Forty-nine children with large optic disc cups were examined over a 4-year period who met the selection criterion of nonglaucomatous optic disc cupping, based on previous clinical diagnosis during routine care in a comprehensive pediatric ophthalmology practice. We purposely did not stipulate measurement parameters as inclusion criteria; rather, we sought to define a typical clinical population and analyze measurement parameters as the outcome of the study. Nonglaucomatous cupping was defined as optic disc cupping in the absence of glaucoma, optic atrophy, or other optic disc anomaly, but allowed for physiologic optic disc cupping and cupping in a setting of prematurity. Patients were excluded if they had ocular hypertension; glaucoma; history of congenital anterior segment anomalies; history of trauma; prior eye surgery; history of intraocular inflammation; optic atrophy, or history of intracranial tumor, increased intracranial pressure, or optic nerve tumor; presence of optic nerve pits, optic nerve colobomas, optic disc hypoplasia, or other optic disc anomalies; cicatricial retinopathy of prematurity or peripheral retinal ablation treatment; myopia greater than 5 D; or age greater than 17 years. Optic atrophy was defined as pallor affecting the optic rim and was excluded from the cohort; all discs had neuroretinal rims of good color. In children with significant developmental delay, neuroimaging data excluded compressive optic nerve or optic chiasm lesions. In many cases, information from multiple prior visits was available to corroborate early-onset, nonprogressive optic disc cupping. Complete dilated eye examinations were performed on each child. The intraocular pressure by hand-held tonometry (Tono-Pen XL; Medtronic, Jacksonville, FL) or Goldmann applanation tonometry measured 21 mm Hg or less in all children, with the exception of three children whose developmental delay and level of cooperation did not allow measurement. Two of the three children had been seen for prematurity in infancy with large cups noted, and all three had no progression of cupping over follow-up and thus were believed to have nonglaucomatous cupping.
Where age and cooperation allowed, digital fundus photography of the optic discs (Topcon retinal camera TRC; Topcon Medical Systems, Inc., Paramus, NJ) was performed. Forty-two of 49 children with large cups allowed digital fundus photography. Children ranged in age from 1 year, 4 months to 16 years, 5 months. Since in many cases fellow eyes did not correlate with each other in obeying the ISNT rule (
Table 1, the Results section), both eyes of each patient were included in the data analysis if the eyes otherwise met the inclusion criteria. Eighty-three images of discs with large cups were analyzed (cup/disc ratio, >0.50). The images were compared with 48 images of normal optic discs in children with small to medium cups (cup/disc ratio, <0.45). The cohort of normal discs was derived from photographs taken for focal retinal defects in healthy patients or patients who had disease in the opposite eye not affecting the optic nerve. Eyes with diffuse macular defects were excluded, but photographs from normal fellow eyes were included. Eyes with small localized retinal pigment epithelial defects or congenital hypertrophy of the retinal pigment epithelium were included. The optic disc image analysis included no identifiable patient information. Parental consent was given for examination, the study was approved by the local institutional review board (IRB), and the research adhered to the tenets of the Declaration of Helsinki.
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Optic disc images were analyzed with the measuring software component of a digital imaging system (IMAGEnet; Topcon Medical Systems, Inc., Paramus, NJ). The measurements are calibrated for the particular camera and working distance used, to give reproducible anatomic measurements. All digital photographs and measurements were taken from the same camera. Measurements were obtained by projecting an enlarged digital image of the optic disc on the computer monitor and drawing with a cursor over the image the linear distance or circular area to be measured. The drawing was completed with the operator masked as to the remainder of the data and masked to the measurement results. The drawings were performed in the following order: the vertical disc diameter from 12 to 6 o'clock; the horizontal disc diameter from 3 to 9 o'clock; the temporal disc margin to fovea distance, done by drawing a line from the temporal end of the horizontal disc diameter line to the center of the fovea; the optic disc area, done by drawing a continuous curve tracing the optic disc margin fully around from 12 o'clock to 12 o'clock; the optic cup area, done by drawing a continuous curve tracing the internal margin of the optic disc rim fully around from 12 o'clock to 12 o'clock; the vertical cup diameter from 12 to 6 o'clock, starting at 12 o'clock on the circular cup curve already drawn and ending at 6 o'clock on the circular cup curve; the horizontal cup diameter from 3 to 9 o'clock on the circular cup curve; the neuroretinal rim width, measuring from the drawn interior (cup) curve to the drawn exterior (disc margin) curve at the 12, 3, 6 and 9 o'clock disc diameter lines. The placement of the neuroretinal rim width lines was thus already determined based on the closed disc and cup curves and the disc diameter lines. When the location of the optic disc margin was selected, the position of the outer limit of the disc neural tissue was used, not including any pigmentary changes adjacent to the disc. The location of the outer border of the optic cup (inner margin of the optic rim) was determined by the contour of the cup, not specifically by the pale color of the cup, using the stereoscopic disc viewer and blood vessel contour when needed. The edge of the cup was determined by the location of the smallest radius of curvature of the disc contour, at the transition zone from the cup to the nearly planar rim, which was seen as the position of maximum change in the angle of the blood vessels traversing to and over the rim, a strategy that was especially useful in cases of gradually sloping cups. Blood vessels adjacent to the internal border of the neuroretinal rim were not included as part of the rim. Assessment of the precise location of the rim was meant to substantiate the clinical decision-making on which the ISNT rule is generally based, using the gold standard of planimetric photography. Reproducibility of measurements was validated by repeatedly measuring the superior rim width from disc margin curve to cup curve on the digital projection of a sample eye 30 times and finding a mean of 0.4033 mm and an SE of measurement (SD) of 0.0035 mm (0.87%).
Once the drawings for a disc had been completed, the measurements were obtained (IMAGEnet software; Topcon Medical Systems, Inc.) and recorded. The vertical cup/disc ratio was calculated as the vertical optic cup diameter divided by the vertical optic disc diameter; the horizontal cup/disc ratio was calculated as the horizontal optic cup diameter divided by the horizontal optic disc diameter; the rim/disc ratio was calculated as the rim width at a given meridian (inferior, superior, nasal, or temporal) divided by the average of the vertical and horizontal disc diameters.
The Topcon fundus camera is not telecentric, and the measurements among different eyes are subject to magnification error. Adjustments for magnification error using parameters of ametropia, keratometry, and axial length were beyond the scope of this study in children, because of the constraints of age and cooperation, especially for axial length measurements. We did exclude myopic refractive errors greater than 5.00 D. Magnification errors were felt to be insignificant to the primary outcome measures of our study, in that magnification would not affect analysis of optic rim and disc shape or application of the ISNT rule. Absolute size measurements have been shown to depend on instrumentation used, and thus are interpreted based on published data for our camera system.
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We analyzed data for both fellow eyes when they were available and met inclusion criteria, to determine overall adherence and intereye variation with respect to the ISNT rule. We then randomly assigned only one fellow eye of each pair for analysis of optic disc parameters and statistical comparison of groups to assure independent data sets. Statistical comparison of means to determine level of significance was performed with unpaired Student's t-tests. The percentage of each group obeying the rule was compared for statistical significance by χ2 test.