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北美接触性皮炎组斑贴试验结果:2009 年至 2010 年。

North American Contact Dermatitis Group patch test results: 2009 to 2010.

机构信息

Department of Dermatology, Minneapolis VA Health Care System and University of Minnesota, Minneapolis, MN, USA.

出版信息

Dermatitis. 2013 Mar-Apr;24(2):50-9. doi: 10.1097/DER.0b013e3182819c51.

Abstract

BACKGROUND

Patch testing is an important diagnostic tool for determination of substances responsible for allergic contact dermatitis.

OBJECTIVE

This study reports the North American Contact Dermatitis Group (NACDG) patch testing results from January 1, 2009, to December 31, 2010.

METHODS

At 12 centers in North America, patients were tested in a standardized manner with a screening series of 70 allergens. Data were manually verified and entered into a central database. Descriptive frequencies were calculated, and trends were analyzed using χ2 statistics.

RESULTS

A total of 4308 patients were tested. Of these, 2614 (60.7%) had at least 1 positive reaction, and 2284 (46.3%) were ultimately determined to have a primary diagnosis of allergic contact dermatitis. Four hundred twenty-seven (9.9%) patients had occupationally related skin disease. There were 6855 positive allergic reactions. As compared with the previous reporting period (2007-2008), the positive reaction rates statistically decreased for 20 allergens (nickel, neomycin, Myroxylon pereirae, cobalt, formaldehyde, quaternium 15, methydibromoglutaronitrile/phenoxyethanol, methylchlorisothiazolinone/methylisothiazolinone, potassium dichromate, diazolidinyl urea, propolis, dimethylol dimethylhydantoin, 2-bromo-2-nitro-1,3-propanediol, methyl methacrylate, ethyl acrylate, glyceryl thioglycolate, dibucaine, amidoamine, clobetasol, and dimethyloldihydroxyethyleneurea; P < 0.05) and statistically increased for 4 allergens (fragrance mix II, iodopropynyl butylcarbamate, propylene glycol, and benzocaine; P < 0.05). Approximately one quarter of tested patients had at least 1 relevant allergic reaction to a non-NACDG allergen. Hypothetically, approximately one quarter of reactions detected by NACDG allergens would have been missed by TRUE TEST (SmartPractice Denmark, Hillerød, Denmark).

CONCLUSIONS

These results affirm the value of patch testing with many allergens.

摘要

背景

斑贴试验是确定引起变应性接触性皮炎物质的重要诊断工具。

目的

本研究报告了 2009 年 1 月 1 日至 2010 年 12 月 31 日期间北美接触性皮炎组(NACDG)的斑贴试验结果。

方法

在北美 12 个中心,以标准化方式对患者进行了一项 70 种过敏原的筛查系列检测。数据经过人工验证并输入中央数据库。使用 χ2 统计数据计算描述性频率,并分析趋势。

结果

共有 4308 名患者接受了检测。其中,2614 名(60.7%)至少有 1 次阳性反应,2284 名(46.3%)最终被诊断为过敏性接触性皮炎。427 名(9.9%)患者患有职业性皮肤病。共有 6855 次阳性变应反应。与前一报告期(2007-2008 年)相比,20 种过敏原(镍、新霉素、秘鲁香脂、钴、甲醛、季铵 15、甲溴二甘氨酸/苯氧乙醇、甲基氯异噻唑啉酮/甲基异噻唑啉酮、重铬酸钾、二氮杂环丁烷、蜂胶、二羟甲基二羟乙内酰脲、2-溴-2-硝基-1,3-丙二醇、甲基丙烯酸甲酯、丙烯酸乙酯、甘油硫代乙醇酸、丁卡因、酰胺胺、卤倍他索、二羟甲基海因脲)的阳性反应率统计学上有所下降(P<0.05),4 种过敏原(香薰混合物 II、碘丙炔基丁基氨甲酸酯、丙二醇和苯佐卡因;P<0.05)的阳性反应率统计学上有所上升。约四分之一接受测试的患者对非 NACDG 过敏原至少有 1 种相关过敏反应。假设通过 NACDG 过敏原检测到的反应中,约有四分之一可能会被 TRUE TEST(丹麦希勒勒的 SmartPractice Denmark)遗漏。

结论

这些结果证实了使用多种过敏原进行斑贴试验的价值。

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