The Impact of Optical Coherence Tomography in the Early Identification of Children with Sickle Cell Retinopathy

Author:

Abdelkader Ashraf12ORCID,Shaaban Mohamed1ORCID,Zahran Mahmoud M.1ORCID,Mohammed Mostafa F.3ORCID,Ebrahim Anas M.3ORCID,Galhoom Ahmed I.3ORCID

Affiliation:

1. Department of Pediatrics, Faculty of Medicine for Boys, Al-Azhar University, Cairo, Egypt

2. Scientific Research and Continuous Medical Education Unit, Al Ansari Specialist Hospital, Yanbu, Saudi Arabia

3. Department of Ophthalmology, Faculty of Medicine for Boys, Al-Azhar University, Cairo, Egypt

Abstract

Introduction. Sickle cell disease is characterized by the production of abnormal hemoglobin, which affects hemoglobin molecule stability during hypoxia and leads to the formation of sickle cells, resulting in increased hematic viscosity, hemolysis, and microvascular blockage. Vasoocclusion is assumed to be the primary cause of vision-threatening retinopathy in sickle cell disease. The aim of this study was to improve the early detection of sickle cell retinopathy (SCR) in children with sickle cell disease (SCD) and investigate the link between systemic and ocular symptoms. Methods. This cross-sectional study comprised children with SCD. The patient files provided a detailed medical history. The laboratory tests included a blood count, reticulocyte count, and Hb electrophoresis. The slit lamp, fundus, optical coherence tomography (OCT), and optical coherence tomography angiography (OCTA) were all part of the ophthalmological examination. Results. The study comprised 15 children with sickle cell disease who met the inclusion and exclusion criteria, with a mean age of 11.15 ± 1.29 years. Nine of the children were males (60%) and six were females (40%). 8 (53.3%) of the children had Hb SS, three (20%) had Hb SC, three (20%) had Hb SB+, and one (6.7%) had Hb SB0. Four children (26.7%) had poor visual acuity. A fundus examination revealed significant abnormal findings in 12 of the 7 children’s eyes (40 percent). Macular thinning was detected by OCT in 10 eyes of 7 children (33.3%). Flow voids at the deep retinal capillary plexus were detected by OCTA in 10 eyes of 7 children (33.3%). Longer disease duration, higher reticulocytic percent, more painful crises, and noncompliance with hydroxyurea medication were all linked to the existence of eye abnormalities on fundus examination and OCT. Conclusion. OCTA can show early retinal damage in sickle cell patients with macular changes. Sickle cell retinopathy is usually associated with more severe disease.

Publisher

Hindawi Limited

Subject

General Medicine

Reference27 articles.

1. Sickle cell retinopathy: a literature review;M. V. M. R. Ribeiro;Journal of the Brazilian Medical Association,2017

2. Sickle-cell disease;D. C. Rees;The Lancet,2010

3. Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical sub phenotypes;G. J. Kato;Blood Reviews,2007

4. Sickle Cell Vaso-Occlusion

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Longitudinal Assessment of Macular Thickness and Microvascular Changes in Children with Sickle Cell Disease;Ophthalmology Retina;2024-02

2. Seltene vaskuläre Erkrankungen der Netzhaut – Teil 1;Klinische Monatsblätter für Augenheilkunde;2023-08-16

3. Seltene vaskuläre Erkrankungen der Netzhaut – Teil 1;Augenheilkunde up2date;2023-08

4. EVO-Based Optimization of Deep Learning Models for Diabetic Retinopathy Diagnosis;2022 OPJU International Technology Conference on Emerging Technologies for Sustainable Development (OTCON);2023-02-08

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3