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Safety of segmental allergen challenge in human allergic asthma.

机译:分段过敏原挑战在人类过敏性哮喘中的安全性。

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BACKGROUND: Segmental allergen challenge is widely used to study mechanisms of human allergic asthma. Despite the relatively large dissemination, limited information is available about the safety of this method. OBJECTIVE: Observational, retrospective study to report the adverse events of segmental allergen challenge in a large group of volunteers with asthma. METHODS: In total, 78 cases from several studies performed between 1994 and 2007 were pooled for this analysis. Volunteers underwent allergen challenge using either a fixed dose of allergen (7 cases) or an individually standardized allergen dose defined by an inhaled allergen test before the challenge (71 cases). A subgroup of 13 volunteers underwent repeated challenges, with more than 6 months between the challenges. RESULTS: With a fixed dose instilled during bronchoscopy, 43% of the participants developed wheezing and coughing, requiring 2-6 puffs of a ss(2)-agonist after segmental allergen challenge. In volunteers with individually standardized doses, a ss(2)-agonist was required in only 19% of the cases. No severe adverse events occurred in all cases studied. Volunteers who underwent repeated challenges did not develop more adverse events than those who underwent 1 challenge. CONCLUSIONS: Segmental allergen challenge is a safe tool to study the mechanisms of human allergic asthma, even when repeated challenges are performed in the same patient. It is associated with only a few, tolerable adverse events, especially when the dose of allergen is standardized individually.
机译:背景:节段性过敏原攻击被广泛用于研究人类过敏性哮喘的机制。尽管传播相对较大,但有关此方法安全性的信息有限。目的:观察性回顾性研究报告了一大批哮喘志愿者中分段过敏原激发的不良事件。方法:总共收集了1994年至2007年间进行的几项研究的78例病例进行了分析。志愿者使用固定剂量的变应原(7例)或通过在激发前进行吸入性变应原测试定义的单独标准化变应原剂量(71例)进行了变应原挑战。一个由13名志愿者组成的小组经历了多次挑战,两次挑战之间的间隔时间超过6个月。结果:在支气管镜检查期间以固定剂量滴注,有43%的参与者出现了喘息和咳嗽,在节段性变应原攻击后需要2-6喷的ss(2)激动剂。在单独标准化剂量的志愿者中,仅19%的病例需要使用ss(2)激动剂。在所有研究的病例中均未发生严重的不良事件。经历反复挑战的志愿者没有比经历一次挑战的志愿者产生更多的不良事件。结论:即使同一位患者反复进行挑战,节段性过敏原攻击仍是研究人类过敏性哮喘机制的安全工具。它仅与少数可忍受的不良事件有关,特别是当过敏原剂量单独标准化时。

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