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Efficacy and safety of fexofenadine in the treatment of pruritus associated with eczema가려움증을 동반한 습진 치료에서의 Fexofenadine 경구요법의 유효성 및 안전성 평가

Other Titles
가려움증을 동반한 습진 치료에서의 Fexofenadine 경구요법의 유효성 및 안전성 평가
Authors
Kim, Young HoonKo, Joo YoenMoon, Kee ChanPark, Young MinSeo, Young JoonYoo, Jae HakLee, Kwang HoonLee, Seung ChulLee, Ai YoungKim, Seong-EonJang, Ho SunHaw, Choong LimRo, Young Suck
Issue Date
Feb-2008
Publisher
Korean Journal of Dermatology
Keywords
Allergic contact dermatitis; Antihistamine; Atopic dermatitis; Eczema; Fexofenadine
Citation
Korean Journal of Dermatology, v.46, no.2, pp.151 - 159
Indexed
SCOPUS
KCI
Journal Title
Korean Journal of Dermatology
Volume
46
Number
2
Start Page
151
End Page
159
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/178977
ISSN
0494-4739
Abstract
Background: Fexofenadine (Allegra®) is a Hi-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.
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