Abstract
Aphakic glaucoma is the most common long-term complication seen following congenital cataract surgery. It has a reported incidence of between 15% and 45%. Many risk factors have been identified including microcornea, early surgery, persistent fetal vasculature, congenital rubella syndrome, Lowe syndrome, chronic inflammation and retained lens material. Diagnosis is often difficult as the classic signs of congenital glaucoma such as epiphora, blepharospasm and buphthalmos are usually absent. Additionally, it is also difficult to perform accurate ocular examinations on young children and examination under anaesthesia is usually required. Surgical intervention is often required with medical treatment providing adjunctive therapy. Surgical techniques performed include trabeculectomy with or without antifibrotic agents, glaucoma drainage devices (valved and non-valved), cyclodestructive procedures, goniotomy and trabeculotomy. Trabeculectomy with mitomycin C and glaucoma drainage devices are the two most commonly performed procedures. In spite of considerable advances having been made in the management of aphakic glaucoma, it still poses a significant management dilemma. Despite best standard of care two thirds of aphakic children end up with a mean visual acuity of ≤ 20/400.
Highlights
Aphakic glaucoma is a well recognised sight-threatening complication seen following uncomplicated paediatric cataract extraction
The mechanism and pathophysiology of glaucoma occurring in aphakes with open angles following congenital cataract surgery is largely not understood
This study suggested that nuclear sclerosis imposed increased risk of developing glaucoma
Summary
Aphakic glaucoma is a well recognised sight-threatening complication seen following uncomplicated paediatric cataract extraction. Aphakic glaucoma poses a significant clinical challenge, with regards to diagnosis and treatment These children are hard to diagnose as they can remain asymptomatic for a long period of time despite high intraocular pressures (IOP). Chen et al [13] described glaucoma surgery being required in 57.1% of cases (170 eyes) of aphakic patients following congenital cataract surgery. The mechanism and pathophysiology of glaucoma occurring in aphakes with open angles following congenital cataract surgery is largely not understood. They found a nadir of aphakic glaucoma risk for surgery at 3-4 months of age which they were unable to explain They excluded microcornea and PFV, both significant confounding factors. The incidence of glaucoma was found to be 33% (15 eyes) in the aphakic
Published Version
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