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用于诊断阿司匹林超敏反应的口服阿司匹林激发试验方案的改进。

Improvements in an oral aspirin challenge protocol for the diagnosis of aspirin hypersensitivity.

作者信息

Cormican L J, Farooque S, Altmann D R, Lee T H

机构信息

Department of Asthma, King's College London, Guy's Hospital, London, UK.

出版信息

Clin Exp Allergy. 2005 Jun;35(6):717-22. doi: 10.1111/j.1365-2222.2005.02261.x.

Abstract

Oral aspirin challenge (OAC) is used to confirm aspirin hypersensitivity (AHs) but there is no consensus on a standardized protocol. As a prior clinical history of adverse reactions to aspirin is poorly predictive of a positive result from formal aspirin challenge, many patients have an OAC performed. We retrospectively identified and prospectively validated how a 1-day OAC protocol could be modified, and patient selection improved, to deliver a safe and more efficient service. In a retrospective audit of 45 OACs using a 2 h dose interval, all reactions occurred within 90 min of the threshold dose. Forty OACs were then performed using a 90-min dose interval. This reduced the mean duration of a positive and negative OAC from 6 to 5 h and from 8 to 6 h, respectively. Histories of multiple manifestations of AHs were found in 91.6% (11) of those with asthma, 87.5% (7) with angiooedema, 70.6% (12) with rhinosinusitis, 63.6% (7) with chronic non-vasculitic urticaria and all with anaphylaxis, who developed a positive OAC. None of those with anaphylaxis, 8.3% (1) with asthma and 12.5% (1) with angiooedema, with a positive OAC, had a history of a single manifestation of AHs. The efficiency of an OAC service can safely be improved by reduction of the dose interval from 2 to 1 (1/2) h, and more targeted patient selection, as the likelihood of a positive OAC increases among patients with a history of asthma, angiooedoema or anaphylaxis with multiple manifestations of AHs.

摘要

口服阿司匹林激发试验(OAC)用于确诊阿司匹林超敏反应(AHs),但目前尚无关于标准化方案的共识。由于既往阿司匹林不良反应的临床病史对正式阿司匹林激发试验阳性结果的预测性较差,许多患者都接受了OAC。我们回顾性地确定并前瞻性地验证了如何修改1天的OAC方案以及改进患者选择,以提供安全且更高效的服务。在一项对45例采用2小时剂量间隔的OAC的回顾性审计中,所有反应均在阈值剂量的90分钟内发生。随后进行了40例采用90分钟剂量间隔的OAC。这分别将阳性和阴性OAC的平均持续时间从6小时缩短至5小时,从8小时缩短至6小时。在哮喘患者中,91.6%(11例)、血管性水肿患者中87.5%(7例)、鼻窦炎患者中70.6%(12例)、慢性非血管性荨麻疹患者中63.6%(7例)以及所有发生过敏反应的患者中,出现OAC阳性的患者均有多种AHs表现的病史。在OAC阳性的患者中,发生过敏反应的患者、8.3%(1例)哮喘患者和12.5%(1例)血管性水肿患者均无单一AHs表现的病史。通过将剂量间隔从2小时缩短至1.5小时以及更有针对性地选择患者,可以安全地提高OAC服务的效率,因为在有哮喘、血管性水肿或过敏反应病史且有多种AHs表现的患者中,OAC阳性的可能性会增加。

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