Effects of Rebamipide for Dry Eye on Optical Quality and Efficacy: A Systematic Review and Meta-Analysis.

IF 1.9 4区 医学 Q2 OPHTHALMOLOGY
Yu-Ling Yan, Jing-Yao Chang, Xin-Ru Ling, Chun-Yan Xue
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Abstract

Purpose: To evaluate the effects of rebamipide ophthalmic suspension on optical quality and efficacy of patients with dry eye under different conditions. Methods: A comprehensive search across five databases (PubMed, Cochrane Library, Web of Science, China National Knowledge Infrastructure, and Wan Fang) was conducted for studies published through May 13, 2024, focusing on rebamipide for dry eye treatment. Results: A total of 11 studies including 334 patients with dry eye were included. Tear breakup time (TBUT) values of patients with dry eye increased significantly after 2 weeks (standardized mean difference [SMD] =1.07, 95% confidence interval [CI] = [0.05, 2.09]), 4 weeks (SMD = 1.26, 95% CI = [0.77, 1.75]), and 12 weeks (SMD = 1.04, 95% CI = [0.37, 1.71]) of rebamipide treatment. Subgroup analysis revealed that patients with dry eye wearing soft contact lens (SCL) exhibited higher TBUT values after 4 weeks of rebamipide treatment compared with those who received rebamipide alone. In addition, rebamipide significantly improved fluorescein staining score of patients with dry eye after 4 weeks of treatment (SMD = -0.34, 95% CI = [-0.63, -0.06]). However, 4 weeks of rebamipide treatment showed no significant effect on Schirmer I test values (SMD = -0.04, 95%, CI = [-0.43, 0.35]) and higher-order aberrations (SMD = -0.73, 95% CI = [-1.77, 0.30]). Conclusions: These results indicate a significant improvement in the efficacy of rebamipide treatment for patients with dry eye, particularly for those wearing SCL. The effect of rebamipide on visual quality was found to correlate with the underlying dry eye status.

瑞巴派特治疗干眼症对光学质量和疗效的影响:系统回顾与元分析》。
目的:评估瑞巴派特眼用混悬液在不同条件下对干眼症患者光学质量和疗效的影响。方法在五个数据库(PubMed、Cochrane Library、Web of Science、中国国家知识基础设施和万方数据库)中对截至 2024 年 5 月 13 日发表的研究进行了全面检索,重点关注瑞巴派特用于干眼症治疗的研究。研究结果共纳入 11 项研究,包括 334 名干眼症患者。干眼症患者的泪液破裂时间(TBUT)值在接受瑞巴咪啶治疗 2 周(标准化平均差 [SMD] =1.07,95% 置信区间 [CI] = [0.05,2.09])、4 周(SMD =1.26,95% CI = [0.77,1.75])和 12 周(SMD =1.04,95% CI = [0.37,1.71])后显著增加。亚组分析显示,与单独接受瑞巴咪啶治疗的患者相比,佩戴软性隐形眼镜(SCL)的干眼症患者在接受 4 周瑞巴咪啶治疗后的 TBUT 值更高。此外,治疗 4 周后,干眼症患者的荧光素染色评分明显提高(SMD = -0.34,95% CI = [-0.63, -0.06])。然而,4周的雷帕米特治疗对Schirmer I测试值(SMD = -0.04,95% CI = [-0.43,0.35])和高阶像差(SMD = -0.73,95% CI = [-1.77,0.30])没有明显影响。结论:这些结果表明,对干眼症患者,尤其是佩戴 SCL 的干眼症患者而言,瑞贝美的疗效显著提高。研究发现,瑞巴派特对视觉质量的影响与干眼症的基本状况有关。
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来源期刊
CiteScore
4.60
自引率
4.30%
发文量
72
审稿时长
1 months
期刊介绍: Journal of Ocular Pharmacology and Therapeutics is the only peer-reviewed journal that combines the fields of ophthalmology and pharmacology to enable optimal treatment and prevention of ocular diseases and disorders. The Journal delivers the latest discoveries in the pharmacokinetics and pharmacodynamics of therapeutics for the treatment of ophthalmic disorders. Journal of Ocular Pharmacology and Therapeutics coverage includes: Glaucoma Cataracts Retinal degeneration Ocular infection, trauma, and toxicology Ocular drug delivery and biotransformation Ocular pharmacotherapy/clinical trials Ocular inflammatory and immune disorders Gene and cell-based therapies Ocular metabolic disorders Ocular ischemia and blood flow Proliferative disorders of the eye Eyes on Drug Discovery - written by Gary D. Novack, PhD, featuring the latest updates on drug and device pipeline developments as well as policy/regulatory changes by the FDA.
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