The screening examination consisted of a structured interview about occupation, health history, surgery and trauma history, and smoking habits. Experienced examiners measured the body weight, height, and BP; and ophthalmologists performed ocular examinations that included measurement of the uncorrected and best-corrected visual acuity (VA), refraction using an autorefractometer (ARK-730; Topcon, Tokyo, Japan), IOP, CCT by specular microscopy (SP-2000; Topcon), central anterior chamber depth, and axial length (using the IOLMaster; Carl Zeiss Meditec), slit-lamp examination, ophthalmoscopy, fundus photography (45° of the visual angle) and sequential stereoscopic disc photographs at a parallax of approximately 8° (30° of the visual angle) using a digital nonmydriatic fundus camera (TRC-NW7; Topcon), and visual field (VF) testing using frequency-doubling technology (FDT) perimetry with the C-20-1 screening program (Carl Zeiss Meditec). The IOP was measured three times using a Goldmann applanation tonometer under topical anesthesia and the median value was recorded. The peripheral anterior chamber depth was scored according to the van Herick method and the gonioscopic findings according to Shaffer's grading system using a Goldmann two-mirror lens. Participants were referred for a definitive examination if they had one or more of the following: corrected VA of 20/30 or less; IOP of 19 mm Hg or higher; an abnormality suggestive of glaucoma or other ocular diseases on ophthalmoscopy, fundus photographs, or stereoscopic disc photographs including a v-C/D of 0.6 or higher, superior (11 to 1 o'clock hours) or inferior (5 to 7 o'clock hours) R/D ratio of 0.2 or lower, bilateral asymmetry of the v-C/D of 0.2 or higher, a nerve fiber layer defect, a splinter disc hemorrhage, any abnormalities on slit-lamp examination, an angle width of grade 2 or less (van Herick method), and at least one abnormal test point (P ≤ 0.05) on FDT VF testing. An independent photograph screening committee judged the fundus and stereo disc photographs.
The definitive examination included detailed slit-lamp, gonioscopic, and fundus examinations and VF testing with a field analyzer (Humphrey Field Analyzer [HFA]; Carl Zeiss Meditec), central 24-2 Swedish interactive threshold algorithm standard program. In eyes without contraindications, the pupils were dilated to observe the fundus by direct and indirect ophthalmoscopy; in eyes with a contraindication, examinations were performed with undilated pupils.
The details of the disc, fundus, and VF examination and diagnosis of glaucoma were essentially the same as those previously reported.
11,44 A photograph reading committee, comprised of members who were different from the members of the photograph screening committee and did not have other information about the eyes, evaluated the pairs of digital stereo color fundus photographs of all the participants undergoing a definitive examination. When the assessments by the committee members did not agree with each other, consensus was obtained by a discussion with reference to all available photographs. The VF reading committee examined results of the HFA tests and did not have access to other ocular information. VFs with fixation loss below 33% and false positives and negatives below 20% were considered reliable and abnormal VFs, defined as the presence of at least one abnormal hemifield that was determined based on the criteria of Anderson and Patella.
11,45 A panel of glaucoma specialists, including those who were members of the photograph reading committee, determined the final glaucoma diagnosis based on clinical records obtained during all examinations. Glaucoma was diagnosed based on evaluations of the disc, RNFL, and VFs based on the ISGEO criteria.
9 In glaucoma diagnosis, anomalous discs, including tilted discs, were excluded.