眼科 ›› 2026, Vol. 35 ›› Issue (2): 103-108.doi: 10.13281/j.cnki.issn.1004-4469.2026.02.004

• 论著 • 上一篇    下一篇

微脉冲经巩膜睫状体光凝术治疗难治性青光眼的短期疗效

陶德1,2   苏玉芳  杨亚军2   

  1. 1内蒙古科技大学包头医学院,内蒙古包头014040; 2包头朝聚眼科医院,内蒙古包头014000
  • 收稿日期:2025-06-17 出版日期:2026-03-25 发布日期:2026-03-25
  • 通讯作者: 杨亚军,Email:yangyajun@chaojueye.com
  • 基金资助:
    包头市卫生健康科技计划(2023wsjkkj99、2023wsjkkj100)

The short-term efficacy of micro-pulse transscleral cyclophotocoagulation for the treatment of refractory glaucoma

Tao De1,2, Su Yufang2, Yang Yajun2   

  1. 1Baotou Medical College, Inner Mongolia University of Science and Technology, Baotou Inner Mongolia 014040, China; 2Baotou Chaoju Eye Hospital, Baotou Inner Mongolia 014000, China
  • Received:2025-06-17 Online:2026-03-25 Published:2026-03-25
  • Contact: Yang Yajun, Email: yangyajun@chaojueye.com
  • Supported by:
    Baotou Health Science and Technology Plan(2023wsjkkj99, 2023wsjkkj100)

摘要:  目的  评估微脉冲经巩膜睫状体光凝术(MP-TSCPC)对难治性青光眼的短期疗效与安全性。 设计  回顾性病例系列。研究对象  2023年8月至2025年1月在包头朝聚眼科医院接受MP-TSCPC治疗的29例(31眼)曾经多次手术或眼压无法控制的难治性青光眼患者。方法  手术使用Cyclo G6激光系统,配合MicroPulse P3探头进行治疗。将MicroPulse P3光纤探头置于距角巩膜缘约1 mm处,探头紧密与球结膜接触,以适中的压力在四个象限角膜缘后连续各扫45~60 s,能量2000 mW。术前和术后3个月观察患者的眼压、最佳矫正视力(BCVA),记录患者抗青光眼药物使用数量,采用美国国立眼科研究所视功能问卷-25(NEI-VFQ-25)了解患者的生活质量,视觉模拟疼痛评分(VAS)评价患者疼痛情况。主要指标  眼压、抗青光眼药物使用数量、BCVA、VAS评分以及NEI-VFQ-25量表评分。结果  术后1天、1周、1个月、3个月眼压分别为(18.61±7.97)mmHg、(14.16±3.86)mmHg、(18.90±7.84)mmHg、(20.97±9.00)mmHg,均低于术前的(46.35±15.02)mmHg(F=57.302,P<0.001)。抗青光眼药物使用数量由术前的3种减少至2种(Z=-3.973,P<0.001)。术后3个月BCVA与术前视力比较无统计学差异(Z=-0.618,P=0.536)。术前VAS评分为(1.74±3.15),术后1天为(0.58±1.45)、术后1周为(0.10±0.53),均较术前明显下降(P=0.025、0.002)。至术后1个月所有眼疼痛完全消失。NEI-VFQ-25量表在整体健康、总体视力及眼球疼痛感方面显著改善。术前11眼有疼痛感,术后1天减少至5眼,术后1周只有1眼轻度疼痛,无疼痛眼的比例从术前64.5%增加至术后1周的99.6%。术后1个月及3个月所有眼均无疼痛。术后3个月内3眼发生并发症,其中2眼脉络膜脱离,1眼角膜上皮损伤,经药物治疗后脉络膜均复位,角膜上皮损伤修复,未见其他并发症发生。结论  MP-TSCPC术后3个月内能有效降低难治性青光眼患者的眼压、减少降眼压药物依赖,并改善患者的生活质量和疼痛症状。

关键词: 微脉冲经巩膜睫状体光凝术, 难治性青光眼, 眼压

Abstract:  Objective To assess the short-term efficacy and safety of micro-pulse transscleral cyclophotocoagulation (MP-TSCPC) in refractory glaucoma. Design Retrospective case series. Participants  Twenty-nine patients (31 eyes) with refractory glaucoma whose intraocular pressure (IOP) was uncontrolled despite prior medical or surgical treatment, treated at Baotou Chaoju Eye Hospital between August 2023 and January 2025. Methods The MP-TSCPC procedure was performed using a Cyclo G6 laser system with a MicroPulse P3 probe. The fiberoptic probe was positioned approximately 1 mm posterior to the limbus, maintaining gentle contact with the conjunctiva, and swept continuously for 45~60 seconds in each quadrant at a power setting of 2000 mW. IOP, best-corrected visual acuity (BCVA), number of glaucoma medications, NEI-VFQ-25 quality-of-life score, and visual analog scale (VAS) pain score were assessed preoperatively and at 3 months postoperatively. Main Outcome Measures IOP, number of glaucoma medications, BCVA, score of VAS and NEI-VFQ-25. Results The mean IOP at 1 day, 1 week, 1 month, and 3 months postoperatively was (18.61±7.97) mmHg, (14.16±3.86) mmHg, (18.90±7.84) mmHg, and (20.97±9.00) mmHg, respectively, all significantly lower than the preoperative value of (46.35±15.02) mmHg (F=57.302, P<0.001). The median number of glaucoma medications decreased from 3 preoperatively to 2 postoperatively (Z=-3.973, P<0.001). BCVA showed no significant change (Z=-0.618, P=0.536). The preoperative VAS score was (1.74±3.15), while it decreased significantly to (0.58±1.45) on postoperative day 1 and to (0.10±0.53) on postoperative week 1, with statistical significance (P=0.025, 0.002). By postoperative month 1, all ocular pain had completely resolved. NEI-VFQ-25 scores improved significantly in the domains of general health, overall vision, and ocular pain. Preoperatively, 11 eyes experienced pain; this decreased to 5 eyes at postoperative day 1 and to 1 eye (mild) at postoperative week 1. The proportion of pain-free eyes increased from 64.5% preoperatively to 99.6% at 1 week postoperatively. All eyes were pain-free at 1 month and 3 months postoperatively. Within 3 months, 3 eyes developed complications: 2 eyes of choroidal detachment and 1 case of corneal epithelial injury, all of which resolved with medical treatment. No other complications were observed. Conclusions MP-TSCPC effectively lowers IOP and reduces medication burden within 3 months postoperatively, while improving quality of life and alleviating ocular pain in patients with refractory glaucoma, with a favorable safety profile.

Key words:  Micro-pulse transscleral cyclophotocoagulation, Refractory glaucoma, Intraocular pressure