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PHYSICAL PRINCIPLES
Luminescence- Emission of light from any source other then high temp.
Fluorescence- luminescence maintained only by continuous excitation. (stop as soon as exciting stimulus withdrawn)
FFA
PURPOSE
Evaluate, Diagnose -Retinal, Choroidal vascular & Macular diseases Guide - for laser treatment Monitor-effect of treatment
1871-Adolf Baeyer-first to synthesize dye Na. Fluorescien 1910-Burke examine the Retina & choroid after administration of fluorescien in coffee 1925-Nordenson fundus camera 1961-Novotny & Alvis- First Successful FFA in human.
HISTORY
TECHNIQUE
seated in front of fundus camera Color & Red-free image is capture Fluorescein dye 5ml of 10% or 3ml 25%(for opaque media) injected. Images taken approx 1-sec intervals ,5-12 sec after inj. After transit phase photograph in one eye control picture of opposite eye.
Flourescene enters in the eye through ophthalmic artery Passing into the choroidal circulation.post ciliary A. Retina-central retinal a.
PHASES OF ANGIOGRAM
Choroidal (10-12 sec) Arterial (1-3 sec) A-V (capillary) Venous (20-25 sec) Recirculation(30 sec ) Late phase(10 min)
ARTERIAL PHASE
Filling of CRA.
Dye from smaller venules enter the vein along their wall-laminar flow Dye sticks to the wall of vein At the junction of two vein ,inner lamina of each merge creating a trilaminar flow
A-V PHASE
Dye completely fill the lumen of vein Perifoveal capillary network best visualized (dye max concentration) Fovea appears hypofluo.
RECIRCULATION PHASE
Begins about 30 sec of dye inj Dye in lower concentration
LATE PHASE
Vessels are empty(10 min after inj) Diffuse background fluo (d/t staining of bruchs memb. choroid & sclera ) Large vessels seen in silhouette against this background Disc remain hyperfluo in late film (staining)
WATERSHED ZONE
Post ciliary a. supply the lat. & medial halves of disc & choroid Four (sometime 6-7) post ciliary vein (vertex vein) drain into sup. & inf ophthalmic veins quadrantric pattern Segmental drainage exists vertical & horizontal watershed FA-patchy choroidal filling
ABNORMAL FLUORESCENCE
d/t LEAKAGE (a) Abnormal choro.vasculatureCNV Early lacy filling pattern which increase in size & intensity
b)(Breakdown of inner retinal barrier-CME Beginning of A-V phase which increase in size and intensity Flower-petal pattern (late phase)
CSR
(b) In the sub-RPE space- PED early hyperfluo which increases in intensity but not in size
STAINING
Attachment of the dye molecule to tissue May be seen in late phase of angiogram It occur in normal structure (sclera) or pathological states (Scar ,drusen) Margins do not go beyond
CAUSES OF HYPOFLUORESCENCE
Reduction or absence of fluo. (a) Blockage(masking)-retinal / choroidal (b) Filling defects
FILLING DEFECTS
1-Vascular occlusion-prevent access dye to the tissue Occlusion may choroidal circulation / retinal a./r.vein/capillaries(capillary drop out) 2 loss of vascular bed-severe myopic deg or choroideremia