The present study was part of the Chennai Glaucoma Study (CGS), a population-based survey of glaucoma in Southern India. The study was previously approved by the Institutional Review Board, and written informed consent was obtained from all participants. The study was conducted in accordance with the tenets of the Declaration of Helsinki.
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The methodology of the CGS has been described in detail in a previous publication.
8 In brief, the study had rural and urban components. The urban component included five randomly chosen clusters in Chennai city. Permanent residents (
n = 960) 40 years of age or older were enumerated from each cluster. Persons examined from the last two clusters were included in the present study, as only participants from these two clusters had the keratometry readings necessary to correct for ocular magnification.
Eligible residents were contacted by social workers to collect demographic information and confirm eligibility and were asked to participate in a comprehensive ophthalmic examination at the base hospital. Written informed consent was obtained from all participants at the examination center. A detailed medical and ophthalmic history was recorded. The participants then underwent visual acuity testing with a logarithm of minimum angle of resolution (log MAR) 4-m charts (Light House Low Vision Products, New York, NY) and objective and subjective refraction. Spherical equivalent refraction was calculated as spherical error plus half of the cylindrical error. A minus cylindrical error was noted. The participants then underwent slit lamp examination and applanation tonometry, pachymetry, gonioscopy, frequency-doubling perimetry (C-20-1 screening and N-30 threshold, FDP; Carl Zeiss Meditec, Inc., Dublin, CA), and detailed lens, optic disc, and fundus examination after pupillary dilation. All subjects with sufficient media clarity to permit good-quality fundus photographs underwent fundus photography. A fundus camera (FF450-plus with VISUPAC; Carl Zeiss Meditec) with digital image–archiving system was used. Photography included one stereo-pair (nonsimultaneous) of 20° optic disc photographs for each eye. Axial length measurement was performed using an ultrasonic biometer (Ocuscan; Alcon Laboratories, Fort Worth, TX) on every fifth subject, the first subject in the series having been selected at random.
In addition, subjects from the last two clusters also underwent keratometry (Bausch & Lomb Ophthalmic Instruments, Rochester, NY) before any contact procedures. Among persons from the last two clusters examined, further eligibility criteria for the current planimetric study were absence of any cataract (based on the Lens Opacities Classification System [LOCS II]
9 grading), media haze or other ocular abnormality, and reliable, normal FDP screening examinations. Reliability criteria for FDP were no fixation errors or false positives.
Patients with glaucoma were excluded from the present study. For the CGS, glaucoma was diagnosed based on the recommendations of the International Society for Geographic and Epidemiologic Ophthalmology (ISGEO).
10 11 Ocular hypertensives (high IOP plus normal Humphrey 24-2 visual fields) were, however, included.
Other exclusion criteria from the planimetric study were any cataract or other media haze, aphakia, pseudophakia, nonavailability of keratometry measurements, poor-quality optic disc photographs including blurred photographs and/or poor stereo and any defect(s) on FDP and myopia >−8.0 D.
The labeled optic disc photographs were exported from the VISUPAC system as high-quality JPEG images and saved in an external storage device to be analyzed later.
Planimetry was performed using custom planimetry software, which was developed specifically for this purpose (MatLab ver. 7; Mathworks Inc., Natick, MA). The custom software was tested against the commercial VISUPAC software. Vertical and horizontal disc diameters and disc areas were marked on 50 optic disc pictures (of 50 subjects) and the values were noted. The pictures were then exported as described, and the same measurements were made using the custom software. Excellent correlation was found between the two measurement methods. The mean difference between the results of the two methods of vertical linear measures was 0.005 ± 0.004, intraclass correlation coefficient (ICC) 0.99; for horizontal lines it was 0.001 ± 0.004, ICC 0.99; and for area measures it was 0.011 ± 0.02, ICC 0.99.