Outcomes of the Paul Glaucoma Implant in Refractory Secondary Glaucoma.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-01-18 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S505220
Mohamed M Khodeiry, Amr K Hassan, Abdelrahman M Elhusseiny, Richard K Lee, Mohamed S Sayed
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Abstract

Purpose: To evaluate the efficacy and safety of the Paul Glaucoma Implant (PGI) surgery in patients with secondary glaucomas.

Patients and methods: Retrospective chart review of adult patients with medically recalcitrant secondary glaucoma who underwent PGI implantation at a single tertiary center between August 2022 and June 2023. The primary outcome measure was surgical success. Surgical success was defined as intraocular pressure (IOP) between 6 and 21 mmHg with a ≥20% reduction compared to baseline (with or without medications) with no need for implant removal, further glaucoma reoperation, or development of vision-threatening complications at 1 year of follow-up. The secondary outcomes were IOP, glaucoma medication numbers, visual acuity, and surgical complications.

Results: Thirty eyes of 30 patients were identified. Nine patients (30%) had neovascular glaucoma, and 9 patients (30%) had silicone-oil-induced glaucoma. At 12 months postoperatively, 28 eyes (93.3%) fulfilled the success criteria. The mean IOP at 12 months was 15.2 ± 4.6 mmHg compared to the mean baseline IOP of 32.6 ± 10 mmHg (p < 0.001). A significant reduction in the mean number of glaucoma medications at 12 months compared to the baseline was observed. The complication rate was 13.3% (4 eyes), with most complications being mild and transient.

Conclusion: The PGI demonstrated favorable efficacy and safety profiles in the management of medically uncontrolled secondary glaucomas.

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Paul青光眼植入治疗难治性继发性青光眼的疗效观察。
目的:评价保罗青光眼植入术(PGI)治疗继发性青光眼的疗效和安全性。患者和方法:回顾性分析2022年8月至2023年6月在单一三级中心接受PGI植入术的成人性难治性继发性青光眼患者的图表。主要观察指标为手术成功。手术成功的定义是眼内压(IOP)在6 - 21 mmHg之间,与基线相比(有或无药物治疗)降低≥20%,随访1年不需要移除植入物、进一步青光眼再手术或出现视力威胁并发症。次要结果是IOP,青光眼药物剂量,视力和手术并发症。结果:30例患者30只眼被识别。新生血管性青光眼9例(30%),硅油性青光眼9例(30%)。术后12个月,28眼(93.3%)达到成功标准。12个月时的平均IOP为15.2±4.6 mmHg,而平均基线IOP为32.6±10 mmHg (p < 0.001)。与基线相比,观察到12个月时青光眼药物的平均数量显著减少。并发症发生率为13.3%(4眼),并发症多为轻度和短暂性。结论:PGI治疗药物控制不佳的继发性青光眼具有良好的疗效和安全性。
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