209 research outputs found
Best mulig behandling med antiepileptika for den enkelte pasient!
Hensikt
«Best mulig behandling med antiepileptika
for den enkelte pasient!» er et
avgjørende
mål for behandling av pasienter
med epilepsi,
men også for stadig nye
pasientgrupper
som bruker antiepileptika.
Hensikten
med artikkelen er å gi en oppdatert
oversikt over metoder og anvendelse av
klinisk farmakologi for antiepileptika, med
fokus på populasjons- og pasientaspekter.
Materiale og metoder
Artikkelen er basert på erfaring og
et utvalg av litteratur fra forfatternes
forskningsbakgrunn.
Resultater
Det er fokusert på to tilnærminger for å
studere
klinisk farmakologi av antiepileptika.
Endring i bruk av antiepileptika ved epilepsi
og andre indikasjoner (smerte og psykiatri),
polyterapi og psykiatrisk komorbiditet
kan
undersøkes ved farmakoepidemiologiske
studier, for eksempel ved bruk av Reseptregisteret.
Slike studier kan være til hjelp
også i behandling av den enkelte pasient.
Farmakokinetisk variabilitet hos enkeltpasienter
og i spesielle pasientgrupper
som barn, gravide og eldre kan studeres
ved bruk av data fra terapeutisk legemiddelmonitorering.
Dermed
kan dosen bedre
tilpasses individuelt for optimalisering av
behandlingen. Utfordringer inkluderer
aldersrelaterte endringer i farmakokinetikk,
interaksjoner, farmakogenetisk variasjon,
stor bivirkningsbelastning og varierende
etterlevelse.
Konklusjon
Kunnskap om bruk og oppfølging av
antiepileptika
i hele populasjonen og i
spesielle pasientgrupper er viktig for å
oppnå en best mulig behandling for den
enkelte pasient
Legemidler og pasientsikkerhet – fokus på eldre
Fagartikkel som beskriver utfordringer knyttet til legemiddelbruk hos eldre.Hensikt: eldre står for en stor andel av det totale legemiddelbruket og bruker ofte flere ulike legemidler samtidig. Legemiddelbruk hos eldre er dermed et stort og viktig område. Hensikten med denne oversiktsartikkelen er å peke på utfordringer relatert til legemiddelbruk hos eldre og vise hvordan feil legemiddelbruk kan oppstå og mer optimal behandling kan tilstrebes. Materiale og metode: artikkelen favner bredt og dekker ulike fagområder som samfunnsfarmasi, galenisk farmasi, farmakologi og legemiddelanalyse. Den er basert på utvalgte forskningsartikler publisert i internasjonale eller norske vitenskapelige tidsskrifter. Egen forskning er trukket frem særskilt. Resultater: sannsynligheten for feil og uhensiktsmessig bruk av legemidler øker hos pasienter med høy alder. Høy alder medfører også ofte polyfarmasi, noe som øker sannsynligheten for feil ytterligere. Fysiologiske endringer kan føre til endret farmakokinetikk, svelgevansker, og at det blir vanskeligere for pasienten å sette seg godt inn i sin egen medikamentelle behandling for dermed å kunne oppdage eventuelle feil. Ulike utfordringer følger av dette, og kan relateres til forskrivningssituasjonen, utfordringer relatert til skifte mellom ulike omsorgsnivå, legemiddelhåndtering og etterlevelse. Konklusjon: optimal legemiddelbruk hos eldre er en utfordrende problemstilling. Valg av indikasjon og legemiddel, formulering, dosering, behov for informasjon og hvorvidt legemiddellistene er samstemte bør vurderes kritisk. En god balanse mellom effekt og tolerabilitet og total legemiddelbelastning bør tilstrebes
Drugs that lower the seizure threshold
Drugs with potential to lower the seizure threshold are numerous and diverse. Whether they contribute to clinically overt seizures depends on the dosage in which they are taken, the time-course of their effects and the susceptibility of the patient. Crucially, however, their contribution to seizure risk is potentially modifiable
A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies
Objective: Clinical care of rare and complex epilepsies is challenging, because evidence-based treatment guidelines are scarce, the experience of many physicians is limited, and interdisciplinary treatment of comorbidities is required. The pathomechanisms of rare epilepsies are, however, increasingly understood, which potentially fosters novel targeted therapies. The objectives of our survey were to obtain an overview of the clinical practice in European tertiary epilepsy centers treating patients with 5 arbitrarily selected rare epilepsies and to get an estimate of potentially available patients for future studies.
