对OMNI®手术系统及其前身的临床有效性、安全性、人性化和经济负担进行系统回顾和荟萃分析。

IF 1.4 4区 医学 Q3 OPHTHALMOLOGY
Obeda Kailani, Sameh Mosaed, Fritz H Hengerer, Rachana Patel, Anna W Świder, Federico Ghinelli, Laura Wells, Patricia Buchholz
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引用次数: 0

摘要

本系统综述和荟萃分析的目的是评估OMNI®手术系统(OMNI)、Visco360和Trab360治疗开角型青光眼(OAG)的临床、人文和经济证据。方法于2024年4月16日在MEDLINE®、Web of Science™、Cochrane(2016年1月- 2024年4月)上应用搜索策略。国会会议记录(2021-2024年)于2024年7月检索。纳入了包含≥15例患者的研究,这些研究报告了与使用OMNI、Visco360或Trab360治疗成人OAG相关的临床、人文或经济结果。结构化摘要用于总结研究结果,荟萃分析用于综合数据。使用纽卡斯尔-渥太华和CHEERS检查表评估偏倚风险。协议在PROSPERO上注册(CRD42024536680)。结果在纳入的29篇文献中,27篇报道临床结果,2篇报道经济结果。OMNI显著降低眼内压(IOP),平均IOP;这是24-36个月。不良事件通常是轻微和短暂的。结论:onomni持续降低IOP和药物使用,持续效果超过24- 36个月,具有良好的安全性,因此支持在OAG患者中使用。本综述的局限性包括缺少随机对照试验。6项研究被评价为质量良好,其余研究显示有偏倚风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systematic review and meta-analysis of the clinical effectiveness, safety, humanistic and economic burden of the OMNI® surgical system and its predecessors.

ObjectiveThe aim of this systematic review and meta-analysis was to assess the clinical, humanistic, and economic evidence of the OMNI® Surgical System (OMNI), Visco360 and Trab360 for open-angle glaucoma (OAG).MethodsSearch strategies were applied across MEDLINE®, Web of Science™, Cochrane (January 2016-April 2024) on 16th April 2024. Congress proceedings (2021-2024) were searched in July 2024. Studies containing ≥15 patients that reported clinical, humanistic or economic outcomes associated with the use of OMNI, Visco360 or Trab360 for the treatment of adults with OAG were included. Structured summaries were used to summarize findings and a meta-analysis synthesized the data. Risk of bias was assessed using the Newcastle-Ottawa and CHEERS checklists. The protocol was registered on PROSPERO (CRD42024536680).ResultsAmong 29 included publications, 27 reported clinical and 2 reported economic outcomes. OMNI significantly reduced intraocular pressure (IOP) with mean IOP <18 mmHg (11.5-17.2 mmHg) at 12 months when used standalone or combined with cataract surgery. The meta-analysis confirmed statistically significant, comparable IOP reductions at months 6, 12 and 24. IOP-lowering medication use decreased from 0.9-3.4 at baseline to 0.1-2.2 at month 12 (standalone and combination); these continued months 24-36. Adverse events were generally mild and transient.ConclusionOMNI consistently reduced IOP and medication use demonstrating sustained effects over 24--36 months with a favorable safety profile, thus supporting its use in patients with OAG. Limitations of this review include the absence of randomized controlled trials. Six studies were assessed as good quality, the remainder showed risk of bias.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
372
审稿时长
3-8 weeks
期刊介绍: The European Journal of Ophthalmology was founded in 1991 and is issued in print bi-monthly. It publishes only peer-reviewed original research reporting clinical observations and laboratory investigations with clinical relevance focusing on new diagnostic and surgical techniques, instrument and therapy updates, results of clinical trials and research findings.
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