选择性激光小梁成形术治疗原发性开角型青光眼的长期疗效和安全性如何?系统回顾和荟萃分析。

IF 2.6
Kai-Yang Chen, Hoi-Chun Chan, Chi-Ming Chan
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引用次数: 0

摘要

背景:选择性激光小梁成形术(SLT)是一种基于激光的干预措施,用于降低原发性开角型青光眼(POAG)患者的眼压(IOP)。它已被采用作为主要和辅助治疗,越来越多的人对其长期疗效感兴趣。本系统综述和荟萃分析旨在评估SLT治疗成年POAG患者的长期疗效和安全性,重点关注持续的IOP控制、减轻药物负担、保持视觉功能和不良事件发生率。方法:本综述按照PRISMA 2020和MOOSE指南进行,并在PROSPERO进行前瞻性注册(CRD420251030192)。于2025年6月16日对PubMed、Embase、Medline和Scopus进行了系统的文献检索,包括从数据库建立到检索日期的所有记录。纳入了报告SLT结果的随机对照试验和观察性研究,随访时间至少为12个月。主要结局包括长期IOP降低和SLT失败率。次要结局包括药物使用、视野改变和不良事件。使用rob2和Newcastle-Ottawa工具评估研究质量。采用随机效应模型综合数据,采用I²统计量量化研究间异质性。结果:从3462份确定的记录中,60份临床研究被纳入定性综合,50份被纳入荟萃分析,代表8,934只眼睛的合并样本。SLT在治疗后6-12个月达到了与局部药物相当的IOP降低(平均差异:0.04 mmHg;95% CI: -0.27 ~ 0.34)。SLT后药物使用显著减少(平均减少:-0.87种药物;95% CI: -1.13 ~ -0.62)。视野平均偏差改善了0.79 dB (95% CI: 0.76 - 0.82), SLT与最小的短期IOP峰值相关。以EQ-5D衡量的与健康有关的生活质量得分显示出适度但持续的改善。大多数领域的偏倚和发表偏倚风险较低。结论:SLT在降低POAG患者眼压和减轻药理学负担方面具有持续的长期疗效。它在长期随访中维持了视觉功能,并具有良好的安全性,包括不良事件发生率低和IOP峰值。这些发现支持将SLT作为POAG的有效和安全的长期治疗选择,并证明其在临床实践中可作为一线或辅助治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
What is the Long-Term Efficacy and Safety of Selective Laser Trabeculoplasty in the Management of Primary Open-Angle Glaucoma? A Systematic Review and Meta-Analysis.

Background: Selective laser trabeculoplasty (SLT) is a laser-based intervention used to lower intraocular pressure (IOP) in patients with primary open-angle glaucoma (POAG). It has been adopted as both a primary and adjunctive therapy, with growing interest in its long-term outcomes. This systematic review and meta-analysis aimed to assess the long-term efficacy and safety of SLT in adult patients with POAG, with a focus on sustained IOP control, reduction in medication burden, preservation of visual function, and adverse event incidence.

Methods: This review was conducted in accordance with PRISMA 2020 and MOOSE guidelines and was prospectively registered in PROSPERO (CRD420251030192). A systematic literature search was performed on June 16, 2025, across PubMed, Embase, Medline, and Scopus, including all records from database inception to the search date. Randomized controlled trials and observational studies reporting SLT outcomes with a minimum follow-up duration of 12 months were included. Primary outcomes included long-term IOP reduction and SLT failure rates. Secondary outcomes included medication use, visual field changes, and adverse events. Study quality was assessed using ROB-2 and Newcastle-Ottawa tools. Data were synthesized using random-effects models, and inter-study heterogeneity was quantified using the I² statistic.

Results: From 3,462 identified records, 60 clinical studies were included for qualitative synthesis and 50 were included in the meta-analysis, representing a pooled sample of 8,934 eyes. SLT achieved IOP reduction comparable to topical medications at 6-12 months post-treatment (mean difference: 0.04 mmHg; 95% CI: -0.27 to 0.34). Medication use significantly decreased following SLT (mean reduction: -0.87 medications; 95% CI: -1.13 to -0.62). Visual field mean deviation improved by 0.79 dB (95% CI: 0.76 to 0.82), and SLT was associated with minimal short-term IOP spikes. The health-related quality-of-life scores, as measured by EQ-5D, showed modest but consistent improvements. Risk of bias and publication bias were low in most domains.

Conclusion: SLT demonstrated sustained long-term efficacy in reducing intraocular pressure and minimizing pharmacological burden in patients with POAG. It maintained visual function over extended follow-up and was associated with a favorable safety profile, including a low incidence of adverse events and IOP spikes. These findings support the use of SLT as an effective and safe long-term management option for POAG and justify its consideration as a first-line or adjunctive therapy in clinical practice.

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