Journal of the Korean Ophthalmological Society 2006;47(3):381-387.
Published online March 31, 2006.
Analysis of Preferential Hyperacuity Perimeter Results in Maculopathy Caused by Various Retinal Diseases.
Eung Suk Kim, Woo Ho Nam, Seung Young Yu, Hyung Woo Kwak
1Department of Ophthalmology, KyungHee University College of Medicine, Seoul, Korea. syyu@khu.ac.kr
2Department of Ophthalmology, Kangnam Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Korea.
황반부이상을 나타내는 여러 망막질환에서 선택적초시력시야계 결과분석
김응석1,남우호2,유승영1,곽형우1
Department of Ophthalmology, KyungHee University College of Medicine1, Seoul, Korea Department of Ophthalmology, Kangnam Sacred Heart Hospital, Hallym University College of Medicine2, Seoul, Korea
Correspondence:  Eung Suk Kim, M.D.1
Abstract
PURPOSE
The Preferential Hyperacuity Perimeter (PHP) is a device designed to monitor the development of choroidal neovascularization in age-related macular degeneration (AMD) patients. Recent studies have reported the efficacy of the PHP in early detection of AMD. To evaluate hyperacuity, a dot deviation signal is flashed to the central 14 degrees of the macular visual field and the patient's perceived hyperacuity defect is recorded. The purpose of our study was to identify the role of the PHP in analyzing visual functions of patients with maculopathy caused by retinal diseases other than AMD. METHODS: Seventy-four eyes of 55 patients with macular abnormalities caused by various retinal diseases (44 eyes of diabetic retinopathy, 6 eyes of central serous chorioretinopathy, 24 eyes of other retinal diseases) underwent PHP, Optical Coherence Tomography (OCT) and fluorescein angiography (FAG). RESULTS: Of the 74 eyes with maculopathy, 60 eyes (81%) were positive on the PHP. By disease, 40 eyes (40/44, 91%) with diabetic retinopathy, 3 eyes (3/6, 50%) with central serous chorioretinopathy and 17 eyes (17/24, 71%) with other retinal diseases were positive. Among them, the location of hyperacuity defect lesions determined by PHP correlated well with the location shown on OCT and FAG in 6 eyes (6/40, 15%) with diabetic retinopathy, 1 eye (1/3, 33%) with central serous chorioretinopathy and 5 eyes (5/17, 29%) with other retinal diseases. CONCLUSIONS: Many retinal diseases that lead to maculopathy revealed a hyperacuity defect on PHP when the lesion was located not only in the retinal pigment epithelium but also in the outer retinal layer. Special attention to the patient's visual acuity and visual field defects is required when analyzing PHP results since these factors can influence the PHP evaluation.
Key Words: Hyperacuity;Maculopathy;PHP


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