2009
DOI: 10.1080/09546630802512646
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Efficacy and tolerability at 3 and 6 months following use of azathioprine for recalcitrant atopic dermatitis in children and young adults

Abstract: Azathioprine reduced the disease severity of AD within 3 months of use in these children. Better efficacy was observed in females at 6 months. Adverse hematologic and biochemical effects appeared acceptable but longer-term monitoring is desirable.

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Cited by 51 publications
(44 citation statements)
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“…After 3 months of therapy, 28 patients (58.3%) showed excellent results and 13 patients (27.1%) showed good improvement, whereas only 7 patients (14.6%) showed little or no improvement. In 2009, another retrospective uncontrolled study including 17 patients (mean age of 16.1 ± 3.9 years) with recalcitrant AD showed significant improvement of SCORAD after 3 months and 6 months of treatment with azathioprine as well as significant reduction in total serum IgE levels [73]. Azathioprine has an intriguing metabolism with several immunosuppressant metabolites, governed by thiopurine methyltransferase activity (TPMT), so that the azathioprine dosage should be determined based on the TPMT genotype or activity levels to limit the possible appearance of myelotoxicity.…”
Section: Methodsmentioning
confidence: 99%
“…After 3 months of therapy, 28 patients (58.3%) showed excellent results and 13 patients (27.1%) showed good improvement, whereas only 7 patients (14.6%) showed little or no improvement. In 2009, another retrospective uncontrolled study including 17 patients (mean age of 16.1 ± 3.9 years) with recalcitrant AD showed significant improvement of SCORAD after 3 months and 6 months of treatment with azathioprine as well as significant reduction in total serum IgE levels [73]. Azathioprine has an intriguing metabolism with several immunosuppressant metabolites, governed by thiopurine methyltransferase activity (TPMT), so that the azathioprine dosage should be determined based on the TPMT genotype or activity levels to limit the possible appearance of myelotoxicity.…”
Section: Methodsmentioning
confidence: 99%
“…Use is generally recommended for those children whose dermatitis is recalcitrant, or when there is significant psychosocial impact on the patient and family unit. 50, 51 Insufficient data exists to recommend an optimal dose, duration of therapy, or to predict the relapse rate upon discontinuation. However, the most common dosage given is 2.5 mg/kg/day, with a higher treatment range maximum of 4 mg/kg/day relative to adult dosing (maximum 3 mg/kg/day).…”
Section: Azathioprinementioning
confidence: 99%
“…Only a few controlled studies with long-term use of AZA in AD patients are published1,19. A significant improvement of the AD lesions, a reduction of total serum IgE levels and moderate side effects have been reported in a recent pediatric study running over three months45. Infections, skin cancer, gastrointestinal disturbances, hepatotoxicity and rare but severe bone marrow suppression are typical side effects of AZA.…”
Section: Systemic Anti-inflammatory Therapymentioning
confidence: 84%