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梅奥诊所接触性皮炎研究组1998 - 2000年的斑贴试验结果。

Patch test results from the Mayo Clinic Contact Dermatitis Group, 1998-2000.

作者信息

Wetter David A, Davis Mark D P, Yiannias James A, Cheng Janet F, Connolly Suzanne M, el-Azhary Rokea A, Farmer Sara A, Fett Debra D, Johnson Janis S, Linehan Diane L Nordberg, Richardson Donna M, Schroeter Arnold L

机构信息

Mayo Clinic Contact Dermatitis Group, Department of Dermatology, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

J Am Acad Dermatol. 2005 Sep;53(3):416-21. doi: 10.1016/j.jaad.2005.04.077.

Abstract

BACKGROUND

Patch testing is a diagnostic tool for the evaluation of patients with suspected allergic contact dermatitis. A standard series of allergens similar to that used by the North American Contact Dermatitis Group (NACDG) is used at Mayo Clinic.

OBJECTIVE

Our aim was to report the results of patch testing with a standard series at Mayo Clinic from July 1, 1998, to Dec 31, 2000 and to compare our findings with those of the NACDG during the same period.

METHODS

The results of patch testing with the standard series at Mayo Clinic were examined. Positive reaction rates were compared between Mayo Clinic and the NACDG.

RESULTS

During the 30-month period, 1324 Mayo Clinic patients were patch tested with a standard series of allergens (mean, 60 allergens), whereas the NACDG standard series during this period included 50 allergens. Overall, 917 patients (69.3%) had at least one positive reaction and 606 patients (45.8%) had two or more positive reactions. The 10 allergens used both by Mayo Clinic and by the NACDG that most frequently caused positive reactions were nickel sulfate hexahydrate, balsam of Peru (Myroxylon pereirae), neomycin sulfate, cobalt chloride, fragrance mix, potassium dichromate (0.25%), thimerosal, bacitracin, formaldehyde, and glutaraldehyde. Statistically significant differences in positive reaction rates (P < .05) were observed for 12 of the 43 allergens common to both Mayo Clinic and the NACDG.

CONCLUSION

With large standard patch test series, one can identify commonly encountered and potentially relevant contact allergens.

摘要

背景

斑贴试验是评估疑似过敏性接触性皮炎患者的一种诊断工具。梅奥诊所使用的标准变应原系列与北美接触性皮炎组(NACDG)所使用的类似。

目的

我们的目的是报告1998年7月1日至2000年12月31日在梅奥诊所进行的标准系列斑贴试验的结果,并将我们的发现与同期NACDG的结果进行比较。

方法

检查了梅奥诊所标准系列斑贴试验的结果。比较了梅奥诊所和NACDG之间的阳性反应率。

结果

在这30个月期间,1324名梅奥诊所患者接受了标准变应原系列的斑贴试验(平均60种变应原),而同期NACDG的标准系列包括50种变应原。总体而言,917名患者(69.3%)至少有1次阳性反应,606名患者(45.8%)有2次或更多次阳性反应。梅奥诊所和NACDG都使用的最常引起阳性反应的10种变应原是六水合硫酸镍、秘鲁香脂(秘鲁胶木)、硫酸新霉素、氯化钴、香料混合物、重铬酸钾(0.25%)、硫柳汞、杆菌肽、甲醛和戊二醛。在梅奥诊所和NACDG共有的43种变应原中,有12种变应原的阳性反应率存在统计学显著差异(P < 0.05)。

结论

通过大型标准斑贴试验系列,可以识别常见且可能相关的接触性变应原。

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