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在一项为期1年的1%吡美莫司乳膏药代动力学研究中,特应性皮炎婴儿的全身暴露量较低* 。

Low systemic exposure in infants with atopic dermatitis in a 1-year pharmacokinetic study with pimecrolimus cream 1%*.

作者信息

Lakhanpaul M, Davies T, Allen B R, Schneider D

机构信息

Division of Child Health, University of Leicester, UK.

出版信息

Exp Dermatol. 2006 Feb;15(2):138-41. doi: 10.1111/j.1600-0625.2006.00398.x.

Abstract

Systemic drug exposure following the application of topical agents is a very important safety consideration, particularly in infants, who have a significantly higher ratio of body surface area to body mass than older children and adults. Here, we report on drug exposure in five infants aged 5.7-11.9 months at baseline, with extensive, moderate-to-severe atopic dermatitis (AD). Patients were treated bid for 1 year, as needed, with pimecrolimus cream 1% in an open-label, non-controlled study. No indication of drug accumulation was found; pimecrolimus blood concentrations were consistently low, ranging from below the limit of quantitation (0.1 ng/ml) to 1.94 ng/ml. Treatment over this prolonged period was well tolerated, with no evidence of any treatment-related adverse events. The results of this 1-year study indicate that long-term management of AD with pimecrolimus cream 1% is associated with consistently very low systemic absorption, even in the youngest patients with extensive disease.

摘要

局部用药后全身药物暴露是一个非常重要的安全性考量因素,对于婴儿而言尤为如此,因为他们的体表面积与体重之比显著高于大龄儿童和成年人。在此,我们报告了5名基线时年龄在5.7至11.9个月、患有广泛性、中度至重度特应性皮炎(AD)的婴儿的药物暴露情况。在一项开放标签、非对照研究中,根据需要,患者每日两次使用1%吡美莫司乳膏进行为期1年的治疗。未发现药物蓄积迹象;吡美莫司血药浓度始终较低,范围从低于定量下限(0.1 ng/ml)至1.94 ng/ml。在这一较长时期的治疗耐受性良好,没有任何与治疗相关不良事件的证据。这项为期1年的研究结果表明,即使是患有广泛性疾病的最年幼患者,使用1%吡美莫司乳膏对AD进行长期管理时,全身吸收始终非常低。

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