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Wiley InterScience

Journal of the European Academy of Dermatology and Venereology

Journal of the European Academy of Dermatology and Venereology

Volume 19 Issue 2, Pages 172 - 175

Published Online: 22 Feb 2005

Journal compilation © 2010 European Academy of Dermatology and Venereology



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ORIGINAL ARTICLE
Oral itraconazole for the treatment of seborrhoeic dermatitis: an open, noncomparative trial
O Kose*, H Erbil , AR Gur
 School of Medicine, Department of Dermatology, 06018 Ankara, Turkey.
  * Corresponding author, Gulhane Military Medical Academy, School of Medicine, Department of Dermatology, 06018 Ankara, Turkey. Current address: Queen Mary School of Medicine, Cutaneous Research Centre, 2nd Floor, 2 Newark Street, Whitechapel, London E1 2AT, UK, E-mail: okose@gata.edu.tr
Copyright © 2005 European Academy of Dermatology and Venereology
KEYWORDS
intermittent therapy • itraconazole • pityrosporum ovale • seborrhoeic dermatitis

ABSTRACT

AbstractMaterials and methodsResultsDiscussionReferences

Background Seborrhoeic dermatitis is an inflammatory cutaneous disorder in which the colonization of the affected area by Malassezia has been proved to play a key role.

Objective To perform a noncomparative open clinical study with oral itraconazole capsule (200 mg/day × 7 days) and consecutive usage 200 mg/day for the first 2 days of the following 2 months in patients with seborrhoeic dermatitis.

Methods Twenty-nine patients were enrolled to determine the efficacy and safety of oral itraconazole. The patients were evaluated according to itching, burning, erythema, desquamation and seborrhoea, each scored on a 0–4 scale on days 15 (T15), 30 (T30), 60 (T 60) and 90 (T90). Itraconazole capsule 100 mg was given twice a day for 1 week and then, after a 3-week interval, patients used itraconazole capsule 200 mg/day for the first 2 days of the following 2 months. The clinical response was graded as markedly effective, effective, moderate or ineffective.

Results A clinical improvement (evaluated as markedly effective or effective) was observed in 23 patients (83%) at T15, 21 (76%) at T30, 20 (72%) at T60 and 17 (61%) at T90. At baseline, the mean ± SD total clinical scores were 10.44 ± 2.45, 1.98 ± 0.5, 2.97 ± 1.12, 3.15 ± 1.74 and 3.30 ± 1.90 at T0, T15, T30, T60 and T90, respectively. Compared with baseline values, itraconazole capsule significantly reduced the mean ± SD total score as well as individual erythema and desquamation (Wilcoxon's signed test-two tailed) (P < 0.0001). No drug-related systemic adverse event was observed during the study.

Conclusions Seborrhoeic dermatitis shows marked reduction in inflammation when treated with itraconazole. The anti-inflammatory activity of oral itraconazole and efficacy on Malessezia suggests that itraconazole capsule will be first oral treatment option in future in severe seborrhoeic dermatitis.


Received 10 December 2003; accepted 4 March 2004

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1468-3083.2005.01090.x About DOI

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