April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Cross-Linking in Keratoconus: Early Changes by Confocal Microscopy
Author Affiliations & Notes
  • R. Cuiña Sardiña
    Ophthalmology, Hospital Clinico San Carlos, Madrid, Spain
  • M. Iradier
    Ophthalmology, Hospital Clinico San Carlos, Madrid, Spain
  • D. Diaz-Valle
    Ophthalmology, Hospital Clinico San Carlos, Madrid, Spain
  • R. Mendez
    Ophthalmology, Hospital Clinico San Carlos, Madrid, Spain
  • P. Arriola
    Ophthalmology, Hospital Clinico San Carlos, Madrid, Spain
  • J. M. Benitez-del-Castillo
    Ophthalmology, Hospital Clinico San Carlos, Madrid, Spain
  • Footnotes
    Commercial Relationships  R. Cuiña Sardiña, None; M. Iradier, None; D. Diaz-Valle, None; R. Mendez, None; P. Arriola, None; J.M. Benitez-del-Castillo, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 5465. doi:
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      R. Cuiña Sardiña, M. Iradier, D. Diaz-Valle, R. Mendez, P. Arriola, J. M. Benitez-del-Castillo; Cross-Linking in Keratoconus: Early Changes by Confocal Microscopy. Invest. Ophthalmol. Vis. Sci. 2009;50(13):5465.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Confocal microscopy permits an in vivo ultrastructural analysis of the cornea. The purpose of this study was to evaluate keratoconic corneas after cross-linking by confocal microscopy in the early postoperative period.

Methods: : We examine five keratoconic corneas using the Heidelberg HRT II with the Rostock module. After the application of a topical anesthesia, mechanical scraping of the epithelium was performed. Preirradiation the cornea was soaked in rivoflavin solution 0.1% (Ricrolin, Italy) every 2.5 minutes for 30 minutes. The corneas were exposed for 30 minutes to UVA radiation (3mW/cm2). Corneas were examined before and one, two, four, twelve and twenty-four weeks after cross-linking.

Results: : An increase in epithelial stratification was observed and all the epithelial cells appeared nucleated one week after treatment. Anterior stroma keratocytes were activated. A clear delimitation line between the middle stroma and the posterior stroma was observed. The endothelium was normal. Epithelial cells started to normalized after two weeks, nevertheless intra and subepithelial nerves were not present until three months after surgery when stromal fibrosis appeared.

Conclusions: : Confocal microscopy is a useful technique for evaluating ultrastructural changes after corneal cross-linking.

Keywords: keratoconus • imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • cornea: clinical science 
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