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Robot-mediated and clinical scales evaluation after upper limb botulinum toxin type A injection in children with hemiplegia

The aim of this pilot study was to examine changes in different
aspects of impairment, including spasticity in the upper limbs, of hemiplegic
children following botulinum toxin type A intervention. Progress was assessed
using standard clinical measurements and a robotic device. DESIGN: Pre-post
multiple baseline. SUBJECTS:
Six children with hemiplegia. METHODS: Botulinium
toxin type A injections were administered into the affected upper limb muscles.
Outcomes were evaluated before and one month after the injection. Outcome
assessments included: Melbourne Scale, Modified Ashworth Scale (MAS) and Passive
Range of Motion. Furthermore, a robotic device was employed as an evaluation
tool. RESULTS: Patients treated with botulinum toxin type A had significantly
greater reduction in spasticity (MAS, p < 0.01), which explains an improvement in
upper limb function and quality movement measured with the Melbourne Scale (p <
0.01). These improvements are consistent with robot-based evaluation results that
showed statistically significant changes (p < 0.01) following botulinum toxin
type A injections. CONCLUSION: The upper limb performs a wide variety of
movements. The multi-joint nature of the task during the robot-mediated
evaluation required active control of joint interaction forces. There was good
correlation between clinical scales and robotic evaluation. Hence the
robot-mediated assessment may be used as an additional tool to quantify the
degree of motor improvement after botulinum toxin type A injections.

Langue : ANGLAIS

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