dc.contributor.author
Raffaelli, Bianca
dc.contributor.author
García-Azorín, David
dc.contributor.author
Boucherie, Deirdre M.
dc.contributor.author
Amin, Faisal Mohammad
dc.contributor.author
Deligianni, Christina I.
dc.contributor.author
Gil-Gouveia, Raquel
dc.contributor.author
Kirsh, Sarah
dc.contributor.author
Lampl, Christian
dc.contributor.author
Sacco, Simona
dc.contributor.author
Uluduz, Derya
dc.contributor.author
Versijpt, Jan
dc.contributor.author
MaassenVanDenBrink, Antoinette
dc.contributor.author
Zeraatkar, Dena
dc.contributor.author
Sanchez-del-Rio, Margarita
dc.contributor.author
Reuter, Uwe
dc.date.accessioned
2025-09-18T11:48:06Z
dc.date.available
2025-09-18T11:48:06Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/49423
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-49145
dc.description.abstract
Objective 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.MethodsA 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.ResultsEight 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)].ConclusionsThere 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.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Migraine Disorders* / drug therapy
en
dc.subject
Patient Satisfaction
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
European Headache Federation (EHF) critical reappraisal and meta-analysis of oral drugs in migraine prevention – part 3: topiramate
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
134
dcterms.bibliographicCitation.doi
10.1186/s10194-023-01671-5
dcterms.bibliographicCitation.journaltitle
The Journal of Headache and Pain
dcterms.bibliographicCitation.number
1
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.volume
24
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
37814223
dcterms.isPartOf.eissn
1129-2377