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FUNDUS FLUORESCEIN ANGIOGRAPHY

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Presentation on theme: "FUNDUS FLUORESCEIN ANGIOGRAPHY"— Presentation transcript:

1 FUNDUS FLUORESCEIN ANGIOGRAPHY
NISHITA AFRIN B.OPTOM 3rd batch ICO,CU

2 INTRODUCTION Fluorescein angiography refers to photographing fluorescein dye in the retinal vasculature following intravenous injection of fluorescein solution

3 FLUORESCENCE C20H12O5 Refers to fluorescein sodium (C20H10Na2O5)
A brown or ornge red crystalline substance, alkaline in nature First synthesized in 1871 in Germany by Von Bayer

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5 CONTINUE… Metabolized by liver and exerted by kidney
Absorbs blue light (490nm ) and emits yellow-green light (530nm) Metabolized by liver and exerted by kidney

6 HAZARDS OF FLUORESCEIN DYE
Reletively safe drug Temporary tan skin coloration Urine discoloration Transient nausea and vomiting More severe : hives ,asthmatic symptoms and laryngeal edema

7 CONTINUE… Myocardial infraction Respiratory and Cardiac arrest
Syncope , anaphylactic reaction to fluorescein Myocardial infraction Respiratory and Cardiac arrest

8 INDOCYANINE GREEN Binds to plasma protein, confined to vascular system
Cyanine dye Binds to plasma protein, confined to vascular system Molecular wt. 775 dalton Half life – dalton Remove from circulation by the liver to bile juice

9 Absorbs 600 nm -900 nm and emits 750 nm to 950 nm

10 General Principles of ICG Angiography
1. Binding 98% bound to proteins Less leakage from choriocapillaris 2. Fluorescence Much less than fluorescein Excitation peak 800 nm Emission at 835 nm 3. Filters Infrared barrier and excitation 4. Safer than fluorescein

11 Side effects of ICG… Sore throats and hot flashes Anaphylactic shock
Risk in pregnancy Sore throats and hot flashes Anaphylactic shock Hypotension Trachycardia Dyspnea and Urticaria

12 CLINICAL USE OF FLUORESCENCE DYE
Clinical use Research Care -treatment protocol for retinal diseases - to understand retinal and choroidal leisons . E.g. Age related macular degeneration, diabetic retinopathy ,retinal detachment…

13 Anatomic Considerations

14 FFA

15 General principles of FA
Fluorescein 85% bound to serum proteins 15% unbound ‘free’ fluorescein Inner blood-retinal barrier (retinal capillaries) Impermeable to fluorescein Outer blood-retinal barrier (zonula occludens) Impermeable to fluorescein Choriocapillaris Permeable only to ‘free’ fluorescein

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18 OPTICAL PRINCIPLE

19 Filters 1.Blue excitation filter 2.Yellow-green filter

20 PROCEDURE… Pupils should well dialed
Patient seat infront of the camera Red free photographs taken Dye injected in the forearm or anticubital vein Photographs with fluorescein - 1 sec interval between 5 and 25 secs - late photographs after mins

21 Syringe with NaF Insertion of needle containing Retractable needle with catheter system Mild hematoma

22 Angiographic phases: Five angiographic phases:
Pre arterial (choroidal 9-15 seconds) Arterial Arteriovenous(capillary) Venous Recirculation

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24 Circulation of NaF Dye injected from peripheral vein
venous circulation heart arterial system INTERNAL CAROTID ARTERY Ophthalmic artery Short posterior ciliary artery) Central retinal artery (choroidal circulation.) ( retinal circulation) N.B. The choroidal filling is 1 second prior to the retinal filling.

25 1-Choroidal flush 2-Arterial phase

26 3-Arteriovenous phase

27 4-Venous phase Mid Phase Late Phase

28 Interpretation of FA

29 Red-free fundus photos
Normal appearance Autofluorescence

30 Abnormal angiographic findings
Hypofluorescence: Filling defect Blocking defect Hyperfluorescence : window defect Leakage Pooling Staining

31 Subretinal neovasculari-
zation Choroid Tumor vessels Chorioretinal anastomosis Vascular tortuosities Dilation and shunts Anastomosis Neovascularization Hyperfluorescence Anomalous vessels Aneurysms Retina Teleangiectasia Tumor vessels Hamatoma Neovascularization Tortuosity Optic nerve head Dilation Hamatoma Tumor vessels

32 Retinal Cystoid edema In a preformed space (pooling) Subretinal Detachment of the pigment epithelium Hyper- fluorescence Leakage Detachment of the sensory retina Retina noncystoid edema Into tissue (staining) Subretinal e.g.dursen

33 Fibers, optic nerve drusen
Drusen of the optic nerve head Autofluorescence Fluorescence without the administration of fluorescein Hamatoma Scleral exudate Scar tissue Pseudofluorescence Foreign body Myelinate nerve Fibers, optic nerve drusen

34 Causes of dark appearance of fovea
Avascularity Blockage of background choroidal fluorescence by: Increased density of xanthophyll Large RPE cells with more melanin

35 Causes of hyperfluorescence
RPE ‘ window’ defect Pooling of dye RPE atrophy (bull’s eye maculopathy Under RPE (pigment epithelial detachment) Under sensory retina (central serous retinopathy)

36 Causes of hyperfluorescence
Leakage of dye Prolonged dye retention ( staining ) Into sensory retina (cystoid macular oedema) From new vessels (choroidal neovascularization Associated with drusen

37 Capillary non-perfusion
Causes of hypofluorescence Vascular occlusion Loss of vascular tissue Capillary non-perfusion (venous occlusion) Choroideremia or high myopia

38 Red-free fundus photos
Normal appearance Autofluorescence

39 Autofluorescence

40 Macular hole

41 CHOROIDAL NAEVUS

42 DIABETIC MACULOPATHY TREATED WITH LASER

43 BACKGROUND DIABETIC RETINOPATHY

44 CENTRAL SEROUS RETINOPATHY

45 PROLIFERATIVE DIABETIC RETINOPATHY (early venous phase)

46 Stargardt's Disease

47 DIABETIC AND HYPERTENSIVE RETINOPATHY

48 Limitations of FFA 1) Does not permit study of choroidal circulation details due to a) melanin in RPE b) low mol wt of fluorescein 2) More adverse reaction 3) Inability to obtain angiogram in patient with excess hemoglobin or serum protein.e.g. polycythemia weldenstrom macroglobulenaemia binding of fluorescein with excess Hb or protein Lack of freely circulating molecule

49 THANKS TO ALL


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