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首页> 外文期刊>Annals of allergy, asthma, and immunology >AAAAI and ACAAI surveillance study of subcutaneous immunotherapy, Year 3: What practices modify the risk of systemic reactions?
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AAAAI and ACAAI surveillance study of subcutaneous immunotherapy, Year 3: What practices modify the risk of systemic reactions?

机译:皮下免疫疗法的AAAAI和ACAAI监测研究,第3年:哪些做法可改变全身反应的风险?

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摘要

Objective: To define the incidence of and clinical practices associated with subcutaneous immunotherapy (SCIT)-related systemic reactions (SRs). Methods: From 2008-2011, American Academy of Allergy, Asthma & Immunology and American College of Allergy, Asthma & Immunology members completed an annual survey of SCIT-related SRs of varying severity (with grade 1 indicating mild; grade 2, moderate; and grade 3, severe anaphylaxis). From 2010-2011 (year 3) data were collected regarding SCIT-related procedures, including screening of patients with asthma, dose adjustment during peak pollen seasons, build-up regimens (conventional, cluster, or rush), and premedication. Results: No fatal reactions were directly or indirectly reported from 2008-2011. The SR rates were similar for all 3 years (0.1% of injection visits; 83% of practices), as were severity grades. On average, for all 3 years, there were 7.1 grade 1, 2.6 grade 2, and 0.4 grade 3 SRs per 10,000 injection visits. Screening for worsening asthma symptoms was highly prevalent (86% always screened). Practices that always reduced doses during peak pollen season were significantly less likely to report grade 2 or 3 SRs (44% vs 65%; P =.04). Cluster and rush build-up were associated with significantly more SRs (P <.001). Practices that premedicated were significantly more likely to report grade 2 and 3 SRs (P <.01). Conclusion: Fatal reactions to SCIT appear to be declining, possibly related to almost universal screening of asthmatic patients. Adjusting doses during the pollen season may be associated with decreased risk for severe SRs. Cluster and rush immunotherapy were associated with increased risk for SRs. Premedication by practices reporting SRs likely reflects past experience with SRs.
机译:目的:确定皮下免疫疗法(SCIT)相关的全身反应(SRs)的发生率和临床实践。方法:从2008年至2011年,美国过敏,哮喘与免疫学会和美国过敏,哮喘与免疫学会成员完成了对SCIT相关严重程度不同的SR的年度调查(1级表示轻度; 2级表示中度; 3级,严重过敏反应)。从2010年至2011年(第3年),收集了与SCIT相关程序的数据,包括筛查哮喘患者,在花粉高峰季节调整剂量,建立治疗方案(常规,整群或急诊)和用药前。结果:2008-2011年没有直接或间接报告致命反应。在所有3年中,SR率均相似(0.1%的注射访视; 83%的实践),以及严重程度等级。平均而言,这3年中,每10,000次注射就诊有7.1级1、2.6级2级和0.4级3级SR。哮喘症状恶化的筛查非常普遍(始终筛查86%)。在高峰花粉季节始终减少剂量的实践报告2级或3级SR的可能性大大降低(44%对65%; P = .04)。集群和仓促积累与更多的SR相关(P <.001)。用药前的实践报告SR和SR的可能性更高(P <.01)。结论:对SCIT的致命反应似乎正在下降,这可能与哮喘患者的几乎所有筛查有关。在花粉季节调整剂量可能与降低严重SR的风险有关。群集和急诊免疫疗法与SR风险增加相关。报告SR的实践进行的预防可能反映了SR的以往经验。

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