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用赖氨酸乙酰水杨酸酯进行剂量计吸入试验以检测阿司匹林诱发的哮喘。

Dosimeter inhalation test with lysine acetylsalicylate for the detection of aspirin-induced asthma.

作者信息

Melillo G, Padovano A, Cocco G, Masi C

机构信息

Foundation Clinica del Lavoro, Division of Pharmacology, Campoli, Italy.

出版信息

Ann Allergy. 1993 Jul;71(1):61-5.

PMID:8328716
Abstract

Inhalation challenge with lysine acetylsalicylate (L-ASA) is often used to diagnose aspirin-induced asthma. The aim of this study was to evaluate the specificity and safety of performing L-ASA inhalation challenge with a dosimeter. Twenty-four subjects entered the study: ten ASA-sensitive asthmatic patients, seven non-ASA-sensitive asthmatic patients, and seven normal control subjects. The investigation was performed on two consecutive days. On day 1 a dosimeter inhalation test with methacholine was performed to establish the provocation dose (PD20). On day 2, patients underwent the L-ASA inhalation test, whereby increasing doses of L-ASA (from 1 to 32 mg cumulative dose) were inhaled using a dosimeter and a dose response curve was constructed. In subjects negative to the top dose, an additional oral dose of 500 mg of aspirin was administered to exclude aspirin sensitivity not revealed with the inhaled drug. The ten ASA-sensitive asthmatic patients developed early reactions within 30 minutes of PD20 administration. Recovery time from induced bronchoconstriction varied from two to three hours to six hours or longer resulting in an "early prolonged reaction." The response was limited to airways. No clear late reactions were observed. There was no correlation between PD20 with methacholine and PD20 with L-ASA. The L-ASA challenge was negative in the seven non-ASA-sensitive asthmatic patients and in the seven normal control subjects. In conclusion the dosimeter method is sensitive, specific, and safe for the detection of aspirin-induced asthma.

摘要

赖氨酸乙酰水杨酸(L-ASA)吸入激发试验常用于诊断阿司匹林诱发的哮喘。本研究的目的是评估使用剂量仪进行L-ASA吸入激发试验的特异性和安全性。24名受试者进入研究:10名对阿司匹林敏感的哮喘患者、7名对阿司匹林不敏感的哮喘患者和7名正常对照受试者。研究在连续两天进行。第1天,使用剂量仪进行乙酰甲胆碱吸入试验以确定激发剂量(PD20)。第2天,患者接受L-ASA吸入试验,使用剂量仪吸入递增剂量的L-ASA(累积剂量从1至32毫克)并构建剂量反应曲线。对于最高剂量试验结果为阴性的受试者,额外口服500毫克阿司匹林以排除吸入药物未显示出的阿司匹林敏感性。10名对阿司匹林敏感的哮喘患者在给予PD20后30分钟内出现早期反应。诱发支气管收缩后的恢复时间从两到三小时到六小时或更长,导致“早期延长反应”。反应仅限于气道。未观察到明显的迟发反应。乙酰甲胆碱的PD20与L-ASA的PD20之间无相关性。7名对阿司匹林不敏感的哮喘患者和7名正常对照受试者的L-ASA激发试验结果为阴性。总之,剂量仪法对于检测阿司匹林诱发的哮喘是敏感、特异且安全的。

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