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Guidelines for performing skin tests with drugs in the investigation of cutaneous adverse drug reactions

机译:在皮肤不良药物反应调查中使用药物进行皮肤测试的指南

摘要

Skin testing with a suspected drug has been reported to be helpful in determining the cause of cutaneous adverse drug reactions (CADR). Many isolated reports of positive drug skin tests are published, but without detailed information concerning the clinical features of the CADR and the method used in performing drug skin tests, such data are not very informative. A working party of the European Society of Contact Dermatitis (ESCD) for the study of skin testing in investigating cutaneous adverse drug reactions, has proposed the herein-reported guidelines for performing skin testing in CADR in order to standardize these procedures. In each reported case, the imputability of each drug taken at the onset of the CADR and a highly detailed description and characterization of the dermatitis need to be given. Drug skin tests are performed 6 weeks to 6 months after complete healing of the CADR. Drug patch tests are performed according to the methods used in patch testing in studying contact dermatitis. The commercialized form of the drug used by the patient is tested diluted at 30% pet. (pet.) and/or water (aq.). The pure drug is tested diluted at 10% in pet. or aq. In severe CADR, drug patch tests are performed at lower concentrations. It is also of value to test on the most affected site of the initial CADR. Drug prick tests are performed on the volar forearm skin with the commercialized form of the drug, but with sequential dilutions in cases of urticaria. Intradermal tests (IDT) are performed with sterile sequential dilutions (10-4, 10-3, 10-2, 10-1) of a pure sterile or an injectable form of the suspected drug with a small volume of 0.04 ml. Drug skin tests need to be read at 20 min and also later at D2 and D4 for patch tests, at D1 for prick tests and IDT. All these tests also need to be read at 1 week. The success of skin tests varies with the drug tested, with a high % of positive results, for example, with betalactam antibiotics, pristinamycin, carbamazepine and tetrazepam on patch testing, or with betalactam antibiotics and heparins on delayed readings of IDT. The results of drug skin tests also depend on the clinical features of the CADR. The use of appropriate control patients is necessary to avoid false-positive results.
机译:据报道,使用可疑药物进行皮肤测试有助于确定皮肤药物不良反应(CADR)的原因。发表了许多孤立的药物皮肤试验阳性报告,但没有有关CADR的临床特征和进行药物皮肤试验所用方法的详细信息,此类数据不是很有用。欧洲接触性皮炎协会(ESCD)的一个工作组,在研究皮肤不良药物反应中进行皮肤测试的研究,提出了本文报告的在CADR中进行皮肤测试的指南,以使这些程序标准化。在每种报道的病例中,需要给出在CADR发作时服用的每种药物的插补性,以及对皮炎的高度详细的描述和表征。在CADR完全愈合后的6周至6个月内进行药物皮肤测试。根据研究接触性皮炎的贴剂测试中使用的方法进行贴剂测试。测试患者使用的药物的商业化形式,稀释度为30%pet。 (宠物)和/或水(水溶液)。测试纯药物在宠物中稀释为10%。或水在严重的CADR中,药物补丁测试以较低的浓度进行。在初始CADR受影响最大的位置进行测试也很有价值。用商品化形式的药物在掌前臂皮肤上进行药物点刺试验,但在荨麻疹的情况下进行连续稀释。皮内试验(IDT)使用纯无菌或可注射形式的可疑药物的无菌顺序稀释液(10-4、10-3、10-2、10-1)进行无菌稀释,稀释量为0.04 ml。需要在20分钟时读取药物皮肤测试,然后在D2和D4读取补丁测试,在D1读取点刺测试和IDT。所有这些测试还需要在1周时阅读。皮肤测试的成功取决于所测试的药物,阳性结果的百分比很高,例如,贴片测试使用的是β-内酰胺类抗生素,倍他霉素,卡马西平和四西p,而IDT的延迟读数则是使用β-内酰胺类抗生素和肝素。药物皮肤测试的结果还取决于CADR的临床特征。必须使用适当的对照患者以避免假阳性结果。

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