Evidence map›Paper›PMID 38573131›Full record

ArticleEpilepsia open2024

Spanish consensus on the management of concomitant antiseizure medications when using cenobamate in adults with drug-resistant focal seizures.

Mar Carreño, Antonio Gil-Nagel, José M Serratosa, Manuel Toledo, Juan Jesus Rodriguez-Uranga, Vicente Villanueva

Open access · goldAbstract readConsensus Statement
In one paragraph

Article in Epilepsia open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Article
  4. Cenobamate: An Appraisal Five Years On.Neurology and therapy · 2026
    Review
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  6. Observational
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  10. Article
  11. Review
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  17. Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 6 institutions in 2 countries.

Mar CarreñoHospital Clinic Barcelona, Epilepsy Unit, Barcelona, Spain.ORCID https://orcid.org/0000-0002-3361-8427
Antonio Gil-NagelDepartment of Neurology, Epilepsy Program, Ruber International Hospital, Madrid, Spain.ORCID https://orcid.org/0000-0003-4515-0793
José M SerratosaDepartment of Neurology, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
Manuel ToledoVall d'Hebron University Hospital, Epilepsy Unit, Barcelona, Spain.
Juan Jesus Rodriguez-UrangaAdvanced Neurological Centre, Seville, Spain.ORCID https://orcid.org/0009-0007-5354-1256
Vicente VillanuevaLa Fe University and Polytechnic Hospital, Refractory Epilepsy Unit, Valencia, Spain.ORCID https://orcid.org/0000-0003-2080-8042
Center for Advanced Aerospace Technologies · ESHebron University · PSHospital Clínic de Barcelona · ESHospital Ruber Internacional · ESHospital Universitari i Politècnic La Fe · ESHospital Universitario Fundación Jiménez Díaz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCenobamate is an antiseizure medication (ASM) associated with high rates of seizure freedom and acceptable tolerability in patients with focal seizures. To achieve the optimal cenobamate dose for maximal potential effectiveness while avoiding or minimizing drug-related adverse events (AEs), the administration of cenobamate with other ASMs must be managed through concomitant ASM load reduction. A panel of Spanish epilepsy experts aimed to provide a Spanish consensus on how to adjust the dose of concomitant ASMs in patients with drug-resistant epilepsy (DRE) in order to improve the effectiveness and tolerability of adjunctive cenobamate.

methodsA three-stage modified Delphi consensus process was undertaken, including six Spanish epileptologists with extensive experience using cenobamate. Based on current literature and their own expert opinion, the expert panel reached a consensus on when and how to adjust the dosage of concomitant ASMs during cenobamate titration.

resultsThe expert panel agreed that tailored titration and close follow-up are required to achieve the best efficacy and tolerability when initiating cenobamate in patients receiving concomitant ASMs. When concomitant clobazam, phenytoin, phenobarbital, and sodium channel blockers are taken at high dosages, or when the patient is receiving two or more sodium channel blockers, dosages should be proactively lowered during the cenobamate titration period. Other concomitant ASMs should be reduced only if the patient reports a moderate/severe AE at any stage of the titration period. SIGNIFICANCE: Cenobamate is an effective ASM with a dose-dependent effect. To maximize effectiveness while maintaining the best tolerability profile, co-medication management is needed. The recommendations included herein provide practical guidance for proactive and reactive management of co-medication in cenobamate-treated patients with DRE and a high drug load. PLAIN LANGUAGE SUMMARY: Patients with epilepsy may continue to have seizures even after treatment with several different antiseizure medications (ASMs). Cenobamate is an ASM that can reduce seizures in these patients. In this study, six Spanish experts in epilepsy discussed the best way to use cenobamate in drug-resistant epilepsy. They provide practical guidance on when and how the dose of other ASMs might be adjusted to reduce side effects and optimize the use of cenobamate.

Indexed as

AnticonvulsantsCarbamatesChlorophenolsDrug Resistant EpilepsyDrug Therapy, CombinationAdultDelphi TechniqueEpilepsies, PartialHumansSeizuresSpainTetrazolesAnticonvulsantsCarbamatesCenobamateChlorophenolsTetrazolesantiseizure medicationcenobamatedosage adjustmentepilepsytitration

Identifiers

PMID38573131
PMCPMC11145622
OpenAlexW4393933177

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.