Retinal Detachment Flashcards
What is retinal detachment?
Retinal detachment (RD) is typically a progressive condition in which the neuroretina separates (detaches) from the retinal pigment epithelium.
Sub-retinal fluid accumulates, and the retina temporarily loses its function. In case of a rhegmatogenous RD, the separation is due to a retinal discontinuity (break, tear).
In the tractional form, RD is caused by proliferative membranes, whether present on the retinal surface or, less commonly, underneath it (sub-retinal strands). No retinal break is present, although it may subsequently develop (combined rhegmatogenous/tractional RD)
What are the risk factors for retinal detachment?
- posterior vitreous detachment
- increasing age
- myopia (exceeding -8D)
- prev cataract surgery
- trauma
- intraocular tumour
What is posterior vitreous detachment?
The development of rhegmatogenous RD is a consequence of vitreoretinal traction (such as a posterior vitreous detachment) leading to the development of one or more breaks in the retina.
Detachment of the posterior vitreous is considered a major factor in the pathogenesis of rhegmatogenous RD.
Normally it is benign and very common
What are the symptoms of posterior vitreous detachment causing retinal detachment?
- floaters (vitreous condensations)
- flashes (retinal stimulation from traction)
- small % → retinal tear (no additional symptoms)
- if untreated, retinal tear can allow fluid from vitreous space behind retina so it peels off (RD)
- black curtain/loss of vision progressing across visual field over hours-days (ie. not like TIA)
- eye will go blind if untreated
How is retinal detachment investigated?
- visual impairment + field loss (O/E)
- RAPD
- visible detachment on fundoscopy
How is retinal detachment treated?
Treatment w/ retinal surgery - vitrectomy / cryotherapy / gas