眼科 ›› 2026, Vol. 35 ›› Issue (4): 278-284.doi: 10.13281/i.cnki.issn.1004-4469.2026.04.007

• 论著 • 上一篇    下一篇

激光强化药物精准穿透治疗新生血管性年龄相关性黄斑变性的短期疗效观察

王祎伟1,2,3  翟羽佳2  蒋宇琦1  黄厚斌2   

  1. 1中国人民解放军医学院,北京 100853;2中国人民解放军总医院眼科医学部,北京 100039;3中国人民解放军联勤保障部队三亚康复疗养中心眼科,海南三亚 572000
  • 收稿日期:2026-03-29 出版日期:2026-07-25 发布日期:2026-07-25
  • 通讯作者: 黄厚斌,Email: 536273642@qq.com

Observation on the short term efficacy of laser enhanced anti-VEGF precise permeation therapy for neovascular age-related macular degeneration

Wang Yiwei1,2,3, Zhai Yujia2, Jiang Yuqi1, Huang Houbin2   

  1. 1 Medical School of Chinese People's Liberation Army, Beijing 100853, China; 2 Senior Department of Ophthalmology, PLA General Hospital, Beijing 100039, China; 3 Sanya Rehabilitation and Recuperation Center, Sanya Hainan 572000, China
  • Received:2026-03-29 Online:2026-07-25 Published:2026-07-25
  • Contact: Huang Houbin, Email: 536273642@qq.com

摘要: 目的  探讨采用基于吲哚青绿血管造影定位的激光强化抗VEGF药物精准穿透(laser enhanced anti-VEGF precise permeation, LEAP)治疗新生血管性年龄相关性黄斑变性(neovascular age-related macular degeneration , nAMD)患者6个月的安全性和有效性。设计  前瞻性、非随机对照研究。 研究对象  2023年9月至2026年3月在解放军总医院第一、第三医学中心接受玻璃体内注射抗血管内皮生长因子(vascular endothelial growth factor,VEGF)药物治疗的nAMD患者112例(122眼)。方法  依据患者主观治疗意愿,将患者分为接受LEAP治疗组(60例)与单纯抗VEGF药物注射治疗组(62例);观察、对比两组患者治疗后6个月的治疗次数及疗效指标,评估两种方案的诊疗负担及治疗有效性。相干光断层扫描(optic coherence tomography,OCT)持续检查提示无积液或仅残留可耐受的、无临床意义的微量积液即为病变稳定。主要指标  玻璃体内注射次数、最佳矫正视力、黄斑中心凹厚度、视网膜下液高度、色素上皮层脱离高度。结果  LEAP治疗组纳入研究前平均注射药物(5.77±3.73)次,LEAP治疗后6个月平均治疗(0.48±0.91)次即可达到病变稳定,显著少于单纯注药组的(2.79±1.03)次(z=-8.568,P<0.001);两组间最佳矫正视力(P=0.058)、黄斑中心凹厚度(P=0.663)、视网膜下液高度(P=0.082)及色素上皮层脱离高度(P=0.242)均无显著差异;各组内疗效指标均较基线显著改善(P均<0.05);研究期间未观察到与LEAP治疗相关的不良事件。结论  LEAP疗法为nAMD提供了显著减少治疗次数的新策略,同时其疗效及安全性与单纯抗VEGF药物注射治疗相当。

关键词:  , 新生血管性年龄相关性黄斑变性;激光疗法;抗血管内皮生长因子;药物精准穿透

Abstract:  Objective To investigate the short-term (6-month) safety and efficacy of laser enhanced anti-VEGF precise permeation (LEAP) therapy based on indocyanine green angiography localization in patients with neovascular age-related macular degeneration (nAMD). Design A prospective, non-randomized controlled study. Participants A total of 112 patients (122 eyes) with nAMD who received intravitreal injection of anti-vascular endothelial growth factor (anti-VEGF) drugs at the First Medical Center and the Third Medical Center of Chinese PLA General Hospital from September 2023 to March 2026. Methods According to patients' voluntary treatment willingness, the subjects were divided into LEAP treatment group and simple anti-VEGF intravitreal injection group. The number of treatments and efficacy indicators at the 6-month follow-up were observed and compared between the two groups, and the differences in treatment burden and efficacy of the two regimens were evaluated. Main Outcome Measures Number of treatments at the 6-month endpoint, best corrected visual acuity (BCVA), central macular thickness (CMT), height of subretinal fluid (SRF), and height of pigment epithelial detachment (PED). Results Before enrollment in the study, the mean number of intravitreal injections in the LEAP treatment group was (5.77±3.73). At the 6-month short-term endpoint, the LEAP group achieved lesion stability with a mean treatment count of only (0.48±0.91) times, which was significantly lower than (2.79±1.03) times in the intravitreal injection alone group (z=-8.568, P<0.001).There were no significant between-group differences in efficacy indicators including best corrected visual acuity (P=0.058), central macular thickness (P=0.663), subretinal fluid height (P=0.082), and pigment epithelial detachment height (P=0.242). All intragroup efficacy parameters were significantly improved compared with baseline (all P<0.05). No adverse events related to LEAP treatment were observed during the study period. Conclusion LEAP therapy serves as a novel strategy to remarkably reduce the treatment frequency for nAMD, with non-inferior efficacy and safety compared with conventional simple anti-VEGF intravitreal injection therapy.


Key words: Neovascular age-related macular degeneration, Laser therapy, Anti-VEGF, Drug permeation