To compare the standardised Nidek EAS-1000 densitometric analysis of the lens with clinical assessment of the nucleus at an early stage of cataract development, 1,200 eyes of 1,204 participants of the VECAT study were assessed at the baseline using both subjective and objective lens grading. Standardisation of the automatic slit image analysis was achieved using a custom-designed EAS-1000 Software version 3.01c. Among 6 measurements of nuclear optical density, the mean pixel luminescence of integrated anterior nuclear density correlated best with clinical assessment (R = 0.662, p < 0.001). Variance components that interfere with the assessment are defined.

Prior vitamin E supplementation may protect VECAT participants from developing at least early cortical cataracts. No apparent protective role in terms of nuclear opacities and nuclear color was found regardless of the level, regularity or duration of intake.

Cataract is the leading cause of blindness in the world today, while age-related macular degeneration is responsible for the majority of new cases of visual impairment in the Western world. There is a growing body of evidence suggesting a role for antioxidant therapy to prevent the progression of these conditions. A 4-year prospective, randomised, controlled trial of an antioxidant versus placebo in a population of healthy volunteers aged 55-80 years at enrolment is described. This paper outlines the primary aims of the Vitamin E, Cataract and Age-related Macular Degeneration (VECAT) Study, the methodology, and the recruitment rates. Additional data on the toxicity and non-ocular effects of vitamin E will also be collected. Standardised clinical grading of macular and lens features, and comparison of serial macular photographs and digital lens photographs will form the basis for assessment of primary study outcomes. Information collected in this study will assist in the assessment of the potential value of antioxidants in preventing the enormous burden imposed on developed communities by age-related eye disease. In addition, important data on prevalence and progression rates of cataract and macular degeneration will be collected.

The VECAT study methodology appears to be highly reliable and to have sufficient power to detect the differences in the four-year progression of soft distinct and indistinct drusen and pigment abnormalities between the treatment groups.

We conducted a study to determine the prevalence of central islands after refractive excimer laser surgery and the factors associated with their occurrence. A VISX Twenty/Twenty excimer laser was used to perform 157 photorefractive keratectomy (PRK) and 263 photorefractive astigmatic keratectomy (PARK) procedures. Corneal topography was assessed in 156 patients three months postoperatively using a topographic analysis system. Central islands were seen in 67% of patients; 26% had islands of 3.0 diopters (D) or more in height. Occurrence was associated with the laser suction nozzle being fixed during the procedure (P < .05). There was no demonstrable effect of central islands on visual acuity or refractive outcome, nor was there any relation to the amount of attempted correction or type of procedure (PARK or PRK). Central islands with a curvature difference of less than 3.0 D were seen more frequently than an absence of islands, suggesting these may be a "normal" postoperative topographic variation. The effect of nozzle position on island formation suggests that plume removal or corneal hydration may be important, as is corneal epithelial healing.