Department of Ophthalmology, Juntendo University Urayasu Hospital, Chiba, Japan.
Department of Ophthalmology, Japanese Red Cross Medical Center, 4-1-22, Hiroo, Shibuya-ku, Tokyo, 156-8935, Japan.
BMC Ophthalmol. 2023 Dec 14;23(1):509. doi: 10.1186/s12886-023-03247-y.
To investigate the outcome of non-valved glaucoma drainage implant surgery (GDIS) in primary open-angle glaucoma (POAG) patients divided in the first GDI group (patients who underwent the first GDIS) and the second GDI group (patients who underwent the second GDIS because of the failed first GDIS).
Intraocular pressure (IOP), visual acuity (VA), visual field defect (VFD), medication score (MS), survival rate of GDIS, complications, and patient background was retrospectively analyzed. Two success criteria were set: Criteria (1) IOP reduction ≥ 20% and 5 < IOP ≤ 21, Criteria (2) IOP reduction ≥ 20% and 5 < IOP ≤ 14.
There were 136 eyes of 109 patients in the first GDI group and 32 eyes of 27 patients in the second GDI group. In the first GDI group and II, mean preoperative IOP was 26.7 ± 6.7 mmHg and 23.7 ± 3.5 mmHg, respectively (P = 0.09). No statistically significant difference in postoperative IOP reduction was found between the two groups (P = 0.39). At 5-years postoperative, the Criteria 1 (Criteria 2) survival rate in the first GDI group and the second GDI group was 60.4% (31.7%) and 61.2% (25.6%), respectively (Criteria 1: hazard ratio [HR]: 0.64, 95% confidence interval [CI]: 0.30-1.35 [P = 0.24]; Criteria 2: HR: 0.81, 95% CI: 0.46-1.44, P = 0.48). No significant difference in VA, VFD change, MS, or complications was observed. Young patient age was the only significant factor for failure in the first GDI group (odds ratio: 0.95, 95% confidence interval: 0.91-1.00, P = 0.03).
The second GDIS may be as effective as the first GDIS for IOP reduction in POAG patients, however, there is a high risk of failure in young-age patients and the surgery may be ineffective in eyes requiring Criteria 2.
本研究旨在探讨原发性开角型青光眼(POAG)患者中初次(第一组)和再次(第二组)行非阀门式青光眼引流植入手术(GDIS)的治疗结局。
回顾性分析两组患者的眼压(IOP)、视力(VA)、视野缺损(VFD)、药物评分(MS)、GDIS 存活率、并发症和患者背景。设定了两个成功标准:标准 1(IOP 降低≥20%,且 5<IOP≤21mmHg)和标准 2(IOP 降低≥20%,且 5<IOP≤14mmHg)。
第一组纳入 109 例患者的 136 只眼,第二组纳入 27 例患者的 32 只眼。第一组和第二组的平均术前 IOP 分别为 26.7±6.7mmHg 和 23.7±3.5mmHg(P=0.09)。两组术后 IOP 降低程度无统计学差异(P=0.39)。术后 5 年,第一组和第二组的标准 1(标准 2)存活率分别为 60.4%(31.7%)和 61.2%(25.6%)(标准 1:危险比[HR]:0.64,95%置信区间[CI]:0.30-1.35[P=0.24];标准 2:HR:0.81,95% CI:0.46-1.44,P=0.48)。VA、VFD 变化、MS 或并发症无显著差异。在第一组中,年轻患者年龄是手术失败的唯一显著因素(优势比:0.95,95%置信区间:0.91-1.00,P=0.03)。
对于 POAG 患者,再次行 GDIS 可能与初次 GDIS 同样有效降低 IOP,但在年轻患者中存在较高的手术失败风险,且对于需要标准 2 的患者,手术可能无效。