Methods: Members of the European Reference Network for rare and complex epilepsies (EpiCARE) were invited to participate in a web-based survey on clinical practice of patients with Dravet syndrome, tuberous sclerosis complex (TSC), autoimmune encephalitis, and progressive myoclonic epilepsies including Unverricht Lundborg and Unverricht-like diseases. A consensus-based questionnaire was generated for each disease.
Results: Twenty-six of 30 invited epilepsy centers participated. Cohorts were present in most responding centers for TSC (87%), Dravet syndrome (85%), and autoimmune encephalitis (71%). Patients with TSC and Dravet syndrome represented the largest cohorts in these centers. The antiseizure drug treatments were rather consistent across the centers especially with regard to Dravet syndrome, infantile spasms in TSC, and Unverricht Lundborg / Unverricht-like disease. Available, widely used targeted therapies included everolimus in TSC and immunosuppressive therapies in autoimmune encephalitis. Screening for comorbidities was routinely done, but specific treatment protocols were lacking in most centers.
Significance: The survey summarizes the current clinical practice for selected rare epilepsies in tertiary European epilepsy centers and demonstrates consistency as well as heterogeneity in the treatment, underscoring the need for controlled trials and recommendations. The survey also provides estimates for potential participants of clinical trials recruited via EpiCARE, emphasizing the great potential of Reference Networks for future studies to evaluate new targeted therapies and to identify novel biomarkers.info:eu-repo/semantics/publishedVersio
A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies
Objective: Clinical care of rare and complex epilepsies is challenging, because evidence‐based treatment guidelines are scarce, the experience of many physicians is limited, and interdisciplinary treatment of comorbidities is required. The pathomechanisms of rare epilepsies are, however, increasingly understood, which potentially fosters novel targeted therapies. The objectives of our survey were to obtain an overview of the clinical practice in European tertiary epilepsy centers treating patients with 5 arbitrarily selected rare epilepsies and to get an estimate of potentially available patients for future studies. /
Methods: Members of the European Reference Network for rare and complex epilepsies (EpiCARE) were invited to participate in a web‐based survey on clinical practice of patients with Dravet syndrome, tuberous sclerosis complex (TSC), autoimmune encephalitis, and progressive myoclonic epilepsies including Unverricht Lundborg and Unverricht‐like diseases. A consensus‐based questionnaire was generated for each disease. /
Results: Twenty‐six of 30 invited epilepsy centers participated. Cohorts were present in most responding centers for TSC (87%), Dravet syndrome (85%), and autoimmune encephalitis (71%). Patients with TSC and Dravet syndrome represented the largest cohorts in these centers. The antiseizure drug treatments were rather consistent across the centers especially with regard to Dravet syndrome, infantile spasms in TSC, and Unverricht Lundborg / Unverricht‐like disease. Available, widely used targeted therapies included everolimus in TSC and immunosuppressive therapies in autoimmune encephalitis. Screening for comorbidities was routinely done, but specific treatment protocols were lacking in most centers. /
Significance: The survey summarizes the current clinical practice for selected rare epilepsies in tertiary European epilepsy centers and demonstrates consistency as well as heterogeneity in the treatment, underscoring the need for controlled trials and recommendations. The survey also provides estimates for potential participants of clinical trials recruited via EpiCARE, emphasizing the great potential of Reference Networks for future studies to evaluate new targeted therapies and to identify novel biomarkers
A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies
