Feng Yan, Meng Ya-Ping, Dong Ying-Ying, Qiu Chang-Yu, Cheng Lei
Department of Otolaryngology-Head and Neck Surgery, The First Hospital, Shanxi Medical University, Taiyuan, China.
Shanxi Key Laboratory of Otorhinolaryngology-Head and Neck Cancer, Taiyuan, China.
Allergy Asthma Clin Immunol. 2021 Jun 29;17(1):62. doi: 10.1186/s13223-021-00564-z.
Inconsistencies remain regarding the effectiveness and safety of leukotriene receptor antagonists (LTRAs) and selective H1-antihistamines (SAHs) for allergic rhinitis (AR). A meta-analysis of randomized controlled trials (RCTs) was conducted to compare the medications.
Relevant head-to-head comparative RCTs were retrieved by searching the PubMed, Embase, and Cochrane's Library databases from inception to April 20, 2020. A random-effects model was applied to pool the results. Subgroup analyses were performed for seasonal and perennial AR.
Fourteen RCTs comprising 4458 patients were included. LTRAs were inferior to SAHs in terms of the daytime nasal symptoms score (mean difference [MD]: 0.05, 95% confidence interval [CI] 0.02 to 0.08, p = 0.003, I = 89%) and daytime eye symptoms score (MD: 0.05, 95% CI 0.01 to 0.08, p = 0.009, I = 89%), but were superior in terms of the nighttime symptoms score (MD: - 0.04, 95% CI - 0.06 to - 0.02, p < 0.001, I = 85%). The effects of the two treatments on the composite symptom score (MD: 0.02, 95% CI - 0.02 to 0.05, p = 0.30, I = 91%) and rhinoconjunctivitis quality-of-life questionnaire (RQLQ) (MD: 0.01, 95% CI - 0.05 to 0.07, p = 0.71, I = 99%) were similar. Incidences of adverse events were comparable (odds ratio [OR]: 0.97, 95% CI 0.75 to 1.25, p = 0.98, I = 0%). These results were mainly obtained from studies on seasonal AR. No significant publication bias was detected.
Although both treatments are safe and effective in improving the quality of life (QoL) in AR patients, LTRAs are more effective in improving nighttime symptoms but less effective in improving daytime nasal symptoms compared to SAHs.
白三烯受体拮抗剂(LTRA)和选择性H1组胺拮抗剂(SAH)用于治疗过敏性鼻炎(AR)的有效性和安全性仍存在不一致之处。我们进行了一项随机对照试验(RCT)的荟萃分析以比较这两种药物。
通过检索PubMed、Embase和Cochrane图书馆数据库,从建库至2020年4月20日,获取相关的直接比较RCT。应用随机效应模型汇总结果。对季节性和常年性AR进行亚组分析。
纳入了14项RCT,共4458例患者。在日间鼻部症状评分(平均差[MD]:0.05,95%置信区间[CI]0.02至0.08,p = 0.003,I = 89%)和日间眼部症状评分方面,LTRA不如SAH(MD:0.05,95%CI 0.01至0.08,p = 0.009,I = 89%),但在夜间症状评分方面更优(MD:-0.04,95%CI -0.06至-0.02,p < 0.001,I = 85%)。两种治疗对综合症状评分(MD:0.02,95%CI -0.02至0.05,p = 0.30,I = 91%)和鼻结膜炎生活质量问卷(RQLQ)(MD:0.01,95%CI -0.05至0.07,p = 0.71,I = 99%)的影响相似。不良事件发生率相当(比值比[OR]:0.97,95%CI 0.75至1.25,p = 0.98,I = 0%)。这些结果主要来自季节性AR的研究。未检测到显著的发表偏倚。
尽管两种治疗在改善AR患者生活质量(QoL)方面均安全有效,但与SAH相比,LTRA在改善夜间症状方面更有效,而在改善日间鼻部症状方面效果较差。