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dc.contributor.authorBurns, Margrete Larsen
dc.contributor.authorNikanorova, Marina
dc.contributor.authorBaftiu, Arton
dc.contributor.authorRasmussen, Jan Borg
dc.contributor.authorJohannessen, Svein Ivar
dc.contributor.authorLandmark, Cecilie Johannessen
dc.date.accessioned2019-03-15T17:22:49Z
dc.date.accessioned2019-03-22T12:23:55Z
dc.date.available2019-03-15T17:22:49Z
dc.date.available2019-03-22T12:23:55Z
dc.date.issued2019-01-01
dc.identifier.citationBurns M, Nikanorova M, Baftiu A, rasmussen jb, Johannessen Si, Landmark CJL. Pharmacokinetic variability and clinical use of lacosamide in children and adolescents in Denmark and Norway. Therapeutic Drug Monitoring. 2019:1-26en
dc.identifier.issn0163-4356
dc.identifier.issn0163-4356
dc.identifier.issn1536-3694
dc.identifier.urihttps://hdl.handle.net/10642/6868
dc.description.abstractBackground: The indication for the antiepileptic drug (AED) lacosamide (LCM) was recently extended to include children from the age of four. Real-life data on the use and serum concentrations of LCM in children and adolescents are limited. The purpose of this study was to investigate the use of LCM in this patient group in relation to age, co medication, dose, serum concentrations and duration of treatment, and to examine pharmacokinetic variability. Methods: Children and adolescents (<18 years) who had serum concentrations of LCM measured from January 2012 to June 2018 were retrospectively identified from the therapeutic drug monitoring (TDM) databases at two national epilepsy centers in Norway and Denmark. Clinical data were collected from request forms and medical records. Results: Data from 124 patients were included, 61 girls/63 boys. Weight was available for 76 patients. Median age was 15 years (range 2-17 years), dose of LCM 300 mg/day (76-600 mg/day) and serum concentration 18 µmol/L (5-138 µmol/L) [4.5 mg/L (1.3-34.5 mg/L)]. Pharmacokinetic variability was demonstrated as the concentration/(dose/kg) ratio ranged from 1.3 to 9.4 (µmol/L)/(mg/kg) and was affected by age. Polytherapy with 1-3 other AEDs was noted in 107 patients (86%). Treatment was continued beyond 1 year in 71% (n=45) of the 63 patients where such information was available, and all of these 45 patients had serum concentrations within the defined reference range. The 1-year retention rate was higher in patients not concomitantly using other sodium channel blocking drugs (82% vs 56%). Conclusion: The study demonstrates pharmacokinetic variability in and between age groups, which indicates usefulness of TDM. More than two thirds of patients continued treatment beyond one year, suggesting reasonable effectiveness.en
dc.language.isoenen
dc.publisherLippincott, Williams & Wilkinsen
dc.relation.ispartofseriesTherapeutic Drug Monitoring;41 (3): 340–347, JUNE 2019
dc.rightsDen aksepterte, fagfellevurderte postprint-versjonen av artikkelene er tillatt å arkivere i institusjonelle arkiv med en embargo på tolv måneder.en
dc.subjectAntiepileptic drugsen
dc.subjectLacosamideen
dc.subjectTherapeutic drug monitoringen
dc.subjectChildrenen
dc.subjectPharmacokinetic variabilitiesen
dc.titlePharmacokinetic variability and clinical use of lacosamide in children and adolescents in Denmark and Norwayen
dc.typeJournal articleen
dc.typePeer revieweden
dc.date.updated2019-03-15T17:22:48Z
dc.description.versionacceptedVersionen
dc.identifier.doihttp://dx.doi.org/10.1097/FTD.0000000000000599
dc.identifier.cristin1685234
dc.source.journalTherapeutic Drug Monitoring


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