姜立学, 朱兴中, 孙军, 范晶晶, 秦基云, 潘冬梅. 变应性鼻炎舌下特异性免疫治疗同步接种新型冠状病毒疫苗的安全性分析[J]. 实用临床医药杂志, 2022, 26(20): 78-80, 84. DOI: 10.7619/jcmp.20222756
引用本文: 姜立学, 朱兴中, 孙军, 范晶晶, 秦基云, 潘冬梅. 变应性鼻炎舌下特异性免疫治疗同步接种新型冠状病毒疫苗的安全性分析[J]. 实用临床医药杂志, 2022, 26(20): 78-80, 84. DOI: 10.7619/jcmp.20222756
JIANG Lixue, ZHU Xingzhong, SUN Jun, FAN Jingjing, QIN Jiyun, PAN Dongmei. Analysis in safety of allergic rhinitis patients with sublingual immunotherapy and simultaneous vaccination of novel coronavirus[J]. Journal of Clinical Medicine in Practice, 2022, 26(20): 78-80, 84. DOI: 10.7619/jcmp.20222756
Citation: JIANG Lixue, ZHU Xingzhong, SUN Jun, FAN Jingjing, QIN Jiyun, PAN Dongmei. Analysis in safety of allergic rhinitis patients with sublingual immunotherapy and simultaneous vaccination of novel coronavirus[J]. Journal of Clinical Medicine in Practice, 2022, 26(20): 78-80, 84. DOI: 10.7619/jcmp.20222756

变应性鼻炎舌下特异性免疫治疗同步接种新型冠状病毒疫苗的安全性分析

Analysis in safety of allergic rhinitis patients with sublingual immunotherapy and simultaneous vaccination of novel coronavirus

  • 摘要:
    目的 分析变应性鼻炎(AR)舌下特异性免疫治疗(SLIT)同步接种新型冠状病毒疫苗的临床安全性。
    方法 选取本院441例AR行SLIT并同步接种新型冠状病毒疫苗的患者为研究对象,观察接种人群不良反应的发生情况。
    结果 441例AR患者中, 51例成人患者在SLIT递增期接种了新型冠状病毒疫苗第1剂,接种后出现局部荨麻疹2例,低热1例,全身乏力及酸痛2例,不良反应发生率为9.8%(5/51); 390例患者在SLIT维持期接种新型冠状病毒疫苗第1剂,接种后出现1例鼻塞、流涕,不良反应发生率为0.26%(1/390)。441例AR患者接种新型冠状病毒疫苗第2剂后出现全身乏力1例,不良反应发生率0.23%(1/441); 423例AR患者接种新型冠状病毒疫苗第3剂后均无不良反应。
    结论 在新型冠状病毒肺炎疫情常态化管理下,建议AR患者在特异性免疫治疗维持期接种新型冠状病毒疫苗,避免在递增期接种,以减少不良反应的发生。若接种第1剂新型冠状病毒疫苗后出现不良反应,在接种第2、3剂新型冠状病毒疫苗时应暂停特异性免疫治疗,无不良反应后再继续特异性免疫治疗,以避免多种免疫应答对机体内环境的影响,提高多种免疫方案同步治疗的安全性。

     

    Abstract:
    Objective To analyze the clinical safety of allergic rhinitis (AR) patients with sublingual immunotherapy (SLIT) and simultaneous vaccination of novel coronavirus.
    Methods A total of 441 patients with AR treated by SLIT and simultaneous vaccination of novel coronavirus were selected as research objects, and incidence of complications related to vaccination was observed.
    Results Among the 441 AR patients, 51 adult patients received the first dose of novel coronavirus vaccine in the incremental period of SLIT, but there were 2 cases of local urticaria, 1 case of low fever and 2 cases of fatigue and pain after the vaccination, and the incidence of adverse reactions was 9.8%(5/51); a total of 390 patients received the first dose of novel coronavirus vaccine in the maintenance period of SLIT, but there was 1 case with stuffy and running nose after vaccination, and the incidence of adverse reactions was 0.26%(1/390). One of 441 AR patients had general fatigue after receiving the second dose of novel coronavirus vaccine, and the incidence of adverse reactions was 0.23%(1/441); a total of 423 AR patients had no adverse reactions after receiving the third dose of novel coronavirus vaccine.
    Conclusion Under the normalization management for epidemic situation of the Coronavirus Disease 2019, it is recommended that AR patients should be inoculated with novel coronavirus vaccine in the maintenance period of specific immunotherapy to avoid vaccination in the incremental period, so as to reduce the incidence of adverse reactions. If adverse reactions occur after receiving the first dose of novel coronavirus vaccine, specific immunotherapy should be suspended when the second and third doses of novel coronavirus vaccine are inoculated, and specific immunotherapy should be carried out after there are no adverse reactions, so as to avoid the impact of multiple immune responses on the internal environment and improve the safety of simultaneous treatment of multiple immune schemes.

     

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