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Updated: May 11, 2026

Three Different Protocols of Corneal Collagen Crosslinking in Keratoconus: Conventional, Accelerated and Iontophoresis
Published on: November 12, 2015
Early confocal microscopy findings after cross-linking treatment
M Ramírez1, E Hernández-Quintela, R Naranjo-Tackman
1Servicio de Córnea y Cirugía Refractiva, Asociación para Evitar la Ceguera en México, Hospital Luis Sánchez Bulnes, Universidad Nacional Autónoma de México, Mexico City, Mexico. mramirezf@medicasur.org.mx
Corneal cross-linking treatment in keratoconus patients showed stromal changes, including activated keratocytes and organized collagen fibers, visible with confocal microscopy up to 300 μm deep.
Area of Science:
- Ophthalmology
- Corneal Science
- Biomedical Engineering
Background:
- Keratoconus is a progressive corneal ectasia.
- Corneal cross-linking (CXL) aims to strengthen the cornea.
- Understanding CXL's in vivo effects is crucial for treatment optimization.
Purpose of the Study:
- To evaluate the in vivo effects of corneal cross-linking treatment.
- To assess changes in corneal stromal depth and cellular activity post-CXL.
Main Methods:
- Corneal cross-linking performed on 18 eyes using riboflavin and UVA radiation.
- In vivo confocal microscopy used for imaging before and after treatment (1 week, 1 month).
Main Results:
- Keratocyte activation and collagen fiber organization observed as hyper-reflective structures.
- Changes noted from the sub-epithelial layer to stromal depths of 275.1 ± 85.9 μm at 1 week.
- At 1 month, changes extended to 324.9 ± 66.0 μm, with deeper linear hyper-reflective structures.
Conclusions:
- In vivo confocal microscopy revealed corneal stromal changes following CXL treatment in humans.
- These changes, including cellular activation and fiber organization, occurred at depths exceeding 300 μm in some cases.
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