It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
We identified clinical characteristics and risk factors of choroidal neovascularization (CNV) in eyes with prior episode of central serous chorioretinopathy (CSC). This retrospective case-control study included those initially diagnosed with CSC and developed CNV secondarily (Group 1, n = 16), those diagnosed with CNV in eyes of previous putative CSC (Group 2, n = 14), and those initially diagnosed with CSC, and did not develop CNV secondarily, as a control group for Group 1 (Group 3, n = 250). Clinical characteristics including treatment outcomes were assessed. Demographics and multimodal imaging at the time of CSC diagnosis of secondary CNV were compared between the groups to identify risk factors. Duration from diagnosis of CSC to development of CNV in Group 1 was 40.2 ± 42.0 months. Classic CNV was noted in 23 (76.7%) eyes. After treatment with intravitreal antiangiogenics with average of 4.9 times, visual acuity improved in Group 1 and Group 2 (p = 0.002). Multivariate analysis revealed that systemic hypertension, pigmentary changes, and double layer sign were associated with development of CNV secondary to CSC (p < 0.05). Hypertension, pigmentary changes, and double layer sign were independent risk factors for CNV secondary to CSC. The CNV’s responded well to treatment, resulting in improved vision.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
; Chang, Cho Soo 2 ; Park, Kyu Hyung 3 ; Kim Sang Jin 4 ; Kim, Kyung Tae 4 1 Samsung Medical Center, Sungkyunkwan University School of Medicine, Department of Ophthalmology, Seoul, Republic of Korea
2 Seoul National University College of Medicine, Seoul National University Bundang Hospital, Department of Ophthalmology, Seongnam, Republic of Korea (GRID:grid.412480.b) (ISNI:0000 0004 0647 3378); Kyungpook National University Hospital, Department of Ophthalmology, Daegu, Republic of Korea (GRID:grid.411235.0) (ISNI:0000 0004 0647 192X)
3 Seoul National University College of Medicine, Seoul National University Bundang Hospital, Department of Ophthalmology, Seongnam, Republic of Korea (GRID:grid.412480.b) (ISNI:0000 0004 0647 3378)
4 Samsung Medical Center, Sungkyunkwan University School of Medicine, Department of Ophthalmology, Seoul, Republic of Korea (GRID:grid.412480.b)




