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研究 0.04%他扎罗汀微球凝胶治疗青春期前痤疮的疗效和耐受性。

Study of the efficacy and tolerability of 0.04% tretinoin microsphere gel for preadolescent acne.

机构信息

Rady Children's Hospital, 8010 Frost St, Suite 602, San Diego, CA 92123, USA.

出版信息

Pediatrics. 2010 Jun;125(6):e1316-23. doi: 10.1542/peds.2009-3447. Epub 2010 May 24.

Abstract

OBJECTIVES

The goals were to assess the degree of improvement of facial acne after treatment with the 0.04% tretinoin microsphere gel (TMG) among patients 8 to 12 years of age and to assess tolerability and safety.

METHODS

An open-label study was conducted with 40 patients 8 to 12 years of age (mean age: 10.7 years) with mild/moderate acne, defined on the basis of Evaluator's Global Severity Score (EGSS) values between 2 and 3. Patients were treated with the 0.04% TMG for 12 weeks and were evaluated at baseline and weeks 3, 6, and 12. Primary end points were changes in EGSS and Alternative Evaluator's Global Severity Score values; the secondary efficacy end point was the Investigator's Global Evaluation of treatment responses at week 12.

RESULTS

The mean EGSS value decreased significantly from baseline to week 12 (2.6 vs 2.1; P < .001), with 75% of cases being graded as almost clear or mild. The mean Alternative Evaluator's Global Severity Score value decreased from 3.1 to 2.4 during the 12-week period (P < .001). The mean Investigator's Global Evaluation score was 3.39 at week 12, indicating moderate improvement of acne. Treatment-associated adverse events were minimal, with mild skin irritation being most commonly recorded, generally in the first 3 weeks of therapy.

CONCLUSIONS

The 0.04% TMG pump was effective and safe for the treatment of acne vulgaris in this 8- to 12-year-old population, and the treatment was generally well tolerated. Additional studies in this population are recommended, to confirm these results.

摘要

目的

评估 0.04%他扎罗汀微球凝胶(TMG)治疗 8 至 12 岁患者痤疮后的改善程度,并评估其耐受性和安全性。

方法

进行了一项开放性研究,共纳入 40 名 8 至 12 岁(平均年龄:10.7 岁)的轻/中度痤疮患者(根据评估者总体严重度评分[EGSS]值为 2 至 3 分定义)。患者接受 0.04%TMG 治疗 12 周,在基线和第 3、6、12 周进行评估。主要终点为 EGSS 和替代评估者总体严重度评分的变化;次要疗效终点为第 12 周时研究者对治疗反应的总体评估。

结果

EGSS 平均值从基线显著下降至第 12 周(2.6 降至 2.1;P<0.001),75%的病例为几乎无痤疮或轻度痤疮。在 12 周期间,替代评估者总体严重度评分均值从 3.1 降至 2.4(P<0.001)。第 12 周时,研究者总体评估评分为 3.39,表明痤疮有中度改善。治疗相关不良反应轻微,最常见的是治疗最初 3 周轻度皮肤刺激。

结论

0.04%TMG 泵对 8 至 12 岁人群的寻常痤疮有效且安全,且治疗通常具有良好的耐受性。建议在该人群中开展更多研究,以验证这些结果。

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