镰状细胞病患儿中央凹无血管区改变

T. ElSadek, Abdelrahman Salman, A. Said, N. Elsherif, M. Saleh
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引用次数: 0

摘要

目的通过光学相干断层血管造影(OCTA)研究镰状细胞病(SCD)患儿中央凹无血管带(FAZ)的形态学变化。患者和方法本研究是在某三级医院进行的前瞻性病例对照研究。共纳入15例SCD患儿(经电泳证实)和15例匹配的健康患儿。进行眼科检查。使用RTVue XR Avanti进行6×6黄斑OCTA扫描。分析中心凹参数包括FAZ面积(mm2)、周长(mm) (PERIM)、圆度指数(AI)和中心凹密度。儿科评估包括疾病变异、镰状危象和当前治疗。结果15例SCD患儿共15眼,健康患儿15眼。6只眼睛出现1期视网膜病变。SCD患儿FAZ面积较对照组宽(P=0.001), PERIM较大(P=0.00), AI较高(P=0.030)。伴有1期视网膜病变的SCD患者与无视网膜病变患者的FAZ参数无明显变化。结论与正常对照相比,SCD患儿FAZ区宽,PERIM大,AI高。OCTA黄斑病变可能是镰状细胞视网膜病变的早期预测因子。建议进一步的随访研究,以了解早期黄斑变化对视网膜病变未来发展的影响。
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Foveal avascular zone changes in children with sickle cell disease
Purpose To study the morphological changes in the foveal avascular zone (FAZ) in children diagnosed with sickle cell disease (SCD) via the optical coherence tomography angiography (OCTA). Patients and methods This was a prospective case–control study that was done in a tertiary hospital. A total of 15 children with SCD (confirmed with electrophoresis) and 15 matched healthy children were included. Ophthalmological assessment was done. RTVue XR Avanti was employed to obtain 6×6 macular OCTA scans. Foveal parameters including FAZ area (mm2), perimeter (mm) (PERIM), acircularity index (AI), and foveal density were analyzed. Pediatric assessment including the disease variant, sickling crisis, and current treatment was done. Results A total of 15 eyes of 15 children with SCD and 15 eyes of healthy children were included. Six eyes showed stage 1 retinopathy. Children with SCD had wider FAZ area (P=0.001) with larger PERIM (P=0.00) and higher AI (P=0.030) in comparison with the control children. No significant changes in the FAZ parameters between patients with SCD with stage 1 retinopathy and patients without retinopathy were found. Conclusion Children with SCD have a wide FAZ area with large PERIM and high AI in comparison with normal controls. OCTA macular changes might be an early predictor of sickle cell retinopathy. Further follow-up studies are recommended to understand the effect of early macular changes on the future development of retinopathy.
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