Cited by 511Epilepsy research and treatmentPharmacological Effects and Toxicity StudiesNeuroscience and Neuropharmacology Research

The DOI matches its Crossref record; 202 of the 205 references it cites were found in a registry or an index; 2 of the 287 sources its claims cite were checked for support.

Benzodiazepines in epilepsy: pharmacology and pharmacokinetics

Open access
Riss, J., Cloyd, J., Gates, J., Collins, S.·2008·Acta Neurologica Scandinavica

Abstract

Benzodiazepines (BZDs) remain important agents in the management of epilepsy. They are drugs of first choice for status epilepticus and seizures associated with post-anoxic insult and are also frequently used in the treatment of febrile, acute repetitive and alcohol withdrawal seizures. Clinical advantages of these drugs include rapid onset of action, high efficacy rates and minimal toxicity. Benzodiazepines are used in a variety of clinical situations because they have a broad spectrum of clinical activity and can be administered via several routes. Potential shortcomings of BZDs include tolerance, withdrawal symptoms, adverse events, such as cognitive impairment and sedation, and drug interactions. Benzodiazepines differ in their pharmacologic effects and pharmacokinetic profiles, which dictate how the drugs are used. Among the approximately 35 BZDs available, a select few are used for the management of seizures and epilepsy: clobazam, clonazepam, clorazepate, diazepam, lorazepam and midazolam. Among these BZDs, clorazepate has a unique profile that includes a long half-life of its active metabolite and slow onset of tolerance. Additionally, the pharmacokinetic characteristics of clorazepate (particularly the sustained-release formulation) could theoretically help minimize adverse events. However, larger, controlled studies of clorazepate are needed to further examine its role in the treatment of patients with epilepsy.

Overview

Integrity signals

Registry

Crossref · 10.1111/j.1600-0404.2008.01004.x

Cites

202 of 202 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

191 Not checked yet · 37 No basis given · 8 Own interpretation · 8 Own result · 2 Supported

Verify all 285 references — free account

Show all 123 claims

  • It may state two separate claims as one. 106
  • Probably not a substantial claim. 28
  • The quote only partly states this claim. 4
123 of 123
  • The paper relies on this without support.

    Changes in simulated plasma DMD peak-to-trough concentrations correspond to clinical risks of breakthrough seizures and drug toxicity.

    “This effect may prevent breakthrough seizures in some patients.”
    “which may reduce the risk of drug toxicity.”
  • The paper relies on this without support.

    Tolerance to antiepileptic drugs is associated with a progressive increase in the number and severity of seizures and an increased risk of withdrawal seizures when the maintenance dose is constant.

    “Tolerance to AEDs is associated with a progressive increase in the number and severity of seizures and an increased risk of withdrawal seizures in the presence of a constant maintenance dose.”
  • The authors state this as an assumption.

    In Bateson's unified model, initial potentiation of the GABA response leads to desensitization, and prolonged desensitization could result in uncoupling as either a signal for or a consequence of receptor internalization.

    “This model assumes that initial potentiation of the GABA response leads to desensitization and that prolonged desensitization could result in uncoupling (as either a signal for or a consequence of receptor internalization, i.e. endocytosis).”
  • The authors state this as an assumption.

    After receptor internalization, degradation of certain receptor subunits could provide a signal for changes in GABA A receptor gene transcription.

    “Subsequent to receptor internalization, degradation of certain receptor subunits could provide a signal for changes in GABA A receptor gene transcription.”
4 of 4

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Citations

Cites

Show all 205 references

Research works printed but not linked: 26

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  4. Hobbs, 1996, Goodman & Gilmans. The pharmacological basis of therapeutics, 361
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  8. Lacy, Anticonvulsants and antimicrobial cytochrome P-450 effects
  9. Goshman, 1999, Clinically significant P450 drug interactions, J Pharm Soc Wisconsin, 23
  10. Riss, The simulation of desmethyldiazepam (DMD) concentrations following missed daily doses of Tranxene-SD and Tranxene T-Tab
  11. Gastaut, 1965, Laction du diazepam (Valium) dans le traitement des formes non-convulsive de lepilepsie generalisee [in French], Rev Neurol (Paris), 112, 99
  12. Schmidt, 2002, Antiepileptic drugs, 206
  13. Schmidt, 1995, Antiepileptic drugs, 705
  14. Sato, 1995, Antiepileptic drugs, 725
  15. Sato, 1977, Clonazepam in the treatment of absence seizures: a double-blind clinical trial [abstract], Neurology, 27, 371
  16. Beck, 1973, Traitement des etats de mal epileptiques par le clonazepam [in French], Sem Hop Paris, 49, 21
  17. Bergamini, 1970, Elektroenzephalographische und klinische Bewertung des neuen Benzodiazepin Ro 54023 [in German], EEG EMG, 1, 182
  18. Bergamini, 1972, LAction du Ro 54023 dans le traitement des differentes formes depilepsie [in French]
  19. Gastaut, 1970, Properties anti-epileptiques exceptionneles dune benzodiazepine nouvelle le Ro 05-4023 [in French], La Vie Medicale, 51, 5175
  20. Gimenez-Roldan, 1972, Un nuevo medicamento eficaz en el trataimento del status epilepticus - Ro 5-4023 [in Spanish], Med Clin (Barc), 58, 133
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  22. 123.Midazolam HCl injection [package insert]. Weston, FL: Apotex Corp, 2000.
  23. Wolf, 1985, Clobazam. Human psychopharmacology and clinical application, 167
  24. Critchley, 1981, Clobazam, 159
  25. Wilson, 1985, Clobazam. Human psychopharmacology and clinical application, 172
  26. Graf, 1987, Clorazepate therapy in children with refractory seizures [abstract], Epilepsia, 28, 606

Cited by

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Metadata

Authors
Riss, J., Cloyd, J., Gates, J., & Collins, S.
Affiliations
  • University of Minnesota (US)
  • Minnesota Epilepsy Group (US)
Corresponding author
Cloyd, J.
Venue
Acta Neurologica Scandinavica
Publisher
Wiley
Published
2008-08
Volume
118
Issue
2
Pages
69-86
ISSN
  • 0001-6314 (ISSN-L)
  • 1600-0404
OpenAlex
W2047978949
Cited by
511
References
205
Citations by year
2026: 10 · 2025: 19 · 2024: 30 · 2023: 26 · 2022: 25 · 2021: 26 · 2020: 40 · 2019: 36 · 2018: 33 · 2017: 25 · 2016: 37 · 2015: 30 · 2014: 39 · 2013: 23 · 2012: 38
FWCI
3.16
Type
journal article
Language
en
Open access
Locations
  • Acta Neurologica Scandinavica (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Clinical Neurology › Epilepsy research and treatment
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmacological Effects and Toxicity Studies
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords
benzodiazepines, epilepsy, pharmacokinetics, pharmacology, clorazepate, clonazepam, diazepam, lorazepam, midazolam, clobazam, drug tolerance, drug interactions, sedation, cognitive impairment, status epilepticus, febrile seizures, alcohol withdrawal seizures
MeSH terms
Benzodiazepines, Epilepsy, Humans

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