Interpretation of retinal angiographic studies has heretofore been largely
qualitative, The temporal properties associated with fluorescein fluorescen
ce of normal and pathologic fundus features are quantified to potentiate pi
xel assignment and fundus feature quantitation for clinical studies where p
recise image metrology is vital. Fluorescein angiography studies were digit
ized, and temporally sequential images were spatially registered with polyn
omial warping algorithms, allowing for the construction of a three-dimensio
nal angiogram vector. Temporal profiles through spatially registered, tempo
rally sequential pixels were computed. Fundus feature fluorescence behavior
was quantified. Fundus features may be discriminated on the basis of spati
o-temporal fluorescein fluorescence properties. Pixel assignment based on s
patio-temporal relationships will facilitate fundus feature quantitation.