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Pediatr Dermatol ; 26(5): 551-8, 2009.
Article in English | MEDLINE | ID: mdl-19840309

ABSTRACT

The aim of this study is to compare twice-daily and once-daily applications of pimecrolimus cream 1% for prevention of atopic dermatitis relapses in pediatric patients. This multicenter trial enrolled 300 outpatients aged 2 to 17 years, with mild-to-severe atopic dermatitis. The patients were initially treated with twice-daily topical pimecrolimus until complete clearance or for up to 6 weeks (open-label period). Those who achieved a decrease of at least 1 point in the Investigator's Global Assessment score were then randomized to double-blind treatment with pimecrolimus cream 1% either twice daily or once daily for up to 16 weeks. Study medication was discontinued during periods of disease remission (Investigator's Global Assessment = 0). The primary efficacy end point of the double-blind phase was disease relapse (worsening requiring topical corticosteroids or additional/alternative therapy and confirmed by Investigator's Global Assessment score > or = 3 and pruritus score > or = 2). Of the 300 patients enrolled in the study, 268 were randomized to treatment with pimecrolimus cream 1% either twice daily or once daily (n = 134 in each group). The relapse rate was lower in the twice-daily dose group (9.9%) than that in the once-daily dose group (14.7%), but analysis of the time to disease relapse, using a Cox proportional model to adjust for confounding variables, did not show a statistically significant difference between treatment arms (hazard ratio: 0.64; 95% CI: 0.31-1.30). Treatment of active atopic dermatitis lesions with pimecrolimus cream 1% twice daily, followed by the once-daily dosing regimen, was sufficient to prevent subsequent atopic dermatitis relapses over 16 weeks in pediatric patients.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Dermatitis, Atopic/drug therapy , Tacrolimus/analogs & derivatives , Administration, Topical , Adolescent , Adrenal Cortex Hormones/administration & dosage , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Child , Child, Preschool , Dose-Response Relationship, Drug , Female , Humans , Male , Proportional Hazards Models , Secondary Prevention , Tacrolimus/administration & dosage , Tacrolimus/adverse effects , Treatment Outcome
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