Abstract

BackgroundFatigue is a common and debilitating symptom of Multiple Sclerosis (MS); however, it is unknown what constitutes a clinically significant change in fatigue. Establishing the minimally important difference (MID) of fatigue outcome measures can inform the interpretation of changes in fatigue by estimating the level of change that is considered clinically relevant. AimDetermine the MID for the Fatigue Severity Scale (FSS) and Modified Fatigue Impact Scale (MFIS) in people with MS. MethodsThis cross-sectional study collected information on self-reported fatigue (FSS and MFIS) and quality of life (EQ-5D and MS Impact Scale 29) through an online survey. Anchor-based methods were used to estimate MID, and ordinal logistic regression models were used to determine the difference in fatigue that would predict a significant effect on quality of life. Results365 people with MS (81.9% female, 69.3% relapsing-remitting MS, mean age 46.2 ± 11.6 years, mean time since diagnosis 9.6 ± 8.7 years) responded to the survey. MID estimates for the FSS and MFIS ranged from 0.45–0.88 and 3.86–8.11 respectively, accounting for 6.4–12.6% of maximum FSS score and 4.6–9.7% of maximum MFIS score. ConclusionsMID estimates derived from this study indicate that a difference of at least 0.45 points on the FSS or 4 points on the MFIS constitutes a clinically significant difference in fatigue. Therefore, these estimates represent a threshold value which can be used to interpret changes in the FSS and MFIS over time or in response to an intervention.

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