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与皮下变应原免疫治疗相关的全身性反应:时间和风险评估。

Systemic reactions associated with subcutaneous allergen immunotherapy: timing and risk assessment.

机构信息

Division of Allergy and Clinical Immunology, The Children's Hospital of Philadelphia, Pennsylvania, USA.

出版信息

Ann Allergy Asthma Immunol. 2011 Jun;106(6):533-537.e2. doi: 10.1016/j.anai.2011.02.007. Epub 2011 Apr 14.

DOI:10.1016/j.anai.2011.02.007
PMID:21624754
Abstract

BACKGROUND

Subcutaneous allergen immunotherapy (SCIT) is associated with risk of systemic reaction. Although risk factors have been identified, the incidence of immunotherapy-related systemic reactions has not changed in recent years.

OBJECTIVES

To examine patterns of systemic reaction and determine whether risk of systemic reaction from SCIT is associated with patterns of response to skin tests to inhalant allergens recorded before receiving SCIT.

METHODS

We carried out a retrospective review from January 2001 to December 2007. Patterns of systemic reaction from immunotherapy were examined. Cases were matched with controls by age (±10 years), sex, and time of injection (±1 week) to determine whether a pattern of more than 33% 3+ and 4+ skin test responses is associated with elevated risk for systemic reaction.

RESULTS

Rate of systemic reaction from SCIT was 0.28% (46/16,375) per injection visit. Twenty patients had 46 systemic reactions. All severe reactions occurred within 30 minutes. The estimated odds of systemic reaction were almost 6 times higher for patients with more than 33% 3 to 4+ positive skin tests (OR = 5.83; 95%CI: 1.23-27.59, P = .026). For each additional 4+ skin test, the estimated odds for systemic reaction increased by 17% (P = .020).

CONCLUSIONS

A small number of patients receiving SCIT account for a large proportion of systemic reactions. Skin test patterns demonstrating a greater number of larger skin tests responses to inhalant skin testing are associated with significantly elevated risk for systemic reaction in patients receiving SCIT.

摘要

背景

皮下变应原免疫治疗(SCIT)与全身性反应的风险相关。尽管已经确定了危险因素,但近年来免疫治疗相关的全身性反应发生率并没有改变。

目的

检查全身性反应的模式,并确定 SCIT 引起的全身性反应风险是否与接受 SCIT 之前记录的吸入性变应原皮肤试验的反应模式相关。

方法

我们进行了一项回顾性研究,时间为 2001 年 1 月至 2007 年 12 月。检查了免疫治疗的全身性反应模式。通过年龄(±10 岁)、性别和注射时间(±1 周)将病例与对照组相匹配,以确定是否存在超过 33%的 3+和 4+皮肤试验反应模式与全身性反应风险增加相关。

结果

SCIT 的全身性反应发生率为每注射 16375 次注射 0.28%(46/16375)。20 例患者发生 46 次全身性反应。所有严重反应均发生在 30 分钟内。对于皮肤试验阳性的 3 至 4+比例超过 33%的患者,全身性反应的估计比值几乎高出 6 倍(OR=5.83;95%CI:1.23-27.59,P=0.026)。每增加 1 个 4+皮肤试验,全身性反应的估计比值增加 17%(P=0.020)。

结论

接受 SCIT 的少数患者占全身性反应的很大比例。皮肤试验模式显示对吸入性皮肤试验的更大数量的更大皮肤试验反应与接受 SCIT 的患者的全身性反应风险显著增加相关。

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