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Three Different Protocols of Corneal Collagen Crosslinking in Keratoconus: Conventional, Accelerated and Iontophoresis
Published on: November 12, 2015
Definitions for Keratoconus Progression and Their Impact on Clinical Practice
Carina Koppen1, Marta Jiménez-García, Elke O Kreps
1Department of Ophthalmology (C.K., M.J.-G., S.N.D., J.J.R.), Antwerp University Hospital (UZA), Edegem, Belgium; Department of Medicine and Health Sciences (C.K., M.J.-G., S.N.D., J.J.R.), University of Antwerp, Antwerp, Belgium; Department of Ophthalmology (E.O.K.), Ghent University Hospital (UZA), Edegem, Belgium; and Department of Medicine and Health Sciences (E.O.K.), University of Ghent, Ghent, Belgium.
Defining keratoconus progression accurately is crucial to avoid overtreatment. Combining multiple diagnostic variables or using wider margins for the ABCD progression display improves consistency and aligns progression rates with clinical observations.
Area of Science:
- Ophthalmology
- Corneal Diseases
- Vision Science
Background:
- Keratoconus (KC) progression criteria lack consensus, leading to potential overtreatment.
- Establishing reliable methods to identify progressive KC is essential for appropriate patient management.
Purpose of the Study:
- To evaluate the performance of various keratoconus progression criteria.
- To compare these criteria against established clinical knowledge of KC evolution.
Main Methods:
- Retrospective analysis of 906 keratoconus patients' data.
- Assessed progression criteria based on keratometry (K MAX), front astigmatism (A F), pachymetry (P MIN), and ABCD progression display.
- Evaluated individual and population consistency of progression detection.
Main Results:
- Single progression criteria yielded high rates of eyes flagged as progressive (R PROG).
- Combining K MAX and P MIN showed better population consistency than K MAX and A F.
- Alternative criteria (K 2F and R mB) demonstrated superior consistency and lower variability.
- Adjusting the ABCD display with wider confidence intervals reduced R PROG to 27.9%.
Conclusions:
- Current progression criteria may lead to overtreatment due to high R PROG values.
- Combining variables or widening margins in progression displays improves consistency.
- Revised criteria bring R PROG closer to observed clinical progression rates (20-30%).
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