Matched case–control comparison of surgical success after XEN45 Gel Stent and PRESERFLO MicroShunt implantation in a Caucasian population

IF 4.9 2区 医学 Q1 OPHTHALMOLOGY
Jan Niklas Lüke MD, Thomas S. Dietlein PhD, Randolf A. Widder PhD, Gernot F. Roessler PhD, Vincent Lüke, Philip Enders PhD, Alexandra Lappa PhD, David Kiessling MD
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Abstract

Background

The aim of this study was to compare the outcome of implantation of a XEN45 Gel Stent with the outcome of implantation of a Preserflo MicroShunt in a matched-pair analysis in eyes being naïve to filtering surgery.

Methods

In this comparative, retrospective study, 50 eyes that had undergone XEN45 Gel Stent implantation were compared with 50 eyes after Preserflo implantation. Follow-up was at least 6 months, and surgical success was measured by criteria A (IOP < 21 mmHg, IOP reduction >20%, no repeat surgery); criteria B (IOP < 18 mmHg, IOP reduction >20%, no repeat surgery); and criteria C (IOP ≤15 mmHg, IOP reduction ≥40%, no repeat surgery).

Results

After a follow-up period of 12 months, mean IOP had decreased from preoperative 25.2 ± 4.8 mmHg in the XEN group to 14.5 ± 4.0 (n = 35) and from 25.3 ± 6.8 mmHg to 11.9 ± 2.9 (n = 41) in the Preserflo group, respectively. The IOP at the last follow-up of the two groups differed significantly (p < 0.01). The probability of surgical success did not differ concerning Criteria A and B, but surgical success was significantly higher in the Preserflo group for Criteria C (60%, p < 0.01).

Conclusion

Both the Preserflo and XEN45 Gel Stent provide an effective and safe treatment option for advanced glaucoma and have a high potential to reduce intraocular pressure. Absolute IOP levels of <16 mmHg after 12 months were significantly more frequent in the Preserflo group.

Abstract Image

白种人植入 XEN45 凝胶支架和 PRESERFLO MicroShunt 后手术成功率的匹配病例对照比较。
研究背景本研究的目的是通过配对分析,比较滤过手术新手植入 XEN45 凝胶支架与植入 Preserflo MicroShunt 的疗效:在这项比较性回顾研究中,50 只接受 XEN45 凝胶支架植入术的眼睛与 50 只接受 Preserflo 植入术的眼睛进行了比较。随访时间至少为 6 个月,手术成功率按照标准 A(眼压降低 20%,无重复手术)、标准 B(眼压降低 20%,无重复手术)和标准 C(眼压≤15 mmHg,眼压降低≥40%,无重复手术)进行衡量:随访12个月后,XEN组的平均眼压从术前的25.2 ± 4.8 mmHg降至14.5 ± 4.0(n = 35),Preserflo组的平均眼压从25.3 ± 6.8 mmHg降至11.9 ± 2.9(n = 41)。两组患者在最后一次随访时的眼压差异显著(P 结论:两组患者在最后一次随访时的眼压差异显著:Preserflo 和 XEN45 凝胶支架都为晚期青光眼提供了有效、安全的治疗方案,并具有降低眼压的巨大潜力。两组患者的绝对眼压水平
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来源期刊
CiteScore
7.60
自引率
12.50%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Clinical & Experimental Ophthalmology is the official journal of The Royal Australian and New Zealand College of Ophthalmologists. The journal publishes peer-reviewed original research and reviews dealing with all aspects of clinical practice and research which are international in scope and application. CEO recognises the importance of collaborative research and welcomes papers that have a direct influence on ophthalmic practice but are not unique to ophthalmology.
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