Multiple Sclerosis Impact Scale (MSIS-29): reliability and validity in hospital based samples

A Riazi1, J C Hobart, D L Lamping

  • 1Neurological Outcome Measures Unit, Institute of Neurology, London, UK.

Abstract

Insights

The Multiple Sclerosis Impact Scale (MSIS-29) demonstrates reliable and valid psychometric properties across diverse hospital patient samples. These findings support its use as an outcome measure in various clinical settings for multiple sclerosis (MS).

Area of Science:

  • Clinical assessment
  • Psychometrics
  • Multiple Sclerosis (MS) research

Background:

  • Rating scales' psychometric properties are sample-dependent, requiring validation in different populations.
  • The Multiple Sclerosis Impact Scale (MSIS-29) was initially developed using a community-based sample.
  • Key characteristics of the initial MSIS-29 development sample were not fully known.

Purpose of the Study:

  • To evaluate the psychometric properties of the MSIS-29 in three distinct hospital-based samples.
  • To assess MSIS-29 performance in patients undergoing rehabilitation, corticosteroid treatment for relapses, and those with primary progressive MS.

Main Methods:

  • Recruitment of individuals with MS from three clinical settings.
  • Administration of the MSIS-29 and other health measures.
  • Evaluation of MSIS-29 data for quality, scaling assumptions, acceptability, reliability, and validity, with comparisons to a community-based study.

Main Results:

  • Data from 233 participants (rehabilitation, corticosteroids, primary progressive MS) were analyzed.
  • Low missing data (or=0.91) were observed across all samples.
  • MSIS-29 correlations with other scales aligned with hypotheses, and findings were consistent with community samples.

Conclusions:

  • The MSIS-29 exhibits consistent psychometric properties across three hospital-based patient groups.
  • Its performance in clinical settings mirrors that observed in community samples.
  • These results reinforce the MSIS-29's utility as an outcome measure in diverse clinical contexts for MS.