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A Comparative Study of Montelukast and Azelastine add on Therapy in Moderate to Severe Allergic Rhinitis Treatment: A Double-Blind Randomized Clinical Trial

医学 氮芥 孟鲁卡斯特 布地奈德 鼻喷雾剂 鼻腔给药 抗组胺药 安慰剂 随机对照试验 哮喘 生活质量(医疗保健) 内科学 皮质类固醇 麻醉 鼻子 临床试验 外科 药理学 替代医学 护理部 病理
作者
Hossein Esmaeilzadeh,Nasrin Mortazavi Far,Seyed Hesamedin Nabavizadeh,Masroor Babaeian,Maryam Hadipour,Soheila Alyasin
出处
期刊:American Journal of Rhinology & Allergy [SAGE Publishing]
卷期号:36 (5): 559-567 被引量:3
标识
DOI:10.1177/19458924221086268
摘要

Background Allergic Rhinitis (AR) is a prevalent chronic inflammatory nasal condition with significant negative effects on the patients’ quality of life. This study aimed to investigate the efficacy of Montelukast and intranasal antihistamine in combination with intranasal corticosteroid (INCS) in moderate to severe allergic rhinitis on the patients’ quality of life and AR control. Method This double-blind randomized clinical trial study was carried out on 66 moderate to severe AR patients referred to Namazi Hospital, Shiraz, Iran from 2020 to 2021, who were randomly divided into 3 groups. Group one received Montelukast add-on therapy and Budesonide nasal spray. The second group received intranasal antihistamine (Azelastine) add-on therapy and Budesonide nasal spray and the third group as the control group received intranasal Budesonide spray with a placebo tablet. To measure the impact of each medication on the patient's quality of life and AR control, we employed the Sino-Nasal Outcome Test-22 questionnaire (SNOT 22). We evaluated the symptoms and compared them at baseline, one and three months after the start of treatments. Spirometry was performed to investigate the possibility of co-morbid asthma at baseline and end of the study. Results The patients’ mean age was 30.13 ± 12.7 years. Most patients experienced perennial AR (65.2%). Reduction of mean scores SNOT22 was statistically different between groups (P-value < 0.001). Three months after treatment, the mean decrease of SNOT-22 in the Azelastine group was statistically significant compared to both Montelukast (P-value < 0.001) and control groups (P-value < 0.001). No significant difference was observed between the Montelukast and control groups (P-value = 0.142). 23 of 66 patients were diagnosed with asthma and asthma treatment was initiated. The amount of FEV1 change after AR treatment was not statistically significant between the groups in asthmatic patients (P-value = 0.351). Conclusion Based on our findings, we recommend Azelastine in conjunction with an intranasal corticosteroid for the treatment of moderate to severe allergic rhinitis. In moderate to severe AR or even asthma management, Montelukast has no greater impact than INCS.
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