Manchester Royal Eye Hospital, Central Manchester University Hospitals NHS Foundation Trust, Oxford Road, Manchester, M13 9WL, UK.
Eye (Lond). 2021 Aug;35(8):2277-2282. doi: 10.1038/s41433-020-01255-6. Epub 2020 Nov 2.
To determine the efficacy and safety of combined phacoemulsification and single first-generation iStent implantation over 84 months.
SUBJECTS/METHODS: Single-surgeon, single-centre, uncontrolled prospective interventional study in real-world settings. Forty-one patients with open-angle glaucoma on at least one antihypertensive drop underwent phaco-iStent surgery. This cohort was monitored over the subsequent 84 months. The primary outcome measure was intraocular pressure (IOP). Secondary outcome measures were number of glaucoma drops, visual acuity, cup-disc-ratio (CDR), mean deviation (MD) and visual field index (VFI). Thirty-one (76%) patients survived to 48 months and 19 (46%) patients to 84 months.
At 84 months, we demonstrate an absolute mean reduction of 4.87 mmHg (95% CI 1.62-7.64) for IOP and 0.59 (95% CI 0.03-1.16) for number of glaucoma drops. At the final clinic visit, LogMAR VA improved by 0.21 (95% CI 0.08-0.34), with no significant change in CDR, MD and VFI. Attrition was mainly due to death (27%) and further glaucoma surgery (12%). A single patient suffered from postoperative hyphaema, with no sequalae. Patients at high risk for progression to filtration surgery were defined as those on oral acetazolamide for IOP control, or those fulfilling all the following criteria: IOP ≥ 20 mmHg, CDR ≥ 0.7, MD ≤ -4.0 dB, number of drops ≥ 2. This group is to be considered for surgery as the next step in management according to NICE glaucoma guidelines. These patients (n = 14) demonstrated a more marked final IOP reduction of 6.85 mmHg (95% CI 3.97-9.75) vs 1.62 mmHg (95% CI 0.04-3.22) in their low-risk counterparts (n = 27). Reduction in glaucoma drops was 0.86 (95% CI 0.07-1.64) for the high-risk and 0.56 (95% CI 0.06-1.05) for the low-risk cohort. Further glaucoma surgery was required for 4 (29%) high-risk and 1 (0.5%) low-risk patients over the study period.
Our results strongly suggest that the expected outcome of phaco-iStent surgery is a maintained reduction in intraocular pressure and number of glaucoma medications over 7 years. This is combined with a negligible rate of complications, a sustained improvement in central visual acuity, and a reliable maintenance of peripheral visual function.
确定白内障超声乳化联合第一代 iStent 植入术 84 个月的疗效和安全性。
受试者/方法:真实环境中单名外科医生、单中心、非对照前瞻性干预研究。41 名至少使用一种抗高血压滴眼剂的开角型青光眼患者接受了超声乳化联合 iStent 手术。随后对该队列进行了 84 个月的监测。主要观察指标为眼内压(IOP)。次要观察指标包括青光眼滴数、视力、杯盘比(CDR)、平均偏差(MD)和视野指数(VFI)。31 名(76%)患者存活至 48 个月,19 名(46%)患者存活至 84 个月。
84 个月时,我们证明 IOP 的平均绝对降低了 4.87mmHg(95%置信区间为 1.62-7.64),青光眼滴数降低了 0.59(95%置信区间为 0.03-1.16)。在最后一次临床就诊时,LogMAR VA 提高了 0.21(95%置信区间为 0.08-0.34),而 CDR、MD 和 VFI 没有显著变化。失访主要归因于死亡(27%)和进一步的青光眼手术(12%)。1 名患者发生术后前房积血,但无后遗症。根据 NICE 青光眼指南,被定义为需要口服乙酰唑胺控制 IOP 或符合以下所有标准的患者为进展为滤过性手术的高危人群:IOP≥20mmHg、CDR≥0.7、MD≤-4.0dB、滴数≥2。这些患者(n=14)的最终 IOP 降低更明显,为 6.85mmHg(95%置信区间为 3.97-9.75),而低危患者(n=27)为 1.62mmHg(95%置信区间为 0.04-3.22)。高危组的青光眼滴数减少 0.86(95%置信区间为 0.07-1.64),低危组减少 0.56(95%置信区间为 0.06-1.05)。研究期间,高危组有 4 名(29%)患者和低危组有 1 名(0.5%)患者需要进一步的青光眼手术。
我们的研究结果强烈表明,白内障超声乳化联合 iStent 手术的预期结果是 7 年内眼压和青光眼药物使用量持续降低。同时,中央视力持续改善,周边视力功能可靠维持,并发症发生率低。