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dc.contributor.authorDikmen, Pınar Yalınay
dc.contributor.authorBaykan, Betül
dc.contributor.authorUludüz, Derya
dc.contributor.authorÖzge, Aynur
dc.contributor.authorAydınlar, Elif Ilgaz
dc.contributor.authorPolat, Burcu
dc.contributor.authorKarlı, Necdet
dc.contributor.authorTepe, Nermin
dc.date.accessioned2024-08-28T11:14:05Z
dc.date.available2024-08-28T11:14:05Z
dc.date.issued2023en_US
dc.identifier.issn1471-2377
dc.identifier.urihttps://doi.org/10.1186/s12883-023-03467-1
dc.identifier.urihttps://hdl.handle.net/20.500.12462/15080
dc.descriptionTepe, Nermin (Balikesir Author)en_US
dc.description.abstractBackground The complexity of clinical practice extends far beyond the controlled settings of trials, and there is a need for real-world studies aimed at identifying which patients will respond to anti-CGRP monoclonal antibodies in different countries. This study aimed to investigate the efficacy and safety of galcanezumab in treating migraine in a real-life setting in Turkey, as well as identify predictors of treatment response. Methods A total of 476 patients who diagnosed with migraine according to ICHD-3 criteria and treated with galcanezumab by headache specialists were voluntarily participated in this cross-sectional study. Galcanezumab is indicated for the prevention of migraine in adults who have at least 4 monthly migraine days in Turkey. All patients filled out a survey on Google Form that comprised 54 questions, addressing various aspects such as demographics, migraine characteristics, previous use of acute symptomatic medication, failures with preventive drug classes, comorbidities, most bothersome symptoms, as well as the interictal burden of migraine. Results Among the participants, 89.3% reported that galcanezumab treatment was beneficial for them. A decrease in the frequency (80.0%), severity (85.7%), and acute medication usage for migraine attacks (71.4%) was reported with galcanezumab treatment. An adverse effect related to galcanezumab was reported in 16.3% of cases, but no serious adverse reactions were observed. Remarkably, 14.3% of participants reported no longer experiencing any headaches, and 18.9% did not require any acute treatment while receiving galcanezumab treatment. A logistic regression model showed that male gender, lack of ictal nausea, and previous failure of more than 2 prophylactic agents may predict the non-responders. Conclusions The first large series from Turkey showed that galcanezumab treatment is safe and effective in most of the patients diagnosed with migraine by headache experts in the real-life setting. Patients reported a significant decrease in both ictal and interictal burden of migraine and expressed satisfaction with this treatment.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.isversionof10.1186/s12883-023-03467-1en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCalcitonin gene-related Peptideen_US
dc.subjectCGRPen_US
dc.subjectGalcanezumaben_US
dc.subjectmAbsen_US
dc.subjectMonoclonal Antibodyen_US
dc.subjectMigraineen_US
dc.subjectMigraine Preventionen_US
dc.subjectAnti-CGRPen_US
dc.titleReal-life experiences with galcanezumab and predictors for treatment response in Turkeyen_US
dc.typearticleen_US
dc.relation.journalBMC Neurologyen_US
dc.contributor.departmentTıp Fakültesien_US
dc.contributor.authorID0000-0003-4148-2539en_US
dc.identifier.volume23en_US
dc.identifier.issue1en_US
dc.identifier.startpage1en_US
dc.identifier.endpage13en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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