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皮下免疫治疗注射后的即刻和迟发性全身反应:ACAAI/AAAAI 皮下免疫治疗监测研究:第 2 年。

Immediate and delayed-onset systemic reactions after subcutaneous immunotherapy injections: ACAAI/AAAAI surveillance study of subcutaneous immunotherapy: year 2.

机构信息

Department of Medicine, Division of Immunology, Allergy and Rheumatology, University of Cincinnati College of Medicine, Ohio, USA.

出版信息

Ann Allergy Asthma Immunol. 2011 Nov;107(5):426-431.e1. doi: 10.1016/j.anai.2011.05.020. Epub 2011 Jun 17.

Abstract

BACKGROUND

Incidences of subcutaneous immunotherapy (SCIT) related systemic reactions (SRs) and fatal reactions (FRs) are not well defined, nor are delayed-onset SRs and their treatment.

OBJECTIVES

To estimate SCIT-related SRs/FRs, and the incidence and treatment of delayed-onset SRs.

METHODS

In 2008 and 2009, American Academy of Allergy, Asthma & Immunology (AAAAI) and American College of Allergy Asthma & Immunology (ACAAI) members completed a survey about SCIT-related SR severity (grade 1 = mild; grade 2 = moderate; grade 3 = severe anaphylaxis). In 2009, members reported the time of onset and use of epinephrine (EPI), with early onset defined as beginning ≤30 minutes, and delayed onset beginning more than 30 minutes after injections.

RESULTS

As in year 1, no FRs were reported during year 2 (630 total practices responded). Among 267 practices providing data on the timing of SRs, 1,816 early-onset SRs (86%) and 289 (14%) delayed-onset SRs were reported. Fifteen percent (226/1,519) of grade 1, 10% (54/538) of grade 2, and 12.5% (9/72) of grade 3 SRs were delayed-onset. Among early-onset SRs, EPI was given for 71% of grade 1, 93% of grade 2, and 94% of grade 3s. Among delayed-onset SRs, EPI was given for 56% of grade 1, 67% of grade 2, and 100% of grade 3s (P = .0008 for difference in EPI administration based on severity; P = .07 based on time of onset).

CONCLUSIONS

Delayed-onset SRs are less frequent than previously reported. Epinephrine was given less frequently for grades 1 and 2 (but not grade 3) delayed-onset SRs compared with early-onset SRs. Further study of prescribing self-injectable EPI for SCIT patients in the event of delayed-onset SRs may be warranted.

摘要

背景

皮下免疫疗法(SCIT)相关全身性反应(SR)和致命反应(FR)的发生率尚不清楚,迟发性 SR 及其治疗也不清楚。

目的

估计 SCIT 相关 SR/FR 以及迟发性 SR 的发生率和治疗方法。

方法

2008 年和 2009 年,美国过敏、哮喘和免疫学学会(AAAAI)和美国过敏、哮喘和免疫学学会(ACAAI)的成员完成了一项关于 SCIT 相关 SR 严重程度(1 级=轻度;2 级=中度;3 级=严重过敏反应)的调查。2009 年,成员报告了注射后出现的时间和肾上腺素(EPI)的使用情况,早期发作定义为开始≤30 分钟,而延迟发作定义为开始≥30 分钟。

结果

与第 1 年一样,第 2 年(630 家诊所做出回应)没有报告 FR。在 267 家提供 SR 时间数据的诊所中,报告了 1816 例早期发作的 SR(86%)和 289 例(14%)迟发性发作的 SR。15%(226/1519)的 1 级、10%(54/538)的 2 级和 12.5%(9/72)的 3 级 SR 为迟发性。在早期发作的 SR 中,71%的 1 级、93%的 2 级和 94%的 3 级给予了 EPI。在迟发性发作的 SR 中,56%的 1 级、67%的 2 级和 100%的 3 级给予了 EPI(基于严重程度的 EPI 给药差异 P =.0008;基于发作时间的 P =.07)。

结论

迟发性 SR 比以前报道的要少见。与早期发作的 SR 相比,1 级和 2 级(但不是 3 级)迟发性 SR 给予 EPI 的频率较低。可能需要进一步研究为接受 SCIT 的患者开具迟发性 SR 情况下的自我注射 EPI 处方。

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