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dc.contributor.authorÖzdemir, Mustafa
dc.contributor.authorBalevi, Ali
dc.date.accessioned10.07.201910:49:13
dc.date.accessioned2019-07-10T20:02:27Z
dc.date.available10.07.201910:49:13
dc.date.available2019-07-10T20:02:27Z
dc.date.issued2017en_US
dc.identifier.citationÖzdemir, M. ve Balevi, A. (2017). Bilateral half-head comparison of 1% anthralin ointment in children with alopecia areata. Pediatric Dermatology, 34(2), 128-132. https://dx.doi.org/10.1111/pde.13049en_US
dc.identifier.issn0736-8046
dc.identifier.issn1525-1470
dc.identifier.urihttps://dx.doi.org/10.1111/pde.13049
dc.identifier.urihttps://hdl.handle.net/20.500.12511/3650
dc.descriptionWOS: 000398113000016en_US
dc.descriptionPubMed ID: 28044367en_US
dc.description.abstractBackground/Objectives: Alopecia areata (AA) is one of the most difficult skin diseases to manage well. In children, anthralin is commonly used for the treatment of AA. Available research consists of a limited number of uncontrolled trials that assessed the effectiveness of anthralin in promoting hair growth in patients with AA. The objective of this study was to validate the clinical effectiveness of short-contact anthralin 1% ointment in children with AA. Methods: Thirty children with chronic, severe, treatment-refractory, extensive AA were treated with 1% anthralin ointment. One side of the scalp was treated with anthralin for 12 months and the other side was left untreated. Outcomes were evaluated according to the Severity of Alopecia Tool (SALT) score. Results: The mean time to first response in terms of new hair growth was 3 months and the mean time to maximal response was 9 months. In the first 12-month period, 10 patients (33.4%) achieved complete response to treatment and 11 patients (36.6%) had a partial response. Of the 11 patients with partial response at the end of the first year, 6 achieved a complete response before the end of the study. Total SALT scores for the entire scalp decreased from the end of the first year to the end of the 2-year period. No serious adverse events were observed. Conclusion: Anthralin 1% is an effective therapy for AA and should be continued at least 9 months. At 9 months of topical anthralin therapy, the patients with at least a 50% reduction in their pretreatment SALT scores should continue the same treatment for at least 1 year. Anthralin is safe in children with chronic, severe, treatment-refractory, extensive AA.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectAlopecia Areataen_US
dc.subjectHalf‐Head Comparisonen_US
dc.subjectTreatment‐Refractoryen_US
dc.titleBilateral half-head comparison of 1% anthralin ointment in children with alopecia areataen_US
dc.typearticleen_US
dc.relation.ispartofPediatric Dermatologyen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Deri ve Zührevi Hastalıklar Ana Bilim Dalıen_US
dc.authorid0000-0002-7022-913Xen_US
dc.authorid0000-0001-5057-0405en_US
dc.identifier.volume34en_US
dc.identifier.issue2en_US
dc.identifier.startpage128en_US
dc.identifier.endpage132en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1111/pde.13049en_US
dc.identifier.wosqualityQ3en_US
dc.identifier.scopusqualityQ2en_US


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