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皮下注射药物的浓度——ENDA/EAACI 药物过敏兴趣小组立场文件。

Skin test concentrations for systemically administered drugs -- an ENDA/EAACI Drug Allergy Interest Group position paper.

机构信息

Department of Dermatology und Allergology Biederstein, Division Environmental Dermatology and Allergology Helmholtz Zentrum München/TUM, Technical University Munich, Munich, Germany.

出版信息

Allergy. 2013 Jun;68(6):702-12. doi: 10.1111/all.12142. Epub 2013 Apr 25.

DOI:10.1111/all.12142
PMID:23617635
Abstract

Skin tests are of paramount importance for the evaluation of drug hypersensitivity reactions. Drug skin tests are often not carried out because of lack of concise information on specific test concentrations. The diagnosis of drug allergy is often based on history alone, which is an unreliable indicator of true hypersensitivity.To promote and standardize reproducible skin testing with safe and nonirritant drug concentrations in the clinical practice, the European Network and European Academy of Allergy and Clinical Immunology (EAACI) Interest Group on Drug Allergy has performed a literature search on skin test drug concentration in MEDLINE and EMBASE, reviewed and evaluated the literature in five languages using the GRADE system for quality of evidence and strength of recommendation. Where the literature is poor, we have taken into consideration the collective experience of the group.We recommend drug concentration for skin testing aiming to achieve a specificity of at least 95%. It has been possible to recommend specific drug concentration for betalactam antibiotics, perioperative drugs, heparins, platinum salts and radiocontrast media. For many other drugs, there is insufficient evidence to recommend appropriate drug concentration. There is urgent need for multicentre studies designed to establish and validate drug skin test concentration using standard protocols. For most drugs, sensitivity of skin testing is higher in immediate hypersensitivity compared to nonimmediate hypersensitivity.

摘要

皮肤试验对于评估药物过敏反应至关重要。由于缺乏特定测试浓度的简明信息,药物皮肤试验通常未进行。药物过敏的诊断通常仅基于病史,这是真正过敏的不可靠指标。为了在临床实践中促进和规范使用安全、非刺激性药物浓度的可重复皮肤试验,欧洲过敏与临床免疫学会(EAACI)药物过敏兴趣小组在 MEDLINE 和 EMBASE 上进行了皮肤试验药物浓度的文献检索,使用 GRADE 系统对文献进行了回顾和评估证据质量和推荐强度。在文献不足的情况下,我们考虑了小组的集体经验。我们建议进行皮肤试验的药物浓度,以实现至少 95%的特异性。已经有可能为β-内酰胺类抗生素、围手术期药物、肝素、铂盐和造影剂推荐特定的药物浓度。对于许多其他药物,没有足够的证据推荐适当的药物浓度。迫切需要进行多中心研究,旨在使用标准方案建立和验证药物皮肤试验浓度。对于大多数药物,与非即刻过敏反应相比,即刻过敏反应的皮肤试验敏感性更高。

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