Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

가려움증을 동반한 습진 치료에서의 Fexofenadine 경구요법의 유효성 및 안전성 평가

Full metadata record
DC Field Value Language
dc.contributor.author김영훈-
dc.contributor.author고주연-
dc.contributor.author문기찬-
dc.contributor.author박영민-
dc.contributor.author서영준-
dc.contributor.author유재학-
dc.contributor.author이광훈-
dc.contributor.author이승철-
dc.contributor.author이애영-
dc.contributor.author김성언-
dc.contributor.author장호선-
dc.contributor.author허충림-
dc.contributor.author노영석-
dc.date.accessioned2022-12-21T04:13:27Z-
dc.date.available2022-12-21T04:13:27Z-
dc.date.created2022-09-19-
dc.date.issued2008-02-
dc.identifier.issn0494-4739-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/178966-
dc.description.abstractBackground: Fexofenadine (AllegraⓇ) is a H1-receptor selective antihistamine which exhibits consistent efficacy and safety in the treatment of allergic diseases. We thought that fexofenadine may be useful in treatment of the pruritus associated with eczema. Objective: The purpose of this study was to evaluate the efficacy and safety of fexofenadine in the treatment of pruritus associated with eczema. Methods: In this study, patients with atopic and allergic contact dermatitis were divided into a group given fexofenadine 180 mg once daily with topical prednicarbate treatment group or a topical prednicarbate treatment only group, for 1 week. The primary efficacy parameter was the mean change from baseline in pruritus score, and the secondary parameters were the mean change in the incidence of scratching, the mean change in visual analogue scale (0∼100 mm) of pruritus, and a comparison of patient satisfaction. Results: 435 patients were included and the mean age was 32.9 years old. The mean pruritus score at baseline was 3.55 point in fexofenadine group and 3.51 point in the control group. Regarding the mean change in pruritus score, fexofenadine significantly decreased the severity of pruritus compared with the control group (p<0.05). There were no significant differences in the decrease in the incidence of scratching between the two groups. A decrease in pruritus levels utilizing visual analogue scale was significant in the fexofenadine group (p<0.05) and patient satisfaction was significantly higher in the fexofenadine group (p=0.0192). There was no significant difference in the incidence of adverse events between two groups (p=0.6237). Conclusion: Fexofenadine administered 180 mg once daily in combination with topical prednicarbate treatment was effective and well tolerated in this study.-
dc.language한국어-
dc.language.isoko-
dc.publisher대한피부과학회-
dc.title가려움증을 동반한 습진 치료에서의 Fexofenadine 경구요법의 유효성 및 안전성 평가-
dc.title.alternativeEfficacy and Safety of Fexofenadine in the Treatment of Pruritus Associated with Eczema-
dc.typeArticle-
dc.contributor.affiliatedAuthor고주연-
dc.contributor.affiliatedAuthor노영석-
dc.identifier.scopusid2-s2.0-41149108157-
dc.identifier.bibliographicCitation대한피부과학회지, v.46, no.2, pp.151 - 159-
dc.relation.isPartOf대한피부과학회지-
dc.citation.title대한피부과학회지-
dc.citation.volume46-
dc.citation.number2-
dc.citation.startPage151-
dc.citation.endPage159-
dc.type.rimsART-
dc.identifier.kciidART001246780-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorAllergic contact dermatitis-
dc.subject.keywordAuthorAntihistamine-
dc.subject.keywordAuthorAtopic dermatitis-
dc.subject.keywordAuthorEczema-
dc.subject.keywordAuthorFexofenadine-
dc.identifier.urlhttps://kiss.kstudy.com/thesis/thesis-view.asp?key=2673259-
Files in This Item
Go to Link
Appears in
Collections
서울 의과대학 > 서울 피부과학교실 > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Ko, Joo Yeon photo

Ko, Joo Yeon
COLLEGE OF MEDICINE (DEPARTMENT OF DERMATOLOGY)
Read more

Altmetrics

Total Views & Downloads

BROWSE