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首页> 外文期刊>Dermatitis: contact, atopic, occupational, drug : official journal of the American Contact Dermatitis Society, North American Contact Dermatitis Group >Positivity ratio and reaction index: patch-test quality-control metrics applied to the north american contact dermatitis group database.
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Positivity ratio and reaction index: patch-test quality-control metrics applied to the north american contact dermatitis group database.

机译:阳性率和反应指数:应用于北美接触性皮炎组数据库的斑贴试验质量控制指标。

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摘要

BACKGROUND: The positivity ratio (PR) and reaction index (RI) characterize the ability of patch-test preparations to produce strong (++ or +++) reactions as opposed to weak (+), questionable, or irritant reactions. OBJECTIVE: This study evaluates these measures for North American Contact Dermatitis Group (NACDG) patch-test preparations. METHODS: The PR and RI were calculated for 79 NACDG standard allergens tested from 1994 to 2006 (n = 26,479 patients). The median values were used as cutoff values for "acceptable" versus "problematic" preparations. RESULTS: The top 10 "acceptable" patch-test preparations (PR < or = 55 and RI > 0.46) were mixed dialkyl thioureas 1% in petrolatum (pet), tixocortol-21-pivalate 1% pet, ethylenediamine dihydrochloride 1% pet, sesquiterpene lactone mix 0.1% pet, nickel sulfate 2.5% pet, bacitracin 20% pet, thimerosal 0.1% pet, epoxy resin 1% pet, colophony 20% pet, and mercaptobenzothiazole 1% pet. The most "problematic" patch-test preparations (PR > 55 and RI < or = 0.46) were cocamidopropyl betaine 1% aqueous (aq), benzalkonium chloride 0.1% aq, jasmine absolute 2% pet, iodopropynyl butyl carbamate 0.1% pet, 2-bromo-2-nitropropane-1,3-diol 0.5% pet, methyldibromoglutaronitrile 0.4% pet, methyldibromoglutaronitrile/phenoxyethanol 2% pet and 2.5% pet, dimethylol dihydroxyethyleneurea 4.5% aq, and clobetasol-17-propionate 1% pet. CONCLUSION: Caution should be used when interpreting reactions to "problematic" patch-test preparations with a high proportion of weak, irritant, and questionable reactions.
机译:背景:阳性率(PR)和反应指数(RI)表征了斑贴测试制剂产生强(++或+++)反应的能力,而不是弱(+),可疑或刺激性反应。目的:本研究评估了北美接触性皮炎组(NACDG)贴剂测试制剂的这些措施。方法:对1994年至2006年期间测试的79种NACDG标准过敏原(n = 26,479名患者)的PR和RI进行了计算。中值用作“可接受的”制剂与“有问题的”制剂的临界值。结果:前10种“可接受的”贴剂测试制剂(PR <或= 55,RI> 0.46)是在凡士林(宠物)中混合1%的二烷基硫脲,1%宠物用替考克多醇-21-新戊酸酯,1%宠物用乙二胺二盐酸盐,倍半萜烯内酯混合物0.1%宠物,硫酸镍2.5%宠物,杆菌肽20%宠物,硫柳汞0.1%宠物,环氧树脂1%宠物,松香20%宠物和巯基苯并噻唑1%宠物。最“有问题的”贴剂测试制剂(PR> 55,RI <或= 0.46)是椰油酰胺丙基甜菜碱1%水溶液(水溶液),苯扎氯铵0.1%水溶液,茉莉绝对2%宠物,碘丙炔基氨基甲酸丁酯0.1%宠物,2 -溴2-硝基硝基-1,3-二醇0.5%宠物,甲基二溴戊二腈0.4%宠物,甲基二溴戊二腈/苯氧基乙醇2%宠物和2.5%宠物,二羟甲基二羟基亚乙基脲4.5%水溶液和氯倍他索17-丙酸酯1%宠物。结论:在解释对“问题性”斑贴试验制剂的反应时,应谨慎使用,这些反应中弱,刺激性和可疑反应的比例很高。

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