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.
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.
Background:
Acute central nervous system (CNS) complications are common and well described among pediatric patients undergoing haematopoietic cell transplantation (HCT). However, their long-term outcomes are not known. The aim of this study is to describe the incidence, characteristics, and risk factors of long-term epilepsy in pediatric patients with acute CNS complications of HCT.
Methods:
This retrospective study included pediatric patients who developed acute CNS complications from autologous or allogeneic HCT between 2000 and 2022. Clinical, therapeutic and prognostic data including long-term outcomes were analyzed. A diagnosis of epilepsy was provided if unprovoked seizures occurred during follow-up.
Results:
Ninety-four patients (63 males, 31 females, median age 10 years, range 1-21 years) were included. The most common acute CNS complications were posterior reversible encephalopathy syndrome (n = 43, 46 %) and infections (n = 15, 16 %). Sixty-five patients (69 %) had acute symptomatic seizures, with 14 (16 %) having one or more episodes of status epilepticus (SE). Nine patients (9.6 %) were diagnosed with long-term focal epilepsy during the follow-up (5-year cumulative incidence from the acute complication, 13.3 %). Acute symptomatic SE during neurological complications of HCT was associated with an increased risk of long-term epilepsy (OR=14, 95 % CI 2.87-68.97).
Conclusions:
A higher occurrence of epilepsy has been observed in our cohort compared to the general population. Acute symptomatic SE during HCT was associated with a higher risk of long-term epilepsy. Pediatric patients with CNS complications during HCT could benefit from specific neurological follow-up. Further studies are needed to characterize mechanisms of epileptogenesis in pediatric patients undergoing HCT.
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