[A preliminary study on the short-term effectiveness and safety of sublingual immunotherapy-spray for patients with respiratory allergy].

Q3 Medicine
X Y Dai, H D Lou, X Y Wang, S Chen, J Zhang, H B Ding, J Li, L Cheng
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引用次数: 0

Abstract

To investigate the short-term effectiveness and safety of sublingual allergen immunotherapy with allergen sprays (SLIT-sprays) in Chinese patients with allergic rhinitis (AR) with or without asthma using real-world data. The retrospective cohort study included 100 patients who received SLIT-sprays in the ENT departments in Hainan Shulan (Boao) Hospital and Boao Super Hospital between October 2023 and August 2024. A questionnaire survey was conducted to collect clinical data on the effectiveness and safety of SLIT-sprays, examining the types and incidence of adverse events (AEs) during treatment, treatments after the occurrence of AEs, and changes in Visual Analog Scale (VAS) scores before and after SLIT-sprays. Self-reports from 100 patients were collected. The results showed that the average treatment duration for the 100 patients was (90.7±58.9) days, median 78.5 days. Using changes in VAS scores as the effectiveness assessment, the average VAS score increased by 4.2 (95%CI: 4.06-4.34). The incidence of AEs during the SLIT-sprays was 17.0% (17/100), all of which were mild to moderate local reactions, with no serious AEs reported. There were no significant differences in AE incidence among patients with different diseases (AR or AR with asthma and asthma alone) (χ2=1.831,P>0.05), different age group (χ2=1.477,P>0.05), different types of allergen extracts (χ2=1.613,P>0.05), or the number of allergen extracts used (patients using one or two allergen extracts) (Fisher's exact test,P>0.05). In conclusion, Chinese patients showed good safety and tolerability to SLIT-sprays, with all AEs being mild to moderate local reactions and no serious or systemic AEs occurring. Patients reported positive subjective evaluations of the early treatment effects.

[舌下免疫治疗喷雾剂对呼吸道过敏患者短期疗效及安全性的初步研究]。
目的:探讨舌下过敏原喷雾剂(SLIT-sprays)对伴有或不伴有哮喘的中国变应性鼻炎(AR)患者的短期有效性和安全性。该回顾性队列研究纳入了2023年10月至2024年8月在海南舒兰(博鳌)医院和博鳌超级医院耳鼻喉科接受裂隙喷雾剂治疗的100例患者。通过问卷调查收集sslit喷雾剂的有效性和安全性的临床资料,检查治疗过程中不良事件(ae)的类型和发生率,ae发生后的治疗情况,以及sslit喷雾剂前后视觉模拟评分(VAS)的变化。收集了100例患者的自我报告。结果显示,100例患者的平均治疗时间为(90.7±58.9)d,中位治疗时间为78.5 d。以VAS评分变化作为疗效评价,VAS评分平均提高4.2分(95%CI: 4.06-4.34)。喷施过程中不良反应发生率为17.0%(17/100),均为轻度至中度局部反应,无严重不良反应报告。不同疾病(AR、AR合并哮喘和单独哮喘)、不同年龄组(χ2=1.477,P>0.05)、不同过敏原提取物类型(χ2=1.613,P>0.05)、不同过敏原提取物使用次数(使用一种或两种过敏原提取物)患者的AE发病率差异无统计学意义(Fisher精确检验,P>0.05)。综上所述,中国患者对slit喷雾剂表现出良好的安全性和耐受性,所有不良反应均为轻度至中度局部反应,未发生严重或全身性不良反应。患者报告了对早期治疗效果的积极主观评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
中华预防医学杂志
中华预防医学杂志 Medicine-Medicine (all)
CiteScore
1.20
自引率
0.00%
发文量
12678
期刊介绍: Chinese Journal of Preventive Medicine (CJPM), the successor to Chinese Health Journal , was initiated on October 1, 1953. In 1960, it was amalgamated with the Chinese Medical Journal and the Journal of Medical History and Health Care , and thereafter, was renamed as People’s Care . On November 25, 1978, the publication was denominated as Chinese Journal of Preventive Medicine . The contents of CJPM deal with a wide range of disciplines and technologies including epidemiology, environmental health, nutrition and food hygiene, occupational health, hygiene for children and adolescents, radiological health, toxicology, biostatistics, social medicine, pathogenic and epidemiological research in malignant tumor, surveillance and immunization.
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