Effects of Botulinum Toxin-A and casting treatment on assessed spasticity, muscle morphology and gait kinematics in spastic paresis

Abstract (2017)
Authors

Guido Weide (Amsterdam UMC, Vrije Universiteit Amsterdam)

Lizeth Sloot (Amsterdam UMC)

Laura Oudenhoven (Amsterdam UMC)

Richard T. Jaspers (Vrije Universiteit Amsterdam)

J. Harlaar (TU Delft - Biomechatronics & Human-Machine Control, Amsterdam UMC)

Annemieke Buizer (Amsterdam UMC)

Lynn Bar-On (Katholieke Universiteit Leuven, Amsterdam UMC)

Research Group
Biomechatronics & Human-Machine Control
To reference this document use:
https://doi.org/10.1016/j.gaitpost.2017.06.314
More Info
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Publication Year
2017
Language
English
Research Group
Biomechatronics & Human-Machine Control
Issue number
Supplement 1
Volume number
57
Pages (from-to)
104-105
DOI:
https://doi.org/10.1016/j.gaitpost.2017.06.314

Abstract

Spasticity as part of a central neurological disorder is characterized by a ‘velocity dependent hyperactive stretch-reflex’ [1]. Secondary, morphological adaptations of the muscle-tendon complex reduce the passive joint angle-moment relationship (i.e. passive ROM) [2]. Potentially, joint hyper-resistance, as a result of either the neurological disorder, muscle morphology or both, can be clinically assessed [3]. Botulinum Toxin-A (BoNT-A), in combination with casting and physiotherapy are regularly used as conservative treatment in children with a spastic paresis to improve gait. While in some studies improvements resulting from this approach are reported, large treatment response variability persists [4]. Heterogeneity in treatment effectiveness may be due to a clinical focus at the joint impairment level rather than on the contributing mechanisms of joint hyper-resistance. In recent years great advances have been made in standardized, objective assessments of stretch reflexed induced joint hyper resistance [5]. 3D ultrasound (3DUS), allows morphometry of the muscle-tendon complex in children with spastic paresis [6]. The combination of instrumented assessments of neurological, muscle morphology and gait characteristics following treatment has not been carried out.

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