High Dose Intravitreal Bevacizumab for Refractory Pigment Epithelial Detachment in Age-related Macular Degeneration
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Purpose: Intravitreal anti-vascular endothelial growth factor (anti-VEGF) is the first choice of treatment forage-related macular degeneration. However, quite a few eyes treated using conventional dose anti-VEGF(CDAV) have persistent pigment epithelial detachment (PED) on optical coherence tomography. This studyinvestigated the efficacy and safety of high dose anti-VEGF (HDAV) for refractory PED. Methods: In this retrospective study, 31 eyes of neovascular age-related macular degeneration patients withpersistent PED findings despite six or more intravitreal injections of CDAV (bevacizumab 1.25 mg or ranibizumab2.5 mg) were analyzed. Changes in visual outcome, central foveal thickness, and PED height werecompared before and after HDAV (bevacizumab 5.0 mg) for these refractory PED cases. Results: The mean age of patients was 67.7 years. The number of CDAV injections was 12.1. The number ofHDAV injections was 3.39. Best-corrected visual acuity in logarithm of the minimum angle of resolution beforeand after HDAV was 0.49 and 0.41 (p < 0.001), respectively. Central foveal thickness before and afterHDAV was 330.06 and 311.10 μm (p = 0.125), respectively. PED height before and after HDAV was 230.28 and204.07 μm (p = 0.014), respectively. There were no serious adverse reactions in all the eyes. Conclusions: Increasing the dose of bevacizumab in refractory PED may be a possible treatment option.
Abstract
Purpose: Intravitreal anti-vascular endothelial growth factor (anti-VEGF) is the first choice of treatment forage-related macular degeneration. However, quite a few eyes treated using conventional dose anti-VEGF(CDAV) have persistent pigment epithelial detachment (PED) on optical coherence tomography. This studyinvestigated the efficacy and safety of high dose anti-VEGF (HDAV) for refractory PED. Methods: In this retrospective study, 31 eyes of neovascular age-related macular degeneration patients withpersistent PED findings despite six or more intravitreal injections of CDAV (bevacizumab 1.25 mg or ranibizumab2.5 mg) were analyzed. Changes in visual outcome, central foveal thickness, and PED height werecompared before and after HDAV (bevacizumab 5.0 mg) for these refractory PED cases. Results: The mean age of patients was 67.7 years. The number of CDAV injections was 12.1. The number ofHDAV injections was 3.39. Best-corrected visual acuity in logarithm of the minimum angle of resolution beforeand after HDAV was 0.49 and 0.41 (p < 0.001), respectively. Central foveal thickness before and afterHDAV was 330.06 and 311.10 μm (p = 0.125), respectively. PED height before and after HDAV was 230.28 and204.07 μm (p = 0.014), respectively. There were no serious adverse reactions in all the eyes. Conclusions: Increasing the dose of bevacizumab in refractory PED may be a possible treatment option.
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