Abstract

Purpose. Keratolimbal allograft (KLAL) is a treatment for limbal stem cell deficiency. One disadvantage is systemic immunosuppression to avoid rejection. Our purpose was to examine the adverse effects of systemic immunosuppression in KLAL. Methods. A retrospective case review of 16 patients with KLAL who received systemic immunosuppression consisting of a corticosteroid, an antimetabolite, and/or a calcineurin inhibitor was performed. Patients were monitored for signs, symptoms, or laboratory evidence of toxicity. Results. Eleven of 16 patients (68%) experienced an adverse effect. The average age of those with adverse effects was 43.5 years and without was 31.4 years. Ten of 11 patients (91%) had resolution during mean followup of 16.4 months. No serious adverse effects occurred. The most common included anemia, hyperglycemia, elevated creatinine, and elevated liver function tests. Prednisone and tacrolimus were responsible for the most adverse effects. Patients with comorbidities were more likely to experience an adverse effect (82% versus 20%, P = 0.036). Conclusions. KLAL requires prolonged systemic immunosuppression. Our data demonstrated that systemic immunosuppression did not result in serious adverse effects in our population and is relatively safe with monitoring for toxicity. In addition, we demonstrated that adverse effects are more likely in older patients with comorbidities.

Highlights

  • Limbal stem cell deficiency can develop following destruction of the limbal epithelial stem cells, or in conditions that impair the development or differentiation of the limbal stem cells

  • In one series of aniridia patients treated with Keratolimbal allograft (KLAL), the success rate was 90% in patients receiving systemic immunosuppression compared to 40% in patients treated with only topical immunosuppression [2]

  • A retrospective case review was conducted on 16 patients (19 eyes) with documented limbal stem cell deficiency that underwent keratolimbal allograft at the University of Illinois at Chicago Medical Center (UIMC) between January 2006 and June 2009

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Summary

Introduction

Limbal stem cell deficiency can develop following destruction of the limbal epithelial stem cells (e.g., chemical injury), or in conditions that impair the development or differentiation of the limbal stem cells (e.g., aniridia). In limbal stem cell deficiency, the cornea becomes covered by ingrowing conjunctival epithelium leading to recurrent epithelial breakdown, neovascularization, and scarring with subsequent loss of vision. Limbal stem cell transplantation is currently the main surgical treatment for visually disabling, total limbal stem cell deficiency. Keratolimbal allograft (KLAL) is the surgical procedure of transplanting cadaveric limbal grafts for patients with bilateral limbal stem cell deficiency, with a reported success rate of around 73% at 5 years [1]. In one series of aniridia patients treated with KLAL, the success rate was 90% in patients receiving systemic immunosuppression compared to 40% in patients treated with only topical immunosuppression [2]

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