Retinal detachment (RD) is the separation of the neurosensory retina from the underlying retinal pigment epithelium. This can be due to a break/tear in the retina (rhegmatogenous), traction from surrounding structures (tractional), or accumulation of subretinal fluid (exudative).
RD can be precipitated by trauma, inflammatory conditions (such as uveitis), posterior vitreous detachment, or associated with causative comorbidities.
While prompt treatment typically leads to good prognosis, RD left untreated can result in blindness
Risk Factors
Risk factors for RD can be effectively broken down by the subcategory of RD which they precipitate:
Rhegmatogenous – Trauma - typically blunt (open or closed globe), myopia, previous cataract surgery, previous RD, family history of RD
Note that symptoms of traumatic RD may not develop for up to days after a traumatic event
Tractional – Increasing age, diabetes/diabetic retinopathy.
Exudative – Inflammatory eye conditions such as uveitis or scleritis, congenital eye conditions such as glaucoma or cataracts, local malignancy.
Likely next steps by specialist care
In the absence of clearer information from specialty care, patients with suspected RD could be advised to expect:
- Further examination of visual acuity, fundoscopy, pressure testing, and slit lamp examination with drug adjuncts
- Surgical intervention if RD confirmed which could include laser therapy/cryotherapy, vitrectomy, insertion of silicone ‘buckle’ on the sclera, or injection into the vitreous cavity