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周边虹膜切除术联合房角粘连分离术及房角切开术与小梁切除术治疗晚期原发性闭角型青光眼的随机临床试验

Peripheral Iridectomy With Goniosynechialysis and Goniotomy vs Trabeculectomy for Advanced PACG: A Randomized Clinical Trial.

作者信息

Lin Fengbin, Lv Aiguo, Li Fei, Song Yunhe, Xie Lin, Zhu Xiaomin, Tang Li, Zhang Yao, Huang Jingjing, Tang Guangxian, Zhang Hengli, Lu Lan, Xiao Meichun, Xu Jiangang, Nie Xin, Liao Mengfei, Yang Yangfan, Gao Kai, Yuan Huiping, Song Wulian, Zuo Chengguo, Lu Ping, Yan Xiaowei, Zhou Fengqi, Wang Zhenyu, Jin Ling, Peng Yuying, Chen Weirong, Barton Keith, Park Ki Ho, Aung Tin, Lam Dennis S C, Weinreb Robert N, Wang Ningli, Tham Clement C, Fan Sujie, Zhang Xiulan

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Guangdong Provincial Clinical Research Center for Ocular Diseases, Guangzhou, China.

Handan City Eye Hospital (The Third Hospital of Handan), Handan, China.

出版信息

JAMA Ophthalmol. 2025 Jun 1;143(6):472-479. doi: 10.1001/jamaophthalmol.2025.0757.

Abstract

IMPORTANCE

The safety and effectiveness of combining surgical peripheral iridectomy (SPI) with goniosynechialysis (GSL) and goniotomy (GT) vs trabeculectomy for intraocular pressure (IOP) reduction remains unknown.

OBJECTIVE

To investigate the safety and effectiveness at 1 year of SPI + GSL + GT vs trabeculectomy in advanced primary angle-closure glaucoma (PACG) without cataract.

DESIGN, SETTING, AND PARTICIPANTS: This noninferiority randomized clinical trial was conducted at 8 tertiary eye centers in China. A total of 88 Chinese patients (88 eyes) with advanced PACG without cataract were enrolled from January 2022 to July 2023. Data were analyzed from August 2024 to September 2024. Mean (SD) patient age was 60.3 (7.3) years, and 52 patients (59.1%) were female. Forty-three patients were randomized to SPI + GSL + GT and 45 were randomized to trabeculectomy; 86 patients (97.7%) completed the 12-month follow-up.

INTERVENTIONS

Participants were randomized 1:1 to receive SPI + GSL + GT or trabeculectomy.

MAIN OUTCOMES AND MEASURES

The primary outcome was IOP at 12 months (noninferior margin: 4 mm Hg). Secondary outcomes included surgical success (IOP: 5-18 mm Hg, ≥20% reduction from baseline, with or without antiglaucoma medications); postoperative complications and interventions, including bleb massage, suture lysis, or releasable sutures; and number of antiglaucomatous medications prescribed.

RESULTS

At 12 months, the SPI + GSL + GT group had a mean (SD) IOP of 15.6 (4.0) mm Hg vs 14.9 (4.2) mm Hg in the trabeculectomy group (difference, 0.5 mm Hg; 95% CI, -1.2 to 2.2; P = .55), which was within the 4-mm Hg noninferiority margin. Qualified success rates were 38 of 43 participants (88.4%) for SPI + GSL + GT and 42 of 45 participants (93.3%) for trabeculectomy (difference, -5.0%; 95% CI, -19.6% to 8.5%; P = .48). However, complete success rates were lower in the SPI + GSL + GT group (26 participants [60.5%]) vs the trabeculectomy group (37 participants [82.2%]; difference, -21.8%; 95% CI, -40.2% to -2.4%; P = .03). Postoperative complications were present for 8 participants (18.6%) in the SPI + GSL + GT group vs 9 participants (20.0%) in the trabeculectomy group (difference, -1.4%; 95% CI, -17.9% to 15.1%; P = .71). Postoperative interventions were lower in the SPI + GSL + GT group (3 participants [7.0%] vs 25 participants [55.6%]; difference, 48.6%; 95% CI, 32.2%-65.0%; P < .001). Median (IQR) numbers of medications used decreased from 2 (0-3) to 0 (0-1) in the SPI + GSL + GT group and from 2 (2-3) to 0 (0-0) in the trabeculectomy group (difference, -0.81; 95% CI, -1.36 to -0.26; P = .004).

