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Botulinum toxin with and without casting in ambulant children with spastic diplegia: a clinical and functional
M Bottos1, M G Benedetti, P Salucci
1Childhood Neuromotor Disabilities Centre, Azienda USL, Bologna, Italy.
Insights
Botulinum toxin A (BTX-A) injections reduce spasticity in children with dynamic equinus foot. Combining BTX-A with casting yields more significant and lasting improvements in functional performance like walking.
Area of Science:
- Pediatric Orthopedics
- Neurology
- Rehabilitation Medicine
Background:
- Dynamic equinus foot in children with spastic diplegia can impair motor function.
- Botulinum toxin A (BTX-A) is a common treatment for reducing spasticity.
Purpose of the Study:
- To compare the clinical and functional outcomes of BTX-A treatment alone versus BTX-A combined with casting in children with dynamic equinus foot.
Main Methods:
- Ten children with mild spastic diplegia received either BTX-A injections with an ankle-foot orthosis or BTX-A injections with casting.
- Clinical assessments included the Ashworth scale, GMFM, range of motion, and gait analysis at baseline and 1, 4, and 12 months post-treatment.
Main Results:
- Both groups showed significant spasticity reduction at 1 month. Group 2 (BTX-A plus casting) demonstrated significant improvements in Gross Motor Function Measure (GMFM) for standing and walking at 4 months.
- Gait analysis revealed a significant increase in walking speed in Group 2. No significant changes were observed in ankle kinematics, kinetics, or muscle activity.
Conclusions:
- BTX-A effectively reduces spasticity and enhances functional performance in standing and walking.
- The combination of BTX-A with casting provides more pronounced and sustained improvements compared to BTX-A alone in children with dynamic equinus foot.
Abstract:
This study compared clinical and functional outcomes after treatment with botulinum toxin A (BTX-A) and BTX-A with casting in children with dynamic equinus foot. Ten children (seven males, three females; mean age 6 years 4 months, SD 2 years 7 months; range 4 to 11 years) with mild spastic diplegia and independent walking were divided into two groups: group 1, BTX-A and group 2, BTX-A plus casting. BTX-A was injected in the triceps surae bilaterally at multiple sites while the children were sedated with mask anaesthesia. Dysport toxin was used, 15 to 20 IU/kg in each muscle. Immediately after injection an ankle-foot orthosis was applied to children in group 1 and a cast to children in group 2. Clinical assessment using the Ashworth scale, Gross Motor Function Measure (GMFM), range of movement measurement, and gait analysis was performed before treatment and 1, 4, and 12 months after treatment. Spasticity decreased significantly at 1-month examination in both groups (p = 0.002), at 4-month examinations (Wilcoxon test p = 0.003), and 12 month (p = 0.052) examinations in group 2. GMFM highlighted a significant improvement in group 2 at the 4-month examination (p = 0.052 for standing,p = 0.007 for walking). Gait analysis showed a significant increase in the walking speed in group 2 (p = 0.04). No change was detected in ankle kinematics and kinetics or in muscular activity during the gait cycle. We confirmed that BTX-A reduces spasticity and improves functional performance in standing and walking; association with casting provides more marked and enduring results.
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