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The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review
INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) have been the first-line choice for the acute treatment of migraine attacks for decades; however, the safety of a particular NSAID is related to its treatment dose, duration, and mechanism of action. Although adverse event (AE) risks differ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Healthcare
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199993/ https://www.ncbi.nlm.nih.gov/pubmed/37093356 http://dx.doi.org/10.1007/s40122-023-00501-5 |
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author | Ailani, Jessica Nahas, Stephanie J. Friedman, Deborah I. Kunkel, Todd |
author_facet | Ailani, Jessica Nahas, Stephanie J. Friedman, Deborah I. Kunkel, Todd |
author_sort | Ailani, Jessica |
collection | PubMed |
description | INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) have been the first-line choice for the acute treatment of migraine attacks for decades; however, the safety of a particular NSAID is related to its treatment dose, duration, and mechanism of action. Although adverse event (AE) risks differ substantially among individual migraine treatments, increased or prolonged exposure to any NSAID elevates risks and severity of AEs. METHODS: For this narrative review, we conducted a literature search of PubMed until July 2022, focusing on the history, mechanism of action, and treatment guidelines informing the safety and efficacy of celecoxib oral solution for the acute treatment of migraine attacks. RESULTS: Here we discuss the mechanisms of action of nonselective NSAIDs vs. cyclooxygenase-2 (COX-2) inhibitors, and how these mechanisms underlie the AEs associated with these treatments. We review the clinical trials that influenced the regulatory history of NSAIDs, specifically COX-2 inhibitors, the role of traditional and new formulations of NSAIDs including celecoxib oral solution, and special considerations in the acute treatment of migraine attacks. CONCLUSIONS: Low-dose formulations of NSAIDs, such as celecoxib oral solution, provide acute migraine analgesia with similar or fewer associated cardiovascular and gastrointestinal events than previous formulations. |
format | Online Article Text |
id | pubmed-10199993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-101999932023-05-22 The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review Ailani, Jessica Nahas, Stephanie J. Friedman, Deborah I. Kunkel, Todd Pain Ther Review INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) have been the first-line choice for the acute treatment of migraine attacks for decades; however, the safety of a particular NSAID is related to its treatment dose, duration, and mechanism of action. Although adverse event (AE) risks differ substantially among individual migraine treatments, increased or prolonged exposure to any NSAID elevates risks and severity of AEs. METHODS: For this narrative review, we conducted a literature search of PubMed until July 2022, focusing on the history, mechanism of action, and treatment guidelines informing the safety and efficacy of celecoxib oral solution for the acute treatment of migraine attacks. RESULTS: Here we discuss the mechanisms of action of nonselective NSAIDs vs. cyclooxygenase-2 (COX-2) inhibitors, and how these mechanisms underlie the AEs associated with these treatments. We review the clinical trials that influenced the regulatory history of NSAIDs, specifically COX-2 inhibitors, the role of traditional and new formulations of NSAIDs including celecoxib oral solution, and special considerations in the acute treatment of migraine attacks. CONCLUSIONS: Low-dose formulations of NSAIDs, such as celecoxib oral solution, provide acute migraine analgesia with similar or fewer associated cardiovascular and gastrointestinal events than previous formulations. Springer Healthcare 2023-04-24 2023-06 /pmc/articles/PMC10199993/ /pubmed/37093356 http://dx.doi.org/10.1007/s40122-023-00501-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Review Ailani, Jessica Nahas, Stephanie J. Friedman, Deborah I. Kunkel, Todd The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review |
title | The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review |
title_full | The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review |
title_fullStr | The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review |
title_full_unstemmed | The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review |
title_short | The Safety of Celecoxib as an Acute Treatment for Migraine: A Narrative Review |
title_sort | safety of celecoxib as an acute treatment for migraine: a narrative review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199993/ https://www.ncbi.nlm.nih.gov/pubmed/37093356 http://dx.doi.org/10.1007/s40122-023-00501-5 |
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