Rhegmatogenous Retinal Detachment
Also known as: RRD
Separation of the neurosensory retina from the retinal pigment epithelium caused by a full-thickness retinal break through which liquefied vitreous passes into the subretinal space. Incidence is about 1 in 10,000 people per year.
- Requirements: a retinal break, vitreous liquefaction (syneresis) and traction at the break site.
- Risk factors: myopia (above 3 dioptres raises risk several-fold), posterior vitreous detachment, lattice degeneration, previous cataract surgery (0.5 to 3 percent of pseudophakic eyes, higher after posterior capsule rupture), ocular trauma, previous detachment in the fellow eye, family history, Stickler syndrome, Marfan syndrome, and age 50 to 70 years.
- Break types: horseshoe (flap) tear from vitreous traction, round atrophic hole (lattice, young myopes), giant tear (more than 90 degrees), retinal dialysis (disinsertion at the ora serrata, often traumatic, inferotemporal).













