Department of Ophthalmology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo, Tokyo, 113-8655, Japan.
Yotsuya Shirato Eye Clinic, Tokyo, Japan.
Graefes Arch Clin Exp Ophthalmol. 2024 Jan;262(1):191-201. doi: 10.1007/s00417-023-06209-8. Epub 2023 Aug 25.
To investigate the postoperative intraocular pressure (IOP) control and identify the factors associated with failure of initial Ex-PRESS surgery in patients with open-angle glaucoma for 3 years.
A total of 79 patients with medically uncontrolled open-angle glaucoma (55 normal-tension glaucoma and 24 primary open-angle glaucoma) were enrolled. All patients underwent Ex-PRESS implantation (including combined cataract surgery). The outcome measure was the survival rate using life table analysis, the failure was defined as IOP of > 18 mmHg (criterion A), > 15 mmHg (criterion B) or > 12 mmHg (criterion C) and/or IOP reduction of < 20% from baseline (each criterion) without any glaucoma medications. The Cox proportional hazards model was used to identify risk factors for IOP management defined as the above criterion. RESULTS: The mean preoperative IOP was 19.3 ± 5.8 mmHg. At 36 months, the mean IOP was 11.8 ± 3.6 mmHg with a mean IOP change of 7.5 mmHg (reduction rate 39.0%). The cumulative probability of success was 58% (95%CI: 42-64%) (criterion A), 48% (95%CI: 37-59%) (criterion B) and 30% (95%CI: 20-40%) (criterion C). In multivariate analyses, factors that predicted poor IOP control included the intervention of bleb needling after 6 months after the surgery (HR: 2.43; 95%CI: 1.35-4.37; P = 0.032). Transient hypotony was observed in 4 patients.
The implementation of bleb needling after Ex-PRESS surgery in the late postoperative period was suggested to be the main risk factor for achieving lower IOP.
研究术后眼内压(IOP)的控制情况,并确定与 3 年内开角型青光眼患者 Ex-PRESS 手术初始失败相关的因素。
共纳入 79 例药物治疗无法控制的开角型青光眼(55 例正常眼压性青光眼和 24 例原发性开角型青光眼)患者。所有患者均行 Ex-PRESS 植入术(包括联合白内障手术)。采用寿命表分析评估患者的生存率,将眼压>18mmHg(标准 A)、>15mmHg(标准 B)或>12mmHg(标准 C)和/或与基线相比眼压降低<20%(每个标准)定义为失败,且不使用任何抗青光眼药物。采用 Cox 比例风险模型确定与上述标准定义的 IOP 控制相关的危险因素。
术前平均 IOP 为 19.3±5.8mmHg。36 个月时,平均 IOP 为 11.8±3.6mmHg,IOP 平均变化 7.5mmHg(降低率 39.0%)。累积成功率为 58%(95%CI:42-64%)(标准 A)、48%(95%CI:37-59%)(标准 B)和 30%(95%CI:20-40%)(标准 C)。多因素分析显示,术后 6 个月行滤枕针刺干预是预测 IOP 控制不佳的因素(HR:2.43;95%CI:1.35-4.37;P=0.032)。4 例患者出现短暂低眼压。
建议在 Ex-PRESS 手术后的晚期行滤枕针刺,这可能是实现较低 IOP 的主要危险因素。