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Updated: Apr 5, 2026

Methods to Quantify Pharmacologically Induced Alterations in Motor Function in Human Incomplete SCI
Published on: April 18, 2011
Hemiparetic gait and changes in functional performance due to OnabotulinumtoxinA injection to lower limb muscles
Alberto Esquenazi1, Daniel Moon1, Amanda Wikoff1
1MossRehab Gait & Motion Analysis Laboratory and Department of PM&R MossRehab, Elkins Park, PA, USA.
Objective:
To review gait alterations and evaluate the effects of OnabotulinumtoxinA on spatiotemporal walking parameters of patients with hemiparetic gait.
Design:
Retrospective pre- and post-intervention analysis.
Setting:
Gait analysis laboratory in a tertiary level rehabilitation hospital.
Participants:
42 patients with hemiparesis. 19 males and 23 females, age 18-78 years were included.
Intervention:
Spatiotemporal parameters collected before and within 4-10 weeks after OnabotA injection to the ankle muscles. Data was recorded at self-selected velocity on a 12 m instrumented walkway. The most common muscles injected were medial and lateral gastrocnemius, soleus and tibialis posterior. Average total OnabotulinumtoxinA dose was 320 ± 107 units.
Main Outcome:
Spatiotemporal parameters of walking assessed before (T0) and within 4-10 weeks post injection (T1). Paired t-test was used to compare pre- and post-intervention data. A sequential Holm-Bonferroni procedure was used to adjust for multiple comparisons and minimize the risk of type I error. Statistical significance was set at p < 0.05.
Results:
Statistically significant increases were seen for walking velocity (20%) (T0 = 0.40 ± 0.26 m/s and T1 = 0.48 ± 0.29 m/s; p = 0.006), and increased cadence (T0 = 63.48 ± 23.93 steps/min, and T1 = 70.88 ± 23.65 steps/min; p = 0.006) following OnabotulinumtoxinA injections.
Conclusion:
This study demonstrates that injection of OnabotulinumtoxinA 320 units to ankle muscles selected with the aid of dynamic electromyography can significantly increase gait velocity and enhance functional ambulation in adults with hemiparesis due to upper motor neuron syndrome.

