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抗生素过敏管理的最新进展。

Update on the management of antibiotic allergy.

机构信息

Department of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Singapore.

出版信息

Allergy Asthma Immunol Res. 2010 Apr;2(2):77-86. doi: 10.4168/aair.2010.2.2.77. Epub 2010 Mar 24.

Abstract

Drug allergy to antibiotics may occur in the form of immediate or non-immediate (delayed) hypersensitivity reactions. Immediate reactions are usually IgE-mediated whereas non-immediate hypersensitivity reactions are usually non-IgE or T-cell mediated. The clinical manifestations of antibiotic allergy may be cutaneous, organ-specific (e.g., blood dyscracias, hepatitis, interstitial nephritis), systemic (e.g., anaphylaxis, drug induced hypersensitivity syndrome) or various combinations of these. Severe cutaneous adverse reactions manifesting as Stevens Johnson syndrome or toxic epidermal necrolysis (TEN) may be potentially life-threatening. The management of antibiotic allergy begins with the identification of the putative antibiotic from a detailed and accurate drug history, complemented by validated in-vivo and in-vitro allergological tests. This will facilitate avoidance of the putative antibiotic through patient education, use of drug alert cards, and electronic medical records with in-built drug allergy/adverse drug reaction prescription and dispensing checks. Knowledge of the evidence for specific antibiotic cross-reactivities is also important in patient education. Apart from withdrawal of the putative antibiotic, immunomodulatory agents like high-dose intravenous immunoglobulins may have a role in TEN. Drug desensitization where the benefits outweigh the risks, and where no alternative antibiotics can be used for various reasons, may be considered in certain situations. Allergological issues pertaining to electronic drug allergy alerts, computerized physician prescriptions and decision support systems, and antibiotic de-escalation in antimicrobial stewardship programmes are also discussed.

摘要

抗生素药物过敏可能表现为即刻或迟发(延迟)超敏反应。即刻反应通常为 IgE 介导,而非即刻超敏反应通常为非 IgE 或 T 细胞介导。抗生素过敏的临床表现可能为皮肤、器官特异性(例如血液学异常、肝炎、间质性肾炎)、全身性(例如过敏反应、药物诱导的超敏反应综合征)或这些表现的各种组合。严重皮肤不良反应表现为史蒂文斯-约翰逊综合征或中毒性表皮坏死松解症(TEN),可能危及生命。抗生素过敏的管理始于从详细准确的药物史中确定可疑抗生素,辅以前瞻性和体外过敏学检测加以证实。这将通过患者教育、使用药物警示卡和内置药物过敏/药物不良反应处方和配药检查的电子病历来促进避免使用可疑抗生素。了解特定抗生素交叉反应的证据对患者教育也很重要。除了停用可疑抗生素外,免疫调节剂如大剂量静脉注射免疫球蛋白在 TEN 中可能也有作用。在某些情况下,如果获益大于风险,并且由于各种原因无法使用其他抗生素,则可以考虑进行药物脱敏。还讨论了与电子药物过敏警报、计算机化医生处方和决策支持系统以及抗菌药物管理计划中抗生素降阶梯相关的过敏问题。

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