摘要
PURPOSE: To report the feasibility and safety profile of 2-mg and 6-mg fluoc inolone acetonide implants after longterm follow-up in eyes with choroidal neov ascularization (CNV)DESIGN: Prospective, noncomparative, interventional case ser ies of patients with non-age-related subfoveal choroidal neovascularization en rolled in a compassionate use protocol METHODS: Sustained drug delivery devices containing either 2 mg (eight eyes) or 6 mg (six eyes) of fluocinolone acetonide were implanted through the pars plana into the vitreous cavity of 14 patients w ith predominantly classic, subfoveal CNV. The main outcome measures were complic ations related to the device. Secondary outcome measures were involution of esta blished CNV, inhibition of recurrent CNV, and visual acuity RESULTS: Patients ha d a diagnosis of ocular histoplasmosis (seven), myopic degeneration (four), angi oid streaks (two), and punctate inner choroidopathy (one). Patients were followe d for an average of 33 months (range, 16 to 40 months). All 14 eyes developed el evated intraocular pressure and cataract. Four eyes developed nonischemic centra l retinal vein occlusion. Complications required implant removal in 8 eyes. Ten of 14 eyes demonstrated involution of CNV or inhibition of recurrent CNV. Ten ey es had stable or improved visual acuity. Median initial visual acuity was 20/64. Median final visual acuity was 20/40 CONCLUSIONS: Longterm follow-up demonstra tes a significant complication rate with the sustained release of high-dose int raocular corticosteroids. The complications are treatable, and eyes can retain g ood vision. This therapeutic approach warrants further study to identify if lowe r doses of corticosteroids may reduce the complication rate yet still be effecti ve in treating ocular disease.
PURPOSE: To report the feasibility and safety profile of 2-mg and 6-mg fluoc inolone acetonide implants after longterm follow-up in eyes with choroidal neov ascularization (CNV)DESIGN: Prospective, noncomparative, interventional case ser ies of patients with non-age-related subfoveal choroidal neovascularization en rolled in a compassionate use protocol METHODS: Sustained drug delivery devices containing either 2 mg (eight eyes) or 6 mg (six eyes) of fluocinolone acetonide were implanted through the pars plana into the vitreous cavity of 14 patients w ith predominantly classic, subfoveal CNV. The main outcome measures were complic ations related to the device. Secondary outcome measures were involution of esta blished CNV, inhibition of recurrent CNV, and visual acuity RESULTS: Patients ha d a diagnosis of ocular histoplasmosis (seven), myopic degeneration (four), angi oid streaks (two), and punctate inner choroidopathy (one). Patients were followe d for an average of 33 months (range, 16 to 40 months). All 14 eyes developed el evated intraocular pressure and cataract. Four eyes developed nonischemic centra l retinal vein occlusion. Complications required implant removal in 8 eyes. Ten of 14 eyes demonstrated involution of CNV or inhibition of recurrent CNV. Ten ey es had stable or improved visual acuity. Median initial visual acuity was 20/64. Median final visual acuity was 20/40 CONCLUSIONS: Longterm follow-up demonstra tes a significant complication rate with the sustained release of high-dose int raocular corticosteroids. The complications are treatable, and eyes can retain g ood vision. This therapeutic approach warrants further study to identify if lowe r doses of corticosteroids may reduce the complication rate yet still be effecti ve in treating ocular disease.
出处
《世界核心医学期刊文摘（眼科学分册）》
2005年第8期18-19,共2页
Digest of the World Core Medical Journals:Ophthalmology
