Table 1

Sensitivity of WF-OCTA in comparison to UWF-FA in diagnosing PDR and agreement between devices in detecting NVE

UWF-FAWF-OCTA
Diagnosis PDR, n of eyes (%)59 (100%)56 (95%)*TPR=0.95 (95% CI 0.85 to 0.98)
Eyes with NVD16 (27.1%)16 (27.1%)*
Eyes with NVD only4 (6.8%)5 (8.5%)*
Eyes with NVE55 (93.2%)51 (86.4%)*
Eyes with NVE only43 (72.9%)40 (67.8%)*
Eyes with NVD and NVE12 (20.3%)11 (18.6%)*
No of NVE seen on UWF-FA242 (100%)174 (71.9%)*
No of NVE in quadrants
 Superotemporal75 (30.9%)71 (29.3%)*
 Inferotemporal78 (32.2%)71 (29.3%)*
 Superonasal43 (17.7%)14 (5.8%)*
 Inferonasal46 (19%)18 (7.4%)*
Median n of NVE/eye
 In total (IQR)3 (1–7)2 (1–4)κ=0.76 (95% CI 0.6 to 0.91)
 Superotemporal1 (0–2)1 (0–2)κ=0.98 (95% CI 0.95 to 1)
 Inferotemporal1 (0–2)1 (0–2)κ=0.94 (95% CI 0.88 to 1)
 Superonasal0 (0–1)0 (0–0)κ=0.24 (95%CI −0.04–0.5)
 Inferonasal0 (0–1)0 (0–0)κ=0.42 (95%CI 0.17 to 0.66)
  • Distribution of NVD and NVE in eyes on UWF-FA and WF-OCTA.

  • *Percentage of the total number of eyes or NVEs seen on UWF-FA.

  • NVD, neovascularisation at the disc; NVE, neovascularisation elsewhere; OCTA, optical coherence tomography angiography; PDR, proliferative diabetic retinopathy; TPR, true positive results; UWF-FA, ultrawidefield fluorescein angiography; WF-OCTA, widefield-OCTA.