Clinical and functional outcome after alcohol neurolysis of the tibial nerve for ankle-foot spasticity

Citation
Ksg. Chua et Kh. Kong, Clinical and functional outcome after alcohol neurolysis of the tibial nerve for ankle-foot spasticity, BRAIN INJUR, 15(8), 2001, pp. 733-739
Citations number
17
Categorie Soggetti
Neurology
Journal title
BRAIN INJURY
ISSN journal
02699052 → ACNP
Volume
15
Issue
8
Year of publication
2001
Pages
733 - 739
Database
ISI
SICI code
0269-9052(200108)15:8<733:CAFOAA>2.0.ZU;2-8
Abstract
Purpose: To report one's experience of using 50-100% alcohol for neurolysis of the tibial nerve in chronic ankle-foot spasticity. Methods: The records of patients who received alcohol neurolysis of the tib ial nerve were retrospectively reviewed. Repetitive monopolar nerve stimula tion was used to localize the tibial nerve. Outcome measures included muscl e tone as measured by the Modified Ashworth Score (MAS), passive ankle rang e of motion (PROM), effect on clonus, plantar flexor motor strength, visual gait analysis and use of orthoses. Results: A total of 21 tibial nerves were neurolysed in 18 patients (mean a ge 38.9 +/- 15.8 years, 12 males, six females). Mean duration post-event wa s 14.8 +/- 3.9 months. The mean pre-neurolysis MAS was 2.50 +/- 0.77 and th is improved to 0.97 +/- 0.88 ( p <0.001) and 0.93 +/- 0.85 ( p <0.001) at 1 and 6 months post-procedure, respectively. Average duration of effect was 10.5 +/- 8.9 months. Eleven out of 12 patients (91.7%) with sustained ankle clonus had complete abolishment lasting 6 months. Mean gain in PROM was 24 .6 +/- 16.1 degrees and 32.6 +/- 19.0 degrees at 1 and 3 months post-neurol ysis, respectively ( p <0.001, <0.02). No decrease in motor strength was se en post-neurolysis. All 13 ambulant patients had visible improvements in ga it. Complications were transient and included dysesthetic pain (4), sensory loss (1) and distal limb oedema (1). Conclusion: Alcohol neurolysis (50-100%) of the tibial nerves is an effecti ve and safe method of managing ankle-foot spasticity.