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. 2024 Jan 8;14:4. doi: 10.1186/s13613-023-01213-x

Table 1.

Clinical characteristics of attacks requiring orotracheal intubation versus attacks not requiring orotracheal intubation

All attacks, N = 73 OTI-attacks, N = 8 (11.0%) Non-OTI-attacks, N = 65 (89.0%) P-value
Gender: female/male 64 (87.7) 7 (87.5) 57 (87.7) 0.925
Place of birth
 France—metropolitan area 34 (46.6) 1 (12.5) 33 (50.8)
 France–West indies–Guyana 6 (8.2) 4 (50.0) 2 (3.1)
 Asia 6 (8.2) 0 (0.0) 6 (9.2)
 North Africa 6 (8.2) 0 (0.0) 6 (9.2)
 Sub-Saharan Africa 20 (27.4) 2 (25.0) 18 (27.7)
 Middle East 1 (1.4) 1 (12.5) 0 (0.0)
Age at start of the disease, years, median (IQR) 33.20 [21.30, 46.90] 47.15 [33.18, 55.70] 32.90 [19.60, 43.40] 0.662
Age at attack onset, years 43 (31–53) 50 (42–56) 43 (28–53) 0.834
First attack of NMOSD-AQP4 disease 22 (30.1) 4 (50) 18 (27.7) 0.592
Attack occurring in the first 6 months of NMOSD-AQP4 disease 28 (38.9) 7 (87.5) 21 (32.8) 0.411
Any active NMOSD disease modifying therapy (DMT)a 36 (49.3) 0 (0) 36 (55.4)
Type of DMT
 Azathioprine 8 (11) 8 (12.3)
 Mycophenolate mofetil 11 (15.1) 11 (16.9)
 Rituximab 8 (11) 8 (12.3)
 Cyclophosphamide 3 (4.1) 3 (4.6)
 Methotrexate 4 (5.5) 4 (6.2)
 TPE 6 (8.2) 6 (9.2)
EDSS before attack 2.0 (0–3.5) 1.0 (0–3.5) 2.0 (0–3.5) 0.460
Modified Rankin scale before attack 1 (0–2) 0.5 (0–3.25) 1 (0–2) 0.380
Clinical examination at the hospital entry
 EDSS at admission 6.0 (3.5–8) 7.5 (6.0–8.5) 6.0 (3.5–8) 0.029
 Lower limb paresis 46 (63) 6 (75) 40 (61.5) 0.460
 Upper limb paresis 25 (34.2) 6 (75) 19 (29.2) 0.366
 Dyspnea (number of patients with available data) 7 (9.7) (71) 3 (50) (6) 4 (6.6) (65) 0.002

Results are expressed in median (interquartile range) or N (%) unless otherwise specified

NA number of observations non available, OTI orotracheal intubation, DMT disease modifying therapy

P-value is estimated with binomial generalized linear mixed model, with a random intercept for patient ID. Due to separation issues, p-value has not been estimated for some variables

aActive DMT was defined if it has been received for at least 3 months before the attack first symptoms