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. 1998 Jan;82(1):18–25. doi: 10.1136/bjo.82.1.18

Clinical results of implantation of the Chirila keratoprosthesis in rabbits

C Hicks 1, T Chirila 1, A Clayton 1, J Fitton 1, S Vijayasekaran 1, P Dalton 1, X Lou 1, S Platten 1, B Ziegelaar 1, Y Hong 1, G Crawford 1, I Constable 1
PMCID: PMC1722337  PMID: 9536874

Abstract

AIMS/BACKGROUND—An ideal keratoprosthesis (KPro) would closely resemble a donor corneal button in terms of its surgical handling, optics, and capacity to heal with host tissue in order to avoid many of the complications associated with the KPros which are currently in clinical use. This study was carried out to assess the long term clinical outcomes on implantation of the core and skirt poly(2-hydroxyethyl methacrylate) KPro in animals.
METHODS—20 KPros were made and implanted as full thickness corneal replacements into rabbits and followed for up to 21 months to date.
RESULTS—80% of the prostheses have been retained, with a low incidence of complications such as cataract, glaucoma, and retroprosthetic membrane formation which are frequently associated with KPro surgery.
CONCLUSIONS—KPros of this type may offer promise in the treatment of patients for whom penetrating keratoplasty with donor material carries a poor prognosis. Refinement of the KPro and further animal trials, including implantation into abnormal corneas, are however mandatory before human implantation could be planned.

 Keywords: complications; keratoprosthesis; optics; PHEMA

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Figure 1  .

Figure 1  

The Chirila KPro.

Figure 2  .

Figure 2  

Peroperative appearance (rabbit D3) during formation of the conjunctival flap.

Figure 3  .

Figure 3  

Postoperative appearance (rabbit D6) at 6 months.

Figure 4  .

Figure 4  

Histological section stained with toluidine blue of the skirt of the KPro removed 2 months after implantation in rabbit D4, showing fibroblasts (× 400).

Figure 5  .

Figure 5  

Histological section of the skirt of the KPro removed 5 months after implantation in rabbit M1, stained with 2% alizarin red; specks of calcium can be seen (× 100).

Figure 6  .

Figure 6  

(a) Histological section of a PHEMA gel in which pores can be seen (× 400). (b) Photograph of a whole mount preparation of a PHEMA gel after 1 week in an in vitro calcifying solution, stained with 2% Alizarin red and destained with acetone to demonstrate calcium deposition within a pore in the gel (× 400).

Figure 7  .

Figure 7  

Rabbit corneal epithelial cell outgrowth from a donor button onto a PHEMA sponge specimen in vitro (a) in section, stained with toluidine blue (×200) and (b) surface view (arrow indicates the edge of the advancing sheet of cells).

Selected References

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