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. 2023 Oct 5;55:4257. doi: 10.2340/jrm.v55.4257

Table I.

Patient characteristics

Parameter Baseline population N = 384
Age, years, mean ± SD 53.9 ± 13.8
Sex; Male, n (%) 255 (66.4)
Employment status, n (%)
 Employed (full-time, part-time, student, and sick-leave)
 Unemployed
 Retired
75 (19.5)
162 (42.2)
147 (38.3)
Diagnosis of condition leading to upper limb spasticity, n (%)
 Acquired brain injury (stroke/trauma/other)
 Spinal cord injury
 Other
374 (97.4)
8 (2.1)
2 (0.5)
Aetiology, n (%)
 Vascular (infarct or haemorrhage)
 Trauma
 Hypoxic
 Inflammatory
 Tumour
 Degenerative
 Other
328 (85.4)
44 (11.5)
1 (0.3)
5 (1.3)
2 (0.5)
2 (0.5)
2 (0.5)
Affected leg, n (%)
 Left
 Right
219 (57.0)
165 (43.0)
Affected by upper limb spasticity, n (%)
 Dominant arm
 Non-dominant arm
 Both
 No
156 (47.6)
170 (51.8)
2 (0.6)
56 (14.6)
Time since onset of the event leading to lower limb spasticity, years
 Mean ± SD
 Median (IQR)
6.9 ± 7.9
4.7 (1.7, 8.6)
Prior BoNT treatment; n (%)
 BoNT naïve
 Previously treated
96 (24.0)
288 (76.0)
Time interval between onset of event and first BoNT injection, years
 Mean ± SD
 Median (IQR)
N = 309
3.6 ± 6.9
1.3 (0.6, 3.3)

SD: standard deviation; IQR: interquartile range; BoNT: botulinum toxin type A.