Patients were non-Hispanic White (85 %) males (100 %), aged 33–72 years (55.3 ± 10.8; mean ± SD) (see Table 1). Table 1 Demographic variables of 20 MS patients on dalfampridine [mean ± SD (range) or n (%) where applicable] Grouping variables Sample Age (years) 55.3 ± 10.8 Sex (M:F) 20:0 Ethnicity (White/Black) 17:3 Age of MS onset (years) 35.2 ± 11.9 (20–58) MS duration (years) 23.5 ± 14.5 (5–47) MS types [n (%)] Relapsing-remitting 11 (55) Secondary-progressive 6 (30) Primary-progressive 3 (15) On initial evaluation MMSE 28.0 ± 3.2 Visual (n = 17)
3 (18) Upper limb muscle strength (n = 19) 4.2 ± 0.9 Lower limb muscle strength check details (n = 19) 3.9 ± 0.9 Sensory complaints [yes] (n = 17) 9 (53) Cerebellar complaints [yes] (n = 17) 10 (59) Gait Normal 4 (20) Ataxic 3 (15) Spastic 9 (45) Unable 1 (5) Unknown 3 (15) LEMMT 3.9 ± 0.9 (2–5) 10-meter walk test (sec), initial (n = 19) 28.4 ± 18.7
2-minute walk test (ft), A-1210477 nmr initial (n = 13) 155.4 ± 94.5 Modified Ashworth Score, initial (n = 15) 0.5 ± 0.7 (0–2) EDSS score, initial (n = 19) 5.5 ± 1.9 (1.5–7.5) TFIM score, initial (n = 17) 83.7 ± 13.3 (57–104) Immunomodulators [n (%)]a 13 (65) Avonex 4 (20) Copaxone 8 (40) Natalizumab 1 (5) EDSS Expanded Disability Status Scale, F female, LEMMT Lower Extremity Manual Muscle Test, M male, MMSE Mini-Mental State Examination, MS multiple sclerosis, TFIM Total Functional Independence Measure aConcurrent Florfenicol treatment with interferon, glatiramer, natalizumab Data collected from the charts of
the 20 patients included demographic information, MS characterization, and initial and follow-up scores for the following: Medical Research Council (MRC) lower extremity muscle strength (LEMMT), Total Functional Independence Measure (TFIM), Modified Ashworth Scale (MAS), 10M walk time, and 2MWT distance. Consistent with Veterans Affairs (VA) guidelines for veterans on dalfampridine, response to treatment, compliance, adverse effects, and withdrawals were assessed at 4, 3, 6, and 12 months following treatment initiation. All data were prospectively recorded in the computerized patient record system as part of patient care by a clinician who was unaware of the study hypothesis. 2.2 Primary Outcome Measures The 10M and 2MWT were administered to the MS patients to assess general walking speed and capacity [21, 22]. The 10M walk test measures walking speed (in seconds) of the patient over a set distance. The patient was instructed to walk at usual speed using Selleck Repotrectinib whatever aid was needed as in everyday life. This test was selected as it is simple and quick to administer, inexpensive, and is easily generalizable to community walking [21]. It has been found to be a reliable, valid, and sensitive measure [23–25].