scholarly journals Optical coherence tomography angiography in glaucoma: analysis of the vessel density—visual field sensitivity relationship

2020 ◽  
Vol 8 (18) ◽  
pp. 1203-1203
Author(s):  
Gábor Holló
2018 ◽  
Vol 103 (5) ◽  
pp. 585-591 ◽  
Author(s):  
Joong Won Shin ◽  
Junki Kwon ◽  
Jiyun Lee ◽  
Michael S Kook

AimsTo investigate the global and regional relationships between peripapillary vessel density (pVD) and visual field mean sensitivity (VFMS) in glaucomatous eyes with and without high myopia in comparison with those between peripapillary retinal nerve fibre layer thickness (pRNFLT) and VFMS.MethodsA total of 130 eyes from 130 patients with glaucoma consisting of those with and without high myopia were included in a consecutive manner. High myopia was defined as a spherical equivalent <−6.0 dioptres or axial length >26.5 mm. The pVD and pRNFLT were evaluated using optical coherence tomography angiography (OCT-A) and spectral-domain optical coherence tomography. VFMS was assessed using a linear unlogged 1/L scale. The vasculature–function or structure–function relationships were analysed by comparing the pVD or pRNFLT to the corresponding VFMS, according to Garway-Heath map regionalisation.ResultsThe global pVD-VFMS association was significantly stronger than the pRNFLT-VFMS association in glaucomatous eyes with high myopia (p=0.009). However, there were no significant differences between global pVD-VFMS and pRNFLT-VFMS associations in glaucomatous eyes without high myopia (p=0.343). Regionally, the pVD-VFMS association was significantly greater than the pRNFLT-VFMS association at the superonasal, nasal and temporal sectors (all p<0.05) in glaucomatous eyes with high myopia.ConclusionsThe pVD assessment by OCT-A shows a better global and regional correlation with VFMS than a pRNFLT assessment in glaucoma patients with high myopia. The pVD may be a useful parameter in monitoring disease progression of highly myopic glaucomatous eyes.


Ophthalmology ◽  
2016 ◽  
Vol 123 (12) ◽  
pp. 2498-2508 ◽  
Author(s):  
Adeleh Yarmohammadi ◽  
Linda M. Zangwill ◽  
Alberto Diniz-Filho ◽  
Min Hee Suh ◽  
Siamak Yousefi ◽  
...  

2020 ◽  
Vol 9 (4) ◽  
pp. 1094 ◽  
Author(s):  
Luisa Pierro ◽  
Alessandro Arrigo ◽  
Emanuela Aragona ◽  
Michele Cavalleri ◽  
Francesco Bandello

The aim of this study was to perform quantitative optical coherence tomography angiography (OCTA) assessment of arteritic and non-arteritic anterior ischemic optic neuropathies (AION; NAION). The study was designed as an observational, cross-sectional case series. All patients underwent complete ophthalmologic evaluation including LogMAR best-corrected visual acuity (BCVA), structural optical coherence tomography (OCT) and OCTA images, and dye-based angiography. Retinal nerve fiber layer (RNFL) thickness was obtained from structural OCT, and vessel density (VD) and vessel tortuosity (VT) were measured for each optic nerve head vascular plexus. After selecting the quadrants showing visual field defects, measured by Humphrey 30.2 perimetry (Zeiss Meditec, Dublin, CA, USA), we assessed the correlation between the localization of visual field defects and the quadrants showing impairments of RNFL, VD, and VT. Thirty naïve AION patients (15 arteritic AION (AAION) and 15 non-arteritic AION (NAION)) were included. LogMAR BCVA was 0.6 ± 0.2 for AAION and 0.3 ± 0.3 for NAION (p < 0.01). AAION and NAION eyes showed significant differences in terms of visual field involvement as well as VD and VT values, with remarkably worse alterations affecting AAION eyes. VD values perfectly matched with the quadrants showing RNFL and visual field defects. On the contrary, VT resulted remarkably decreased in all the quadrants, with even worse values in the quadrants showing RNFL and visual field alterations. The present study showed that AAION eyes are more injured than NAION ones. VD represents a good parameter for the detection of the main site on vascular impairment. Remarkably, VT resulted in a more sensitive parameter for the quantitative detection of blood flow impairment in AION disease.


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