CONCLUSIONS AND RELEVANCE

In this randomized clinical trial among patients with advanced PACG without cataract, SPI + GSL + GT demonstrated noninferiority (4-mm Hg margin) to trabeculectomy for IOP at 12 months, with fewer interventions (including bleb massage, suture lysis, or releasable sutures) but no difference in postoperative medication use. This suggests SPI + GSL + GT as a potential alternative to trabeculectomy for similar cases, pending validation in larger sample sizes with smaller noninferiority margins.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT05163951.

摘要

重要性

对于降低眼压,将手术周边虹膜切除术(SPI)与房角分离术(GSL)及房角切开术(GT)联合使用与小梁切除术相比,其安全性和有效性尚不清楚。

目的

探讨在无白内障的晚期原发性闭角型青光眼(PACG)患者中,SPI + GSL + GT与小梁切除术在1年时的安全性和有效性。

设计、设置和参与者:这项非劣效性随机临床试验在中国的8个三级眼科中心进行。2022年1月至2023年7月,共纳入88例无白内障的晚期PACG中国患者(88只眼)。2024年8月至2024年9月进行数据分析。患者平均(标准差)年龄为60.3(7.3)岁,52例患者(59.1%)为女性。43例患者被随机分配至SPI + GSL + GT组,45例患者被随机分配至小梁切除术组;86例患者(97.7%)完成了12个月的随访。

干预措施

参与者按1:1随机分组,接受SPI + GSL + GT或小梁切除术。

主要结局和测量指标

主要结局为12个月时的眼压(非劣效界值:4 mmHg)。次要结局包括手术成功率(眼压:5 - 18 mmHg,较基线降低≥20%,无论是否使用抗青光眼药物);术后并发症及干预措施,包括滤过泡按摩、缝线松解或可拆除缝线;以及开具的抗青光眼药物数量。

结果

12个月时,SPI + GSL + GT组的平均(标准差)眼压为15.6(4.0)mmHg,小梁切除术组为14.9(4.2)mmHg(差值为0.5 mmHg;95%置信区间为 - 1.2至2.2;P = 0.55),在4 mmHg的非劣效界值范围内。SPI + GSL + GT组43例参与者中有38例(88.4%)达到合格成功率,小梁切除术组45例参与者中有42例(93.3%)达到合格成功率(差值为 - 5.0%;95%置信区间为 - 19.6%至8.5%;P = 0.48)。然而,SPI + GSL + GT组的完全成功率低于小梁切除术组(26例参与者[60.5%]对37例参与者[82.2%];差值为 - 21.8%;95%置信区间为 - 40.2%至 - 2.4%;P = 0.03)。SPI + GSL + GT组有8例参与者(18.6%)出现术后并发症,小梁切除术组有9例参与者(20.0%)出现术后并发症(差值为 - 1.4%;95%置信区间为 - 17.9%至15.1%;P = 0.7)。SPI + GSL + GT组的术后干预措施较少(3例参与者[7.0%]对25例参与者[55.6%];差值为48.6%;95%置信区间为32.2% - 65.0%;P < 0.001)。SPI + GSL + GT组使用药物的中位数(四分位间距)从2(0 - 3)降至0(0 - 1),小梁切除术组从2(2 - 3)降至0(0 - 0)(差值为 - 0.81;95%置信区间为 - 1.36至 - 0.26;P = 0.004)。

结论与相关性

在这项针对无白内障的晚期PACG患者的随机临床试验中,SPI + GSL + GT在12个月时降低眼压方面显示出与小梁切除术非劣效(4 mmHg界值),干预措施较少(包括滤过泡按摩、缝线松解或可拆除缝线),但术后用药无差异。这表明对于类似病例,SPI + GSL + GT可能是小梁切除术的一种潜在替代方法,有待在更大样本量和更小非劣效界值的研究中进行验证。

试验注册

ClinicalTrials.gov标识符:NCT05163951

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Primary Angle-Closure Disease Preferred Practice Pattern®.原发性闭角型青光眼首选诊疗模式®
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