Rehman Abdur, Arshad Muhammad, Asif Namra, Khan Muhammad Shuaib, Malik Farhat, Aslam Mohammad Moaviz, Ansar Shahroz, Zafar Mahtab, Khan Imran, Maqbool Shahzaib, Nashwan Abdulqadir J
Otolaryngology - Head and Neck Surgery, Rawalpindi Medical University, Rawalpindi, PAK.
Otolaryngology, Watim Medical and Dental College, Islamabad, PAK.
Cureus. 2025 Aug 17;17(8):e90306. doi: 10.7759/cureus.90306. eCollection 2025 Aug.
This systematic review and meta-analysis aimed to compare the efficacy and safety of olopatadine and rupatadine in the treatment of allergic rhinitis (AR). By synthesizing data from randomized controlled trials (RCTs), this study aimed to evaluate symptom reduction, specifically in terms of the Total Nasal Symptom Score (TNSS), and assess the incidence of adverse effects between these two second-generation antihistamines. A comprehensive literature search was conducted in PubMed, Google Scholar, Web of Science, Embase, and Cochrane databases from November 2024 to February 2025. Studies were selected based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Clinical trials comparing olopatadine and rupatadine in AR patients were included, with a focus on TNSS reduction and adverse event incidence. The Jadad scale was used for quality assessment. Data were analyzed using the DerSimonian and Laird random effects model, with mean differences and risk ratios (RR) calculated. Heterogeneity was assessed using the chi-square test and I² statistic. A total of four RCTs involving 304 patients (153 in the olopatadine group, 151 in the rupatadine group) met the inclusion criteria. Olopatadine demonstrated superior TNSS reduction (mean difference: 2.51; 95% CI: 1.58 to 3.44; p<0.0001), with low heterogeneity (I²=0%). Adverse events were comparable between groups (RR=0.66; 95% CI: 0.29-1.50; P=0.33), with dry mouth, headache, and mild sedation being the most frequently reported. Olopatadine showed greater efficacy in reducing symptoms of allergic rhinitis compared to rupatadine, while both drugs had similar safety profiles. These findings suggest that olopatadine may be preferred for more symptom relief, though larger trials are needed for further validation.
本系统评价和荟萃分析旨在比较奥洛他定和卢帕他定治疗变应性鼻炎(AR)的疗效和安全性。通过综合随机对照试验(RCT)的数据,本研究旨在评估症状减轻情况,特别是总鼻症状评分(TNSS)方面,并评估这两种第二代抗组胺药之间不良反应的发生率。于2024年11月至2025年2月在PubMed、谷歌学术、科学网、Embase和Cochrane数据库中进行了全面的文献检索。研究根据系统评价和荟萃分析的首选报告项目(PRISMA)指南进行选择。纳入了比较奥洛他定和卢帕他定治疗AR患者的临床试验,重点关注TNSS降低情况和不良事件发生率。采用Jadad量表进行质量评估。使用DerSimonian和Laird随机效应模型分析数据,计算平均差和风险比(RR)。使用卡方检验和I²统计量评估异质性。共有4项RCT涉及304例患者(奥洛他定组153例,卢帕他定组151例)符合纳入标准。奥洛他定在降低TNSS方面表现更优(平均差:2.51;95%CI:1.58至3.44;p<0.0001),异质性较低(I²=0%)。两组间不良事件相当(RR=0.66;95%CI:0.29 - 1.50;P=0.33),最常报告的是口干、头痛和轻度镇静。与卢帕他定相比,奥洛他定在减轻变应性鼻炎症状方面疗效更佳,而两种药物的安全性相似。这些发现表明,奥洛他定可能更有助于缓解症状,不过需要更大规模的试验进行进一步验证。