Publication:
CLB add-on treatment in patients with epileptic encephalopathy: a single center experience with long-term follow-up

dc.contributor.authorTÜRKDOĞAN, DİLŞAD
dc.contributor.authorsTurkdogan, Dilsad; Ozturk, Gulten
dc.date.accessioned2022-03-12T22:55:27Z
dc.date.accessioned2026-01-11T13:17:32Z
dc.date.available2022-03-12T22:55:27Z
dc.description.abstractClobazam (CLB) is an effective anticonvulsant used as an adjunctive treatment for several seizures and epilepsy syndromes. Data are limited on efficacy and safety of CLB as add-on therapy for epileptic encephalopaties (EEs) other than Lennox-Gastaut syndrome (LGS). This retrospective study aimed to assess efficacy and safety of long-term CLB add-on therapy for various EE syndromes. Data on CLB add-on therapy were assessed in 74 children (60.8% male) after 3 months (early) and 12 months (late) follow-up as well as in 57 (77%) patients who had been on CLB therapy longer than 12 months (mean:39.11 +/- 30.29; range:12-129 months) (very late) were reported. Data on CLB add-on therapy were assessed in 74 children (60.8% male) after 3 months (early) and 12 months (late) follow-up as well as in 57 (77%) patients who had been on CLB therapy longer than 12 months (mean:39.11 +/- 30.29; range:12-129 months) (very late) were reported. Good response rate (> 50%) for seizures was achieved in 24% at early follow-up, 30% at late follow-up, and 35% during very late follow-up. Complete seizure remission was achieved for 15% seizures; 72.7% occurred at very late follow-up. Myoclonic seizures were the most responsive (35%); this response increased during late follow-up (46%), whereas 27.3% of myoclonic-atonic/atonic seizures had good response at early and very late follow-up. At late follow-up, comparison of mean effective doses of CLB did not show significant difference among types of seizures with good response. Adverse effects reported in 15% of patients did not require stopping CLB therapy. Generalized epileptogenic potentials significantly decreased while focal epileptogenic potentials significantly increased at first year of treatment in comparison to basal EEG findings (p < 0.001). CLB should be considered as an optional antiepileptic that is well tolerated, particularly in EEs with myoclonic and myoclonic-atonic/atonic seizures.
dc.identifier.doi10.1007/s13760-021-01606-4
dc.identifier.eissn2240-2993
dc.identifier.issn0300-9009
dc.identifier.pubmed33782854
dc.identifier.urihttps://hdl.handle.net/11424/236748
dc.identifier.wosWOS:000634715300001
dc.language.isoeng
dc.publisherSPRINGER HEIDELBERG
dc.relation.ispartofACTA NEUROLOGICA BELGICA
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectClobazam
dc.subjectEfficacy
dc.subjectEpileptic encephalopathies
dc.subjectTolerance
dc.subjectMyoclonic-atonic
dc.subjectatonic seizures
dc.subjectsafety
dc.titleCLB add-on treatment in patients with epileptic encephalopathy: a single center experience with long-term follow-up
dc.typearticle
dspace.entity.typePublication
oaire.citation.titleACTA NEUROLOGICA BELGICA

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