Abstract
1. Introduction
2. Materials and Methods
Figure 1. The add-on UWF adapter (left) and the adapter mounted on the device (right).
3. Results
3.1. OCT Measurements
Figure 2. OCT image of a patient with a dome-shaped macula (female, age 46): (A) 10 mm wide scan; (B) 22 mm wide scan. The arrows point at the vitreoretinal traction.
Another figure (Figure 3) demonstrates posterior staphyloma due to high myopia, which extends both vertically and horizontally over a significant area. With a full-range UWF scan that is 22 mm wide and 6 mm high, we can trace the significant depression in the central part of the retina (asterisk) and the strongly curved shape of the posterior pole.
Figure 3. Posterior staphyloma due to high myopia (male, age 43). (A). Colour fundus photograph showing extensive atrophy. (B). A 22 mm wide UWF full-range OCT scan of the posterior pole. The asterisk indicates a localized outpouching around the optic disc.
Figure 4 depicts a patient with a choroidal tumour. The UWF scan reveals a solid choroidal structure (asterisk) with no large vessels, along with overlying drusen temporal to the macula, while the centre of the scan shows a normal retina and choroid.
Figure 4. Choroidal tumour (female, age 55). (A). Colour fundus photograph revealing a darker area temporal to the macula. (B). A 22 mm wide UWF OCT scan of the posterior pole. The asterisk shows a solid choroidal structure.
The next two figures illustrate the use of UWF OCT scanning for en-face analysis. In Figure 5, the central area of atrophy (asterisk) can be seen to be surrounded by only a few small drusen. OCT fundus reconstruction at the choroidal level clearly visualises the boundaries of the area of increased light penetration into the choroid at the site of retinal pigment epithelial atrophy. The outer retina thickness map made from OCT data reveals a reduction in the thickness of the retinal layers in the centre. Figure 6 shows the fundus of a patient with epiretinal membrane (asterisks). In this case, by reconstructing the inner retinal thickness map, the extent of the membrane can be visualised in detail. In addition, the post-operative retinal damage is visible as an area of inner retinal atrophy (arrow).
Figure 6. Patient with epiretinal membrane (male, age 62). (A) Colour fundus photograph. (B) UWF OCT thickness map of the inner retina. The red arrow indicates the site of iatrogenic damage to the retina. (C) A 22 mm wide UWF OCT scan. The asterisks indicate epiretinal membrane.
The last two figures in this section demonstrate surgical cases. Figure 7 shows an example of the preoperative assessment of a strongly adherent vitreous traction (arrow) to the optic disc due to proliferative diabetic retinopathy (DR). A three-dimensional reconstruction of the vitreoretinal interface from a 22 mm wide OCT scan visualises the reciprocal relationship of the two structures on a single image. Figure 8, on the other hand, shows the eye after vitrectomy for retinal detachment. A typical 6 mm OCT scan reveals a shallow pocket of fluid (arrows) under the sensory retina in the macula. Unfortunately, such a scan does not show how far into the periphery the fluid extends. It is only with a 22 mm UWF scan that all the fluid can be visualised.
Figure 7. Vitreoretinal traction in proliferative diabetic retinopathy (female, age 53). (A) Colour fundus photograph. (B) Three-dimensional UWF OCT reconstruction of the interface between the retina and vitreous body. (C) A 22 mm wide UWF OCT scan of the retina across the posterior pole. The arrow points at a strongly adherent vitreous traction.
Figure 8. Patient after vitrectomy for retinal detachment (male, age 37). (A) Colour fundus photograph. (B) A 6 mm wide macular scan showing a flat pocket of fluid in its temporal part. (C) A 22 mm wide UWF OCT scan revealing the entire area of sensory retinal detachment. The arrows point at subretinal fluid.
3.2. Angio-OCT Measurements
Figure 9. OCT angiography of a patient with branch retinal vein occlusion (female, age 46). (A) Measurement with a scan area of 6 × 6 mm. (B) Angiography taken over an area of 15 × 15 mm. (C) UWF OCT angiography covering an area 22 mm in diameter.
