钯贴片反应性

J. Fowler, J. Hayden
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引用次数: 5

摘要

对2000年期间在一个中心进行的所有斑贴试验进行了回顾性审查。所有对钯贴片试验阳性的患者均被选中。其中,还注意到对镍或金的贴片试验呈阳性。未分析阳性试验的假定临床相关性。所有患者均采用北美接触性皮炎组标准筛选系列(见附录)进行测试,其中包括硫酸镍(2.5% pet)和硫代硫酸金钠(0.5% pet)。此外,还对氯化钯(1% pet)进行了测试。所有过敏原均由瑞典马尔默Chemotechnique公司提供。Finn Chambers在Scanpor胶带上进行了测试(Allerderm, Inc., Petaluma, california, USA)。贴片应用约48小时,最终读数约48小时后贴片去除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Palladium Patch Reactivity
A retrospective review of all patch tests performed at 1 center during the year 2000 was undertaken. All patients with positive patch tests to palladium were selected. Of these, the presence of a positive patch test to nickel or gold was also noted. Putative clinical relevance of a positive test was not analyzed. All patients were tested with the North American Contact Dermatitis Group Standard Screening Series (see Appendix), which included nickel sulfate (2.5% pet.) and gold sodium thiosulfate (0.5% pet.). In addition, they were tested to palladium chloride (1% pet.). All allergens were supplied by Chemotechnique, Malmo, Sweden. Tests were applied on Finn Chambers on Scanpor tape (Allerderm, Inc., Petaluma, Calif., USA). Patches were applied for approximately 48 h, with the final reading about 48 h after patch removal.
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