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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
When should children and young adults with sickle cell disease be referred for eye assessment?
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.
Abstract:
Children and young adults who suffer from sickle cell disease (SCD) are at risk of blindness from retinopathy and other complications. The incidence of proliferative retinopathy in SCD patients varies from 5 to 10% depending on the genotype, being commoner in SC than SS and S-thal. 'Sudden' blinding sequelae such as vitreous haemmorrhage and tractional retinal detachment can eventuate from vasculo-proliferative retinal lesions, known as sea fans, in otherwise 'quiet' eyes. This risk can be minimised considerably if the lesions are detected in a timely fashion and treated, usually with laser photocoagulation and possibly with cryotherapy. This communication aims, by a review of relevant literature and through our original data, to highlight a time frame for the development of proliferative sickle retinopathy to enable paediatricians decide on an appropriate time of referral for ophthalmic assessment. Ninety patients with SCD (88 SS, 2 SC) aged 5-36 years were examined for anterior and posterior ocular signs of SCD using dilated binocular indirect ophthalmoscopy. Other relevant literature was reviewed. Twenty-four percent of these patients had some form of SCD related posterior pathology, 5.6% of which was pre-proliferative or proliferative. This included a 14-year-old SS patient with arterio-venous anastomosis. The literature reveals that patients begin to exhibit evidence of proliferative retinopathy from about the age of 10 and the frequency tends to increase with age. However, though rare, vitreous haemmorhage has been known to occur below the age of 20. Children with SCD should, from about the age of ten, be referred for at least biennial dilated binocular indirect ophthalmoscopy preferably with fluorescein angiography if such facilities are available, so that neovascular lesions can be treated before blinding sequelae occur. From the age of 20, the frequency of eye examination should increase to yearly. Antisickling remedies, such as NIPRISAN may be beneficial in prophylaxis.
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