About this item:

78 Views | 23 Downloads

Author Notes:

Edward Faught, Department of Neurology, Emory University School of Medicine, 12 Executive Park Drive, NE, Atlanta, GA, 30329, USA, Tel +1 404 778-3444, Email rfaught@emory.edu

All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.

Medical writing support was provided at the direction of the authors by Laura J. Herold, MA, of The Curry Rockefeller Group, LLC (Tarrytown, NY), which also provided additional editorial assistance including formatting and proofreading. This support was funded by Neurelis, Inc. (San Diego, CA). Portions of this paper were presented at the Academy of Managed Care Pharmacy 2020 Annual Meeting, the Academy of Managed Care Pharmacy Nexus 2020, and the American Epilepsy Society 2020 Annual Meeting as poster presentations with interim findings. Final results were presented at the American Academy of Neurology 2021 Annual Meeting and the 2021 International Epilepsy Congress as poster presentations.

Drs Rabinowicz and Cook are employees of and have received stock options from Neurelis, Inc. Dr Faught has been a member of scientific advisory boards for Eisai Ltd., Neurelis, Inc., SK Life Science, Sage Pharmaceuticals, and Biogen, and has received research support from UCB Pharma. Dr Carrazana is an employee of and has received stock and stock options from Neurelis, Inc. The authors report no other conflicts of interest in this work.

Subject:

Research Funding:

This study was funded by Neurelis, Inc.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Clinical Neurology
  • Psychiatry
  • Neurosciences & Neurology
  • diazepam
  • midazolam
  • nasal
  • rectal
  • acute repetitive seizures
  • twenty-four hours
  • DIAZEPAM RECTAL GEL
  • UNITED-STATES
  • EPILEPSY
  • PHARMACOKINETICS
  • INTRANASAL
  • CHILDREN
  • ADULTS
  • COSTS

Implications of Seizure-Cluster Treatment on Healthcare Utilization: Use of Approved Rescue Medications

Tools:

Journal Title:

NEUROPSYCHIATRIC DISEASE AND TREATMENT

Volume:

Volume 18

Publisher:

, Pages 2431-2441

Type of Work:

Article | Final Publisher PDF

Abstract:

Purpose: People with epilepsy may experience seizure clusters despite a stable regimen of antiseizure medications. Such clusters have the potential to last ≥24 hours, typically occur in the community setting, and may progress to medical emergencies, such as status epilepticus, if untreated. Thus, long-acting rescue therapy for seizure clusters is needed that can be administered by nonmedical individuals outside a hospital. Benzodiazepines are the foundation of rescue therapy for seizure clusters. The approved outpatient treatments (ie, diazepam, midazolam) have differing profiles that may affect multiple aspects of health-care utilization. The current labeling of these medications allows for a second dose if needed to control the cluster. Although no head-to-head studies directly comparing rescue treatments have been conducted, differences between studies with generally similar designs may provide context for the potential importance of second doses of rescue therapy on health-care utilization. Methods: For this analysis, large, long-term, open-label studies of approved seizure-cluster treatments designed for use by nonmedical caregivers were reviewed, and the percentage of seizure clusters for which a second dose was used or that were not controlled at 6, 12, and 24 hours was examined. Available data on hospitalizations were also collected. Results: The 3 identified studies meeting the inclusion criteria were for use of diazepam rectal gel, intranasal midazolam, and diazepam nasal spray. Across these studies, the use of a second dose ranged from <40% at 6 hours to <13% at 24 hours. Hospitalizations and serious treatment-emergent adverse events were reported variably across these studies. Conclusion: These results demonstrate the importance of second doses of rescue therapy for seizure clusters for optimizing healthcare utilization. Need for second doses should be included as one component. In turn, when second doses are needed, they have the potential to curtail emergency department use and hospitalization and to prevent further seizure clusters.

Copyright information:

© 2022 Rabinowicz et al.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License (https://creativecommons.org/licenses/by-nc/3.0/).
Export to EndNote