Australian children undergoing selective dorsal rhizotomy: protocol for a national registry of multidimensional

Jennifer Lewis1, Natasha Bear2, Felicity Baker3

  • 1The Children's Hospital at Westmead, Kids Rehab, Sydney, New South Wales, Australia.

BMJ Open
|May 4, 2019
PubMed

Insights

Selective dorsal rhizotomy (SDR) helps reduce spasticity in children with cerebral palsy (CP). This study tracks outcomes and adverse events to guide families considering this neurosurgical intervention.

Area of Science:

  • Neurosurgery
  • Pediatric Neurology
  • Rehabilitation Medicine

Background:

  • Selective dorsal rhizotomy (SDR) is a surgical option for reducing lower limb spasticity in children with cerebral palsy (CP).
  • Existing evidence on SDR's effectiveness in improving gait, function, and participation is limited, with varying study methodologies complicating clinical guidance.
  • There is significant interest in SDR among families, with some seeking the procedure internationally.

Purpose of the Study:

  • To establish the Australian SDR Research Registry for collecting multidimensional outcomes and adverse event data in Australian children undergoing SDR.
  • To enhance understanding of the short-, medium-, and long-term effects of SDR.
  • To provide crucial data for clinicians to guide families considering SDR for their children with CP.

Main Methods:

  • The Australian SDR Research Registry will collect data for up to 10 years post-surgery.
  • Data includes surgical details, admission information, adverse events, and outcomes across ICF domains (body structure/function, activity, participation).
  • Data collection points are baseline, inpatient stay, and 1, 2, 5, and 10 years post-surgery.

Main Results:

  • This is a pre-results study; no main results are available yet.
  • The study aims to capture comprehensive data on the effectiveness and safety of SDR.
  • Long-term outcome data will be collected to address current evidence gaps.

Conclusions:

  • The Australian SDR Research Registry will provide valuable insights into the outcomes of SDR for children with CP.
  • This national registry aims to improve evidence-based decision-making for clinicians and families.
  • Dissemination of findings will occur through peer-reviewed publications and conference presentations.
Abstract

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