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Three Different Protocols of Corneal Collagen Crosslinking in Keratoconus: Conventional, Accelerated and Iontophoresis
Published on: November 12, 2015
Outcome indicators for cross linking in pediatric keratoconus
Denise Wajnsztajn1, Or Shmueli1, Yehuda Tarnovsky1
1Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Insights
Corneal collagen cross-linking (CXL) effectively treats pediatric keratoconus (KC). Non-accelerated CXL showed better outcomes, particularly for corneas with advanced disease, indicating its efficacy in improving visual acuity and corneal shape.
Area of Science:
- Ophthalmology
- Corneal Surgery
- Pediatric Eye Care
Background:
- Keratoconus (KC) is a progressive corneal ectasia affecting pediatric patients.
- Corneal collagen cross-linking (CXL) is a standard treatment to halt KC progression.
- Predictive factors for CXL success in pediatric KC require further elucidation.
Purpose of the Study:
- To identify predictive factors for successful corneal collagen cross-linking (CXL) in pediatric patients diagnosed with keratoconus (KC).
- To analyze the impact of various clinical and treatment parameters on CXL outcomes in children.
Main Methods:
- Retrospective analysis of a prospectively built database of pediatric KC patients (≤18 years) undergoing CXL.
- Evaluation of outcomes including changes in maximal corneal power (Kmax) and LogMAR visual acuity.
- Statistical analysis of factors such as CXL type, age, sex, ocular allergy, ethnicity, preoperative visual acuity, corneal power, pachymetry, and follow-up duration.
Main Results:
- Corneal collagen cross-linking (CXL) demonstrated significant improvement in Kmax and LogMAR visual acuity in pediatric KC patients.
- Univariate analysis indicated that longer follow-up, lower preoperative central corneal thickness, higher preoperative Kmax, higher preoperative LogMAR visual acuity, and non-accelerated CXL were associated with corneal flattening.
- Multivariate analysis identified higher preoperative Kmax and non-accelerated CXL as significant predictors of corneal flattening.
Conclusions:
- Corneal collagen cross-linking (CXL) is an effective therapeutic option for pediatric keratoconus (KC).
- Non-accelerated CXL appears to be more effective than accelerated CXL in this pediatric cohort.
- Corneas with more advanced disease stages may exhibit a more pronounced positive response to CXL treatment.
Purpose:
To evaluate the predictive factors for successful corneal collagen cross-linking (CXL) in pediatric patients with Keratoconus (KC).
Methods:
This retrospective study was conducted using a prospectively built database. Patients (18 years old or younger) underwent CXL for KC between 2007 and 2017, with a 1-year follow-up period or longer. The outcomes included changes in Kmax (delta [Δ] Kmax = Kmaxlast - Kmaxpre) and LogMAR visual acuity (ΔLogMAR = LogMARlast - LogMARpre).The effects of CXL type (accelerated or non-accelerated), demographics (age, sex, background of ocular allergy, ethnicity), preoperative LogMAR visual acuity, maximal corneal power (Kmax), pachymetry (CCTpre), refractive cylinder, and follow-up (FU) time on the outcomes were analyzed.
Results:
One hundred thirty-one eyes of 110 children were included (mean age, 16 ± 2 years; range, 10-18 years). Kmax and LogMAR improved from baseline to last visit: from 53.81 D ± 6.39 D to 52.31 D ± 6.06 D (p < 0.001) and from 0.27 ± 0.23 LogMAR units to 0.23 ± 0.19 LogMAR units (p = 0.005), respectively. A negative ΔKmax (meaning corneal flattening) was associated with a long FU, low CCTpre, high Kmaxpre, high LogMARpre, and non-accelerated CXL on univariate analysis. High Kmaxpre and non-accelerated CXL were associated with negative ΔKmax in the multivariate analysis.A negative ΔLogMAR (meaning vision improvement) was associated with a high LogMARpre in univariate analysis.
Conclusion:
CXL is an effective treatment option in pediatric patients with KC. Our results showed that the non-accelerated treatment was more effective than the accelerated treatment. Corneas with advanced disease had a greater effect on CXL.
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