Narayanaswamy Arun, Leung Christopher K, Istiantoro Donny V, Perera Shamira A, Ho Ching-Lin, Nongpiur Monisha E, Baskaran Mani, Htoon Hla M, Wong Tina T, Goh David, Su Daniel H, Belkin Michael, Aung Tin
Singapore Eye Research Institute, Singapore National Eye Centre, Singapore.
Department of Ophthalmology and Visual Sciences, Chinese University of Hong Kong, Hong Kong.
JAMA Ophthalmol. 2015 Feb;133(2):206-12. doi: 10.1001/jamaophthalmol.2014.4893.
Selective laser trabeculoplasty (SLT) should be explored as a therapeutic option in eyes with angle closure.
To assess the intraocular pressure (IOP)-lowering efficacy of SLT in eyes with primary angle closure (PAC) and PAC glaucoma (PACG).
DESIGN, SETTING, AND PARTICIPANTS: Randomized clinical trial at tertiary eye care institutions of 100 patients diagnosed as having PAC or PAC glaucoma in which the angles had opened at least 180° (visible posterior trabecular meshwork on gonioscopy) after laser iridotomy. Recruitment and baseline were completed from June 2009 to April 2012 and 6-month follow-up was completed from December 2009 to November 2012.
Eligible patients with a baseline IOP greater than 21 mm Hg were randomized to either SLT or prostaglandin analog (PGA; travoprost, 0.004%). The SLT was repeated if the IOP reduction was less than 20.0% from baseline at the 1- or 3-month follow-up visit.
The primary outcome measure was the change in IOP from baseline to the final follow-up visit (at 6 months). The frequency of additional postoperative treatments and complications were secondary outcomes.
Fifty patients (96 eyes) were randomized to SLT and 50 patients (99 eyes) to PGA medical therapy. At 6 months, 49 patients in the SLT group and 47 in the PGA group completed follow-up. Analysis was based on intent to treat. At 6 months, IOP decreased by 4.0 mm Hg (95% CI, 3.2-4.8) in the SLT group (P < .001) and by 4.2 mm Hg (95% CI, 3.5-4.9) in the PGA group (P < .001). There were no differences between the SLT and PGA groups in the absolute mean reduction of IOP (4.0 vs 4.2 mm Hg, respectively; P = .78) or in the percentage of reduction in IOP (16.9% vs 18.5%, respectively; P = .52). Complete success (IOP ≤21 mm Hg without medications) was achieved in 60.0% eyes of the SLT group, compared with 84.0% of eyes in the PGA group (P = .008). No patients required glaucoma surgery. Additional medications were required in 22.0% of patients in the SLT group compared with 8.0% in the PGA group (P = .05). One patient in the SLT group (2.0%) had a transient posttreatment IOP spike greater than 5 mm Hg. The mean endothelial cell count showed a significant decrease from baseline in the SLT arm (4.8% decrease; P = .001). No other events such as persistent uveitis or increase in peripheral anterior synechiae were noted in eyes that underwent SLT. Two patients in the PGA group exited owing to drug-related complications (1 patient with uveitis and 1 with allergic conjunctivitis).
Eyes with PAC or PACG respond to SLT in the short term, but the overall long-term therapeutic effectiveness needs further evaluation.
clinicaltrials.gov Identifier: NCT01004900.
对于闭角型青光眼,应探索选择性激光小梁成形术(SLT)作为一种治疗选择。
评估SLT对原发性闭角型青光眼(PAC)和原发性闭角型青光眼(PACG)患者降低眼压(IOP)的疗效。
设计、地点和参与者:在三级眼科保健机构进行的一项随机临床试验,研究对象为100例被诊断为PAC或PACG的患者,这些患者在激光虹膜切开术后房角至少开放180°(房角镜检查可见后小梁网)。2009年6月至2012年4月完成招募和基线检查,2009年12月至2012年11月完成6个月的随访。
基线眼压高于21 mmHg的符合条件的患者被随机分为SLT组或前列腺素类似物(PGA;曲伏前列素,0.004%)组。如果在1个月或3个月的随访中眼压降低幅度低于基线的20.0%,则重复进行SLT。
主要结局指标是从基线到最终随访(6个月时)眼压的变化。术后额外治疗的频率和并发症为次要结局。
50例患者(96只眼)被随机分配至SLT组,50例患者(99只眼)被随机分配至PGA药物治疗组。6个月时,SLT组49例患者和PGA组47例患者完成随访。分析基于意向性治疗原则。6个月时,SLT组眼压降低4.0 mmHg(95%CI,3.2 - 4.8)(P <.001),PGA组眼压降低4.2 mmHg(95%CI,3.5 - 4.9)(P <.001)。SLT组和PGA组在眼压绝对平均降低值(分别为4.0 vs 4.2 mmHg;P = 0.78)或眼压降低百分比(分别为16.9% vs 18.5%;P = 0.52)方面无差异。SLT组60.0%的眼达到完全成功(眼压≤21 mmHg且无需药物治疗),而PGA组为84.0%(P = 0.008)。无患者需要青光眼手术。SLT组22.0%的患者需要额外用药,而PGA组为8.0%(P = 0.05)。SLT组1例患者(2.0%)治疗后眼压出现短暂升高超过5 mmHg。SLT组平均内皮细胞计数较基线有显著下降(下降4.8%;P = 0.001)。接受SLT的眼中未发现其他事件,如持续性葡萄膜炎或周边前粘连增加。PGA组2例患者因药物相关并发症退出研究(1例葡萄膜炎,1例过敏性结膜炎)。
PAC或PACG患者的眼在短期内对SLT有反应,但总体长期治疗效果需要进一步评估。
clinicaltrials.gov标识符:NCT01004900。