Suppr超能文献

支气管过敏原激发试验:剂量与浓度

Bronchial allergen challenge: dose versus concentration.

作者信息

Frølund L, Madsen F, Scharling B, Heinig J H, Svendsen U G

机构信息

Allergy Unit, State University Hospital, Copenhagen, Denmark.

出版信息

Clin Exp Allergy. 1992 Feb;22(2):219-25. doi: 10.1111/j.1365-2222.1992.tb03076.x.

Abstract

This study was designed to investigate if two equivalent doses of allergen administered by different dosing regimes--two breaths and 10 breaths of each concentration--would result in the same magnitude of the early and late asthmatic response. Fifteen patients with extrinsic allergic asthma were challenged twice with either two or 10 breaths of twofold increasing allergen concentrations. The challenge was continued until a 20% decrease in FEV1 had been achieved. A non-cumulative PC20FEV1 allergen was derived, and the cumulative dose of allergen given was similarly derived. In order to assess the reproducibility of the challenge, seven patients were challenged twice with two-breath regime. The mean value of allergen PC20 obtained by the two-breath regime was 4.1 fold (95% CI: 2.3-7.1 fold) greater than those obtained by the 10-breath regime (P less than 0.05), whereas the difference was 1.4 fold (95% CI: -3.3-0.5 fold) for the cumulative dose (P greater than 0.05). A statistically significant larger magnitude of the early asthmatic response, as determined by the maximum per cent fall in FEV1, and late asthmatic response determined by the maximum per cent fall in peak expiratory flow domiciliary recorded during the following 24 hr after challenge, was observed in favour of the 10-breath regime compared to the two-breath regime (mean difference 6%, 95% CI: 0.6-11%). The reproducibility of the provocation test was acceptable (+/- 1.8 two-fold concentration difference). These results confirm the 'equivalent dose hypothesis', and demonstrates that dosage rather than concentration appears to determine the early and late asthmatic response after bronchial allergen challenge.

摘要

本研究旨在调查通过不同给药方案给予两种等效剂量变应原(每种浓度分别为两次呼吸量和十次呼吸量)是否会导致相同程度的早发和迟发哮喘反应。15名外源性过敏性哮喘患者接受了两次激发试验,每次激发试验中变应原浓度成倍增加,分别给予两次呼吸量或十次呼吸量。激发试验持续进行,直至第一秒用力呼气量(FEV1)下降20%。得出非累积性使FEV1下降20%的变应原浓度(PC20FEV1),并以同样方式得出变应原的累积给药剂量。为评估激发试验的可重复性,7名患者接受了两次两次呼吸量给药方案的激发试验。两次呼吸量给药方案得出的变应原PC20平均值比十次呼吸量给药方案得出的结果高4.1倍(95%可信区间:2.3 - 7.1倍)(P < 0.05),而累积剂量的差异为1.4倍(95%可信区间:-3.3 - 0.5倍)(P > 0.05)。与两次呼吸量给药方案相比,十次呼吸量给药方案观察到具有统计学显著意义的更大程度的早发哮喘反应(通过FEV1的最大下降百分比确定)和迟发哮喘反应(通过激发试验后接下来24小时内家庭记录的呼气峰值流速的最大下降百分比确定)(平均差异6%,95%可信区间:0.6 - 11%)。激发试验的可重复性是可接受的(±1.8倍浓度差异)。这些结果证实了“等效剂量假说”,并表明剂量而非浓度似乎决定了支气管变应原激发试验后的早发和迟发哮喘反应。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验