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不同微脉冲巩膜激光睫状体光凝术持续时间方案在视力良好眼的疗效和安全性比较。

Comparative efficacy and safety of micropulse transscleral laser cyclophotocoagulation using different duration protocols in eyes with good visual acuity.

机构信息

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.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2021 Nov;259(11):3359-3369. doi: 10.1007/s00417-021-05265-2. Epub 2021 Jul 5.

Abstract

PURPOSE

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

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