Department of Ophthalmology, Ankara University Faculty of Medicine, Ankara, Turkey.
Department of Ophthalmology, Ankara University Faculty of Medicine, Mamak caddesi, Cebeci, 06340, Ankara, Turkey.
Graefes Arch Clin Exp Ophthalmol. 2022 Apr;260(4):1225-1235. doi: 10.1007/s00417-021-05314-w. Epub 2021 Nov 27.
To evaluate the long-term visual, refractive, tomographic, and aberrometric outcomes of corneal collagen crosslinking (CXL) with or without hypoosmolar riboflavin solution in the treatment of progressive keratoconus patients with thin corneas.
Charts of consecutive progressive keratoconus patients with thinnest corneal thickness less than 470 µm who underwent corneal collagen CXL with or without hypoosmolar riboflavin solution and using a standardized protocol for treatment and examinations were analyzed retrospectively. The indication for hypoosmolar riboflavin use was a central corneal thickness less than 400 µm as measured by ultrasound pachymetry after epithelial debridement and before exposure to ultraviolet A (UVA) light. Uncorrected distance visual acuity (UDVA), best spectacle-corrected distance visual acuity (CDVA), manifest refraction, slit lamp biomicroscopy, corneal tomography, corneal aberrometry, and endothelial cell counts were evaluated at baseline and yearly at all postoperative follow-up examinations until month 36. The outcomes of corneal CXL procedure performed using hypoosmolar riboflavin were compared to those performed using the standard procedure.
Twenty-three eyes (19 patients) were treated using hypoosmolar riboflavin application, and 30 eyes (28 patients) were treated using the standard procedure. Compared to baseline, the mean UDVA, CDVA, and keratometric readings improved statistically significantly in both groups at postoperative year 3, without any statistically significant between-group differences. Progression was not observed in any patient eye in either group. No significant endothelial cell loss and no sight threating complication were observed in any patient eye.
At 3 years follow-up, the safety and efficacy of CXL using hypoosmolar riboflavin solution seems to be similar to that of standard CXL in progressive keratoconic eyes with thin corneas. The visual, refractive, keratometric, tomographic and aberrometric outcomes of the two procedures were comparable, as well.
评估角膜胶原交联术(CXL)联合或不联合低渗核黄素溶液治疗薄角膜进行性圆锥角膜患者的长期视力、屈光、断层扫描和像差结果。
回顾性分析了连续进行性圆锥角膜患者的图表,这些患者的最薄角膜厚度小于 470μm,他们接受了角膜胶原 CXL 联合或不联合低渗核黄素溶液治疗,并使用标准化的治疗和检查方案。低渗核黄素的使用指征为上皮清创后和暴露于紫外线 A(UVA)光之前超声角膜测厚仪测量的中央角膜厚度小于 400μm。在所有术后随访检查中,在基线和每年评估未矫正距离视力(UDVA)、最佳矫正距离视力(CDVA)、验光、裂隙灯生物显微镜、角膜断层扫描、角膜像差和内皮细胞计数,直至 36 个月。比较了使用低渗核黄素进行的 CXL 程序的结果与使用标准程序进行的结果。
23 只眼(19 名患者)接受了低渗核黄素应用治疗,30 只眼(28 名患者)接受了标准治疗。与基线相比,两组患者在术后 3 年时的平均 UDVA、CDVA 和角膜曲率读数均有统计学显著改善,两组间无统计学显著差异。在两组患者中均未观察到任何患眼进展。在任何患者眼中均未观察到明显的内皮细胞丢失和视力威胁性并发症。
在 3 年随访时,使用低渗核黄素溶液的 CXL 的安全性和有效性似乎与薄角膜进行性圆锥角膜眼中的标准 CXL 相似。两种手术的视力、屈光、角膜曲率、断层扫描和像差结果也相当。