Department of Ophthalmology, Faculty of Medicine, Ankara University, Mamak Street, Ankara, 06620, Turkey.
Ankara Üniversitesi Tıp Fakültesi Göz Hastalıkları Anabilim Dalı, Vehbi Koç Göz Hastanesi, Balkiraz Mahallesi, Mamak Cd. 6 A, Mamak/Ankara, 06620, Turkey.
Graefes Arch Clin Exp Ophthalmol. 2021 Nov;259(11):3359-3369. doi: 10.1007/s00417-021-05265-2. Epub 2021 Jul 5.
To compare the success rates and safety of micropulse transscleral laser cyclophotocoagulation (MP-TSCPC) for the treatment of refractory glaucoma using the 240-s and 160-s duration protocols in eyes with good visual acuity.
A retrospective analysis of patients with refractory glaucoma who underwent MP-TSCPC from December 2017 to September 2019 with baseline best-corrected visual acuity (BCVA) of ≥ 20/60. Laser treatments for the moderate and short duration protocols were defined as 240 s and 160 s with settings of 2000 mW/Cm2 and a duty cycle of 31.3%. Follow-up examinations were performed regularly until 12 months after the procedure.
Seventy-six eyes of 76 patients were included with BCVA ranging from 20/60 to 20/20. Forty-four eyes were treated with 240 s and 32 eyes were treated with 160-s duration protocols. There was no significant reduction in mean logMAR BCVA and visual field parameters from baseline at any follow-up point in both groups. Visual acuity remained unchanged or improved in 39 of 44 patients (88.6%) in 240-s group and in 28 of 32 patients (87.5%) in 160-s group. Seven of 44 eyes (15.9%) in 240-s group and 12 of 32 eyes (37.5%) in 160-s group required re-treatment for adequate IOP control. After the re-treatments, both protocols showed similar success rates of 79.5% in 240-s group and 75% in 160-s group at 12 months, respectively (p > 0.05).
MP-TSCPC can be offered as a primary surgical treatment for the management of refractory glaucoma in patients with good visual acuity. Considering the high re-treatment rates in 160-s group, the 240-s duration protocol appears to be more effective than 160-s protocol for adequate IOP control.
比较使用 240 秒和 160 秒时长方案的微脉冲经巩膜激光睫状体光凝术(MP-TSCPC)治疗视力良好的难治性青光眼的成功率和安全性。
回顾性分析 2017 年 12 月至 2019 年 9 月期间接受 MP-TSCPC 治疗的难治性青光眼患者,纳入标准为基线最佳矫正视力(BCVA)≥20/60。中短时长方案的激光治疗定义为 240 秒和 160 秒,设定为 2000 mW/Cm2 和 31.3%的占空比。定期进行随访检查,直至术后 12 个月。
76 例患者的 76 只眼纳入研究,BCVA 范围为 20/60 至 20/20。44 只眼接受 240 秒时长方案治疗,32 只眼接受 160 秒时长方案治疗。两组在任何随访点的平均 logMAR BCVA 和视野参数均无显著下降。240 秒时长方案组的 44 名患者中有 39 名(88.6%)视力保持不变或提高,160 秒时长方案组的 32 名患者中有 28 名(87.5%)视力保持不变或提高。240 秒时长方案组的 44 只眼中有 7 只(15.9%),160 秒时长方案组的 32 只眼中有 12 只(37.5%)需要再次治疗以控制眼压。再次治疗后,240 秒时长方案组和 160 秒时长方案组在 12 个月时的成功率分别为 79.5%和 75%(p>0.05)。
MP-TSCPC 可作为视力良好的难治性青光眼患者的主要手术治疗方法。考虑到 160 秒时长方案组的高复发率,240 秒时长方案似乎比 160 秒时长方案更能有效控制眼压。