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• W2088888960 abstract "PurposeTo assess the incidence of immunologic corneal graft rejection episodes in a prospective case series of patients treated 4 times a day with topical cyclosporine 0.05%.DesignProspective, single-center, institutional review board–approved study.ParticipantsFifty-two cornea transplant recipients considered low risk for graft rejection.MethodsPrimary indications for transplantation were keratoconus, Fuchs’ dystrophy, or nonherpetic, nonvascularized scars. Subjects completely tapered off prednisolone acetate 1% by 13 weeks after transplantation and used topical cyclosporine 0.05% 4 times a day, beginning either 1 or 10 weeks posttransplant, with use continued until 1 year posttransplant. One subgroup supplemented cyclosporine use with pulsed prednisolone acetate 1% dosing, 4 times a day for 4 days every 6 weeks. The incidence of immunologic corneal graft rejection episodes was compared with that in Fuchs’ and keratoconus historical control subjects, who used topical steroids a median of 7 months after penetrating keratoplasty.Main Outcome MeasureIncidence of immunologic graft rejection episodes.ResultsGraft rejection episodes occurred earlier and with higher incidence in subjects using cyclosporine 0.05% compared with historical control subjects who used steroids for a longer period of time (P<0.0001). Cyclosporine subjects who pulse-dosed prednisolone had a significantly higher incidence of graft rejection compared with those who did not pulse steroids (P = 0.04).ConclusionThe results suggest that 4 times daily dosing with topical cyclosporine 0.05% is not as effective as use of topical prednisolone acetate 1% for prevention of graft rejection episodes in low-risk corneal transplants, and that periodic pulsing with corticosteroids may increase the risk of rejection episodes. To assess the incidence of immunologic corneal graft rejection episodes in a prospective case series of patients treated 4 times a day with topical cyclosporine 0.05%. Prospective, single-center, institutional review board–approved study. Fifty-two cornea transplant recipients considered low risk for graft rejection. Primary indications for transplantation were keratoconus, Fuchs’ dystrophy, or nonherpetic, nonvascularized scars. Subjects completely tapered off prednisolone acetate 1% by 13 weeks after transplantation and used topical cyclosporine 0.05% 4 times a day, beginning either 1 or 10 weeks posttransplant, with use continued until 1 year posttransplant. One subgroup supplemented cyclosporine use with pulsed prednisolone acetate 1% dosing, 4 times a day for 4 days every 6 weeks. The incidence of immunologic corneal graft rejection episodes was compared with that in Fuchs’ and keratoconus historical control subjects, who used topical steroids a median of 7 months after penetrating keratoplasty. Incidence of immunologic graft rejection episodes. Graft rejection episodes occurred earlier and with higher incidence in subjects using cyclosporine 0.05% compared with historical control subjects who used steroids for a longer period of time (P<0.0001). Cyclosporine subjects who pulse-dosed prednisolone had a significantly higher incidence of graft rejection compared with those who did not pulse steroids (P = 0.04). The results suggest that 4 times daily dosing with topical cyclosporine 0.05% is not as effective as use of topical prednisolone acetate 1% for prevention of graft rejection episodes in low-risk corneal transplants, and that periodic pulsing with corticosteroids may increase the risk of rejection episodes." @default.
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• W2088888960 date "2006-10-01" @default.
• W2088888960 modified "2023-10-16" @default.
• W2088888960 title "Efficacy of Topical Cyclosporine 0.05% for Prevention of Cornea Transplant Rejection Episodes" @default.
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• W2088888960 doi "https://doi.org/10.1016/j.ophtha.2006.05.022" @default.
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