The methodology of the Bridlington Eye Assessment Project has not been described previously and is therefore detailed herein. As just stated, the project systematically invited all the town of Bridlington’s elderly population (over the age of 65 years) for a comprehensive screening eye examination by one of four trained optometrists. Patients aged 65 or older on May 11, 2002, and registered with a general practitioner in Bridlington were eligible to attend the examination. Patients known to be registered as blind or partially sighted, bed-bound or demented, or moving into or out of the area during the study were excluded. The Project saw it’s first patient on May 11, 2002, and had seen 1246 patients when this study commenced in January 2004. Informed consent was obtained from all participants, and a local research ethics committee approved all methodology. All methods adhered to the guidelines of the Declaration of Helsinki for research in human subjects.
A relevant standardized medical history was obtained (diabetes, stroke, hypertension) together with the patient’s drug history. Distance and reading spectacle requirements were noted in addition to any history of amblyopia, ocular surgery, or any other ocular disease. Specifically, any history of glaucoma, diabetic retinopathy, or macular degeneration was noted. Family history of glaucoma was determined, together with the patient’s driving status and social circumstances. Uncorrected, corrected, and pinhole logMAR (logarithm of the minimum angle of resolution) visual acuity was then obtained (Bailey-Lovie no. 4 Chart; National Vision Research Institute of Australia, Carlton, Victoria, Australia). The patient was then examined by one of four optometrists trained specifically for the project. Standardized slit lamp examination of the anterior segment and Goldmann applanation tonometry were performed. After instillation of dilation drops, automated visual field analysis was performed with a perimeter (Henson Pro 5000) with software version 3.1.4 (Tinsley Instruments, Croydon, UK). A single-stimulus, suprathreshold, central 26-point test was used. This was automatically extended to a 68-point test if a defect was detected. The patient’s lens, optic disc, macula, and peripheral retina were then specifically examined by slit lamp biomicroscopy with 90-D lens. Decisions on appropriate further management of the patient were made before high-resolution digital fundus photographs (TRC NW6S; Topcon, Tokyo, Japan) and HRT II images (HRT II software ver. 1.4.1.0; Heidelberg Engineering GmbH) were obtained.