TY - JOUR
T1 - Sampling the visual field based on individual retinal nerve fiber layer thickness profile
AU - Ballae Ganeshrao, Shonraj
AU - Turpin, Andrew
AU - McKendrick, Allison M.
N1 - Funding Information:
Presented at the annual meeting of the Association for Research in Vision and Ophthalmology, Seattle, Washington, United States, May 2016. Supported by the Australian Research Council Linkage Project LP100100250, ARC LP130100055 (AMM, AT) with Heidelberg Engineering, GmBH and by the Australia Research Council Future Fellowship FT0991326 (AT). Disclosure: S. Ballae Ganeshrao, None; A. Turpin, CenterVue SpA (C, F), Haag-Streit AG (F), Heidelberg Engineering GmBH (F); A.M. McKendrick, CenterVue SpA (C, F), Haag-Streit AG (F), Heidelberg Engineering GmBH (F)
Publisher Copyright:
© 2018 The Authors.
PY - 2018/2
Y1 - 2018/2
N2 - PURPOSE. Current perimeters use fixed grid patterns. We test whether a grid based on an individual’s retinal nerve fiber layer (RNFL) thickness profile would find more visual field (VF) defects. METHODS. We describe the defect-based method for choosing test locations. First, the 26 VF locations with the highest positive predictive value to detect glaucoma from the 24-2 pattern are chosen. An additional 26 locations are chosen from a 2 × 2 degree grid based on RNFL thickness. An individualized map was used to relate VF locations to peripapillary RNFL thickness. To test whether the 52 locations chosen by the defect-based method find more defects than other test grids, we collected a 386-location (2 × 2 degree grid) VF measurement on 23 glaucoma participants and classed each location in the dataset as either abnormal or normal using a suprathreshold test. Using this data, defect-based sampling was compared to: a method that sampled VF locations uniformly around the optic nerve head (ONH); the 24-2 pattern; a polar pattern; and a reduced polar pattern. The outcome measure was the number of abnormal points that were selected as test locations. RESULTS. For 8 eyes, no method found more abnormal points than would be expected by chance (hypergeometric distribution, P < 0.05). Of the remaining 15 eyes, the defect-based method identified more abnormal locations on nine eyes, which was significantly better than the other three sampling schemes (24-2: 2 eyes, P < 0.001; polar: 2 eyes, P < 0.001; reduced polar: 2 eyes, P < 0.004; and uniform: 1 eye, P < 0.001). CONCLUSIONS. Using structural information to choose locations to test in a VF for individual patients identifies more abnormal locations than using existing grid patterns and uniform sampling based on structure.
AB - PURPOSE. Current perimeters use fixed grid patterns. We test whether a grid based on an individual’s retinal nerve fiber layer (RNFL) thickness profile would find more visual field (VF) defects. METHODS. We describe the defect-based method for choosing test locations. First, the 26 VF locations with the highest positive predictive value to detect glaucoma from the 24-2 pattern are chosen. An additional 26 locations are chosen from a 2 × 2 degree grid based on RNFL thickness. An individualized map was used to relate VF locations to peripapillary RNFL thickness. To test whether the 52 locations chosen by the defect-based method find more defects than other test grids, we collected a 386-location (2 × 2 degree grid) VF measurement on 23 glaucoma participants and classed each location in the dataset as either abnormal or normal using a suprathreshold test. Using this data, defect-based sampling was compared to: a method that sampled VF locations uniformly around the optic nerve head (ONH); the 24-2 pattern; a polar pattern; and a reduced polar pattern. The outcome measure was the number of abnormal points that were selected as test locations. RESULTS. For 8 eyes, no method found more abnormal points than would be expected by chance (hypergeometric distribution, P < 0.05). Of the remaining 15 eyes, the defect-based method identified more abnormal locations on nine eyes, which was significantly better than the other three sampling schemes (24-2: 2 eyes, P < 0.001; polar: 2 eyes, P < 0.001; reduced polar: 2 eyes, P < 0.004; and uniform: 1 eye, P < 0.001). CONCLUSIONS. Using structural information to choose locations to test in a VF for individual patients identifies more abnormal locations than using existing grid patterns and uniform sampling based on structure.
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U2 - 10.1167/iovs.17-21979
DO - 10.1167/iovs.17-21979
M3 - Article
C2 - 29490343
AN - SCOPUS:85042521497
SN - 0146-0404
VL - 59
SP - 1066
EP - 1074
JO - Investigative Ophthalmology
JF - Investigative Ophthalmology
IS - 2
ER -