When should children and young adults with sickle cell disease be referred for eye assessment?

O E Babalola1, C O Wambebe

  • 1Rachel Eye Center, Garki, Abuja, Nigeria. Rachel@alpha.linkserve.com

Insights

Children with sickle cell disease (SCD) risk blindness from retinopathy. Early ophthalmic screening from age ten, with increased frequency after age twenty, can prevent vision loss by detecting lesions early.

Area of Science:

  • Ophthalmology
  • Hematology
  • Pediatrics

Background:

  • Sickle cell disease (SCD) poses a significant risk of blindness due to retinopathy in children and young adults.
  • Proliferative retinopathy incidence in SCD patients ranges from 5-10%, varying by genotype (SC, SS, S-thal).
  • Sudden visual loss can occur from proliferative retinal lesions like 'sea fans', leading to vitreous hemorrhage and retinal detachment.

Purpose of the Study:

  • To determine an optimal timeframe for ophthalmic screening in pediatric SCD patients.
  • To guide pediatricians on appropriate referral timing for eye assessments.
  • To review literature and original data on the onset and progression of proliferative sickle retinopathy.

Main Methods:

  • Reviewed relevant literature on sickle cell retinopathy.
  • Examined 90 patients with SCD (88 SS, 2 SC, aged 5-36) for ocular signs.
  • Utilized dilated binocular indirect ophthalmoscopy for posterior segment examination.

Main Results:

  • 24% of examined patients showed SCD-related posterior ocular pathology.
  • 5.6% of patients presented with pre-proliferative or proliferative retinopathy.
  • Literature indicates proliferative retinopathy onset around age 10, increasing with age; rare vitreous hemorrhage seen before 20.

Conclusions:

  • Children with SCD should undergo at least biennial dilated eye exams starting at age 10.
  • Annual eye examinations are recommended from age 20 onwards.
  • Timely detection and treatment (laser photocoagulation, cryotherapy) of retinopathy can minimize blinding sequelae.

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