眼科 ›› 2025, Vol. 34 ›› Issue (5): 359-365.doi: 10.13281/j.cnki.issn.1004-4469.2025.05.005

• 论著 • 上一篇    下一篇

圆锥角膜患者配戴巩膜镜的6个月矫治效果观察

齐艳 胡艳 薛劲松 徐英男   

  1. 南京医科大学附属眼科医院,南京 210029
  • 收稿日期:2025-04-02 出版日期:2025-09-25 发布日期:2025-09-12
  • 通讯作者: 徐英男,Email:xyn20051151187@163.com

Observation of the effect of wearing scleral lenses for 6 months in patients with keratoconus

Qi Yan, Hu Yan, Xue Jinsong, Xu Yingnan   

  1. Affiliated Eye Hospital of Nanjing Medical University, Nanjing 210029, China 
  • Received:2025-04-02 Online:2025-09-25 Published:2025-09-12
  • Contact: Xu Yingnan, Email: xyn20051151187@163.com

摘要:  目的  观察圆锥角膜患者配戴巩膜镜的临床矫治效果。设计  回顾性病例系列。研究对象  南京医科大学附属眼科医院完成期3级及以下的圆锥角膜并验配巩膜镜的患者21例(29眼)。方法  所有患者均经规范程序验配巩膜镜。观察比较患者戴镜1周、1个月、3个月及6个月时巩膜镜配适状态即镜片与角膜中央及各方位周边泪液间隙的差异,比较戴镜前,戴镜后1周、1个月、3个月及6个月时视力、屈光度、角膜参数等指标的差异。使用NEI-VFQ-25中文版评估患者配戴巩膜镜6个月的视觉相关生活质量。主要指标  矫正视力、眼压、角膜前表面平坦屈光力值(K1)、角膜前表面陡峭屈光力值(K2)、角膜前表面最大屈光力值(Kmax)、角膜最薄点厚度(TCT)、中央角膜厚度(CCT)、角膜染色评分(CSS)、角膜内皮细胞密度(ECD)、NEI-VFQ-25评分、巩膜镜下泪液间隙。结果   戴镜6个月时,镜片中央区、鼻侧、颞侧、上方、下方泪液间隙分别为221(177,274)μm、98(68,133)μm、138(81,213)μm、145(95,190)μm和360(289,478)μm,较戴镜1周时的240(184,282)μm、98(62,121)μm、120(95,207)μm、145(82,192)μm和326(270,450)μm未见明显统计学差异(P均>0.05)。戴镜1周、6个月时巩膜镜矫正视力分别为0.30(0.05,0.40)LogMAR和0.22(0.02,0.30)LogMAR,均较框架眼镜矫正视力0.52(0.22,0.76)LogMAR明显改善(P=0.013,P=0.001)。戴镜前,戴镜1周、6个月时,K1分别为(57.70±10.71)D、(58.05±10.90)D和(58.43±11.20)D,K2分别为(63.25±13.17)D、(63.42±13.22)D和(63.24±13.00)D,Kmax分别为(72.60±16.94)D、(72.46±16.47)D和(72.30±16.04)D,TCT分别为410(356,453)μm、416(362,457)μm和400(336,462)μm,CCT分别为(410.55±74.25)μm、(416.93±80.98)μm和(421.31±81.56)μm,眼压分别为(10.38±3.91)mmHg、(10.41±4.63)mmHg和(9.79±4.29)mmHg,CSS分别为0(0,1)、0(0,1)和0(0,1),各指标在各时间点差异均无统计学意义(P均>0.05)。戴镜6个月,ECD为2905(2542,3019.5)个/mm2,较戴镜前2876(2659,3148.5)个/mm2未见明显变化(P=0.691)。戴镜6个月,患者NEI-VFQ-25总评分2175(1925,2450),较配戴前1750(1337.5,2025)明显提升(P=0.001)。结论  本小样本量的6个月观察结果表明,巩膜镜在完成期3级及以下的圆锥角膜患者具有良好的矫正效果及安全性,且配戴巩膜镜在改善圆锥角膜患者视功能同时提升了生活质量。


