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变应性鼻炎患者皮下免疫治疗的不良反应:一项真实世界研究。

Adverse reactions to subcutaneous immunotherapy in patients with allergic rhinitis, a real-world study.

机构信息

Department of Otolaryngology-Head and Neck Surgery, Renmin Hospital of Wuhan University, 238 Jiefang Rd, Wuhan, 430060, China.

Research Institute of Otolaryngology-Head and Neck Surgery, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Eur Arch Otorhinolaryngol. 2021 Nov;278(11):4353-4360. doi: 10.1007/s00405-021-06736-2. Epub 2021 Mar 13.

Abstract

PURPOSE

The efficacy of subcutaneous immunotherapy (SCIT) for allergic rhinitis (AR) have been proven but application is still limited by concerns about the safety. The aims of this study were to investigate the incidence of adverse reactions and to ascertain possible risk factors in patients treated with SCIT in central China.

METHODS

This study retrospectively analyzed the application of SCIT from 2016 to 2018, in 236 patients with AR. After each injection, allergen dosage and details about local reactions (LRs)/systemic reactions (SRs) were recorded.

RESULTS

Totaling 236 patients received 5844 injections. The rates of LR were 3.0% per injection and 34.7% per patient, while the rates of SR were 0.48% per injection and 10.6% per patient. 86.9 percent LRs were small. Most SRs were grade 1 (16/57.1%), followed by grade 2 (8/28.6%), grade 3 (4/14.3%). No fatal SRs was recorded. Children, high sensitization and absence of premedication were identified as risk factors for LRs. Recurrent LRs increased the risk of SRs. Premedication could reduce the number and severity of LRs, but not SRs. Dual therapy with antihistamine and montelukast did not provide additional benefit when compared with antihistamine alone.

CONCLUSION

The incidence of SRs was low while LRs were common in SCIT. Children may be prone to develop LRs, while pretreatments could reduce the number and severity of LRs. Recurrent LRs was a risk factor for SRs.

摘要

目的

皮下免疫疗法(SCIT)治疗过敏性鼻炎(AR)的疗效已得到证实,但由于对安全性的担忧,其应用仍然有限。本研究旨在调查不良反应的发生率,并确定在华中地区接受 SCIT 治疗的患者中可能的危险因素。

方法

本研究回顾性分析了 2016 年至 2018 年 236 例 AR 患者接受 SCIT 的应用情况。每次注射后,记录过敏原剂量和局部反应(LRs)/全身反应(SRs)的详细信息。

结果

共有 236 例患者接受了 5844 次注射。LR 的发生率为每注射 3.0%,每患者 34.7%,而 SR 的发生率为每注射 0.48%,每患者 10.6%。86.9%的 LRs 为轻度。大多数 SR 为 1 级(16/57.1%),其次为 2 级(8/28.6%),3 级(4/14.3%)。无致命性 SR 报告。儿童、高致敏和无预处理被确定为 LRs 的危险因素。反复发生 LRs 增加了发生 SRs 的风险。预处理可减少 LRs 的数量和严重程度,但不能减少 SRs。与单独使用抗组胺药相比,抗组胺药和孟鲁司特联合治疗并未提供额外益处。

结论

SCIT 中 SRs 的发生率较低,而 LRs 较为常见。儿童可能容易发生 LRs,而预处理可减少 LRs 的数量和严重程度。反复发生 LRs 是发生 SRs 的危险因素。

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