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既往阿司匹林诱发的哮喘与口服阿司匹林激发试验期间诱发的哮喘严重程度之间的关系。

The relationship between historical aspirin-induced asthma and severity of asthma induced during oral aspirin challenges.

作者信息

Williams Adam N, Simon Ronald A, Woessner Katharine M, Stevenson Donald D

机构信息

Division of Allergy, Asthma, and Immunology, Scripps Clinic, San Diego, CA 92130, USA.

出版信息

J Allergy Clin Immunol. 2007 Aug;120(2):273-7. doi: 10.1016/j.jaci.2007.03.020. Epub 2007 May 3.

Abstract

BACKGROUND

Historical aspirin- or nonsteroidal anti-inflammatory drug (NSAID)-induced reactions might provide predictive information about the severity of reactions in patients with aspirin-exacerbated respiratory disease (AERD) undergoing oral aspirin challenge (OAC).

OBJECTIVE

We sought to assess the relationship between historical aspirin- or NSAID-induced bronchial reactions and the severity of bronchial reactions during OAC in patients with AERD.

METHODS

Data regarding the provoking doses, treatments, and treatment settings of historical aspirin/NSAID-induced reactions were recorded, analyzed, and compared with the provoking doses, maintenance regimens, and observed decreases in FEV(1) that occurred during OAC in 210 consecutive patients referred with suspected AERD.

RESULTS

Of 147 patients who reported seeking acute medical care for their historical aspirin/NSAID-induced asthma attacks, 101 (69%) were treated in an emergency department and released, and 46 (31%) required hospitalization. During OAC in these 147 subjects, 23 (16%) had a 20% to 29% decrease and 14 (10%) had a 30% or greater decrease in FEV(1) values from baseline. Of the 46 patients previously hospitalized for aspirin/NSAID-induced asthma attacks, 9 (20%) had a 20% to 29% decrease and 6 (13%) had a 30% or greater decrease in FEV(1) during OAC. By contrast, of the 63 patients who treated their prior aspirin/NSAID-induced reactions at home, 5 (8%) had a 20% to 29% decrease and 5 (8%) had a 30% or greater decrease in FEV(1) during OAC (P = not significant for both).

CONCLUSION

The severity of the historical aspirin/NSAID-induced asthma attack was not predictive of asthma severity during OAC.

CLINICAL IMPLICATIONS

These data provide further reassurance regarding the safety of outpatient aspirin desensitization.

摘要

背景

既往阿司匹林或非甾体抗炎药(NSAID)诱发的反应可能为正在接受口服阿司匹林激发试验(OAC)的阿司匹林加重性呼吸系统疾病(AERD)患者的反应严重程度提供预测信息。

目的

我们试图评估既往阿司匹林或NSAID诱发的支气管反应与AERD患者OAC期间支气管反应严重程度之间的关系。

方法

记录、分析既往阿司匹林/NSAID诱发反应的激发剂量、治疗方法及治疗环境的数据,并与210例因疑似AERD前来就诊的连续患者在OAC期间的激发剂量、维持方案及观察到的第一秒用力呼气容积(FEV₁)下降情况进行比较。

结果

在147例报告因既往阿司匹林/NSAID诱发哮喘发作而寻求紧急医疗护理的患者中,101例(69%)在急诊科接受治疗后出院,46例(31%)需要住院治疗。在这147例受试者的OAC期间,23例(16%)的FEV₁值较基线下降了20%至29%,14例(10%)下降了30%或更多。在46例既往因阿司匹林/NSAID诱发哮喘发作而住院的患者中,9例(20%)在OAC期间FEV₁下降了20%至29%,6例(13%)下降了30%或更多。相比之下,在63例在家中治疗其既往阿司匹林/NSAID诱发反应的患者中,5例(8%)在OAC期间FEV₁下降了20%至29%,5例(8%)下降了30%或更多(两者P值均无统计学意义)。

结论

既往阿司匹林/NSAID诱发哮喘发作的严重程度不能预测OAC期间哮喘的严重程度。

临床意义

这些数据为门诊阿司匹林脱敏的安全性提供了进一步的保证。

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