The Sydney Myopia Study is a survey of refractive errors and other eye diseases in a large stratified random cluster sample of year-1 (6- to 7-year-old) and year-7 (12- to 13-year-old) schoolchildren. The study was approved by the Human Ethics Committee of the University of Sydney and by the New South Wales Department of Education. Written, informed consent was obtained from parents, and participants provided verbal consent on the day of the examination. The research adhered to the tenets of the Declaration of Helsinki. Details of survey methods are described elsewhere.
29 In brief, 34 primary schools across the Sydney Metropolitan region were selected using random cluster sampling, based on socioeconomic status, to provide a representative sample of children in Sydney schools. A proportional mix of public and private or religious schools was included.
Procedures included a 193-item questionnaire for parents, asking for estimates of time spent by each child engaging in close-up activities and distance activities. Sociodemographic information, including ethnicity, country of birth, education, occupations, age of parents, and type of current housing were collected, in addition to the mother’s obstetric history, child’s birth history, past and current medical history, and a detailed family history of eye disorders. The examination included a detailed assessment of visual acuity, identification of amblyopia and strabismus, cycloplegia using cyclopentolate, autorefraction, and keratometry (Canon RK-F1 autorefractor; Canon Inc., USA, Lake Success, NY) and ocular biometry (axial length, anterior chamber depth, corneal radius of curvature; IOLMaster, Carl Zeiss Meditec AG, Jena, Germany).
The eye drop protocol included amethocaine hydrochloride 0.5% (Minims; Chauvin Pharmaceuticals Ltd., Romford, UK) which was instilled into each eye to provide anesthesia and enhance the absorption of the subsequent eye drops, and two cycles of cyclopentolate 1% (1 drop) and tropicamide 1% (1 drop) applied 5 minutes apart, after corneal anesthesia. The autorefractor was set to generate five valid readings of refraction in each eye automatically, taking place 20 to 30 minutes after instillation of the eye drops. Cycloplegia was considered full when the pupil was fixed and ≥6 mm in diameter. The average refraction was used for analysis.
The ocular biometer (IOLMaster; Carl Zeiss Meditec AG) was used to measure five valid readings of axial length and anterior chamber depth and three keratometry readings. Measures were taken on the entire cohort before the instillation of eye drops and on a subsample after pupil dilation. Predilation measurements for ocular biometry are reported in this study. Anterior chamber depth refers to predilation measurement, unless otherwise stated.