Khodeiry Mohamed M, Hassan Amr K, Elhusseiny Abdelrahman M, Lee Richard K, Sayed Mohamed S
Department of Ophthalmology and Visual Sciences, University of Louisville, Louisville, KY, USA.
Department of Ophthalmology, Bascom Palmer Eye Institute University of Miami Miller School of Medicine, Miami, FL, USA.
Clin Ophthalmol. 2025 Jan 18;19:167-174. doi: 10.2147/OPTH.S505220. eCollection 2025.
To evaluate the efficacy and safety of the Paul Glaucoma Implant (PGI) surgery in patients with secondary glaucomas.
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.
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.
The PGI demonstrated favorable efficacy and safety profiles in the management of medically uncontrolled secondary glaucomas.
评估保罗青光眼植入物(PGI)手术治疗继发性青光眼患者的疗效和安全性。
对2022年8月至2023年6月期间在单一三级中心接受PGI植入术的药物治疗无效的成年继发性青光眼患者进行回顾性病历审查。主要结局指标为手术成功率。手术成功定义为随访1年时眼压(IOP)在6至21 mmHg之间,与基线相比(无论是否使用药物)降低≥20%,且无需取出植入物、再次进行青光眼手术或出现威胁视力的并发症。次要结局指标为眼压、青光眼药物使用数量、视力和手术并发症。
共纳入30例患者的30只眼。9例患者(30%)患有新生血管性青光眼,9例患者(30%)患有硅油性青光眼。术后12个月时,28只眼(93.3%)达到成功标准。术后12个月时平均眼压为15.2±4.6 mmHg,而基线平均眼压为32.6±10 mmHg(p<0.001)。与基线相比,术后12个月时青光眼药物平均使用数量显著减少。并发症发生率为13.3%(4只眼),大多数并发症为轻度且短暂性。
PGI在治疗药物控制不佳的继发性青光眼中显示出良好的疗效和安全性。