Buffet Jenna, Brasnu Emmanuelle, Baudouin Christophe, Labbé Antoine
Department of Ophthalmology III, Quinze-Vingts Hospital.
Quinze-Vingts Hospital, DHU Sight Restore, INSERM-DHOS CIC.
J Glaucoma. 2017 Dec;26(12):1149-1154. doi: 10.1097/IJG.0000000000000808.
The purpose of the current study was to evaluate the efficacy and adverse event profile of 2 trabecular micro-bypass stents implanted during standard phacoemulsification cataract surgery in patients with mild to advanced open-angle glaucoma whose intraocular pressure (IOP) was well controlled by topical medications.
This study was a retrospective analysis of patients with mild to advanced chronic open-angle glaucoma who underwent phacoemulsification and implantation of 2 stents. For all patients, preoperative and postoperative characteristics were evaluated, including number of medications and IOP. Postoperative visits were scheduled at 7 days and at months 1, 6, 12, and 24 after surgery. At each visit, IOP and the number of medications were noted.
In total, 63 eyes of 41 patients were included in the study. The vast majority of eyes (85.7%) were diagnosed with primary open-angle glaucoma. Preoperative mean IOP at baseline was 16.8±3.0 mm Hg (range, 10 to 24 mm Hg) with a mean of 2.3±0.9 medications. The mean IOP reduction represented a 13% decrease at 1 month (P<0.001), 13% at 6 months (P<0.001), 12% at 1 year (P<0.001), and 10% at 2 years (P<0.001), concomitant with a 23% reduction in the mean number of medications (P<0.001), 35% (P<0.001), 40% (P<0.001), and 40% (P<0.001), respectively, at each scheduled follow-up visit. At 24 months postoperatively, 19 of 23 (83%) patients experienced an IOP decrease compared with the preoperative visit. No severe device-related adverse events were observed.
Patients with mild to advanced glaucoma can benefit from micro-bypass implantation even if their IOP is well controlled with topical hypotensive medications. Expectations for these reductions should be moderate.
本研究旨在评估在标准超声乳化白内障手术期间植入2个小梁微旁路支架对轻度至重度开角型青光眼患者的疗效及不良事件情况,这些患者的眼压(IOP)通过局部用药得到良好控制。
本研究是对轻度至重度慢性开角型青光眼患者进行超声乳化及植入2个支架的回顾性分析。对所有患者评估术前和术后特征,包括用药数量和眼压。术后随访安排在术后7天以及术后1、6、12和24个月。每次随访时,记录眼压和用药数量。
本研究共纳入41例患者的63只眼。绝大多数眼睛(85.7%)被诊断为原发性开角型青光眼。术前基线平均眼压为16.8±3.0 mmHg(范围10至24 mmHg),平均用药2.3±0.9种。平均眼压降低情况为:1个月时降低13%(P<0.001),6个月时降低13%(P<0.001),1年时降低12%(P<0.001),2年时降低10%(P<0.001),同时每次预定随访时平均用药数量分别减少23%(P<0.001)、35%(P<0.001)、40%(P<0.001)和40%(P<0.001)。术后24个月时,23例患者中有19例(83%)眼压较术前降低。未观察到严重的与器械相关的不良事件。
轻度至重度青光眼患者即使眼压通过局部降压药物得到良好控制,也可从微旁路植入中获益。对这些降低幅度的预期应适度。