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. 2022 Oct 26;66(6):715–722. doi: 10.1002/mus.27722

TABLE 1.

Demographics and clinical data from 30 patients with CIDP

Variable Median (IQR)
Age (years) 66.0 (48.0‐73.0)
Sex, M:F (n) 22:8
Age at onset (years) 47.5 (34.0‐58.0)
Time since onset of CIDP (years) 14.6 (11.5‐19.0)
Time since first contact to neurologist (years) 14.0 (11.0‐16.0)
Duration of CIDP until treatment initiation (years) 0.75 (0.25‐1.5)
Interval between initial and follow‐up assessments (years) 13.4 (10.9‐15.8)
Acute, GBS‐like onset (n) 5
Walking status at initial visit (n)
Walking independently 22
Walking with aids 3
No ambulation 5
Walking status at follow‐up (n)
Walking independently 28
Walking with aids 1
No ambulation 1
I‐RODS score at follow‐up (a.u.) 73.0 (67.0‐88.0)
NIS score at follow‐up (a.u.) 23.0 (15.0‐30.5)
Isokinetic strength, normalized (%) 56.1 (44.4‐68.7)
Current treatment (n)
IgG 14
Azathioprine 1
Rituximab 1
Prednisolone 1
No treatment 15
Combined axonal Z score
Initial −3.6 (−6.3 to −2.3)
Follow‐up a −3.2 (−4.8 to −1.4)
Combined demyelination Z score
Initial −4.1 (−4.8 to −2.5)
Follow‐up b −3.0 (−4.0 to −1.1)

Abbreviations: CIDP, chronic inflammatory demyelinating polyneuropathy; F, female; GBS, Guillain‐Barré syndrome; IgG, immunoglobulin G; I‐RODS, Inflammatory Rasch‐built Overall Disability Scale; IQR, interquartile range; M, male; NIS, neuropathy impairment score.

a

P = .1.

b

P = .02.