Royal Surrey County Hospital, Guildford, GU2 7XX, UK.
University Hospital Southampton, Southampton, SO16 6YD, UK.
Eye (Lond). 2019 Mar;33(3):469-477. doi: 10.1038/s41433-018-0243-8. Epub 2018 Oct 24.
To assess the efficacy of Xen in reducing intraocular pressure (IOP) in varying glaucoma subtypes. To assess the effect of combined phacoemulsification. To determine the frequency of complications and explore further bleb management needed.
Retrospective case note review of all patients undergoing Xen implantation across four centres from August 2015 to May 2017.
In total, 259 consecutive surgeries of 226 patients were reviewed. IOP reduced from 19.3 (SD ± 6.0) mmHg preoperatively to 14.2 (SD ± 4.4) at month 12 and 13.5 (SD ± 3.3) at month 18 (p < 0.0001). Medication usage reduced from 2.6 (±1.1) preoperatively to 0.8 (±1.0) at month 12 (p < 0.0001) and 1.1 (±1.3) medications at month 18 (p < 0.0001). Simultaneous phacoemulsification did not alter outcomes as Xen IOP was 14.3 (SD ± 4.7) mmHg and Phaco-Xen was 13.8 (SD ± 2.6) mmHg at month 12 (p = 0.5367). Xen appears to be effective in previous failed filtration surgery. Adverse events included: IOP spikes of ≥30 mmHg in 33 (12.7%) cases, secondary filtration surgery required in 24 (9.3%) cases; implant exposure in 6 (2.3%) cases; persistent hypotonous maculopathy in 5 (1.9%) cases; persistent choroidal effusions in 4 (1.5%) cases; a cyclodialysis cleft secondary to implant insertion in 1 (0.5%) case; and 1 (0.5%) case of endophthalmitis post-implant bleb resuturing. In all, 40.9% of cases required postoperative bleb needling or antimetabolite injection.
Xen reduces IOP and medications at 18 months. Adverse events are uncommon. Careful postoperative surveillance and low threshold for bleb management is needed. Xen is safe and effective in mild to moderate glaucoma.
评估 Xen 在降低各种青光眼亚型的眼内压 (IOP) 方面的疗效。评估联合超声乳化术的效果。确定并发症的发生频率,并探讨进一步的滤过泡管理需求。
对 2015 年 8 月至 2017 年 5 月期间在四个中心接受 Xen 植入术的所有患者进行回顾性病历审查。
共回顾了 226 名患者的 259 例连续手术。IOP 从术前的 19.3(SD±6.0)mmHg 降低到 12 个月时的 14.2(SD±4.4)mmHg 和 18 个月时的 13.5(SD±3.3)mmHg(p<0.0001)。术前用药从 2.6(±1.1)种减少到 12 个月时的 0.8(±1.0)种(p<0.0001)和 18 个月时的 1.1(±1.3)种(p<0.0001)。同时行超声乳化术并不会改变结果,因为 Xen 的 IOP 在 12 个月时为 14.3(SD±4.7)mmHg,Phaco-Xen 为 13.8(SD±2.6)mmHg(p=0.5367)。Xen 在既往滤过手术失败的情况下似乎有效。不良事件包括:33 例(12.7%)眼压升高≥30mmHg,24 例(9.3%)需要二次滤过手术;6 例(2.3%)植入物暴露;5 例(1.9%)持续性低眼压性黄斑病变;4 例(1.5%)持续性脉络膜积液;1 例(0.5%)由植入物插入引起的睫状体分离;1 例(0.5%)植入物后滤泡再缝合发生眼内炎。总的来说,40.9%的病例需要术后滤泡穿刺或抗代谢物注射。
Xen 在 18 个月时降低 IOP 和药物用量。不良事件并不常见。需要仔细的术后监测和低阈值的滤泡管理。Xen 在轻度至中度青光眼患者中安全有效。