圆锥角膜合并角膜缘干细胞缺乏症患者胶原交联的疗效。

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI:10.2147/OPTH.S548579
Rashmi Deshmukh, Eeshita Agarwal, Swapna Shanbhag, Rasik B Vajpayee
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引用次数: 0

摘要

目的:分析角膜结膜炎(VKC)致进行性圆锥角膜(KC)伴继发性角膜缘干细胞缺乏症(LSCD)的胶原交联(CXL)治疗效果。方法:纳入2016年5月至2023年10月行CXL的进行性KC和VKC合并LSCD患者。术前、术后1个月、3个月、6个月和1年分别收集人口统计资料、临床资料和角膜地形图资料。记录了CXL手术的细节和术后早期并发症。观察患者1年时的未矫正视力(UCVA)、最佳矫正视力(BCVA)和地形指标,包括最平坦角膜度数(K1)、最陡峭角膜度数(K2)、平均角膜度数(Km)、最大角膜度数(Kmax)和最薄角膜厚度(TCT),并与术前进行比较。结果:11例患者15只眼纳入研究。部分LSCD有14只眼接受了上皮外移植,全LSCD有1只眼接受了上皮外移植。cxl前UCVA最小分辨角(logMAR)的平均对数为0.67±0.38,cxl后6个月为0.54±0.32 (p=0.05), 1年后为0.65±0.35 logMAR (p= 0.005)。cxl前Km为53.5±4.77(中位51.95 d), 6个月时为51.72±3.65 (p=0.014), 1年时为52.34±3.83(中位51.95 d) (p=0.09)。Kmax从cxl前的63.41±7.11(中位63.7 d)降至6个月时的60.65±5.31(中位59.6)(p=0.05), cxl后1年的61.4±6.01(中位61.9 d) (p=0.115)。在14只眼中,2只眼(14.28%)存在持续性上皮缺损(PEDs),其中1只眼需要羊膜移植(AMG)。结论:在我们的研究中,大多数圆锥角膜合并LSCD的眼睛在cxl后没有复杂的眼表愈合,并在1年内保持稳定,视力显著改善。我们的研究表明,在圆锥角膜合并LSCD的病例中,CXL可以成功地进行,没有任何严重的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Outcomes of Collagen Crosslinking in Patients with Keratoconus and Co-Existent Limbal Stem Cell Deficiency.

Outcomes of Collagen Crosslinking in Patients with Keratoconus and Co-Existent Limbal Stem Cell Deficiency.

Outcomes of Collagen Crosslinking in Patients with Keratoconus and Co-Existent Limbal Stem Cell Deficiency.

Purpose: To analyse the outcomes of collagen crosslinking (CXL) in eyes with progressive keratoconus (KC) and secondary limbal stem cell deficiency (LSCD) caused by vernal keratoconjunctivitis (VKC).

Methods: Patients with progressive KC and VKC having co-existent LSCD who underwent CXL from May 2016 to October 2023 were included. Demographic details, clinical and corneal topography data were collected preoperatively, at 1-months, 3-months, 6-months and 1-year. Details of the CXL procedure and early postoperative complications were noted. Uncorrected visual acuity (UCVA), best-corrected visual acuity (BCVA) and topographic indices including flattest keratometry (K1), steepest keratometry (K2), mean keratometry (Km), maximum keratometry (Kmax) and thinnest corneal thickness (TCT) were noted at 1-year and compared with the preoperative data.

Results: Fifteen eyes of 11 patients were included in the study. Partial LSCD was present in 14 eyes and underwent epithelium-off CXL and 1 eye with total LSCD underwent transepithelial CXL. The mean logarithm of the minimum angle of resolution (logMAR) UCVA pre-CXL was 0.67±0.38 which improved to 0.54±0.32 at 6-months (p=0.05) and 0.65±0.35 logMAR at 1-year post-CXL (p = 0.005). Pre-CXL Km was 53.5±4.77 (median-51.95D) which decreased to post-cxl value of 51.72±3.65 at 6-months (p=0.014) and 52.34±3.83 (median-51.3D) at 1-year (p=0.09). Kmax reduced from 63.41±7.11 (median-63.7D) pre-CXL to 60.65±5.31 (median-59.6) (p=0.05) at 6-months and 61.4±6.01 (median-61.9D) at 1-year post-CXL (p=0.115). Of the 14 eyes that underwent epi-off CXL, 2 eyes (14.28%) had persistent epithelial defects (PEDs), one of which needed amniotic membrane graft (AMG).

Conclusion: In our series, most eyes with keratoconus having co-existent LSCD had uncomplicated ocular surface healing post-CXL and remained stable at 1-year with significant improvement in visual acuity. Our study shows that CXL can be successfully performed in cases of Keratoconus with co-existing LSCD without any serious complications.

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