Singhal Aditya, Agrawal Pooja, Chatterji Probal, Matreja Pritpal Singh, Mahmood Tariq
Department of ENT, Teerthanker Mahaveer Medical College and Research Centre, Moradabad, Uttar Pradesh India.
Department of Pharmacology, Teerthanker Mahaveer Medical College and Research Centre, Moradabad, Uttar Pradesh India.
Indian J Otolaryngol Head Neck Surg. 2024 Oct;76(5):4025-4030. doi: 10.1007/s12070-024-04770-0. Epub 2024 Jun 1.
Antihistamines has always remained the mainstay drug treatment for Allergic Rhinitis (AR). Bilastine is a novel, non-sedative antihistamine with a super-selective H1 receptor antagonist property. Both bilastine and fexofenadine are second generation antihistamine drugs commonly used to manage AR and Chronic Urticaria (CU). Autologous Skin Serum Test (ASST) is a practical test for histamine release in CU. These tests have been studied in AR patients with limited data studies.
114 patients diagnosed with perennial AR were recruited and divided into two groups of 57 each. One group was started Bilastine 20 mg once a day and other group, fexofenadine 180 mg once a day. Total Nasal Symptom Score (TNSS) was calculated at presentation and two weeks of antihistamine therapy. ASST was hypothesized to be the test for AR and performed at the time of presentation and at two weeks follow-up. Intergroup and Intragroup assessment of TNSS, ASST and its variables were done using unpaired and paired t test respectively.
Patients showed reduction in symptoms of AR with both antihistamines. A significant improvement of sneezing and rhinorrhoea was seen in Fexofenadine group as compared to Bilastine group. TNSS showed statistically significant improvement in both the groups. ASST had statistically significant reduction in both the groups.
Both Bilastine and fexofenadine were found to be effective in reduction of symptoms of allergic rhinitis. Bilastine was found to be more effective in overall as well as sneezing and rhinorrhoea noted two weeks after therapy.
The online version contains supplementary material available at 10.1007/s12070-024-04770-0.
抗组胺药一直是过敏性鼻炎(AR)的主要药物治疗手段。比拉斯汀是一种新型、非镇静性抗组胺药,具有超选择性H1受体拮抗剂特性。比拉斯汀和非索非那定都是常用于治疗AR和慢性荨麻疹(CU)的第二代抗组胺药。自体皮肤血清试验(ASST)是一种用于检测CU中组胺释放的实用试验。这些试验在AR患者中的研究数据有限。
招募了114例诊断为常年性AR的患者,分为两组,每组57例。一组开始每天服用一次20毫克比拉斯汀,另一组每天服用一次180毫克非索非那定。在就诊时以及抗组胺治疗两周后计算总鼻症状评分(TNSS)。假设ASST可用于AR检测,并在就诊时和两周随访时进行。分别使用未配对和配对t检验对TNSS、ASST及其变量进行组间和组内评估。
两种抗组胺药治疗后患者的AR症状均有所减轻。与比拉斯汀组相比,非索非那定组的打喷嚏和流涕症状有显著改善。两组的TNSS均有统计学意义的改善。两组的ASST均有统计学意义的降低。
比拉斯汀和非索非那定均被发现可有效减轻过敏性鼻炎症状。发现比拉斯汀在总体上以及治疗两周后观察到的打喷嚏和流涕方面更有效。
在线版本包含可在10.1007/s12070-024-04770-0获取的补充材料。