April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
Surface Epithelialization of the Type I Boston Keratoprosthesis Front Plate
Author Affiliations & Notes
  • Lee Kiang
    Ophthalmology,
    The Margaret M. Dyson Vision Research Institute,
    Weill Cornell Medical College, New York, New York
  • Mark I. Rosenblatt
    Ophthalmology,
    The Margaret M. Dyson Vision Research Institute,
    Weill Cornell Medical College, New York, New York
  • Rachel Sartaj
    The Margaret M. Dyson Vision Research Institute,
    Weill Cornell Medical College, New York, New York
  • Donald J. D'Amico
    Ophthalmology,
    Weill Cornell Medical College, New York, New York
  • Kimberly C. Sippel
    Ophthalmology,
    Weill Cornell Medical College, New York, New York
  • Footnotes
    Commercial Relationships  Lee Kiang, None; Mark I. Rosenblatt, None; Rachel Sartaj, None; Donald J. D'Amico, None; Kimberly C. Sippel, None
  • Footnotes
    Support  This work was supported in part by an unrestricted departmental grant from Research to Prevent Blindness. LK was supported by NIH MSTP grant GM07739.
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 344. doi:
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    • Get Citation

      Lee Kiang, Mark I. Rosenblatt, Rachel Sartaj, Donald J. D'Amico, Kimberly C. Sippel; Surface Epithelialization of the Type I Boston Keratoprosthesis Front Plate. Invest. Ophthalmol. Vis. Sci. 2011;52(14):344.

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

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Abstract

Purpose: : To investigate whether a transparent tissue layer partially covering the anterior surface of the Boston type I Keratoprosthesis front plate in four patients represents bona fide epithelium. Presence of this tissue could signify biointegration of these sight saving devices whose use has historically been complicated by infection and tissue necrosis.

Methods: : In two cases, the tissue over the front plate was easily scrolled back as a single transparent layer using a sponge. This was removed several times and each time regrew in the same configuration within one month. Visual acuity was unchanged after removal. Microscopic analysis was undertaken and immunofluorescent staining against cytokeratin 3, specific to corneal epithelium in the eye, was performed.

Results: : Microscopic analysis of samples from two patients revealed the tissue to be multi-layered, non-keratinized squamous epithelium. No goblet cells were seen, suggesting the cells were of corneal, and not conjunctival, epithelial origin. Immunofluorescent staining of all cells was positive for cytokeratin 3, signifying corneal epithelium.

Conclusions: : The demonstration of the growth of regenerating, multi-layered, non-keratinized squamous corneal epithelium on the keratoprosthesis front plate represents a novel aspect of biointegration with potential ramifications for clinical outcomes. A device over which there is an intact epithelial layer would be expected to decrease the risk of endophthalmitis and tissue necrosis associated with permanent keratoprosthesis. Advances in keratoprosthesis composition, design, and surface modifications may be used to elucidate the surface epithelialization mechanism and to accelerate this process to improve outcomes.

Keywords: keratoprostheses • cornea: epithelium • cornea: clinical science 
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