眼科 ›› 2026, Vol. 35 ›› Issue (4): 314-319.doi: 10.13281/i.cnki.issn.1004-4469.2026.04.012

• 论著 • 上一篇    下一篇

巩膜镜治疗圆锥角膜的短期效果及安全性研究

刘晶1  张照程2  叶芙蓉2  赵雪美1  张玉坤1  吴彬阁1  接英3  田磊3   

  1. 1内蒙古科技大学包头医学院第二附属医院眼科,内蒙古包头 014000; 2首都医科大学附属北京同仁医院 北京同仁验光配镜中心,北京 100730; 3首都医科大学附属北京同仁医院 北京同仁眼科中心 北京市眼科研究所,北京 100730
  • 收稿日期:2025-12-29 出版日期:2026-07-25 发布日期:2026-07-25
  • 通讯作者: 田磊,Email: tianlei0131@163.com
  • 基金资助:
    北京市科技新星交叉项目(20240484600)

Study on the effectiveness and short-term safety of scleral lens treatment for keratoconus 

Liu Jing1, Zhang Zhaocheng2, Ye Furong2, Zhao Xuemei1, Zhang Yukun1, Wu Binge1, Jie Ying3, Tian Lei3   

  1. 1 Department of Ophthalmology, The Second Affiliated Hospital of Baotou Medical College, Inner Mongolia University of Science and Technology, Baotou Inner Mongolia 014000, China; 2 Tongren Vision Care, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China; 3 Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China
  • Received:2025-12-29 Online:2026-07-25 Published:2026-07-25
  • Contact: Tian Lei, Email: tianlei0131@163.com
  • Supported by:
    Beijing Science and Technology Star Crossing Project (20240484600)

摘要: 目的  评估巩膜镜治疗圆锥角膜的有效性及短期安全性。 设计  回顾性病例系列。研究对象  北京同仁医院验配巩膜镜的圆锥角膜患者22例(34眼),其中12例(17眼)完成1个月随访。方法  患者均经标准化验配流程佩戴巩膜镜,分别于戴镜前、戴镜后即刻、戴镜沉降60~90分钟及戴镜后1个月(日均戴镜时长为3.3±1.7小时),检测患者的BCVA、等效球镜度(spherical equivalent,SE)、非接触眼压,泪液镜厚度(中央、角膜缘及周边);采用眼前节OCTA于戴镜前及戴镜沉降60~90分钟时,以镜片着陆区“上、下、鼻、颞”象限边缘为定位点,分别对5 mm×5 mm、7 mm×7 mm、9 mm×9 mm区域的平均血流密度百分比进行定量分析。主要指标  BCVA、SE、非接触眼压、泪液镜厚度、平均血流密度百分比。结果  戴镜即刻BCVA为(0.08±0.12)logMAR,较基线框架镜的(0.38±0.33)logMAR显著提高(P<0.0001);戴镜沉降60~90分钟时BCVA为(0.07±0.12)logMAR,与戴镜即刻比较差异无统计学意义(P=0.2054);1个月完成随访的17眼BCVA为(0.07±0.09)logMAR,较基线框架镜的(0.46±0.31)logMAR显著改善(P<0.0001),且与戴镜沉降60~90分钟时(0.06±0.09)logMAR相比保持稳定(P=0.9847)。戴镜沉降60~90分钟时各区域泪液镜厚度[水平中央:(224.1±56.9) μm;垂直中央:(218.6±50.7) μm;上方边缘:(133.9±49.1) μm;下方边缘:(300.3±90.2) μm;鼻侧边缘:(212.8±86.0) μm;颞侧边缘:(228.0±71.8) μm]均较戴镜即刻显著降低(P均<0.05),且处于理想范围内;1个月随访时,各区域泪液镜厚度较戴镜即刻显著降低(P均<0.0001),与戴镜沉降60~90分钟时比较除颞侧有统计学差异外(P=0.0097),余各区域泪液镜厚度差异均无统计学意义(P均>0.05),且均值均在安全范围。OCTA显示戴镜沉降60~90分钟时各网格区域平均血流密度百分比(5 mm×5 mm区域:61.17%±7.50%;7 mm×7 mm区域:57.91%±6.38%;9 mm×9 mm区域:55.50%±5.50%)与戴镜前裸眼的血流密度百分比(61.82%±6.34%、58.48%±5.75%、56.71%±5.51%)相比均无显著差异(P均>0.05)。 结论  巩膜镜可显著提高圆锥角膜患者BCVA,1个月随访期内视力保持稳定,泪液镜厚度维持在安全范围,不引起眼前节血流密度显著减少,具有良好的短期安全性。

