PT - JOURNAL ARTICLE AU - D Mitry AU - J Singh AU - D Yorston AU - M A Rehman Siddiqui AU - A L Murphy AU - A F Wright AU - B W Fleck AU - H Campbell AU - D G Charteris TI - The fellow eye in retinal detachment: findings from the Scottish Retinal Detachment Study AID - 10.1136/bjo.2010.194852 DP - 2012 Jan 01 TA - British Journal of Ophthalmology PG - 110--113 VI - 96 IP - 1 4099 - http://bjo.bmj.com/content/96/1/110.short 4100 - http://bjo.bmj.com/content/96/1/110.full SO - Br J Ophthalmol2012 Jan 01; 96 AB - Aim To characterise the predisposing pathology and clinical features in the fellow eyes of patients recruited as part of the Scottish Retinal Detachment Study.Methods The Scottish Retinal Detachment Study was a 2-year prospectively recruited population-based epidemiology study that sought to recruit all incident cases of primary rhegmatogenous retinal detachment (RRD) in Scotland.Results A total of 1202 incident cases of primary RRD were recruited in Scotland, over a 2-year period and in 94% (1130 cases) detailed data on the clinical features of fellow eyes with RRD were available. Full-thickness retinal breaks were found in 8.4% (95/1130) of fellow eyes on presentation. Lattice degeneration was present in 14.5% (164/1130) of fellow eyes. Thirteen per cent (148/1130) of affected fellow eyes had a best corrected visual acuity of 6/18 or worse with previous RRD, the second most common cause of poor vision. Overall, 7.3% (88/1202) of cases had RRD in both eyes; 60% of cases with consecutive bilateral RRD presented before the macula were affected.Conclusions Rhegmatogenous pathology in the fellow eye represents an important threat to vision. Fellow-eye detachments are more common in pseudophakic individuals and those with a more myopic refractive error. Fellow-eye RRD has a greater likelihood of prompt presentation.