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脱敏止嚏汤治疗变应性鼻炎的临床疗效

Clinical Efficacy of Tuomin Zhiti Decoction in Allergic Rhinitis.

作者信息

Zhang Jian-Xin, Wang Wen-Yan

机构信息

Department of Oto-Rhino-Laryngology Head and Neck Surgery, Weihai Municipal Hospital, Weihai, Shandong, China.

出版信息

Evid Based Complement Alternat Med. 2022 Jun 21;2022:8616075. doi: 10.1155/2022/8616075. eCollection 2022.

Abstract

Allergic rhinitis (AR) is a noninfectious inflammatory disease seriously affecting the quality of life. This study aimed to assess the efficacy of the Tuomin Zhiti decoction in allergic rhinitis and to provide a reference for clinical treatment. One hundred patients with AR treated in the Department of Otolaryngology of our hospital from January 2019 to December 2020 were recruited and assigned via a random number table method (1 : 1) to receive either oral loratadine and mometasone nasal spray (control group) or the Tuomin Zhiti decoction plus oral loratadine and mometasone nasal spray (study group). The total clinical efficacy was 86% (43/50) in the study group, which was significantly higher than that of 64% (32/50) in the control group. After treatment, the Total Nasal Symptoms Scores (TNSS) and Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ) scores between the two groups were similar, but 12 weeks after treatment, the study group had significantly lower TNSS and RQLQ scores than the control group. After treatment, the study group obtained lower levels of interleukin (IL)-4 and higher levels of interferon- (IFN-) than the control group. Significantly lower post-treatment peripheral blood eosinophil count (EOS) and eosinophil cationic protein (ECP) levels were observed in the study group in contrast to those of the control group. The Tuomin Zhiti decoction for the treatment of AR patients alleviates their clinical symptoms, reduces the inflammatory responses, enhances the immune function of patients by regulating IL-4 and IFN-, and lowers the long-term recurrence rate.

摘要

变应性鼻炎(AR)是一种严重影响生活质量的非感染性炎症性疾病。本研究旨在评估脱敏止嚏汤治疗变应性鼻炎的疗效,为临床治疗提供参考。选取2019年1月至2020年12月在我院耳鼻咽喉科治疗的100例AR患者,采用随机数字表法(1∶1)分为两组,分别给予口服氯雷他定和糠酸莫米松鼻喷雾剂(对照组)或脱敏止嚏汤联合口服氯雷他定和糠酸莫米松鼻喷雾剂(研究组)。研究组总临床有效率为86%(43/50),显著高于对照组的64%(32/50)。治疗后,两组间总鼻症状评分(TNSS)和鼻结膜炎生活质量问卷(RQLQ)评分相近,但治疗12周后,研究组TNSS和RQLQ评分显著低于对照组。治疗后,研究组白细胞介素(IL)-4水平低于对照组,干扰素(IFN)-水平高于对照组。与对照组相比,研究组治疗后外周血嗜酸性粒细胞计数(EOS)和嗜酸性粒细胞阳离子蛋白(ECP)水平显著降低。脱敏止嚏汤治疗AR患者可缓解其临床症状,减轻炎症反应,通过调节IL-4和IFN-增强患者免疫功能,并降低远期复发率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7abd/9239797/3c7b348f68d9/ECAM2022-8616075.001.jpg

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