关键词: 巩膜镜, 圆锥角膜, 视力, 血流密度, 眼前节相干光断层扫描血管成像

Abstract: Objective To evaluate the effectiveness and short-term safety of scleral lenses in treating  keratoconus. Design Retrospective case series study. Participants Twenty-two patients (34 eyes) with keratoconus fitted with scleral lenses at the Beijing Tongren Hospital, Capital Medical University, including 12 patients (17 eyes) who completed one-month follow-up. Methods All patients underwent a standardized fitting process for scleral lenses. BCVA, spherical equivalent (SE), non-contact intraocular pressure (IOP), and tear film thickness under the lens (central, limbal, and peripheral regions) were measured before lens insertion, immediately after insertion, 60-90 minutes post-insertion, and at one month follow-up (the average daily wearing time was 3.3±1.7 hours). Anterior segment optical coherence tomography angiography (OCTA) was used to quantitatively analyze the average blood flow density percentages within 5 mm×5 mm, 7 mm×7 mm, and 9 mm×9 mm grid areas centered on the superior, inferior, nasal, and temporal quadrants of the lens landing zone, both before lens insertion and 60-90 minutes post-insertion. Main Outcome Measures BCVA, SE, IOP, tear film thickness, and average blood flow density percentage. Results Immediately after lens insertion, BCVA improved significantly from baseline spectacle correction 0.38±0.33 logMAR to 0.08±0.12 logMAR (P<0.0001). At 60-90 minutes post-insertion, BCVA was 0.07±0.12 logMAR, which showed no significant difference from the immediate post-insertion values (P=0.2054). At one-month follow-up, BCVA remained stable at 0.07±0.09 logMAR, showing significant improvement over baseline spectacle correction (0.46±0.31 logMAR) (P<0.0001), and no significant change compared to values at 60-90 minutes post-insertion (0.06±0.09 logMAR) (P=0.9847). Tear film thickness at 60-90 minutes post-insertion was significantly reduced across all regions compared to immediately after insertion (horizontal center: 224.1±56.9 μm; vertical center: 218.6±50.7 μm; superior edge: 133.9±49.1 μm; inferior edge: 300.3±90.2 μm; nasal edge: 212.8±86.0 μm; temporal edge: 228.0±71.8 μm) (all P<0.05), and remained within ideal ranges. At one-month follow-up, tear film thickness in all regions continued to be significantly reduced compared to immediately after lens insertion (all P<0.0001). Compared to values at 60-90 minutes post-insertion, only the temporal region showed a statistically significant difference (P=0.0097), other regions showed no significant changes (all P>0.05), and all mean values remained within safe limits. OCTA showed no statistically significant differences in the average blood flow density percentages across grid areas at 60-90 minutes post-insertion (5 mm×5 mm area: 61.17%±7.50%; 7 mm×7 mm area: 57.91%±6.38%; 9 mm×9 mm area: 55.50%±5.50%) compared to before lens insertion uncorrected eyes (61.82%±6.34%, 58.48%±5.75%, 56.71%±5.51%, respectively) (all P>0.05). Conclusion Scleral lenses can significantly improve BCVA in patients with keratoconus, maintain stable visual acuity during one-month follow-up, keep tear film thickness within a safe range, and do not cause notable reductions in anterior segment blood flow density, demonstrating good short-term safety.


Key words:  Scleral lens, Keratoconus, Visual acuity, Blood flow density, Anterior segment optical coherence tomography angiography