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一管通用:在三级中心改用保罗青光眼植入物后的1年结果。

One tube for all: 1-year outcomes after transition to Paul glaucoma implant at a tertiary centre.

作者信息

Studsgaard Anne, Nielsen Stine Elkjær, Telinius Niklas

机构信息

Department of Ophthalmology, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Acta Ophthalmol. 2025 Jun;103(4):461-468. doi: 10.1111/aos.17443. Epub 2025 Jan 24.

Abstract

PURPOSE

To evaluate the intraocular pressure (IOP) lowering effect and success rate of Paul glaucoma implant (PGI) in refractory glaucoma after changing practice pattern from Ahmed and Baerveldt tubes to PGI.

METHODS

A prospective observational study of the first 50 consecutive PGI surgeries at a single Danish tertiary centre from January 2022 to October 2023. Primary endpoints were IOP and success rates after 12 months. Secondary endpoints were the use of IOP-lowering medications and complications. All cases had a risk of failure for traditional glaucoma surgery (neovascular glaucoma, oil-filled eye or uveitis).

RESULTS

Preoperative IOP was 29.9 ± 8.6 mmHg and the mean number of topical IOP-lowering medications used was 3.4 ± 0.76 with 14 cases of systemic acetazolamide. Twelve months after surgery IOP was reduced to 11.4 ± 3.1 mmHg and complete success rate with (a) IOP≤21 mmHg was achieved in 43%, (b) IOP≤18 mmHg in 43%, (c) IOP≤15 mmHg in 41% and (d) IOP≤12 mmHg in 33%. Qualified success rate (on topical glaucoma medications) was achieved in (a) 96%, (b) 94%, (c) 86% and (d) 71% of the cases. The number of topical IOP-lowering medications was 0.9 ± 0.9 after surgery and 47% were medication free. Early (<3 months) and late (>3 months) complications were observed in 22% and 16% of patients respectively.

CONCLUSION

This study indicates that PGI provides a good IOP-lowering effect after 12 months in a population with risk factors for failure for traditional glaucoma surgery.

摘要

目的

评估在将手术方式从艾哈迈德管和贝尔维尔德管改为保罗青光眼植入物(PGI)后,PGI对难治性青光眼的眼压降低效果和成功率。

方法

对丹麦一家三级中心在2022年1月至2023年10月期间连续进行的首批50例PGI手术进行前瞻性观察研究。主要终点是12个月后的眼压和成功率。次要终点是降眼压药物的使用情况和并发症。所有病例均存在传统青光眼手术失败的风险(新生血管性青光眼、硅油填充眼或葡萄膜炎)。

结果

术前眼压为29.9±8.6mmHg,使用的局部降眼压药物平均数量为3.4±0.76种,14例使用全身乙酰唑胺。术后12个月,眼压降至11.4±3.1mmHg,完全成功率为:(a)眼压≤21mmHg的占43%,(b)眼压≤18mmHg的占43%,(c)眼压≤15mmHg的占41%,(d)眼压≤12mmHg的占33%。合格成功率(使用局部青光眼药物)为:(a)96%,(b)94%,(c)86%,(d)71%。术后局部降眼压药物数量为0.9±0.9种,47%的患者无需用药。分别有22%和16%的患者观察到早期(<3个月)和晚期(>3个月)并发症。

结论

本研究表明,对于存在传统青光眼手术失败风险因素的人群,PGI在12个月后具有良好的眼压降低效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa53/12069969/0f0d7582a1a0/AOS-103-461-g002.jpg

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