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贝尔维尔德青光眼引流装置:疗效、安全性及在治疗中的地位。

The Baerveldt Glaucoma Drainage Device: Efficacy, Safety, and Place in Therapy.

作者信息

Poelman Huub J, Wolfs Roger C W, Ramdas Wishal D

机构信息

Department of Ophthalmology, Erasmus Medical Center, Rotterdam, the Netherlands.

出版信息

Clin Ophthalmol. 2020 Sep 24;14:2789-2797. doi: 10.2147/OPTH.S219271. eCollection 2020.

Abstract

OBJECTIVE

This review summarizes published findings concerning the Baerveldt-350 glaucoma drainage device (GDD). Most studies focus on the comparison between different treatments; in this review, the primary focus is efficacy, safety, and place in therapy for the Baerveldt implant.

METHODS

A systematic review was performed using the PubMed database for literature on March 13th, 2020. Efficacy was estimated by performing multiple meta-analyses to calculate the weighted mean difference in intraocular pressure (IOP) and IOP-lowering medication after surgery. In order to get an indication of the safety of the Baerveldt implant, all recorded peri- and postoperative complication were summarized.

RESULTS

A total of 21 studies, including 12 randomized controlled trials, were included with a follow-up up to 5 years, covering a mix of glaucoma types. At the last follow-up point, at 5 years postoperative, the mean (95% confidence interval) reduction in IOP was 15.57 mmHg (14.43-16.71) and the mean (95% confidence interval) reduction in IOP-lowering medication after surgery was 1.81 (1.61-2.01). Most frequently observed postoperative complications were corneal edema (2-34%) and tube complications (4-33%). Rates of required re-intervention ranged from 0% to 51% across all included studies.

CONCLUSION

The efficacy of the Baerveldt implant is a significant reduction in IOP in the long term. The safety profile of the Baerveldt implant in terms of complication incidence is similar to those reported for other GDD's. For treatment of secondary glaucoma, we suggest the Baerveldt (or any other similar GDD) as the choice of treatment in patients where highest IOP reduction is desired.

摘要

目的

本综述总结了已发表的关于Baerveldt-350青光眼引流装置(GDD)的研究结果。大多数研究集中在不同治疗方法之间的比较;在本综述中,主要关注Baerveldt植入物的疗效、安全性及在治疗中的地位。

方法

于2020年3月13日使用PubMed数据库对相关文献进行系统综述。通过进行多项荟萃分析来计算术后眼内压(IOP)和降低IOP药物的加权平均差异,以此评估疗效。为了解Baerveldt植入物的安全性,总结了所有记录的围手术期和术后并发症。

结果

共纳入21项研究,包括12项随机对照试验,随访时间长达5年,涵盖多种青光眼类型。在术后5年的最后随访点,IOP的平均(95%置信区间)降低值为15.57 mmHg(14.43 - 16.71),术后降低IOP药物的平均(95%置信区间)减少量为1.81(1.61 - 2.01)。最常观察到的术后并发症是角膜水肿(2 - 34%)和引流管并发症(4 - 33%)。在所有纳入研究中,所需再次干预的发生率从0%到51%不等。

结论

Baerveldt植入物的疗效是长期显著降低IOP。Baerveldt植入物在并发症发生率方面的安全性与其他GDD报道的相似。对于继发性青光眼的治疗,我们建议在期望最大程度降低IOP的患者中选择Baerveldt(或任何其他类似的GDD)作为治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f390/7522304/4cdcd01d8de2/OPTH-14-2789-g0001.jpg

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