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Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc
Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc
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Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc
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Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc
Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc

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Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc
Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc
Journal Article

Visual field progression patterns in the ocular hypertension treatment study correspond to vulnerability regions of the disc

2024
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Overview
Objectives To determine the locations on the 24-2 visual field (VF) testing grid that are most likely to progress in patients with ocular hypertension (OHTN). Based on a structural model of superior and inferior areas of relative vulnerability at the optic disc, we hypothesized that the nasal and paracentral regions are more prone to show a reduction in sensitivity. Methods Posthoc analysis of data collected in phases 1 and 2 of the Ocular Hypertension Treatment Study (OHTS). A pointwise analysis was applied to determine the progression patterns in the early and delayed treatment groups. Each group’s progression rate and frequency were calculated for each of the 52 locations corresponding to the 24-2 VF strategy, using trend- and event-based analyses, respectively. Results For the event-based analysis, the events were most commonly found in the nasal and paracentral regions. The same regions, with some modest variation, were found to have the fastest rates of progression (ROP) measured with trend analysis. A similar pattern of progression was observed in both the early and delayed treatment groups. The difference in event rates and ROP between the early and delayed treatment groups was also greatest in the nasal and paracentral regions. Conclusions Development of VF loss in ocular hypertensive eyes appears to be consistent with the vulnerability zones previously described in glaucomatous eyes with established VF loss. Ocular hypotensive treatment likely helps to slow the rate of progression in these regions. This suggests that careful monitoring of these locations may be useful.