Beckman Kenneth A
Comprehensive EyeCare of Central Ohio, Westerville, OH, USA.
The Ohio State University, Columbus, OH, USA.
Clin Ophthalmol. 2021 Jul 7;15:2921-2932. doi: 10.2147/OPTH.S318317. eCollection 2021.
Epithelium-off cross-linking (epi-off CXL) has long been established as the gold standard treatment for progressive keratoconus. Several protocols for epithelium-on (epi-on) CXL have been proposed to help reduce post-operative pain and facilitate visual recovery, but there is no epi-on treatment approach that is currently approved in the United States. The hydrophilic and macromolecular characteristics of conventional epi-off riboflavin formulations may create clinical challenges for absorption through an intact epithelium. This study investigates the clinical efficacy of a dextran-free hypotonic riboflavin ophthalmic solution (Photrexa, Glaukos, Burlington, MA, USA), approved for epi-off CXL, in a novel epi-on CXL protocol.
Twenty-five eyes of 17 patients were treated in this prospective, single-arm study using a hypotonic riboflavin formulation without dextran and low irradiance UVA (3mW/cm) for epi-on CXL. Visual acuity, as well as refractive and keratometry outcomes, were observed over 12 months.
At 12 months, Kmax was stable with no clinically or statistically significant change from a mean pre-op of 55.4D to 55.9D (p=0.13). Uncorrected and best corrected logMAR visual acuity significantly improved from 0.77 to 0.62 and from 0.17 to 0.12, respectively. There were no significant adverse safety events.
Patients who underwent epi-on CXL with dextran-free hypotonic riboflavin demonstrated improvements in uncorrected and best corrected visual acuity with stable keratometry at 12 months post-operatively. The efficacy is consistent with other epi-on studies to date but remains lower than standard epi-off CXL. New technologies, including supplemental oxygen and transepithelial riboflavin ophthalmic solutions, are currently under clinical evaluation and may offer a path forward for epi-on CXL in the USA.
长期以来,上皮去除交联术(epi-off CXL)一直是进行性圆锥角膜的金标准治疗方法。已经提出了几种上皮在位(epi-on)CXL方案,以帮助减轻术后疼痛并促进视力恢复,但目前美国尚未批准任何epi-on治疗方法。传统的epi-off核黄素制剂的亲水性和大分子特性可能给通过完整上皮的吸收带来临床挑战。本研究调查了一种无右旋糖酐的低渗核黄素滴眼液(Photrexa,Glaukos,美国马萨诸塞州伯灵顿)在一种新型epi-on CXL方案中的临床疗效,该滴眼液已被批准用于epi-off CXL。
在这项前瞻性单臂研究中,使用不含右旋糖酐的低渗核黄素制剂和低辐照度UVA(3mW/cm)对17例患者的25只眼进行epi-on CXL治疗。在12个月内观察视力以及屈光和角膜曲率测量结果。
在12个月时,最大角膜曲率(Kmax)稳定,从术前平均55.4D至55.9D无临床或统计学上的显著变化(p = 0.13)。未矫正和最佳矫正logMAR视力分别从0.77显著提高到0.62和从0.17提高到0.12。没有显著不良安全事件。
接受无右旋糖酐低渗核黄素epi-on CXL治疗的患者在术后12个月时未矫正和最佳矫正视力均有改善,角膜曲率测量结果稳定。其疗效与迄今为止的其他epi-on研究一致,但仍低于标准的epi-off CXL。包括补充氧气和经上皮核黄素滴眼液在内的新技术目前正在临床评估中,可能为美国的epi-on CXL提供一条前进的道路。