Publication:
The efficacy and safety of omalizumab in refractory chronic spontaneous urticaria: Real-life experience in Turkey

dc.contributor.authorBulur, Isil
dc.contributor.authorBaşkan, Emel Bülbül
dc.contributor.authorÖzdemir, Mustafa
dc.contributor.authorBalevi, Ali
dc.contributor.authorGoncu, Emek Kocaturk
dc.contributor.authorAltunay, Ilknur
dc.contributor.authorGonul, Muzeyyen
dc.contributor.authorErgin, Can
dc.contributor.authorErtam, İlgen
dc.contributor.authorErdogan, Hilal Kaya
dc.contributor.authorBilgin, Muzaffer
dc.contributor.authorErdem, Mustafa Teoman
dc.contributor.buuauthorBÜLBÜL BAŞKAN, EMEL
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentDermatoloji Bölümü
dc.contributor.researcheridAAH-1388-2021
dc.date.accessioned2024-11-19T12:57:18Z
dc.date.available2024-11-19T12:57:18Z
dc.date.issued2018-01-01
dc.description.abstractIntroduction: This study used real-world data to evaluate the effectiveness and reliability of omalizumab in treating recalcitrant chronic spontaneous urticaria in Turkish patients.Methods: Study data were collected retrospectively from eight tertiary-care hospitals in Turkey. This study included 132 patients with chronic spontaneous urticaria that were resistant to H-1 antihistamine treatment in a dose up to four times the licensed dose and were treated with 300 mg/month of omalizumab for 6 months.Results: The mean weekly urticarial activity score (UAS(7)) after omalizumab treatment improved significantly compared to the pretreatment score (p < 0.001). Treatment response was detected primarily in the 1st and 2nd months after treatment. No significant association was observed between omalizumab's treatment effectiveness and disease-related parameters or laboratory data. The mean dermatology life quality index was 23.12 +/- 6.15 before treatment and decreased to 3.55 +/- 3.60 6 months after treatment (p < 0.001). No side effects were reported in 89.4% (118) of the patients.Conclusion: This study showed that UAS(7) decreased significantly and quality of life improved in omalizumab-treated patients. Moreover, treatment effectiveness was mainly observed in the first 2 months after treatment. However, no association was observed between omalizumab treatment effectiveness and disease-related parameters or laboratory data.
dc.identifier.doi10.15570/actaapa.2018.25
dc.identifier.eissn1581-2979
dc.identifier.endpage126
dc.identifier.issn1318-4458
dc.identifier.issue3
dc.identifier.startpage121
dc.identifier.urihttps://doi.org/10.15570/actaapa.2018.25
dc.identifier.urihttps://acta-apa.mf.uni-lj.si/journals/acta-dermatovenerol-apa/papers/10.15570/actaapa.2018.25/actaapa.2018.25.pdf
dc.identifier.urihttps://hdl.handle.net/11452/48127
dc.identifier.volume27
dc.indexed.wosWOS.ESCI
dc.language.isoen
dc.publisherDermatovenerological Soc Slovenia
dc.relation.journalActa Dermatovenerologica Alpina Pannonica Et Adriatica
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectQuality-of-life
dc.subjectInducible urticaria
dc.subjectDisease-activity
dc.subjectTherapy
dc.subjectValidation
dc.subjectManagement
dc.subjectIndex
dc.subjectIge
dc.subjectChronic spontaneous urticaria
dc.subjectOmalizumab
dc.subjectDermatology life quality
dc.subjectUas(7)
dc.subjectSide effects
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectDermatology
dc.titleThe efficacy and safety of omalizumab in refractory chronic spontaneous urticaria: Real-life experience in Turkey
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Dermatoloji Bölümü
relation.isAuthorOfPublication5bd3accb-bb59-411b-8d6c-46d06d35b5a4
relation.isAuthorOfPublication.latestForDiscovery5bd3accb-bb59-411b-8d6c-46d06d35b5a4

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