis (MS) presents a significant disability burden.
    • Existing assessment tools may lack standardization for international comparison.
    • Effective resource allocation requires accurate disability data.

    Purpose of the Study:

    • To develop a Minimal Record of Disability (MRD) for Multiple Sclerosis (MS).
    • To create a simple dataset reflecting personal disability and environmental factors in MS.
    • To facilitate local, regional, national, and international planning and evaluation of MS services.

    Main Methods:

    • Collaborative international study over 5 years.
    • Development of a standardized data set.
    • Patterned on the World Health Organization taxonomy for disability.

    Main Results:

    • A Minimal Record of Disability (MRD) for MS has been successfully developed.
    • The MRD is available in nine languages.
    • The record captures personal disability and environmental situations.

    Conclusions:

    • The MRD is ready for implementation in service studies.
    • This tool can improve planning and resource allocation for MS care.
    • International comparisons of system effectiveness are now feasible.

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