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Table 1 Patient demographics and baseline characteristics

From: Real-world effectiveness and safety of fingolimod in patients with multiple sclerosis in the Czech Republic: results from core and extension parts of the GOLEMS study up to 48 months

Parameter

N = 240

Age, years

 Mean (± SD)

37.4 (± 9.27)

 Median (Q1; Q3)

37.0 (31.0; 43.0)

 Min; Max

18; 67

Sex, n (%)

 Male

71 (29.6)

 Female

169 (70.4)

Time since first MS symptom prior to study entry, years

 Mean (± SD)

10.35 (± 6.70)

 Median (Q1; Q3)

9.42 (5.22; 14.26)

 Min; Max

0.4; 38.5

Frequency of relapses during the year prior to fingolimod treatment, n (%) [95% CI]

 Patients with no relapse

47 (19.6) [14.8; 25.2]

 Patients with 1 relapse

54 (22.5) [17.4; 28.3]

 Patients with 2 relapses

102 (42.5) [36.2; 49.0]

 Patients with > 2 relapses

37 (15.4) [11.1; 20.6]

Number of MS relapses within the year prior to fingolimod treatment

 Mean (± SD)

1.6 (± 1.02)

 Median (Q1; Q3)

2.0 (1.0; 2.0)

 Min; Max

0; 4

Frequency of relapses in the 2 years prior to fingolimod treatment, n (%) [95% CI]

 Patients with no relapse

35 (14.6%) [10.4; 19.7]

 Patients with 1 relapse

27 (11.3) [7.6; 15.9]

 Patients with 2 relapses

70 (29.2) [23.5; 35.4]

 Patients with > 2 relapses

108 (45.0) [38.6; 51.5]

Number of MS relapses in the 2 years prior to fingolimod treatment

 Mean (± SD)

2.3 (± 1.46)

 Median (Q1; Q3)

2.0 (1.0; 3.0)

 Min; Max

0; 9

EDSS score for the 3 months prior to study entry or at the start of fingolimod treatment

 Mean (± SD)

3.4 (± 1.26)

 Median (Q1; Q3)

3.5 (2.5; 4.5)

 Min; Max

0; 6

Number of missed days of work during the 3 months prior to study entry

 Mean (± SD)

7.9 (± 19.66)

 Median (Q1; Q3)

0.0 (0.0; 6.0)

 Min; Max

0.0; 90.0

  1. CI Confidence interval, EDSS Expanded Disability Status Scale, Max Maximum, Min Minimum, N Number of patients, Q1 Lower quartile, Q3 Upper quartile, SD Standard deviation