Figure 10. Comparison of the same size central 6 × 6 mm area of different-sized OCT angiographies of the patient in Figure 9. (A) Reference OCT angiography of 6 mm diameter. (B) The central area of the OCT examination with a width of 15 mm. This angio-OCT examination has a lower scanning density and hence lower quality than the other two images. (C) Enlarged UWF OCT centre of angiography taken with a diameter of 22 mm.
Figure 11 shows a case of a patient with central retinal vein occlusion. The prominent haemorrhages obscure the view of the central macula on the colour fundus photo and cast small optical shadows in OCT angiography. The visualisation of the central circulation in a 22 × 22 mm UWF OCT scan is similar to that of a 6 × 6 mm measurement. By using a wide scan, however, extensive zones of non-perfusion (asterisks) throughout the mid-periphery can be easily seen at the same time.
Figure 11. Central retinal vein occlusion (female, age 69). (A) Colour fundus photograph of the central 6 × 6 mm area. (B) OCT angiography measurement of the size of a colour fundus photograph. (C) UWF OCT angiography covering an area that is 22 mm in diameter. The asterisks indicate non-perfusion zones.
The next two cases present patients with proliferative DR. Figure 12 shows a 6 × 6 mm scan of the macula. It presents an enlargement of the foveal avascular zone and small areas of non-perfusion around it. It does not provide any other retinal or flow information. In contrast, the 22 mm UWF scan shows extensive zones of non-perfusion (asterisks) in the periphery and vascular proliferation (arrows), in addition to the above-mentioned changes in the centre. Thus, it indicates an urgent need for extended treatment. Figure 13 relates the 22 mm UWF angio-OCT scan to the wide-angle fluorescein angiography (FA) mosaic. Both examinations reveal vascular proliferation (red arrow), capillary dropout (blue arrow), and non-perfusion zones (asterisk). However, angio-OCT shows vascular structures more clearly due to the lack of background fluorescence, as well as the staining of other lesions.
Figure 12. Proliferative diabetic retinopathy (female, age 54). (A). Colour fundus photograph and 6 × 6 mm OCT angiography. (B). UWF OCT angiography from a 22 mm wide area. The asterisks indicate non-perfusion zones and the arrows point to vascular proliferation. (C). UWF OCT scan of the posterior pole.
Figure 13. Proliferative diabetic retinopathy (male, age 37). (A) A wide-angle fluorescein angiography mosaic. (B) UWF OCT angiography covering a 22 mm wide area. The red arrows point at the vascular proliferation, whereas the blue arrows indicate capillary dropout. The asterisks show non-perfusion zones.
3.3. OCT and Angio-OCT Measurements
Figure 14. Patient after vitrectomy for retinal detachment (male, age 54). (A–C) OCT scans with widths of 10, 15, and 22 mm, respectively. (D) UWF OCT retinal thickness map. The arrow points at the retinal detachment. (E) UWF OCT angiography of the 22 mm area. The asterisks indicate extensive zones of non-perfusion.
3.4. UWF Angio-OCT Mosaics
Figure 15. Healthy individual (female, age 26). The figure shows a 140-degree mosaic of 22 mm wide UWF OCT angiography measurements, showing increased imaging field of view (140-degree external field of view is equal to 210-degree internal field of view—nomenclature as in UWF Optos devices).
Figure 16. Eales disease (male, age 27). The figure shows a 100-degree OCT angiography montage of 22 mm UWF scans, showing extensive peripheral ischaemia and collateral formation (100-degree external field of view is equal to 150-degree internal field of view—nomenclature as in UWF Optos devices). The asterisks indicate non-perfusion zones and the arrows point at collateral vessels.
3.5. Retinal Thickness Measurements
Figure 17. Bland–Altman plots for a thickness profile comparison between UWF and a standard retina scan (Retina 3D) in ETDRS sectors.
4. Discussion
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
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