Cognitive, adaptive, and behavioral effects of adjunctive rufinamide in Lennox–Gastaut syndrome: A prospective observational clinical study

Lennox–Gastaut syndrome (LGS) is a severe pediatric epilepsy syndrome characterized by multiple drug-resistant seizure types. Children with LGS usually experience cognitive regression, and LGS is almost always associated with moderate to severe cognitive impairment. Rufinamide (RFM) was approved by...

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Veröffentlicht in:Epilepsy & behavior 2020-11, Vol.112, p.107445-107445, Article 107445
Hauptverfasser: Operto, Francesca Felicia, Verrotti, Alberto, Marrelli, Alfonso, Ciuffini, Roberta, Coppola, Giangennaro, Pastorino, Grazia Maria Giovanna, Striano, Pasquale, Sole, Michela, Zucca, Claudio, Manfredi, Valentina, Città, Santina, Elia, Maurizio
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container_title Epilepsy & behavior
container_volume 112
creator Operto, Francesca Felicia
Verrotti, Alberto
Marrelli, Alfonso
Ciuffini, Roberta
Coppola, Giangennaro
Pastorino, Grazia Maria Giovanna
Striano, Pasquale
Sole, Michela
Zucca, Claudio
Manfredi, Valentina
Città, Santina
Elia, Maurizio
description Lennox–Gastaut syndrome (LGS) is a severe pediatric epilepsy syndrome characterized by multiple drug-resistant seizure types. Children with LGS usually experience cognitive regression, and LGS is almost always associated with moderate to severe cognitive impairment. Rufinamide (RFM) was approved by the European Medicines Agency in 2007 for the adjunctive treatment of seizures associated with LGS in patients ≥4 years of age. The primary objective of our study was to assess cognitive, adaptive, and behavior functioning of patients with LGS after 12 months of RFM therapy. This was an observational, multicenter, prospective study involving 16 patients diagnosed with LGS aged between 7 and 58 years (mean = 22 ± 16.3). Fourteen of 16 patients were already on therapy with 3 antiseizure drugs and 2/16 with 4 antiseizure drugs; RFM has been added with 100 mg/week increments up to a dose of 300–2400 mg/day. The participants and their parents underwent a neuropsychological evaluation for the assessment of intellectual, adaptive, and emotional/behavioral functioning (Leiter International Performance Scale-Revised (LEITER-R), Vineland, and Child Behavior CheckList (CBCL), respectively) before the RFM introduction (baseline) and 12 months after the RFM therapy (T2). Physical and neurological examination, electroencephalography (EEG) recording, seizure type and frequency, and adverse reactions were also considered. After 12 months, the total intelligence quotient (IQ) assessed by LEITER-R did not show statistical significant changes, such as there were no statistically significant changes in adaptive functions, assessed by Vineland. Furthermore, there were no statistically significant changes in internalizing and externalizing problems assessed by CBCL. Adjunctive treatment with RFM did not negatively affect cognitive, adaptive function, and emotional profile in patients with LGS after 1 year of follow-up. •We assessed cognitive, adaptive, and behavioral profile after 12 months of RFM therapy in LGS.•The intelligence quotient assessed by Leiter-R did not show statistically significant changes.•There were no statistically significant changes in adaptive functions assessed by Vineland.•There were no statistically significant changes in behavioral problems assessed by CBCL.•Adjunctive treatment with RFN did not negatively affect cognitive, adaptive, and behavioral profile.
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Children with LGS usually experience cognitive regression, and LGS is almost always associated with moderate to severe cognitive impairment. Rufinamide (RFM) was approved by the European Medicines Agency in 2007 for the adjunctive treatment of seizures associated with LGS in patients ≥4 years of age. The primary objective of our study was to assess cognitive, adaptive, and behavior functioning of patients with LGS after 12 months of RFM therapy. This was an observational, multicenter, prospective study involving 16 patients diagnosed with LGS aged between 7 and 58 years (mean = 22 ± 16.3). Fourteen of 16 patients were already on therapy with 3 antiseizure drugs and 2/16 with 4 antiseizure drugs; RFM has been added with 100 mg/week increments up to a dose of 300–2400 mg/day. 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Children with LGS usually experience cognitive regression, and LGS is almost always associated with moderate to severe cognitive impairment. Rufinamide (RFM) was approved by the European Medicines Agency in 2007 for the adjunctive treatment of seizures associated with LGS in patients ≥4 years of age. The primary objective of our study was to assess cognitive, adaptive, and behavior functioning of patients with LGS after 12 months of RFM therapy. This was an observational, multicenter, prospective study involving 16 patients diagnosed with LGS aged between 7 and 58 years (mean = 22 ± 16.3). Fourteen of 16 patients were already on therapy with 3 antiseizure drugs and 2/16 with 4 antiseizure drugs; RFM has been added with 100 mg/week increments up to a dose of 300–2400 mg/day. The participants and their parents underwent a neuropsychological evaluation for the assessment of intellectual, adaptive, and emotional/behavioral functioning (Leiter International Performance Scale-Revised (LEITER-R), Vineland, and Child Behavior CheckList (CBCL), respectively) before the RFM introduction (baseline) and 12 months after the RFM therapy (T2). Physical and neurological examination, electroencephalography (EEG) recording, seizure type and frequency, and adverse reactions were also considered. After 12 months, the total intelligence quotient (IQ) assessed by LEITER-R did not show statistical significant changes, such as there were no statistically significant changes in adaptive functions, assessed by Vineland. Furthermore, there were no statistically significant changes in internalizing and externalizing problems assessed by CBCL. Adjunctive treatment with RFM did not negatively affect cognitive, adaptive function, and emotional profile in patients with LGS after 1 year of follow-up. •We assessed cognitive, adaptive, and behavioral profile after 12 months of RFM therapy in LGS.•The intelligence quotient assessed by Leiter-R did not show statistically significant changes.•There were no statistically significant changes in adaptive functions assessed by Vineland.•There were no statistically significant changes in behavioral problems assessed by CBCL.•Adjunctive treatment with RFN did not negatively affect cognitive, adaptive, and behavioral profile.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32920379</pmid><doi>10.1016/j.yebeh.2020.107445</doi><tpages>1</tpages></addata></record>
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subjects Adolescent
Adult
Anticonvulsants - therapeutic use
Child
Cognition
Cognitive profile
Humans
Lennox Gastaut Syndrome - drug therapy
Lennox–Gastaut syndrome
Middle Aged
Prospective Studies
Rufinamide
Triazoles
Young Adult
title Cognitive, adaptive, and behavioral effects of adjunctive rufinamide in Lennox–Gastaut syndrome: A prospective observational clinical study
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