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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorPensato, Umberto
dc.contributor.authorOrnello, Raffaele
dc.contributor.authorRosignoli, Chiara
dc.contributor.authorCaponnetto, Valeria
dc.contributor.authorOnofri, Agnese
dc.contributor.authorBraschinsky, Mark
dc.contributor.authorPozo-Rosich, Patricia
dc.contributor.authorMuñoz-Vendrell, Albert
dc.date.accessioned2025-10-29T08:50:38Z
dc.date.available2025-10-29T08:50:38Z
dc.date.issued2025-08-15
dc.identifier.citationPensato U, Ornello R, Rosignoli C, Caponnetto V, Onofri A, Braschinsky M, et al. Longitudinal assessment of migraine burden in resistant and refractory migraine – Data from the prospective REFINE study. J Headache Pain. 2025 Aug 15;26:184.
dc.identifier.issn1129-2377
dc.identifier.urihttp://hdl.handle.net/11351/13952
dc.descriptionChronic migraine; Disability; Gepants
dc.description.abstractBackground: Some individuals with migraine fail to respond adequately to preventive treatments, bearing most of migraine burden. The European Headache Federation (EHF) classifies these individuals into resistant migraine (ResM) or refractory migraine (RefM) according to treatment failures, debilitating headache days, and disease duration. We investigated the evolution of these categories over six months in patients treated at tertiary headache centers and whether they accurately reflect disability and burden. Methods: Participants from the multicenter, prospective REFINE study were classified into three categories of treatment responsiveness, namely RefM, ResM, and non-refractory non-resistant migraine (NRNRM). The primary objective was to determine the trajectories of category changes over six months. Secondary outcomes included changes in the 6-item Headache Impact Test (HIT-6), Headache-Attributed Lost Time (HALT), and Hospital Anxiety and Depression Scale (HADS-A and HADS-D) scores. Results: Overall, 489 participants were included with a median age of 45 years (IQR = 36-53); 389 participants (79.7%) were female; 256 (52.4%) had NRNRM, 178 (36.4%) ResM, and 55 (11.2%) RefM. At follow-up, 200/256 (78.1%) NRNRM remained stable, while 56/256 (21.9%) progressed to ResM. Among those with ResM, 98/178 (55.1%) remained stable, 72/178 (40.5%) improved to NRNRM, and 8/178 (4.5%) worsened to RefM. Among participants with RefM, 37/55 (67.3%) remained stable, while 18/55 (32.7%) improved to NRNRM. Participants with RefM and ResM presented significantly higher scores at baseline than those with NRNRM. Over time, HIT-6, HALT, and HADS-A scores improved substantially in the overall cohort (p < 0.001, p < 0.001, and p = 0.006, respectively). Improvements were observed in participants with ResM across all scores and HIT-6 and HALT for NRNRM, but no improvement was noted in participants with RefM. Conclusions: Over six months, ~ 40% of ResM and ~ 30% of RefM individuals improved to NRNRM, while ~ 20% of NRNRM developed treatment resistance after receiving care in tertiary headache centers. Participants with ResM had a better prognosis than those with RefM. While both ResM and RefM reflect high migraine disability burden, they might present relevant differences in their management and prognosis.
dc.language.isoeng
dc.publisherBMC
dc.relation.ispartofseriesThe Journal of Headache and Pain;26
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectMigranya - Tractament
dc.subject.meshMigraine Disorders
dc.subject.mesh/drug therapy
dc.titleLongitudinal assessment of migraine burden in resistant and refractory migraine – Data from the prospective REFINE study
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1186/s10194-025-02126-9
dc.subject.decstrastornos migrañosos
dc.subject.decs/farmacoterapia
dc.relation.publishversionhttps://doi.org/10.1186/s10194-025-02126-9
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Pensato U] Department of Neurology, IRCCS Humanitas Research Hospital, Rozzano, Milan, Italy. Department of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy. [Ornello R, Rosignoli C, Onofri A] Department of Biotechnological and Applied Clinical Sciences, University of L’Aquila, L’Aquila, Italy. [Caponnetto V] Department of Life, Health and Environmental Sciences, University of L’Aquila, L’Aquila, Italy. [Braschinsky M] Department of Neurology and Neurosurgery, Institute of Clinical Medicine, Faculty of Medicine, University of Tartu and Neurology Clinic of Tartu University Hospital, Tartu, Estonia. [Pozo-Rosich P, Munoz-Vendrell A] 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
dc.identifier.pmid40817153
dc.identifier.wos001551650300001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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