Last updated: October 2026
Indocyanine green angiography (ICGA) uses a dye that binds strongly to plasma proteins and emits in the near-infrared spectrum — this lets it penetrate the retinal pigment epithelium and image the choroidal circulation in a way FFA and OCTA cannot match, which is exactly where ICGA retains an essential, largely unchallenged role.
Unlike FFA, ICGA has not been substantially displaced by OCTA — OCTA's imaging depth and its inability to show true dye leakage/hyperpermeability limit its usefulness for exactly the diseases where ICGA is most valuable (PCV, CSCR pachychoroid assessment, inflammatory choroidopathies). In current practice, ICGA and OCTA are complementary rather than competing: OCTA for structural/flow detail, ICGA for functional leakage and hyperpermeability of the choroidal circulation.
Key reference: fundamentals of ICGA in choroidal vascular disease remain consistent across recent retina imaging literature; PCV and pachychoroid spectrum disease continue to rely on ICGA as the reference standard.
| Condition | ICGA finding |
|---|---|
| Polypoidal choroidal vasculopathy | Early hyperfluorescent polyps (often with a hypofluorescent halo) at the end of a branching vascular network |
| Central serous chorioretinopathy | Mid-phase multifocal choroidal hyperpermeability; dilated pachyvessels |
| Type 1 (occult) MNV | Late hyperfluorescent plaque; sometimes a focal hot spot (type 3 lesions) |
| VKH and sympathetic ophthalmia | Many hypofluorescent dark dots, fuzzy choroidal vessels, disc hyperfluorescence: sensitive for subclinical activity |
| Birdshot chorioretinopathy | More numerous hypofluorescent spots than seen clinically |
| MEWDS | Hypofluorescent dots and patches in the late phase, often around the disc |
| Serpiginous choroiditis | Hypofluorescent geographic areas throughout |
| Choroidal haemangioma | Very early intense hyperfluorescence with late "wash-out" |
| Choroidal melanoma | Hypofluorescence early with irregular intrinsic vessels later (double circulation) |
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