Keratoprosthesis (artificial cornea) Transplantation

 

An artificial corneal transplant (keratoprosthesis) is a procedure that is typically performed for patients who have had two or more traditional corneal transplants that have failed.  Patients with a history of previous corneal transplant failure often require systemic immunosuppression for a year or longer to decrease the risk of repeat transplant failure, with all of the risks associated with the use of these medications.  Additionally, patients with corneal limbal stem cell failure will also require systemic immunosuppresion for a year or longer if living related or cadaveric donor stem cell transplantation is performed.  Even with the use of systemic immunosuppression, the rate of corneal transplant rejection and failure is high.  Thus, the avoidance of the need for immunosuppression and the increased chance of restoring long term visual clarity for these patients with a keratoprosthesis versus a repeat corneal transplant makes the keratoprosthesis a better, safer option for these patients.

 

Two artificial corneas have been approved for implantation by the US Food and Drug Administration, the Boston (Dohlman-Doane)  Keratoprosthesis (http://www.meei.harvard.edu/shared/ophtho/cornea2.php) and the AlphaCor Keratoprosthesis (http://www.alphacor-ati.com/AlphaCor/AlphaCor.html).  Dr. Aldave performed one of the first AlphaCor keratoprothesis surgeries in the United States in May 2003, and has given courses on implantation of both the Boston and the AlphaCor keratoprostheses at local and national meetings. 

 

  Many of the risks associated with Boston keratoprosthesis implantation are the same as those associated with corneal transplantation (infection in the eye, glaucoma), while some are avoided (corneal transplant rejection and failure and the risks associated with systemic immunosuppression) and others are unique to keratoprostheses (membrane development behind the optic of the keratoprosthesis, wound leak associated with melting of corneal tissue adjacent to the stem of the keratoprosthesis).  As the incidence of intraocular infection and corneal melting has decreased dramatically over the last several years with the use of daily antibiotic drops and modifications in the design of the keratoprosthesis, respectively, these are no longer considered common causes of vision loss after keratoprosthesis implantation.  Additionally, as membrane development behind the optic of the keratoprosthesis can usually be treated easily with an in-office laser treatment, these do not represent an irreversible cause of vision loss.  Glaucoma does, however, and thus the majority of patients undergoing keratoprosthesis implantation are having glaucoma surgery performed at the same time, if not performed previously. 

 

 

 

Photograph of patient two months after implantation of

the Boston type I keratoprosthesis

 

 

 

JSEI Specialists

Anthony J. Aldave, MD

Sophie Deng, MD, PhD