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Title: | Comparative trial of 5% dexpanthenol in water-in-oil formulation with 1% hydrocortisone ointment in the treatment of childhood atopic dermatitis: A pilot study |
Authors: | Udompataikul M. Limpa-o-vart D. |
Keywords: | dexpanthenol hydrocortisone water oil cream absence of side effects adolescent age distribution article atopic dermatitis child clinical article controlled study disease severity drug efficacy drug formulation female human lichenoid eruption male ointment pilot study preschool child randomized controlled trial school child scoring system single blind procedure skin absorption Student t test treatment duration treatment response Administration, Cutaneous Adolescent Case-Control Studies Child Child, Preschool Dermatitis, Atopic Dermatologic Agents Female Humans Hydrocortisone Infant Male Ointments Pantothenic Acid Pilot Projects Single-Blind Method Time Factors Treatment Outcome |
Issue Date: | 2012 |
Abstract: | Background: Atopic dermatitis (AD) is a common chronic relapsing disease particularly affecting children. The emollient used for protection of skin barrier function is the standard treatment for patients with AD. Currently, there is a growing interest in the use of nonsteroidal anti-inflammatory agents such as dexpanthenol (vitamin B5) as an alternative treatment. Objective: To compare the effectiveness of 5% dexpanthenol (DT) ointment with 1% hydrocortisone (HC) ointment in childhood AD therapy. Method: Patients were treated topically with 5% DT ointment on the right side of the body and 1% HC ointment on the other side twice daily for 4 weeks. The clinical responses were evaluated by SCORAD (Scoring Atopic Dermatitis index) with statistical analysis using paired t-test. Result: Of the 30 children enrolled, 26 completed the protocol; mean age was 7.19 years. The average baseline SCORAD score of the DT-treated side and the HC-treated side was 30.95 and 30.54, respectively. There was no statistically significant difference in SCORAD score reduction between the 2 agents. The edematous score of the HC-treated side exhibited faster resolution than that of the DT-treated side, with a statistically significant difference at week 1 and without a statistically significant difference at weeks 2 to 4. The lichenification response rate of HC treatment was more rapid than that of DT treatment; however, there was no statistical group difference. No adverse events were observed with either agent. Conclusion: The effectiveness of 5% DT ointment is equal to that of 1% HC ointment. DT ointment may be used as alternative treatment in mild to moderate childhood AD therapy. Copyright © 2012 Journal of Drugs in Dermatology. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/14370 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84858672070&partnerID=40&md5=e5fdd1b1da2e7f9938ca82c55d0f9a00 |
ISSN: | 15459616 |
Appears in Collections: | Scopus 1983-2021 |
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