Department of Ophthalmology, University of Bonn, Bonn, Germany.
J Glaucoma. 2024 Oct 1;33(10):808-814. doi: 10.1097/IJG.0000000000002457. Epub 2024 Jun 28.
This prospectively collected case series of 56 eyes having PAUL glaucoma implant (PGI) surgery is the first to demonstrate its medium-term safety and effectiveness in what is essentially an exclusively Caucasian population.
To report 2-year outcomes from a single-center cohort undergoing PGI surgery.
Prospectively collected data on patients undergoing PGI surgery at the University Eye Hospital Bonn, Germany, from April 2021 to September 2021.
Of 53 patients, 56 eyes were included. Complete and qualified success rates (95% CI) were 52% (37-66) and 89% (80-96) for criterion A ( intraocular pressure [IOP]≤21 mm Hg), 48% (36-61) and 79% (67-88) for criterion B (IOP≤18 mm Hg), 45% (32-57) and 64% (52-77%) for criterion C (IOP≤15 mm Hg) and 27% (16-40) and 38% (25-50) for criterion D (IOP≤12 mm Hg), respectively. Mean IOP decreased from 25.43 mm Hg (7-48 mm Hg) to 11.25 mm Hg (3-24 mm Hg) (reduction of 50%) after 24 months with a reduction of IOP-lowering agents from 3.50 (1-5) to 0.46 (0-3). One eye needed an injection of viscoelastic due to significant hypotony with AC shallowing; 3 eyes received a Descemet membrane endothelial keratoplasty because of persistent corneal decompensation; 9 eyes developed tube exposure which required conjunctival revision with additional pericardial patch graft, with 5 of these eyes eventually needing tube explantation. An intraluminal prolene stent was removed in 24 eyes (42.9%) after a mean time period of 5.67 months (2-15 m). Mean IOP before removal was 21.4 mm Hg (12-40 mm Hg) and decreased to 11.15 mm Hg (6-20 mm Hg).
PGI surgery is an effective procedure for reducing IOP and pressure-lowering therapy. The use of an intraluminal prolene stent impedes hypotony in the early postoperative phase and enables further noninvasive IOP lowering during the postoperative course.
本研究前瞻性地收集了 56 只接受保罗青光眼植入物(PGI)手术的眼睛的病例系列,这是首个在基本上为纯高加索人群中证明其中期安全性和有效性的研究。
报告单中心队列接受 PGI 手术后的 2 年结果。
对 2021 年 4 月至 2021 年 9 月在德国波恩大学眼科医院接受 PGI 手术的患者进行前瞻性数据收集。
在 53 名患者中,有 56 只眼睛被纳入研究。完全和合格成功率(95%CI)分别为 A 标准(眼压[IOP]≤21mmHg)的 52%(37-66)和 89%(80-96),B 标准(IOP≤18mmHg)的 48%(36-61)和 79%(67-88),C 标准(IOP≤15mmHg)的 45%(32-57)和 64%(52-77%),以及 D 标准(IOP≤12mmHg)的 27%(16-40)和 38%(25-50)。术后 24 个月,平均眼压从 25.43mmHg(7-48mmHg)降至 11.25mmHg(3-24mmHg)(降低 50%),降眼压药物从 3.50(1-5)降至 0.46(0-3)。1 只眼因房水浅导致明显低眼压需要注射粘弹剂;3 只眼因持续角膜失代偿行 Descemet 膜内皮角膜移植术;9 只眼发生引流管暴露,需要进行结膜修正并额外使用心包补片移植,其中 5 只眼最终需要拔管。24 只眼(42.9%)在平均 5.67 个月(2-15 个月)后取出了腔内丙纶支架。取出前平均眼压为 21.4mmHg(12-40mmHg),降至 11.15mmHg(6-20mmHg)。
PGI 手术是降低眼压和降压治疗的有效方法。腔内丙纶支架的使用可在术后早期阻止低眼压,并在术后期间进一步进行非侵入性眼压降低。