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European Headache Federation (EHF) critical reappraisal and meta-analysis of oral drugs in migraine prevention – part 3: topiramate

dc.contributor.authorRaffaelli, Bianca
dc.contributor.authorGarcía-Azorín, David
dc.contributor.authorBoucherie, Deirdre M.
dc.contributor.authorAmin, Faisal Mohammad
dc.contributor.authorDeligianni, Christina I.
dc.contributor.authorGil-Gouveia, Raquel
dc.contributor.authorKirsh, Sarah
dc.contributor.authorLampl, Christian
dc.contributor.authorSacco, Simona
dc.contributor.authorUluduz, Derya
dc.contributor.authorVersijpt, Jan
dc.contributor.authorMaassenVanDenBrink, Antoinette
dc.contributor.authorZeraatkar, Dena
dc.contributor.authorSanchez-del-Rio, Margarita
dc.contributor.authorReuter, Uwe
dc.date.accessioned2023-10-31T10:13:39Z
dc.date.available2023-10-31T10:13:39Z
dc.date.issued2023-12
dc.description.abstractObjective: Topiramate is a repurposed first-line treatment for migraine prophylaxis. The aim of this systematic review and meta-analysis is to critically re-appraise the existing evidence supporting the efficacy and tolerability of topiramate. Methods: A systematic search in MEDLINE, EMBASE, Cochrane CENTRAL, and ClinicalTrials.gov was performed for trials of pharmacological treatment in migraine prophylaxis as of August 13, 2022, following the Preferred Reporting Items for Systematic Reviews (PRISMA). Randomized controlled trials in adult patients that used topiramate for the prophylactic treatment of migraine, with placebo as active comparator, were included. Two reviewers independently screened the retrieved studies and extracted all data. Outcomes of interest were the 50% responder rates, the reduction in monthly migraine days, and adverse events leading to treatment discontinuation. Results were pooled and meta-analyzed, with sensitivity analysis based on the risk of bias of the studies, the monthly migraine days at baseline, and the previous use of other prophylactic treatments. Certainty evidence was judged according to the GRADE framework. Results: Eight out of 10,826 studies fulfilled the inclusion/exclusion criteria, accounting for 2,610 randomized patients. Six studies included patients with episodic migraine and two with chronic migraine. Topiramate dose ranged from 50 to 200 mg/day, and all studies included a placebo arm. There was a high certainty that topiramate: 1) increased the proportion of patients who achieved a 50% responder rate in monthly migraine days, compared to placebo [relative risk: 1.61 (95% confidence interval (CI): 1.29–2.01); absolute risk difference: 168 more per 1,000 (95% CI: 80 to 278 more)]; 2) was associated with 0.99 (95% CI: 1.41–0.58) fewer migraine days than placebo; 3) and had a higher proportion of patients with adverse events leading to treatment discontinuation [absolute risk difference 80 patients more per 1,000 (95% CI: 20 to 140 more patients)]. Conclusions: There is high-quality evidence of the efficacy of topiramate in the prophylaxis of migraine, albeit its use poses a risk of adverse events that may lead to treatment discontinuation, with a negative effect on patient satisfaction and adherence to care.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1186/s10194-023-01671-5pt_PT
dc.identifier.eid85173632210
dc.identifier.issn1129-2369
dc.identifier.pmcPMC10563338
dc.identifier.pmid37814223
dc.identifier.source-work-id6D18-4F7A-E69D/3377211
dc.identifier.urihttp://hdl.handle.net/10400.14/42933
dc.identifier.wos001080615100001
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.titleEuropean Headache Federation (EHF) critical reappraisal and meta-analysis of oral drugs in migraine prevention – part 3: topiramatept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue1pt_PT
oaire.citation.titleJournal of Headache and Painpt_PT
oaire.citation.volume24pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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