Objective: Clinical care of rare and complex epilepsies is challenging, because evidence-based treatment guidelines are scarce, the experience of many physicians is limited, and interdisciplinary treatment of comorbidities is required. The pathomechanisms of rare epilepsies are, however, increasingly understood, which potentially fosters novel targeted therapies. The objectives of our survey were to obtain an overview of the clinical practice in European tertiary epilepsy centers treating patients with 5 arbitrarily selected rare epilepsies and to get an estimate of potentially available patients for future studies. Methods: Members of the European Reference Network for rare and complex epilepsies (EpiCARE) were invited to participate in a web-based survey on clinical practice of patients with Dravet syndrome, tuberous sclerosis complex (TSC), autoimmune encephalitis, and progressive myoclonic epilepsies including Unverricht Lundborg and Unverricht-like diseases. A consensus-based questionnaire was generated for each disease. Results: Twenty-six of 30 invited epilepsy centers participated. Cohorts were present in most responding centers for TSC (87%), Dravet syndrome (85%), and autoimmune encephalitis (71%). Patients with TSC and Dravet syndrome represented the largest cohorts in these centers. The antiseizure drug treatments were rather consistent across the centers especially with regard to Dravet syndrome, infantile spasms in TSC, and Unverricht Lundborg / Unverricht-like disease. Available, widely used targeted therapies included everolimus in TSC and immunosuppressive therapies in autoimmune encephalitis. Screening for comorbidities was routinely done, but specific treatment protocols were lacking in most centers. Significance: The survey summarizes the current clinical practice for selected rare epilepsies in tertiary European epilepsy centers and demonstrates consistency as well as heterogeneity in the treatment, underscoring the need for controlled trials and recommendations. The survey also provides estimates for potential participants of clinical trials recruited via EpiCARE, emphasizing the great potential of Reference Networks for future studies to evaluate new targeted therapies and to identify novel biomarkers
A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies
Objective: Clinical care of rare and complex epilepsies is challenging, because evidence-based treatment guidelines are scarce, the experience of many physicians is limited, and interdisciplinary treatment of comorbidities is required. The pathomechanisms of rare epilepsies are, however, increasingly understood, which potentially fosters novel targeted therapies. The objectives of our survey were to obtain an overview of the clinical practice in European tertiary epilepsy centers treating patients with 5 arbitrarily selected rare epilepsies and to get an estimate of potentially available patients for future studies. Methods: Members of the European Reference Network for rare and complex epilepsies (EpiCARE) were invited to participate in a web-based survey on clinical practice of patients with Dravet syndrome, tuberous sclerosis complex (TSC), autoimmune encephalitis, and progressive myoclonic epilepsies including Unverricht Lundborg and Unverricht-like diseases. A consensus-based questionnaire was generated for each disease. Results: Twenty-six of 30 invited epilepsy centers participated. Cohorts were present in most responding centers for TSC (87%), Dravet syndrome (85%), and autoimmune encephalitis (71%). Patients with TSC and Dravet syndrome represented the largest cohorts in these centers. The antiseizure drug treatments were rather consistent across the centers especially with regard to Dravet syndrome, infantile spasms in TSC, and Unverricht Lundborg / Unverricht-like disease. Available, widely used targeted therapies included everolimus in TSC and immunosuppressive therapies in autoimmune encephalitis. Screening for comorbidities was routinely done, but specific treatment protocols were lacking in most centers. Significance: The survey summarizes the current clinical practice for selected rare epilepsies in tertiary European epilepsy centers and demonstrates consistency as well as heterogeneity in the treatment, underscoring the need for controlled trials and recommendations. The survey also provides estimates for potential participants of clinical trials recruited via EpiCARE, emphasizing the great potential of Reference Networks for future studies to evaluate new targeted therapies and to identify novel biomarkers
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