关键词: 圆锥角膜, 巩膜镜, 矫正效果

Abstract:   Objective  To observe the clinical efficacy of wearing scleral lenses in patients with keratoconus. Design  Retrospective case series. Participants 21 patients (29 eyes) with keratoconus of completion period stage 3 or below and fitted with scleral lenses at the Affiliated Eye Hospital of Nanjing Medical University. Methods All patients underwent a standard fitting procedure for scleral lenses. The fitting status of scleral lenses, as well as the differences in tear film clearance between the lenses and the central and peripheral cornea at 1 week, 1 month, 3 months, and 6 months was observed and compared. Changes in visual acuity, refractive error, corneal parameters, and other indicators were compared between baseline (before wearing glasses), at 1 week, 1 month, 3 months, and 6 months of wearing scleral lenses. Patients completed the NEI-VFQ-25 questionnaire to assess the quality of life and vision of wearing scleral lenses for 6 months. Main Outcome Measures Corrected visual acuity, intraocular pressure (IOP), flat anterior corneal surface refractive power (K1), steep anterior corneal surface refractive power (K2), steepest anterior corneal surface refractive power (Kmax), corneal thinnest point thickness (TCT), center corneal thickness (CCT), corneal staining score (CSS), corneal endothelial cell density (ECD), NEI-VFQ-25 scores, tear film clearance. Results At 6 months of wearing scleral lenses, the tear film clearance in the central, nasal, temporal, upper, and lower regions of the scleral lenses were 221 (177, 274)μm, 98 (68, 133)μm, 138 (81, 213)μm, 145 (95, 190)μm and 360 (289, 478)μm, respectively, there was no significant differences compared to the 240 (184, 282)μm, 98 (62, 121)μm, 120 (95,207)μm, 145 (82,192)μm and 326 (270, 450)μm at 1 week of wearing scleral lenses (all P>0.05). At 1 week and 6 months of wearing scleral lenses, the corrected visual acuity with scleral lenses was 0.30 (0.05, 0.40) LogMAR and 0.22 (0.02, 0.30) LogMAR, respectively, which were significantly improved compared to the corrected visual acuity with frame glasses of 0.52 (0.22, 0.76) LogMAR (P=0.013, P=0.001). Before wearing scleral lenses, at 1 week and 6 months, K1 was (57.70±10.71) D, (58.05±10.90) D and (58.43±11.20) D, K2 was (63.25±13.17) D, (63.42±13.22) D and (63.24±13.00) D, Kmax was (72.60±16.94) D, (72.46±16.47) D and (72.30±16.04) D, TCT was 410 (356, 453)μm, 416 (362, 457)μm and 400 (336, 462)μm, CCT was (410.55±74.25) μm, (416.93±80.98) μm and (421.31±81.56) μm, IOP was (10.38±3.91) mmHg, (10.41±4.63) mmHg and (9.79±4.29) mmHg, CSS was 0 (0,1), 0 (0,1)and 0 (0,1), with no statistically significant differences at each time point (all P>0.05). After wearing scleral lenses for 6 months, the ECD was 2905 (2542, 3019.5) cells/mm2, and there was no significant change compared to 2876 (2659, 3148.5) cells/mm2 before wearing scleral lenses (P=0.691). After wearing scleral lenses for 6 months, the patients'NEI-VFQ-25 score was 2175 (1925, 2450), which was significantly higher than 1750 (1337.5, 2025) before wearing scleral lenses (P=0.001). Conclusions The 6-month observation results of this small sample size indicate that scleral lenses have good corrective effects and safety in patients with keratoconus at completion period stage 3 or below, and wearing scleral lenses significantly improves the visual function and quality of life of keratoconus patients.
  

Key words: Keratoconus, Scleral lens, Clinical correction effectiveness