非甾体抗炎药摄入作为免疫治疗期间过敏反应的危险因素:一个病例系列

D. Fahmy, Jason K. Lee
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引用次数: 3

摘要

背景:皮下过敏原免疫疗法(SCIT)是季节性和/或常年性鼻炎、结膜炎或哮喘的常用治疗方法。不幸的是,在使用过敏原免疫疗法(AIT)治疗期间可能会发生不良事件,包括从皮肤表现到过敏反应的严重程度不等的全身反应。目的:虽然乙酰水杨酸(ASA)和其他非甾体抗炎药(NSAIDs)对肥大细胞的作用以及作为过敏反应的辅助因子已经得到了很好的描述,但它们在AIT中的作用还没有得到很好的描述。目前的实践参数并未将非甾体抗炎药作为AIT过敏反应的潜在危险因素。这篇文章提供了一系列的案例,提供证据,这些药物也应谨慎使用时,给予AIT。结果:我们描述了6例患有各种环境过敏的患者,他们已经接受了AIT并经历了过敏反应。在病史上,这些患者均在注射后24小时内摄入了ASA或NSAIDs。六名患者中有四名选择继续AIT并保持维持剂量,没有发生事故。这些患者除了在注射前24小时避免使用非甾体抗炎药外,没有其他变化。结论:这些病例可能引起对ASA和其他非甾体抗炎药作为SCIT过敏反应辅助因素的关注。提供免疫治疗的医生可能希望确保他们在讨论治疗的风险和益处时,包括在接受治疗前使用ASA和非甾体抗炎药可能会增加全身反应的风险。如果存在,患者可能希望使用更安全的替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-Steroidal Anti-Inflammatory Drug Ingestion as a Risk Factor to Anaphylaxis During Immunotherapy: a Case Series
Background: Subcutaneous allergen immunotherapy (SCIT) is a common treatment for seasonal and/or perennial rhinitis, conjunctivitis, or asthma. Unfortunately, adverse events may occur during treatment with allergen immunotherapy (AIT), including systemic reactions that may range in severity from cutaneous manifestations to anaphylaxis. Objectives: Although the effect of acetasalicylic acid (ASA) and other non-steroidal anti-inflammatory drugs (NSAIDs) on mast cells and as cofactors of anaphylaxis have been well-described, their role in the setting of AIT has not. The current practice parameters do not address NSAIDs as a potential risk factor for anaphylaxis with AIT. This article provides a series of cases that offer evidence that these medications should also be used with caution when administering AIT. Results: We describe six cases of patients with various environmental allergies that had been undergoing AIT and experienced anaphylaxis. On history, each of these patients had ingested ASA or NSAIDs within 24 hours of the injection. Four out of the six described patients elected to continue AIT and remain on maintenance doses without incident. These patients made no additional changes with the exception of avoiding NSAIDs 24 hours prior to injection. Conclusions: These cases may bring to attention the role of ASA and other NSAIDs in acting as a co-factor for anaphylaxis in the setting of SCIT. Physicians providing immunotherapy may wish to ensure that their discussion of the risks and benefits of the treatment include information that ASA and NSAID use prior to receiving therapy may increase the risk of a systemic reaction. Patients may wish to use a safer alternative if such exists.
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