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经巩膜微脉冲睫状体光凝术行睫状体扁平部与睫状体部光凝的一年随访。

One-Year Follow-up of Pars Plicata Versus Pars Plana Application of Transscleral Micropulse Cyclophotocoagulation.

机构信息

Department of Ophthalmology, Medical Faculty Carl Gustav Carus, Technical University, Dresden, Germany.

出版信息

J Glaucoma. 2021 Apr 1;30(4):340-346. doi: 10.1097/IJG.0000000000001775.

Abstract

PURPOSE

To compare the efficacy and safety of micropulse transscleral cyclophotocoagulation applied at the level of the pars plicata transscleral micropulse cyclophotocoagulation (PLI-MPC) versus the pars plana transscleral micropulse cyclophotocoagulation (PLA-MPC).

METHODS

This prospective interventional case series included 44 eyes of 31 medically treated primary open-angle glaucoma patients scheduled for micropulse transscleral cyclophotocoagulation to achieve further intraocular pressure (IOP) reduction. In total, 22 eyes underwent PLI-MPC and PLA-MPC each. Primary endpoints were the reduction of 24-hour mean diurnal IOP (mean of 6 measurements), diurnal IOP fluctuations, and peak IOP, after 3 and 12 months. Secondary outcomes were postoperative complications, a possible deterioration in visual acuity and field, factors influencing IOP reduction, and the number of dropouts.

RESULTS

In the PLI-MPC group, IOP was reduced from 15.9±3.4 mm Hg to 13.6±3.1 mm Hg (n=16; P<0.001) and 12.9±3.7 mm Hg (n=13; P<0.001) at 3 and 12-month follow-up. In the PLA-MPC group, IOP decreased from 16.4±3.5 mm Hg to 12.3±2.6 mm Hg (n=15; P<0.001) and 11.8±2.2 mm Hg (n=14; P<0.001), respectively. At 12 months, 59% of the PLI-MPC and 63% of the PLA-MPC group had a sufficient IOP reduction to reach the individual target pressure. No complications were seen in either group. A higher preoperative IOP was recognized as the only factor influencing the postoperative IOP reduction.

CONCLUSIONS

PLI-MPC and PLA-MPC seem to be safe and effective in further lowering the IOP in about 60% of patients with primary open-angle glaucoma who did not reach target pressure despite maximally tolerated IOP-lowering medication. Although the IOP-lowering effect was not statistically significantly different between groups the pars plicata application was superior and easier to perform and should be recommended as the preferred method of application.

摘要

目的

比较睫状体扁平部经巩膜微脉冲光睫状体光凝术(PLI-MPC)与睫状体平坦部经巩膜微脉冲光睫状体光凝术(PLA-MPC)治疗原发性开角型青光眼的疗效和安全性。

方法

这是一项前瞻性的干预性病例系列研究,纳入了 31 名接受药物治疗的原发性开角型青光眼患者的 44 只眼,这些患者计划接受微脉冲经巩膜睫状体光凝术以进一步降低眼内压(IOP)。共有 22 只眼分别接受了 PLI-MPC 和 PLA-MPC。主要终点是术后 3 个月和 12 个月时 24 小时平均日间 IOP(6 次测量的平均值)、日间 IOP 波动和最高 IOP 的降低。次要结局是术后并发症、视力和视野可能恶化、影响 IOP 降低的因素以及脱落人数。

结果

在 PLI-MPC 组,16 只眼的 IOP 从 15.9±3.4mmHg 降低至 13.6±3.1mmHg(n=16;P<0.001)和 12.9±3.7mmHg(n=13;P<0.001),13 只眼的 IOP 从 16.4±3.5mmHg 降低至 12.3±2.6mmHg(n=15;P<0.001)和 11.8±2.2mmHg(n=14;P<0.001)。在 12 个月时,59%的 PLI-MPC 组和 63%的 PLA-MPC 组患者的 IOP 降低幅度足以达到个体目标压力。两组均未出现并发症。术前较高的 IOP 被认为是唯一影响术后 IOP 降低的因素。

结论

对于未达到目标眼压的原发性开角型青光眼患者,尽管接受了最大限度耐受的降眼压药物治疗,PLI-MPC 和 PLA-MPC 似乎是安全有效的,可以进一步降低约 60%患者的眼压。尽管两组之间的 IOP 降低效果没有统计学上的显著差异,但睫状体扁平部应用效果更好,且更容易操作,应作为首选应用方法。

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