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他克莫司0.03%和0.1%软膏在儿童特应性皮炎中的安全性:一项36个月的随访研究。

Safety of tacrolimus 0.03% and 0.1% ointments in young children with atopic dermatitis: a 36-month follow-up study.

作者信息

Salava A, Perälä M, Pelkonen A, Mäkelä M, Remitz A

机构信息

Helsinki University Hospital, Skin and Allergy Hospital, Helsinki, Finland.

出版信息

Clin Exp Dermatol. 2022 May;47(5):889-902. doi: 10.1111/ced.15024. Epub 2022 Jan 13.

Abstract

BACKGROUND

Topical tacrolimus is used off-label in young children, but data are limited on its use in children under 2 years of age and for long-term treatment.

AIM

To compare safety differences between topical tacrolimus (0.03% and 0.1% ointments) and topical corticosteroids (mild and moderate potency) in young children with atopic dermatitis (AD).

METHODS

We conducted a 36-month follow-up study with 152 young children aged 1-3 years with moderate to severe AD. The children were followed up prospectively, and data were collected on infections, disease severity, growth parameters, vaccination responses and other relevant laboratory tests were gathered.

RESULTS

There were no significant differences between the treatment groups for skin-related infections (SRIs) (P = 0.20), non-SRIs (P = 0.20), growth parameters height (P = 0.60), body weight (P = 0.81), Eczema Area and Severity Index (EASI) (P = 0.19), vaccination responses (P = 0.62), serum cortisone levels (P = 0.23) or serum levels of interleukin (IL)-4, IL-10, IL-12, IL-31 and interferon-γ. EASI decreased significantly in both groups (P < 0.001). In the tacrolimus group, nine patients (11.68%) had detectable tacrolimus blood concentrations at the 1-week visit. There were no malignancies or severe infections during the study, and blood eosinophil counts were similar in both groups.

CONCLUSIONS

Topical tacrolimus (0.03% and 0.1%) and topical corticosteroids (mild and moderate potency) are safe to use in young children with moderate to severe AD, and have comparable efficacy and safety profiles.

摘要

背景

外用他克莫司在幼儿中属超说明书用药,但关于其在2岁以下儿童中的使用及长期治疗的数据有限。

目的

比较外用他克莫司(0.03%和0.1%软膏)与外用皮质类固醇(低、中效)在患有特应性皮炎(AD)的幼儿中的安全性差异。

方法

我们对152名1至3岁患有中度至重度AD的幼儿进行了一项为期36个月的随访研究。对这些儿童进行前瞻性随访,并收集有关感染、疾病严重程度、生长参数、疫苗接种反应及其他相关实验室检查的数据。

结果

治疗组在皮肤相关感染(SRIs)方面(P = 0.20)、非SRIs方面(P = 0.20)、生长参数身高方面(P = 0.60)、体重方面(P = 0.81)、湿疹面积和严重程度指数(EASI)方面(P = 0.19)、疫苗接种反应方面(P = 0.62)、血清可的松水平方面(P = 0.23)或白细胞介素(IL)-4、IL-10、IL-12、IL-31和干扰素-γ的血清水平方面均无显著差异。两组的EASI均显著下降(P < 0.001)。在他克莫司组中,9名患者(11.68%)在第1周就诊时他克莫司血药浓度可测。研究期间未发生恶性肿瘤或严重感染,两组的血嗜酸性粒细胞计数相似。

结论

外用他克莫司(0.03%和0.1%)和外用皮质类固醇(低、中效)在患有中度至重度AD的幼儿中使用安全,且疗效和安全性相当。

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