[Rhizotomy for children with severe spastic cerebral palsy]

Niels Ove Illum1, Lisbeth Torp-Pedersen, Steen Midholm

  • 1Odense Universitetshospital, Børneafdeling H, Børneneurologisk Afsnit, Fysioterapiafdelingen, Odense. niels.illum@ouh.fyns-amt.dk

Ugeskrift for Laeger
|February 28, 2006
PubMed

Insights

Selective dorsal rhizotomy (SDR) significantly reduced spasticity in children with cerebral palsy, with lasting effects observed up to 60 months post-surgery. Functional improvements required dedicated training and time, becoming significant after five years.

Area of Science:

  • Neurosurgery
  • Pediatric Neurology
  • Rehabilitation Medicine

Context:

  • Severe spasticity in children with cerebral palsy significantly hinders motor development.
  • Established treatments like botulinum toxin and baclofen may limit long-term functional gains.
  • Selective dorsal rhizotomy (SDR) preserves motor fibers while cutting sensory afferents to reduce spasticity.

Purpose:

  • To evaluate the efficacy and long-term outcomes of selective dorsal rhizotomy (SDR) in reducing spasticity and improving motor function in children with severe spastic cerebral palsy.
  • To report the first Danish study on SDR for pediatric cerebral palsy.

Summary:

  • Twenty children (ages 4-16) with severe spastic cerebral palsy underwent SDR, with 20-40% of dorsal root filaments (LII-SII) cut.
  • Spasticity scores significantly improved from baseline (median 3.1) to 18 months (median 1.0) and 60 months (median 1.0) post-operation (p < 0.001).
  • While mobility showed initial non-significant improvement at 18 months, it became significant by 60 months (p < 0.05), with younger age correlating with better functional outcomes (r=0.8).

Impact:

  • SDR provides early and sustained spasticity reduction in pediatric cerebral palsy.
  • Significant functional improvements are achievable but necessitate consistent post-operative training and extended follow-up (up to 60 months).
  • This study establishes SDR as a viable, effective treatment option for improving motor function in children with severe spastic cerebral palsy.
Abstract

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