1%吡美莫司乳膏可有效治疗面部和躯干脂溢性皮炎。

E Rallis, A Nasiopoulou, C Kouskoukis, E Koumantaki
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引用次数: 0

摘要

子囊霉素大内酰胺衍生物吡美莫司是一种新型的、非甾体的、细胞选择性炎症细胞因子抑制剂,专门用于治疗炎症性皮肤病。我们的目的是评估1%吡美莫司乳膏治疗脂溢性皮炎的疗效、耐受性和安全性。2003年10月至2004年4月在色雷斯大学皮肤科门诊就诊的患有面部和上躯干脂溢性皮炎的成年人被纳入这项为期9周的开放标签非对照研究。1%吡美莫司乳膏作为单药治疗,每日两次,连续7天,如果需要,此后再使用7天,直到完全清除。复发病例再加5天疗程。在筛选和适当的洗脱期后,受试者在基线(第0天)和第1、3、6和9周的随访中进行评估。脂溢性皮炎的临床严重程度根据红斑、结垢和病变程度分为轻度(总分1-3分)、中度(总分4-6分)和重度(总分7-9分),评分范围为0 ~ 3分。患者还根据局部应用的有效性、安全性和耐受性对其症状进行了从0到5的评估。19例患者(男性12例,女性7例)纳入本研究。在第1、3、6和9周末,完全清除率分别为63%、100%、47%和52%。研究结束时,受试者的平均评估得分为9.73分。除了4例患者局部皮肤灼烧和刺激外,没有其他不良事件被提及。这项初步研究表明,吡美莫司应用每日两次可以是一个安全有效的替代治疗脂溢性皮炎。需要进一步的研究来确定初始和维持治疗。
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Pimecrolimus cream 1% can be an effective treatment for seborrheic dermatitis of the face and trunk.

The ascomycin macrolactam derivative pimecrolimus is a novel, nonsteroidal, cell-selective inhibitor of inflammatory cytokines specifically developed for the treatment of inflammatory skin diseases. Our objective was to assess the efficacy, tolerability and safety of pimecrolimus cream 1% in the treatment of seborrheic dermatitis. Adults with seborrheic dermatitis of the face and upper trunk who were seen from October 2003 to April 2004 at the Dermatologic Outpatient Clinic of the University of Thrace were enrolled in this 9-week open-label uncontrolled study. Pimecrolimus cream 1% was applied as monotherapy twice daily for 7 days and for an additional period of 7 days thereafter, if needed, until complete clearance was achieved. In cases of recurrence a 5-day course was additionally applied. After screening and an appropriate washout period, subjects were evaluated at baseline (day 0) and at follow-up visits at weeks 1, 3, 6 and 9. The clinical severity of seborrheic dermatitis was estimated as mild (total score 1-3), moderate (total score 4-6) and severe (total score 7-9) in terms of erythema, scaling and lesional extent using a scale from 0 to 3 for each. Patients also assessed their symptoms on a scale from 0 to 5 in terms of the efficacy, safety and tolerability of topical application. Nineteen patients (12 males, seven females) were enrolled in this study. At the end of weeks 1, 3, 6 and 9 the percentages of complete clearance were 63%, 100%, 47% and 52%, respectively. At the end of the study, subjects' average assessment score was 9.73. Apart from topical burning and irritation of the skin in four patients, no other adverse event was mentioned. This pilot study indicates that pimecrolimus applied twice daily can be a safe and efficacious alternative in the treatment of seborrheic dermatitis. Further studies are needed to determine the initial and maintenance therapy.

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