Centre for Ophthalmology and Vision Sciences, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK.
Centre for Endocrinology and Diabetes, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester, UK.
Eye (Lond). 2018 Feb;32(2):324-332. doi: 10.1038/eye.2017.162. Epub 2017 Sep 1.
PurposeTo report the efficacy, safety profile, and postoperative management of XEN45 implant at 12-month follow-up.Patients and methodsThis was a retrospective, non-randomised interventional case series involving patients who underwent XEN45 implantation by a single, experienced glaucoma specialist in a tertiary centre. Primary outcome measures were the intraocular pressure (IOP) and the number of medications at 1-year follow-up visit. Two IOP criteria were chosen to measure success: IOP ≤21 mm Hg and ≥20% reduction from baseline (criteria one); and IOP ≤15 mm Hg and ≥30% reduction from baseline (criteria two).ResultsAll 39 eyes completed 1-year follow-up. The mean preoperative IOP was 24.9±7.8 mm Hg on three drops, which reduced to 14.5±3.4 mm Hg at month 12 (P<0.005) on 0.7 drops (P<0.005). On the basis of criteria one, the cumulative probability of success at 1 year was 87.0% without medication and 92.0% with medication. On the basis of criteria two, cumulative probability of success was 62.0% without medication and 64.0% with medication. Bleb intervention with a median of 2 (range 1-4) was required for 51.3% of eyes. Implant was obstructed by iris tissue in three eyes (7.7%); one eye (2.6%) developed hyphaema; eight eyes (20.5%) had numerical hypotony (IOP≤5 mm Hg) at day 1, of which all spontaneously resolved by week 4 apart from one eye.ConclusionsThe XEN45 implant proved to be an effective treatment with a good safety profile at 1-year follow-up period. The high rate of postoperative bleb intervention does not make XEN45 a 'fit-and-forget' procedure and therefore the procedure should ideally be performed by surgeons experienced in bleb management.
报告 XEN45 植入物在 12 个月随访时的疗效、安全性概况和术后管理。
这是一项回顾性、非随机干预性病例系列研究,涉及在一家三级中心由一位经验丰富的青光眼专家进行 XEN45 植入的患者。主要观察指标是 1 年随访时的眼压(IOP)和药物使用数量。选择了两种 IOP 标准来衡量手术的成功:标准一为 IOP≤21mmHg 且较基线降低≥20%;标准二为 IOP≤15mmHg 且较基线降低≥30%。
所有 39 只眼均完成了 1 年随访。术前平均眼压为 24.9±7.8mmHg,使用三种降眼压药物,12 个月时降低至 14.5±3.4mmHg(P<0.005),药物使用数量为 0.7 种(P<0.005)。根据标准一,无药物治疗时 1 年累积成功率为 87.0%,有药物治疗时为 92.0%。根据标准二,无药物治疗时累积成功率为 62.0%,有药物治疗时为 64.0%。51.3%的眼需要中位数为 2 次(范围 1-4 次)的滤枕干预。3 只眼(7.7%)的虹膜组织阻塞了植入物,1 只眼(2.6%)发生了血影细胞性青光眼,8 只眼(20.5%)在第 1 天出现数值性低眼压(IOP≤5mmHg),除了 1 只眼,所有眼在第 4 周前自发缓解。
XEN45 植入物在 1 年随访期内显示出良好的疗效和安全性。高比例的术后滤枕干预并不意味着 XEN45 是一种“一劳永逸”的手术,因此,该手术应由经验丰富的滤枕管理外科医生来完成。