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Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome
BACKGROUND: In October 2011, clobazam was FDA-approved for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS), a debilitating childhood epilepsy characterized by drop attacks, for patients 2 years and older. OBJECTIVES: To assess the budget impact of adding clobazam to a...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Academy of Managed Care Pharmacy
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10437444/ https://www.ncbi.nlm.nih.gov/pubmed/24684645 http://dx.doi.org/10.18553/jmcp.2014.20.4.400 |
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author | Skornicki, Michelle Clements, Karen M. O’Sullivan, Amy K. |
author_facet | Skornicki, Michelle Clements, Karen M. O’Sullivan, Amy K. |
author_sort | Skornicki, Michelle |
collection | PubMed |
description | BACKGROUND: In October 2011, clobazam was FDA-approved for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS), a debilitating childhood epilepsy characterized by drop attacks, for patients
2 years and older. OBJECTIVES: To assess the budget impact of adding clobazam to an antiepileptic drug (AED) portfolio containing topiramate, lamotrigine, and rufinamide in a hypothetical, 100,000-member commercially insured health plan. METHODS: Patient characteristics and AED efficacy (decrease in drop-seizure frequency) were modeled with clinical data. Medical costs were derived from administrative claims data from a large U.S. managed health plan, with the assumption that 2.3% of drop seizures required medical care. Two-year budget impact was measured. Results were expressed as the overall difference in costs (medical and pharmacy) to a health plan and cost per member per month (PMPM) after addition of clobazam. Analyses of alternative scenarios were performed. RESULTS: With the assumption that 0.04% of the plan population had LGS, adding clobazam to the formulary resulted in cost savings of $98,059 in year 1 and $131,690 in year 2 (savings of $0.08 and $0.11 PMPM, respectively). Analyses of alternative scenarios with lower seizure rates upon discontinuation or greater long-term efficacy for lamotrigine and topiramate did not substantially alter conclusions. The assumption that fewer drop seizures required medical care resulted in a savings of approximately $5,000 per year with clobazam, which suggested that medically attended drop seizures drive costs. CONCLUSIONS: Medically attended drop seizures are a major cost driver for LGS patients. Adding clobazam to a health plan formulary can have a positive overall budget impact through decreased medical costs associated with drop seizures. |
format | Online Article Text |
id | pubmed-10437444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Academy of Managed Care Pharmacy |
record_format | MEDLINE/PubMed |
spelling | pubmed-104374442023-08-21 Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome Skornicki, Michelle Clements, Karen M. O’Sullivan, Amy K. J Manag Care Pharm Research BACKGROUND: In October 2011, clobazam was FDA-approved for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS), a debilitating childhood epilepsy characterized by drop attacks, for patients
2 years and older. OBJECTIVES: To assess the budget impact of adding clobazam to an antiepileptic drug (AED) portfolio containing topiramate, lamotrigine, and rufinamide in a hypothetical, 100,000-member commercially insured health plan. METHODS: Patient characteristics and AED efficacy (decrease in drop-seizure frequency) were modeled with clinical data. Medical costs were derived from administrative claims data from a large U.S. managed health plan, with the assumption that 2.3% of drop seizures required medical care. Two-year budget impact was measured. Results were expressed as the overall difference in costs (medical and pharmacy) to a health plan and cost per member per month (PMPM) after addition of clobazam. Analyses of alternative scenarios were performed. RESULTS: With the assumption that 0.04% of the plan population had LGS, adding clobazam to the formulary resulted in cost savings of $98,059 in year 1 and $131,690 in year 2 (savings of $0.08 and $0.11 PMPM, respectively). Analyses of alternative scenarios with lower seizure rates upon discontinuation or greater long-term efficacy for lamotrigine and topiramate did not substantially alter conclusions. The assumption that fewer drop seizures required medical care resulted in a savings of approximately $5,000 per year with clobazam, which suggested that medically attended drop seizures drive costs. CONCLUSIONS: Medically attended drop seizures are a major cost driver for LGS patients. Adding clobazam to a health plan formulary can have a positive overall budget impact through decreased medical costs associated with drop seizures. Academy of Managed Care Pharmacy 2014-04 /pmc/articles/PMC10437444/ /pubmed/24684645 http://dx.doi.org/10.18553/jmcp.2014.20.4.400 Text en Copyright © 2014, Academy of Managed Care Pharmacy. All rights reserved. https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Skornicki, Michelle Clements, Karen M. O’Sullivan, Amy K. Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome |
title | Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome |
title_full | Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome |
title_fullStr | Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome |
title_full_unstemmed | Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome |
title_short | Budget Impact Analysis of Antiepileptic Drugs for Lennox-Gastaut Syndrome |
title_sort | budget impact analysis of antiepileptic drugs for lennox-gastaut syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10437444/ https://www.ncbi.nlm.nih.gov/pubmed/24684645 http://dx.doi.org/10.18553/jmcp.2014.20.4.400 |
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