Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study.

Complications Epilepsy Hematopoietic cell transplantation Seizures Status epilepticus

Journal

Seizure
ISSN: 1532-2688
Titre abrégé: Seizure
Pays: England
ID NLM: 9306979

Informations de publication

Date de publication:
05 Aug 2024
Historique:
received: 16 05 2024
revised: 17 07 2024
accepted: 01 08 2024
medline: 11 8 2024
pubmed: 11 8 2024
entrez: 10 8 2024
Statut: aheadofprint

Résumé

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. 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. 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). 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.

Sections du résumé

BACKGROUND 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 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 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 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.

Identifiants

pubmed: 39126983
pii: S1059-1311(24)00224-3
doi: 10.1016/j.seizure.2024.08.001
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

85-90

Informations de copyright

Copyright © 2024 British Epilepsy Association. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The Authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Luca Bergonzini (L)

IRCCS 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.

Davide Leardini (D)

Pediatric Hematology and Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Roberta Rao (R)

Department of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum - University of Bologna, Bologna, Italy.

Thomas Foiadelli (T)

Clinica Pediatrica, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Maura Faraci (M)

HSCT Unit, Department of Pediatric Hematology-Oncology, IRCCS Istituto G. Gaslini, Genova, Italy.

Maria Margherita Mancardi (MM)

Unit of Child Neuropsychiatry, member of the ERN EpiCare, IRCCS Gaslini, Genova, Italy.

Giulia Nobile (G)

Unit of Child Neuropsychiatry, member of the ERN EpiCare, IRCCS Gaslini, Genova, Italy.

Alessandro Orsini (A)

Pediatric Neurology, Pediatric Department, AOUP Santa Chiara Hospital, Pisa, Italy.

Salvatore Savasta (S)

Clinica Pediatrica, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; Dipartimento di Scienze Mediche e Salute Pubblica, Università di Cagliari, Italy.

Francesca Gottardi (F)

Department of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum - University of Bologna, Bologna, Italy; Pediatric Hematology and Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Anna Fetta (A)

IRCCS 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.

Tommaso Mina (T)

Pediatric Hematology and Oncology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Gabriella Casazza (G)

Pediatric Hematology and Oncology, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.

Maria Cristina Menconi (MC)

Pediatric Hematology and Oncology, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.

Dario Pruna (D)

Pediatric Neurology and Epileptology Unit, Pediatric Department, ARNAS G. Brotzu/ASL, Cagliari, Italy.

Rosa Maria Mura (RM)

Paediatric Hematology and Oncology Unit, Pediatric Hospital "Microcitemico A. Cao", Cagliari, Italy.

Antonio Piroddi (A)

Bone Marrow Transplant Center, Pediatric Hospital "Microcitemico A. Cao", Cagliari, Italy.

Paola Rucci (P)

Department of Biomedical and Neuromotor Sciences (DIBINEM), Alma Mater Studiorum - University of Bologna, Bologna, Italy.

Riccardo Masetti (R)

Department of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum - University of Bologna, Bologna, Italy; Pediatric Hematology and Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Duccio Maria Cordelli (DM)

IRCCS 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. Electronic address: ducciomaria.cordelli@unibo.it.

Classifications MeSH