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. 2023 Jun 30;16:17562864231181177. doi: 10.1177/17562864231181177

Table 1.

Baseline demographics and disease characteristics (data for the safety analysis set, n = 71 and for the effectiveness analysis set, n = 68).

Safety analysis set (n = 71) Effectiveness analysis set (n = 68)
Age, years, mean (SD) 50.7 (13.3) 50.6 (13.2)
Female, n (%) 67 (94.4) 64 (94.1)
Disease duration, years, mean (SD) 6.8 (6.2) 6.9 (6.3)
 <2 years, n (%) 20 (28.2) 20 (29.4)
 ⩾2 years, n (%) 51 (71.8) 48 (70.6)
Symptoms at NMOSD diagnosis, n (%)
 Optic neuritis 34 (47.9) 32 (47.1)
 Transverse myelitis 35 (49.3) 34 (50.0)
 Brain stem symptoms 15 (21.1) 14 (20.6)
 Cerebral symptoms 5 (7.0) 5 (7.4)
 Other 2 (2.8) 2 (2.9)
Any relapse in the 2 years before eculizumab administration, n (%) 51 (71.8) 51 (75.0)
Relapse count in the 2 years before eculizumab administration, n (%)
 1 22 (43.1) 22 (43.1)
 2 14 (27.5) 14 (27.5)
 3 9 (17.6) 9 (17.6)
 ⩾4 6 (11.8) 6 (11.8)
Terminal complement protein C5 genetic polymorphism, n (%)
 Positive 0 (0.0) 0 (0.0)
 Negative 27 (38.0) 27 (39.7)
 Not measured 42 (59.2) 39 (57.4)
 Blank 0 (0.0) 0 (0.0)
Meningococcal vaccination received, n (%) 70 (98.6) 67 (98.5)
Prior NMOSD treatment, n (%)
 Steroids 69 (97.2) 66 (97.1)
 Immunosuppressive therapy 40 (56.3) 40 (58.8)
 Plasma exchange 28 (39.4) 27 (39.7)
 Intravenous immunoglobulin 5 (7.0) 5 (7.4)
 Biologics 3 (4.2) 3 (4.4)
 Other 17 (23.9) 16 (23.5)

NMOSD, neuromyelitis optica spectrum disorder; SD, standard deviation.