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FFA. Dr Aaron Ng. FFA Principles. Fluorescence Stimulated by light of shorter wavelength Emission of light of longer wavelength Flurescein Excitation peak 490nm Emit light of about 530nm. FFA Principles: Filters. 5 Phases of Angiogram. 1. Choroidal (Pre-arterial): 9-15 sec.
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FFA Dr Aaron Ng
FFA Principles • Fluorescence • Stimulated by light of shorter wavelength • Emission of light of longer wavelength • Flurescein • Excitation peak 490nm • Emit light of about 530nm
5 Phases of Angiogram 1. Choroidal (Pre-arterial): 9-15 sec
5 Phases of Angiogram 2. Arterial phase: 1 sec after choroidal phase
5 Phases of Angiogram 3. Arterio-venous (capillary) phase: early venous laminar flow
5 Phases of Angiogram 4a. Venous phase: Laminar venous flow
5 Phases of Angiogram 4b. Venous phase – complete filling • Max perifoveal capillary filling – 20-25 sec • First pass of fluorescein circulation – 30 sec
5 Phases of Angiogram 5. Late (recirculation) phase • Absent after 10 min
Timing of FFA phases • Arm to retina (ONH): 7-12s • Posterior ciliary artery 9s • Choroidal flush, cilio-retinal artery 10s • Retinal arterial phase 10-12s • Capillary transition phase 13s • Early venous/lamellar/a-v phase 14-15s • Venous phase 16-17s • Late venous phase 18-20s • Late phase 5-15 min
Foveal dark appearance • Foveal avascular zone • High density of xanthophyll at the fovea • Foveal RPE larger and rich in melanin and lipofuscin
Causes of hyperfluorescence • Autofluorescence • Pseudofluorescence • RPE window defect • Dye pooling • Dye leaking • Tissue staining-disc, drusen, chorioretinal scar
Autofluorescence Optic disc drusen
Autofluorescence Lipofuscin
Autofluorescence Angioid streaks
RPE window defect Atrophic ARMD
Dye pooling Subretinal - CSCR
Dye pooling Sub-RPE - PED
Dye leaking Proliferative DR Cystoid Macula Oedema
Causes for hypofluorescence • Masking of retinal fluorescence • Pre-retinal lesions block all fluorescence • Deeper retinal lesions e.g. intraretinal haemorrhages and hard exudates block only capillary fluorescence
Pre-retinal lesions Blockage to all fluorescence
Intraretinal lesions Hard exudates Intraretinal haemorrhages
Causes for hypofluorescence • Masking of background choroidal fluorescence • Conditions that block retinal fluorescence • Conditions that block only choroidal • Sub-retinal or subRPE lesions • Increased RPE density • Choroidallesions • Filling defects • Vascular occlusions • Loss of vascular bed (myopic degen, choroidaeraemia)
Increased RPE density CHRPE
Filling defects Capillary drop – out in DR (vascular occlusion) Choroidaeraemia (loss of vascular bed)
Indocyanine Green Angiography • Advantages over FFA • Study of choroidal vasculature otherwise prevented in FFA due to RPE blockage • Near-infrared light utilised penetrates melanin, xanthophylls, exudates and subretinal blood • Infrared is scattered less cf visible light, thus suitable in eyes with media opacities • 98% ICG molecules bound to protein, thus remaining in the blood vessels
ICGA Principles • Infrared excitation (805nm) • Infrared emission (835nm)
Phases of ICGA • Early phase (first 60 sec post injection) – choroidal arteries • Early mid phase (1-3 min) – choroidal veins and retinal vessels • Late mid phase (3-15 min) – choroidal vessels facing but retinal vessels are still visible • Late phase (14-45 min) – hypofluorescent choroidal vessels and gradual fading of diffuse hyperfluorescence
Causes for hyperfluorescence • “Window defect” • Retinal or choroidal vessel leakage • Abnormal retinal or choroidal vessels
Causes for hypofluorescence • Blockage • Pigment, blood, fibrosis, infiltrate, exudate, serous fluid • PED are predominantly hypofluorescent on ICGA as cf FFA • Filling defect • Vascular occlusion • Loss of choroidal or retinal circulation
Clinical indications • PCV • CSCR • Posterior uveitis (extent of disease involvement) • Breaks in Bruch’s (lacquer cracks, angiod streaks) • Contraindication for FFA
CSCR FFA ICGA