Department of Ophthalmology, Jacobs Retina Center at Shiley Eye Center, University of California San Diego, La Jolla, CA, USA.
Retina. 2013 Sep;33(8):1574-83. doi: 10.1097/IAE.0b013e318285cd84.
To evaluate the safety of oral fluorescein angiography (FA) and to compare its efficacy in detection of macular edema (ME) with spectral-domain optical coherence tomography (SD-OCT).
Results of imaging studies for 1,928 eyes of 1,019 patients who had simultaneously undergone both oral FA and SD-OCT by a confocal laser ophthalmoscope were reviewed. Sensitivity in detecting ME, discrepancy rate, and "kappa" agreement were determined for both the techniques and with eyes stratified by disease diagnosis.
No allergic reactions occurred after oral FA. Mild gastric discomfort was noted in <1% of the patients; 1,840 eyes (95.4%) showed concordance between the two techniques, and kappa agreement was 90.3%. For ME, oral FA showed an overall sensitivity of 0.97 and SD-OCT of 0.91. Equivalent sensitivity was found in cases of wet age-related macular degeneration (0.99). Oral FA was more sensitive than SD-OCT in cases of retinovascular diseases. The SD-OCT showed higher sensitivity in cases of macular holes. Detection of ME by SD-OCT was significantly higher in cases of intense leakage on oral FA (P < 0.001).
Oral FA proved to be a safe and an adequate technique to evaluate ME. It is more sensitive than SD-OCT in detection of ME in cases of retinovascular diseases but can fail to detect ME in cases of macular holes. A noninvasive examination with simultaneous oral FA and SD-OCT may be considered to obtain a comprehensive evaluation of the presence of ME from different pathologies.
评估口服荧光素血管造影(FA)的安全性,并比较其与频域光相干断层扫描(SD-OCT)检测黄斑水肿(ME)的效果。
回顾了 1,019 名患者的 1,928 只眼同时进行口服 FA 和共焦激光眼底镜 SD-OCT 的影像学研究结果。确定了两种技术的 ME 检测灵敏度、差异率和“kappa”一致性,并按疾病诊断对眼睛进行分层。
口服 FA 后无过敏反应。<1%的患者出现轻度胃部不适;两种技术的 1,840 只眼(95.4%)显示出一致性,kappa 一致性为 90.3%。对于 ME,口服 FA 的总体敏感性为 0.97,SD-OCT 为 0.91。湿性年龄相关性黄斑变性(0.99)的病例具有相同的敏感性。在血管性疾病的病例中,口服 FA 比 SD-OCT 更敏感。在黄斑裂孔的病例中,SD-OCT 的敏感性更高。在口服 FA 有明显渗漏的情况下,SD-OCT 检测 ME 的灵敏度显著更高(P<0.001)。
口服 FA 被证明是一种安全且足够的评估 ME 的技术。在血管性疾病的 ME 检测中,它比 SD-OCT 更敏感,但在黄斑裂孔的病例中可能无法检测到 ME。可以考虑同时进行口服 FA 和 SD-OCT 的非侵入性检查,从不同的病理角度综合评估 ME 的存在。