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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorNavarro Pérez, María Pilar
dc.contributor.authorGonzalez Quintanilla, Vicente
dc.contributor.authorMuñoz-Vendrell, Albert
dc.contributor.authorMadrigal, Elisabet
dc.contributor.authorLatorre, Germán
dc.contributor.authorAlpuente Ruiz, Alicia
dc.contributor.authorPozo-Rosich, Patricia
dc.date.accessioned2024-07-04T09:59:25Z
dc.date.available2024-07-04T09:59:25Z
dc.date.issued2024-06-13
dc.identifier.citationNavarro-Pérez MP, González-Quintanilla V, Muñoz-Vendrell A, Madrigal E, Alpuente A, Latorre G, et al. Long-term safety of OnabotulinumtoxinA treatment in chronic migraine patients: a five-year retrospective study. Front Neurol. 2024 Jun 13;15:1417831.
dc.identifier.issn1664-2295
dc.identifier.urihttps://hdl.handle.net/11351/11666
dc.descriptionOnabotulinumtoxinA; Chronic migraine; Prophylaxis
dc.description.abstractBackground: Real-world studies have shown the sustained therapeutic effect and favourable safety profile of OnabotulinumtoxinA (BoNTA) in the long term and up to 4 years of treatment in chronic migraine (CM). This study aims to assess the safety profile and efficacy of BoNTA in CM after 5 years of treatment in a real-life setting. Methods: We performed a retrospective chart review of patients with CM in relation to BoNTA treatment for more than 5 years in 19 Spanish headache clinics. We excluded patients who discontinued treatment due to lack of efficacy or poor tolerability. Results: 489 patients were included [mean age 49, 82.8% women]. The mean age of onset of migraine was 21.8 years; patients had CM with a mean of 6.4 years (20.8% fulfilled the aura criteria). At baseline, patients reported a mean of 24.7 monthly headache days (MHDs) and 15.7 monthly migraine days (MMDs). In relation to effectiveness, the responder rate was 59.1% and the mean reduction in MMDs was 9.4 days (15.7 to 6.3 days; p < 0.001). The MHDs were also reduced by 14.9 days (24.7 to 9.8 days; p < 0.001). Regarding the side effects, 17.5% experienced neck pain, 17.3% headache, 8.5% eyelid ptosis, 7.5% temporal muscle atrophy and 3.2% trapezius muscle atrophy. Furthermore, after longer-term exposure exceeding 5 years, there were no serious adverse events (AE) or treatment discontinuation because of safety or tolerability issues. Conclusion: Treatment with BoNTA led to sustained reductions in migraine frequency, even after long-term exposure exceeding 5 years, with no evidence of new safety concerns.
dc.language.isoeng
dc.publisherFrontiers Media
dc.relation.ispartofseriesFrontiers in Neurology;15
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceScientia
dc.subjectMigranya - Tractament
dc.subjectToxina botulínica - Ús terapèutic
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subject.meshMigraine Disorders
dc.subject.mesh/drug therapy
dc.subject.meshBotulinum Toxins, Type A
dc.subject.mesh/therapeutic use
dc.subject.meshTreatment Outcome
dc.titleLong-term safety of OnabotulinumtoxinA treatment in chronic migraine patients: a five-year retrospective study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.3389/fneur.2024.1417831
dc.subject.decstrastornos migrañosos
dc.subject.decs/farmacoterapia
dc.subject.decstoxinas botulínicas de tipo A
dc.subject.decs/uso terapéutico
dc.subject.decsresultado del tratamiento
dc.relation.publishversionhttps://doi.org/10.3389/fneur.2024.1417831
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Navarro-Pérez MP] Hospital Clínico Universitario Lozano Blesa, Zaragoza, Spain. Institute for Health Research Aragon and University of Zaragoza, Zaragoza, Spain. [González-Quintanilla V] Hospital Universitario Marqués de Valdecilla, Universidad de Cantabria e IDIVAL, Santander, Spain. [Muñoz-Vendrell A] Hospital de Bellvitge, Barcelona, Spain. [Madrigal E] Hospital Universitario de Burgos, Burgos, Spain. [Alpuente A, Pozo-Rosich P] Unitat de Cefalees, Servei de Neurologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Grup de Recerca de Cefalea i Dolor Neurològic, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Latorre G] Hospital Universitario de Fuenlabrada, Universidad Rey Juan Carlos, Madrid, Spain
dc.identifier.pmid38938776
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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