Effectiveness of electrical stimulation after administration of botulinum toxin in children with spastic diplegic

Pembe Yiğitoğlu1, Erkan Kozanoğlu2

  • 1Department of Physical Medicine and Rehabilitation, Near East University Faculty of Medicine, Lefkoşa, KKTC.

Insights

Electrical stimulation after Botulinum toxin A (BTX-A) injections did not provide additional benefits for children with spastic diplegic cerebral palsy (SDCP). Both treatment groups showed reduced spasticity, but outcomes were similar.

Area of Science:

  • Pediatric Neurology
  • Rehabilitation Medicine
  • Movement Disorders

Background:

  • Spastic diplegic cerebral palsy (SDCP) is characterized by increased muscle tone, affecting mobility.
  • Botulinum toxin A (BTX-A) injections are used to reduce spasticity in affected muscles.
  • Electrical stimulation is a potential adjunct therapy to enhance BTX-A effects.

Purpose of the Study:

  • To evaluate the effectiveness of electrical stimulation combined with BTX-A injections.
  • To compare outcomes between BTX-A injection with electrical stimulation versus BTX-A injection alone in children with SDCP.

Main Methods:

  • A randomized study included 38 children with SDCP (mean age 6.3 years) with calf muscle spasticity (Modified Ashworth Scale 1+ to 3).
  • Participants received either BTX-A injection plus electrical stimulation (n=19) or BTX-A injection alone (n=19).
  • Evaluations included Modified Ashworth Scale (MAS), Penn Spasm Frequency Scale (PSFS), Gross Motor Function Measure-88 (GMFM-88) Dimensions D and E, and walking velocity.

Main Results:

  • Both groups demonstrated a significant decrease in lower extremity spasticity (p<0.05).
  • No statistically significant differences were observed between the groups in MAS, PSFS, GMFM-88 scores, or walking velocity.

Conclusions:

  • Both treatment approaches (BTX-A with or without electrical stimulation) were beneficial in reducing spasticity.
  • Electrical stimulation applied to gastrocnemius motor points did not offer additional advantages over BTX-A injection alone in this pediatric SDCP cohort.
Abstract

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