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  Vol. 122 No. 12, December 2004 TABLE OF CONTENTS
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Biological Response to a SupraDescemetic Synthetic Cornea in Rabbits

Josef Stoiber, MD; Viviana Fernandez, MD; Stephan Kaminski, MD; Peggy D. Lamar, BS; Sander Dubovy, MD; Eduardo Alfonso, MD; Jean-Marie Parel, PhD

Arch Ophthalmol. 2004;122:1850-1855.

Objective  To evaluate the biocompatibility of a novel nonpenetrating keratoprosthesis (supraDescemetic synthetic cornea) in a rabbit model.

Methods  Seven rabbits received a supraDescemetic synthetic cornea (7-mm diameter, 350-µm-thick optical zone, 100-µm-thick peripheral flange) in their healthy right eyes. A surgical technique was developed that allowed implantation of the device on top of the bare Descemet membrane. Three rabbits received a supraDescemetic synthetic cornea made of hydroxyethyl methacrylate–methyl methacrylate26, 1 received a hydroxyethyl methacrylate–N-vinyl pyrrolidone75 mesoplant, and 3 were implanted with devices made of polymethyl methacrylate. All rabbits were euthanized after 8 weeks; the eyes were enucleated and examined by conventional histological and immunohistochemical evaluations.

Results  All eyes became quiet within several days. The Descemet membrane remained transparent during the observation period. Indirect ophthalmoscopy performed through the prosthesis allowed accurate examination of the posterior pole. Histological evaluation of the implanted corneas displayed no signs of an acute or chronic inflammatory reaction to the supraDescemetic synthetic cornea in 5 eyes; a few inflammatory cells were detected in the corneas of 2 rabbits. The interface between the Descemet membrane and the mesoplant displayed ingrowth of very thin (<10-µm) tissues colonized by keratocytes in 3 of the 7 corneas.

Conclusions  This study validates the biocompatibility of this new type of nonpenetrating keratoprosthesis. Because opening of the anterior chamber is not required with the supraDescemetic synthetic cornea, the risk for intraocular infection is minimal, and the implantation procedure is less traumatic compared with a penetrating device.


Author Affiliations: Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Fla (Drs Stoiber, Fernandez, Dubovy, Alfonso, and Parel and Ms Lamar); Department of Ophthalmology and Optometry, Paracelsus Private Medical University, Salzburg, Austria (Dr Stoiber); and Department of Ophthalmology and Optometry, University of Vienna, Vienna, Austria (Dr Kaminski).



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