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甲氨蝶呤治疗儿童斑块型银屑病:来自儿童 CAPTURE 注册研究的长期每日临床实践结果

Methotrexate in pediatric plaque-type psoriasis: Long-term daily clinical practice results from the Child-CAPTURE registry.

作者信息

van Geel M J, Oostveen A M, Hoppenreijs E P A H, Hendriks J C M, van de Kerkhof P C M, de Jong E M G J, Seyger M M B

机构信息

a Department of Dermatology .

b Department of Pediatric Rheumatology , and.

出版信息

J Dermatolog Treat. 2015 Oct;26(5):406-12. doi: 10.3109/09546634.2014.996515. Epub 2015 Jan 20.

Abstract

BACKGROUND

Evidence on effectiveness and safety of methotrexate (MTX) in pediatric psoriasis is scarce.

OBJECTIVES

To study the effectiveness and safety of MTX in pediatric plaque-type psoriasis and its influence on quality of life (Qol) in daily clinical practice.

METHODS

Subset analysis of prospectively collected data extracted from the Child-CAPTURE registry, a single center, longitudinal, long-term, observational daily practice cohort of pediatric psoriasis patients. A maximum dose between 0.14 and 0.63 mg/kg once weekly was prescribed in 25 children. Primary endpoints were percentages of patients with ≥ 75% improvement in the Psoriasis Area and Severity Index (PASI) at week 12 and 24.

RESULTS

PASI75 was achieved in 4.3% and 33.3% of patients at week 12 and 24, whereas 40% and 28.6% reached PASI 75 at week 36 and 48. Median PASI and body surface area decreased from 10.0 (range 3.8-42.4) and 11.0 (range 3.5-72.0) at baseline to 4.3 (range 0-19.8) and 2.6 (range 0.0-39.6) at week 24, respectively. Physician Global Assessment improved significantly from 3.0 to 1.2 at week 24. A significant decrease in Children's Dermatology Life Quality Index from 9.0 to 3.8 at week 24 was found. Most reported adverse events were severe nausea (n = 5), infections requiring antibiotics (n = 5) and tiredness (n = 4).

CONCLUSIONS

MTX shows a positive effect on PASI scores, improves Qol and has a reasonable safety profile.

摘要

背景

关于甲氨蝶呤(MTX)治疗儿童银屑病有效性和安全性的证据较少。

目的

在日常临床实践中研究MTX治疗儿童斑块型银屑病的有效性、安全性及其对生活质量(Qol)的影响。

方法

对从儿童银屑病前瞻性收集与跟踪登记库(Child-CAPTURE registry)提取的数据进行亚组分析,该登记库是一个针对儿童银屑病患者的单中心、纵向、长期、观察性日常实践队列。25名儿童每周一次服用的最大剂量在0.14至0.63mg/kg之间。主要终点是在第12周和第24周时银屑病面积和严重程度指数(PASI)改善≥75%的患者百分比。

结果

在第12周和第24周时,分别有4.3%和33.3%的患者达到PASI75,而在第36周和第48周时,分别有40%和28.6%的患者达到PASI75。PASI中位数和体表面积分别从基线时的10.0(范围3.8 - 42.4)和11.0(范围3.5 - 72.0)降至第24周时的4.

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