Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A

Luca Bergonzini1, Davide Leardini2, Roberta Rao3

  • 1IRCCS Istituto delle Scienze Neurologiche di Bologna, U.O.C. Neuropsichiatria dell'età pediatrica, Member of the ERN EpiCare, Bologna, , Italy; Department of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum - University of Bologna, Bologna, Italy.

Seizure
|August 10, 2024
PubMed

Insights

Pediatric patients with central nervous system (CNS) complications after haematopoietic cell transplantation (HCT) have a higher risk of developing long-term epilepsy. Acute symptomatic status epilepticus (SE) during HCT significantly increases this risk, warranting specific neurological follow-up.

Area of Science:

  • Neurology
  • Pediatric Hematology/Oncology
  • Transplantation Medicine

Background:

  • Acute central nervous system (CNS) complications are frequent in pediatric hematopoietic cell transplantation (HCT) patients.
  • Long-term outcomes of these CNS complications, particularly epilepsy, remain largely unknown.
  • This study investigates the incidence, characteristics, and risk factors for long-term epilepsy following acute CNS complications in pediatric HCT.

Purpose of the Study:

  • To determine the incidence and characteristics of long-term epilepsy in pediatric HCT survivors with prior acute CNS complications.
  • To identify risk factors associated with the development of epilepsy.
  • To inform potential follow-up strategies for this vulnerable patient population.

Main Methods:

  • Retrospective analysis of pediatric patients undergoing autologous or allogeneic HCT between 2000 and 2022.
  • Inclusion criteria: development of acute CNS complications post-HCT.
  • Epilepsy diagnosis based on unprovoked seizures during follow-up; data on clinical, therapeutic, and prognostic factors were analyzed.

Main Results:

  • Ninety-four pediatric patients were included (median age 10 years).
  • Most common CNS complications were posterior reversible encephalopathy syndrome (46%) and infections (16%).
  • 9.6% of patients developed long-term focal epilepsy (5-year cumulative incidence 13.3%); acute symptomatic status epilepticus (SE) was a significant risk factor (OR=14).

Conclusions:

  • Pediatric HCT patients with CNS complications exhibit a higher epilepsy occurrence compared to the general population.
  • Acute symptomatic SE during HCT is strongly associated with an increased risk of developing long-term epilepsy.
  • These findings support the need for targeted neurological surveillance in pediatric HCT survivors with CNS complications.
Abstract

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