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局部严重反应是儿童皮下免疫疗法全身反应的一个标志吗?

Are large local reactions a marker for systemic reactions to subcutaneous immunotherapy in children?

作者信息

Simsek Isil Eser, Aydogan Metin

机构信息

Division of Pediatric Allergy and Immunology, Kocaeli University, Kocaeli, Turkey.

出版信息

Asian Pac J Allergy Immunol. 2022 Mar;40(1):75-80. doi: 10.12932/AP-020221-1054.

Abstract

BACKGROUND

Previous studies involving predominantly adults concluded that the patients developing frequent large local reactions (LLRs) might be at greater risk for systemic reactions (SRs) during subcutaneous allergen immunotherapy (SCIT).

OBJECTIVE

To determine the rate of side effects to SCIT and evaluate frequency of LLR among pediatric patients with SRs.

METHODS

The retrospective study included pediatric patients receiving SCIT. Data on the demographic features, season at onset of SCIT, the indication for treatment, additional allergic diseases, laboratory results, the allergens applied, side effects after injection, grade of SRs, and the total number of injections for each patient were collected retrospectively from the medical records and injection charts.

RESULTS

A total of 19,562 injections were administered to 261 patients with conventional SCIT. The incidence LLRs was 0.2% per injection; 1.15% of all patients (n = 3) experienced LLRs on at least two consecutive visits. Systemic side effects were seen in 1% of all SCIT injections. No grade 3 or grade 4 SRs were observed. Logistic regression analysis showed that having an LLR was 3.32 times (95% CI, 1.313-8. 440; P = 0.011) and initiation of SCIT in summer and spring was 4.309 and 3.056 times than autumn (95% CI, 1.527-12.157, P = 0.006; 95% CI, 1.358-6.849, P = 0.007), respectively, increased risk for an SR.

CONCLUSIONS

Having LLRs might predict the risk of SRs at any time during immunotherapy in also pediatric patients. Knowing the risk factors is important for developing a personalized protocol in these patients.

摘要

背景

既往主要涉及成人的研究得出结论,在皮下过敏原免疫治疗(SCIT)期间,出现频繁严重局部反应(LLR)的患者发生全身反应(SR)的风险可能更高。

目的

确定SCIT的副作用发生率,并评估发生SR的儿科患者中LLR的频率。

方法

这项回顾性研究纳入了接受SCIT的儿科患者。从病历和注射记录中回顾性收集每位患者的人口统计学特征、SCIT开始时的季节、治疗指征、其他过敏性疾病、实验室检查结果、所应用的过敏原、注射后的副作用、SR的分级以及注射总次数等数据。

结果

对261例患者进行常规SCIT共注射19562次。每次注射LLR的发生率为0.2%;所有患者中有1.15%(n = 3)在至少连续两次就诊时出现LLR。所有SCIT注射中有1%出现全身副作用。未观察到3级或4级SR。逻辑回归分析显示,出现LLR使SR风险增加3.32倍(95%CI,1.313 - 8.440;P = 0.011),在春季和夏季开始SCIT分别使SR风险比秋季增加4.309倍和3.056倍(95%CI,1.527 - 12.157,P = 0.006;95%CI,1.358 - 6.849,P = 0.007)。

结论

出现LLR可能预测儿科患者免疫治疗期间任何时间发生SR的风险。了解风险因素对于为这些患者制定个性化方案很重要。

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