Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Jun 21:79:103999.
doi: 10.1016/j.amsu.2022.103999. eCollection 2022 Jul.

Incidence of eye complications among sickle cell disease patients in Jeddah, Saudi Arabia: A cross-sectional study

Affiliations

Incidence of eye complications among sickle cell disease patients in Jeddah, Saudi Arabia: A cross-sectional study

Eid Ayed Almasoudi et al. Ann Med Surg (Lond). .

Abstract

Introduction: Sickle cell disease (SCD) is a heritable blood disorder resulting in deformed, rigid red blood cells, rendering them more prone to vaso-occlusion. Ocular complications are known to affect multiple organs through the body's vasculature. Here, we evaluated the incidence of eye complications in patients with SCD at King Abdulaziz Medical City in Jeddah, Saudi Arabia.

Materials and methods: We used a cross-sectional approach and collected relevant medical data from nine patients with SCD. Ophthalmic assessment included visual acuity and an in-clinic dilated fundus examination. All patients were asked to attend the ophthalmology clinic to undergo optical coherence tomography (OCT) angiography, macular OCT scan, and fundus photography. The results of the imaging tests were interpreted by a certified ophthalmology consultant specializing in retinal diseases. Descriptive analyses of the results were also performed.

Results: The mean age of the nine patients was 24.78 ± 10.9 years. All patients were non-hypertensive, one had type 1 diabetes, and another had type 2 diabetes. Five patients had normal visual acuity, two had slight impairments in at least one eye, and two had moderate impairment in at least one eye. One of the nine patients exhibited retinal ischemia in the right eye despite normal macular thickness (visual acuity, OD, 6/30; OS, 6/21). The remaining eight patients showed no ocular abnormalities.

Conclusion: Of the nine patients with SCD, five showed no symptoms of ocular complications. One patient showed retinal ischemia in the right eye, despite a normal macular thickness. This study's results suggest routine ophthalmologic examination may not be able to detect or monitor macular or retinal abnormalities unless augmented with detailed imaging techniques.

Keywords: Eye complications; Ophthalmology screening; Retinopathy; Saudi Arabia; Sickle cell disease.

PubMed Disclaimer

Conflict of interest statement

There are no conflicts of interest to declare.

Figures

Fig. 1
Fig. 1
OCT angiography report of the right eye for the patient with retinal abnormalities. Abbreviations: OCT, optical coherence tomography.
Fig. 2
Fig. 2
Wide-angle retinal photography of the patient with retinal abnormalities. Abbreviations: OD, right eye; OS, left eye.

Similar articles

Cited by

References

    1. Rees D.C., Williams T.N., Gladwin M.T. Sickle-cell disease. Lancet. 2010;376(9757):2018–2031. doi: 10.1016/S0140-6736(10)61029-X. - DOI - PubMed
    1. Galadanci A.A., DeBaun M.R., Galadanci N.A. Neurologic complications in children under five years with sickle cell disease. Neurosci. Lett. 2019;706:201–206. doi: 10.1016/j.neulet.2019.04.030. - DOI - PMC - PubMed
    1. Piel F.B., Hay S.I., Gupta S., Weatherall D.J., Williams T.N. Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions. PLoS Med. 2013;10(7) doi: 10.1371/journal.pmed.1001484. - DOI - PMC - PubMed
    1. Pahl D.A., Green N.S., Bhatia M., Lee M.T., Chang J.S., Licursi M., Briamonte C., Smilow E., Chen R.W.S. Optical coherence tomography angiography and ultra-widefield fluorescein angiography for early detection of adolescent sickle retinopathy. Am. J. Ophthalmol. 2017;183:91–98. doi: 10.1016/j.ajo.2017.08.010. - DOI - PMC - PubMed
    1. Hassan T., Badr M., Hanna D., Arafa M., Elhewala A., Dabour S., Shehata S., Rahman D.A. Retinopathy in Egyptian patients with sickle cell disease: a cross-sectional study. Medicine (Baltim.) 2021;100(51) doi: 10.1097/md.0000000000028355. - DOI - PMC - PubMed