TY - JOUR
T1 - Baseline OCT measurements in the idiopathic intracranial hypertension treatment trial, part I
T2 - Quality control, comparisons, and variability
AU - OCT Sub-Study Committee for the NORDIC Idiopathic Intracranial Hypertension Study Group
AU - Kupersmith, Mark J.
N1 - Publisher Copyright:
© 2014 The Association for Research in Vision and Ophthalmology, Inc.
PY - 2014/10/13
Y1 - 2014/10/13
N2 - PURPOSE. Optical coherence tomography (OCT) has been used to investigate papilledema in single-site, mostly retrospective studies. We investigated whether spectral-domain OCT (SDOCT), which provides thickness and volume measurements of the optic nerve head and retina, could reliably demonstrate structural changes due to papilledema in a prospective multisite clinical trial setting.METHODS. At entry, 126 subjects in the Idiopathic Intracranial Hypertension Treatment Trial (IIHTT) with mild visual field loss had optic disc and macular scans, using the Cirrus SD-OCT. Images were analyzed by using the proprietary commercial and custom 3D-segmentation algorithms to calculate retinal nerve fiber layer (RNFL), total retinal thickness (TRT), optic nerve head volume (ONHV), and retinal ganglion cell layer (GCL) thickness. We evaluated variability, with interocular comparison and correlation between results for both methods.RESULTS. The average RNFL thickness > 95% of normal controls in 90% of eyes and the RNFL, TRT, ONH height, and ONHV showed strong (r > 0.8) correlations for interocular comparisons. Variability for repeated testing of OCT parameters was low for both methods and intraclass correlations > 0.9 except for the proprietary GCL thickness. The proprietary algorithm-derived RNFL, TRT, and GCL thickness measurements had failure rates of 10%, 16%, and 20% for all eyes respectively, which were uncommon with 3D-segmentation-derived measurements. Only 7% of eyes had GCL thinning that was less than fifth percentile of normal age-matched control eyes by both methods.CONCLUSIONS. Spectral-domain OCT provides reliable continuous variables and quantified assessment of structural alterations due to papilledema.
AB - PURPOSE. Optical coherence tomography (OCT) has been used to investigate papilledema in single-site, mostly retrospective studies. We investigated whether spectral-domain OCT (SDOCT), which provides thickness and volume measurements of the optic nerve head and retina, could reliably demonstrate structural changes due to papilledema in a prospective multisite clinical trial setting.METHODS. At entry, 126 subjects in the Idiopathic Intracranial Hypertension Treatment Trial (IIHTT) with mild visual field loss had optic disc and macular scans, using the Cirrus SD-OCT. Images were analyzed by using the proprietary commercial and custom 3D-segmentation algorithms to calculate retinal nerve fiber layer (RNFL), total retinal thickness (TRT), optic nerve head volume (ONHV), and retinal ganglion cell layer (GCL) thickness. We evaluated variability, with interocular comparison and correlation between results for both methods.RESULTS. The average RNFL thickness > 95% of normal controls in 90% of eyes and the RNFL, TRT, ONH height, and ONHV showed strong (r > 0.8) correlations for interocular comparisons. Variability for repeated testing of OCT parameters was low for both methods and intraclass correlations > 0.9 except for the proprietary GCL thickness. The proprietary algorithm-derived RNFL, TRT, and GCL thickness measurements had failure rates of 10%, 16%, and 20% for all eyes respectively, which were uncommon with 3D-segmentation-derived measurements. Only 7% of eyes had GCL thinning that was less than fifth percentile of normal age-matched control eyes by both methods.CONCLUSIONS. Spectral-domain OCT provides reliable continuous variables and quantified assessment of structural alterations due to papilledema.
KW - Intracranial hypertension
KW - OCT
KW - Optical coherence tomography
KW - Papilledema
UR - http://www.scopus.com/inward/record.url?scp=84917706932&partnerID=8YFLogxK
U2 - 10.1167/iovs.14-14960
DO - 10.1167/iovs.14-14960
M3 - Article
C2 - 25370510
AN - SCOPUS:84917706932
SN - 0146-0404
VL - 55
SP - 8180
EP - 8188
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
IS - 12
ER -