Plasma Exchange as a Bridge to Recovery in Severe Pediatric Neurological Diseases in Pediatric Intensive Care

Güntülü Şık1, Gamze Başak1, Tuğba Kanar1

  • 1Department of Pediatric Intensive Care, İstanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, İstanbul, Türkiye.

Insights

Therapeutic plasma exchange (TPE) shows promise for pediatric neurocritical care, with 83% of patients improving. Early TPE initiation (within 7 days) correlated with better outcomes, and the procedure was found to be safe in children.

Area of Science:

  • Pediatric Neurology
  • Neurocritical Care
  • Immunology

Background:

  • Therapeutic plasma exchange (TPE) is established in adult neurology but lacks extensive evidence in pediatric neurocritical care.
  • Limited data exists on the safety and efficacy of TPE for immune-mediated neurological disorders in children.

Purpose of the Study:

  • To assess the indications, clinical effectiveness, and safety of TPE in pediatric patients with acute or subacute immune-mediated neurological conditions.
  • To evaluate TPE's role in the pediatric intensive care unit (PICU) setting.

Main Methods:

  • Retrospective cohort study of 24 pediatric patients (1-18 years) treated with TPE.
  • Analysis of diagnoses including multiple sclerosis, Guillain-Barré syndrome, ADEM, transverse myelitis, autoimmune encephalitis, optic neuritis, and myasthenia gravis.
  • Clinical response assessed using modified Rankin Scale (mRS) and GBS disability scores pre- and post-TPE.

Main Results:

  • 83% of patients (20/24) showed clinical improvement, with 33% experiencing moderate improvement.
  • Median mRS/GBS scores significantly decreased from 4.0 to 3.0 (p=0.001).
  • Early TPE initiation (≤7 days from onset) was linked to improved neurological outcomes; no life-threatening complications were observed.

Conclusions:

  • TPE is a safe and potentially effective treatment for severe pediatric neuroimmunological disorders.
  • Earlier TPE initiation may lead to better neurological outcomes, supporting its integration into PICU management.
  • Further research with larger sample sizes is warranted to confirm these findings in diverse pediatric neuroimmunology cases.
Abstract

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