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Updated: Dec 10, 2025

Three Different Protocols of Corneal Collagen Crosslinking in Keratoconus: Conventional, Accelerated and Iontophoresis
Published on: November 12, 2015
Transepithelial Accelerated Corneal Collagen Cross-Linking: Two-Year Results
Ana Maria Cunha1, Tiago Sardinha2, Luís Torrão1
1Department of Ophthalmology, Centro Hospitalar De São João, Porto, Portugal.
Trans-epithelial accelerated corneal collagen crosslinking (TE-ACXL) is a safe and effective treatment for progressive keratoconus over two years. While some patients experienced disease progression, the procedure showed no significant adverse effects.
Area of Science:
- Ophthalmology
- Corneal Surgery
- Vision Science
Background:
- Keratoconus is a progressive corneal ectasia leading to vision impairment.
- Corneal collagen crosslinking (CXL) aims to strengthen the cornea and halt progression.
- Trans-epithelial accelerated corneal collagen crosslinking (TE-ACXL) offers a less invasive alternative.
Purpose of the Study:
- To evaluate the 2-year outcomes of the TE-ACXL procedure in patients with progressive keratoconus.
- To assess the safety and efficacy of TE-ACXL in halting keratoconus progression.
Main Methods:
- A retrospective interventional study included 24 eyes from 24 patients undergoing TE-ACXL.
- Outcome measures included best-corrected visual acuity (BCVA), keratometry, thinnest corneal thickness (PachyMin), and topometric indices.
- Data were analyzed preoperatively and at 6, 12, 18, and 24 months postoperatively.
Main Results:
- No intraoperative or postoperative complications were reported.
- No statistically significant changes were observed in BCVA, Kmax, astigmatism, PachyMin, or various topometric indices at 12 or 24 months.
- Disease progression occurred in 11-33% of patients by 24 months, based on defined progression criteria.
Conclusions:
- TE-ACXL appears to be a safe and effective treatment for keratoconus over a 2-year follow-up.
- Despite its overall efficacy, some patients may still experience disease progression.
- Further research with longer follow-up periods and larger patient cohorts is recommended.
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