Keegel Tessa, Saunders Helen, Milne Roger, Sajjachareonpong Praneet, Fletcher Ashley, Nixon Rosemary
Occupational Dermatology Research and Education Centre, Skin and Cancer Foundation Inc., Melbourne, Australia.
Contact Dermatitis. 2004 Jan;50(1):6-14. doi: 10.1111/j.0105-1873.2004.00275.x.
The reported prevalence of allergic contact dermatitis from topical corticosteroids in clinical populations, in the period 1993-2002, varied from 0.55 to 5.98%. This study is a retrospective analysis of 1153 individuals undergoing routine patch testing in an Occupational Dermatology Clinic in Melbourne, Australia. We report a rate of 0.52% for positive patch test reactions to 5 corticosteroids. Corticosteroids tested were betamethasone-17-valerate, budesonide, Diprosone cream (betamethasone diproprionate 0.05%) (Essex-Pharma, a division of Schering-Plough Pty Ltd, Sydney, Australia), tixocortol-21-pivalate and triamcinolone acetonide. Population characteristics were described using the MOAHL (M = percentage of males tested; O = occupational; A = atopics; H = patients with hand eczema; L = patients with leg ulcers or stasis eczema) index. Prescribing patterns, rate of referral and rate of relevant positive patch test reactions were characterized for the region. These results were compared to the rates of corticosteroid allergy and patch testing methodologies from published international studies. It was noted that many high-sensitization potential corticosteroids were not available in our region. Although a low percentage of leg ulcers and stasis dermatitis may be associated with a lower rate of corticosteroid allergy, this association may be confounded by regional factors such as prescribing habits and the local availability of corticosteroids. We conclude that the low rate of topical corticosteroid contact allergy reported by our clinic is associated with regional availability and prescribing practices and the scarcity of stasis dermatitis and leg ulcers in our clinic population.
1993年至2002年期间,临床人群中报道的外用皮质类固醇引起的过敏性接触性皮炎患病率在0.55%至5.98%之间。本研究是对澳大利亚墨尔本一家职业皮肤病诊所1153例接受常规斑贴试验的个体进行的回顾性分析。我们报告了对5种皮质类固醇斑贴试验阳性反应的发生率为0.52%。所测试的皮质类固醇为倍他米松-17-戊酸酯、布地奈德、适确得乳膏(丙酸倍他米松0.05%)(澳大利亚悉尼先灵葆雅有限公司旗下的埃塞克斯制药公司)、21-特戊酸卤米松和曲安奈德。使用MOAHL(M = 测试男性的百分比;O = 职业性;A = 特应性;H = 手部湿疹患者;L = 腿部溃疡或淤积性皮炎患者)指数描述人群特征。对该地区的处方模式、转诊率和相关斑贴试验阳性反应率进行了特征分析。将这些结果与已发表的国际研究中的皮质类固醇过敏率和斑贴试验方法进行了比较。值得注意的是,我们地区没有许多高致敏性皮质类固醇。虽然低比例的腿部溃疡和淤积性皮炎可能与较低的皮质类固醇过敏率相关,但这种关联可能会被处方习惯和皮质类固醇的当地可获得性等区域因素所混淆。我们得出结论,我们诊所报告的外用皮质类固醇接触过敏率较低与区域可获得性、处方习惯以及我们诊所人群中淤积性皮炎和腿部溃疡的稀缺有关。