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 FLUORESCENCE :- Property of the certain
molecules to emit light energy of longer wave
length when stimulated by a shorter
wavelength.
 Absorbs light in the blue range peaking at
465-490 nm
 Emits light of yellow-green range of visible
spectrum peaking at 520-530nm.
 Diabasic Acid, Yellow Red in color.
 Stable, Highly Water Soluble & Pharmacologically
inert.
 Low Molecular Weight 376.27 D
 Fluoresces at Blood pH
 Peak absorption 465 – 490 nm
 Peak emission 520 – 530 nm
 80% bound to plasma protein and also with RBC
 Can’t pass through tight retinal barriers so allows
study of retinal circulation
 within 24 hours
 Mainly –urine ( yellow orange coloration)
 Small amount-bile
 Some absorbed by kidney
 Skin staining may remain up to 24 hours
 Urine discoloration –24-36 hours
 10 % Solution of 5 ml
 25% Solution of 3 ml (for opaque media)
 Solution above 25% precipitates.
Peripheral vein
venous circulation
heart
arterial system
INTERNAL CAROTID ARTERY
Ophthalmic artery
Short posterior ciliary artery Central retinal Artery
(choroidal circulation) (retinal circulation)
 Patient is informed of the normal procedures, the side
effects and the adverse reactions.
 Dilating the pupil
 Made to sit comfortable.
 3-4 red free photographs taken.(control
photographs)
 5ml of 10% or 3ml of 25% NAF injected through the
anticubital vein
 wait for 10 – 12 seconds( normal arm-retina time)
 Photos are taken at 1 second interval for 10 seconds
 Then every 2 seconds interval for 30 seconds
 Late photographs are usually taken after 3 ,5 and 10 minutes
 Prearterial phase (choroidal phase)
 Arterial phase
 Arterio -venous phase
 Venous phase
early venous
mid venous
late venous
 Late phase
 10 -12 seconds
 Initially patchy filling diffuse filling dye leaks
from choriocapillaris
 no dye reaches retinal arteries
 Cilioretinal artery if present fills in this phase
CHOROIDAL
PHASE
ARTERIAL PHASE
ARTERIO-VENOUS PHASE
EARLY VENOUS PHASE
MID VENOUS PHASE
MID VENOUS LATE VENOUS
 Gradual elimination of dye from choroidal and the retinal
circulation
 Staining of disc :- normal
 After 30 seconds of injection first high concentration
flush of fluoroscein begins to empty and Recirculation
phase follows.
 Vessels completely empty of fluoroscein in approx
10 minutes.
PHASE TIME ( IN Secs)
Injection 0
Choroidal phase 10
Arterial 10-12
Arterio venous 13
Early venous 14-15
Mid venous 16-17
Late venous 18-20
Late ( elimination) 5 MINS
Angiogram
Normal Abnormal Artifact
Hyperfluorescence Hypofluoresence
 HYPERFLUORESCENCE – an area of abnormally
high fluorescence due to increase density of dye
molecule
 HYPOFLUORESCENCE - an area of abnormally
poor fluorescence
 PSEUDOFLUORESCE
NCE
- Non fluorescent light
passes through entire
filter system.
- Decreased contrast
and resolution
Conditions: Any light
colored fundus change
e.g.
Sclera
Scar tissue
Myelinated nerve fibre
Foreign Body
 innate property of fluorescence in certain
ocular tissue
 fluorescence without dye
 Optic nerve head drusen & astrocytic
hamartoma
 Fluorosence of Disc margins from surrounding
capillaries
 Fluorosence of lamina cribrosa
 Fluorosence of Sclera at disc margin if RPE terminates
away from disc as in Optic crescent
 Fluoresence of Sclera if RPE is lightly pigmented.
POOLING –
 accumulation of dye in closed space e.g. RPE
detachment, CSR
SUB-RETINAL SPACE SUB RPE SPACE
Early hyperfluorescence early hyperfluorescence
increase in size & intensity increase intensity only
e.g. CSR,CNVM e.g. PED
 Refers to leakage of fluoroscein into tissue or material
 Must be contrasted from Pooling
 Rule out which tissue involved:
RPE
Bruch’s Memb
Choroid
Sclera
 Evaluation of vascular integrity of retinal &
choroidal vessels
 Disease process affecting macula
 Integrity of the Blood Ocular Barrier.
- outer blood retinal barrier breaks in :- CSR
- inner blood retinal barrier breaks in:-NVD ,NVE
 Determining the extent of damage
 Formulating the treatment strategy for retinal
& choroidal disease.
 Monitoring the result of treatment.
MILD MODERATE SEVERE
Staining of skin,
sclera and mucous
membrane
Nausea ,vomiting laryngeal edema
bronchospasm
Stained secretion
Tear, saliva
Vasovagal
response
Circulatory shock,
MI, cardiac arrest
Orange-yellow urine urticaria Generalized
convulsion
Skin flushing,
tingling lips, pruritus
fainting Skin necrosis
periphlebitis
ABSOLUTE
1) known allergy
2) H/O adverse reaction in past.
 Asthma
 Hay fever
 Renal failure
 Hepatic failure
 Pregnancy ( especially 1st trimester)
Fundus Fluoroscein Angiography

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Fundus Fluoroscein Angiography

  • 1.
  • 2.  FLUORESCENCE :- Property of the certain molecules to emit light energy of longer wave length when stimulated by a shorter wavelength.  Absorbs light in the blue range peaking at 465-490 nm  Emits light of yellow-green range of visible spectrum peaking at 520-530nm.
  • 3.
  • 4.
  • 5.  Diabasic Acid, Yellow Red in color.  Stable, Highly Water Soluble & Pharmacologically inert.  Low Molecular Weight 376.27 D  Fluoresces at Blood pH  Peak absorption 465 – 490 nm  Peak emission 520 – 530 nm  80% bound to plasma protein and also with RBC  Can’t pass through tight retinal barriers so allows study of retinal circulation
  • 6.  within 24 hours  Mainly –urine ( yellow orange coloration)  Small amount-bile  Some absorbed by kidney  Skin staining may remain up to 24 hours  Urine discoloration –24-36 hours
  • 7.  10 % Solution of 5 ml  25% Solution of 3 ml (for opaque media)  Solution above 25% precipitates.
  • 8. Peripheral vein venous circulation heart arterial system INTERNAL CAROTID ARTERY Ophthalmic artery Short posterior ciliary artery Central retinal Artery (choroidal circulation) (retinal circulation)
  • 9.
  • 10.  Patient is informed of the normal procedures, the side effects and the adverse reactions.  Dilating the pupil  Made to sit comfortable.  3-4 red free photographs taken.(control photographs)
  • 11.  5ml of 10% or 3ml of 25% NAF injected through the anticubital vein  wait for 10 – 12 seconds( normal arm-retina time)  Photos are taken at 1 second interval for 10 seconds  Then every 2 seconds interval for 30 seconds  Late photographs are usually taken after 3 ,5 and 10 minutes
  • 12.  Prearterial phase (choroidal phase)  Arterial phase  Arterio -venous phase  Venous phase early venous mid venous late venous  Late phase
  • 13.  10 -12 seconds  Initially patchy filling diffuse filling dye leaks from choriocapillaris  no dye reaches retinal arteries  Cilioretinal artery if present fills in this phase
  • 19. MID VENOUS LATE VENOUS
  • 20.  Gradual elimination of dye from choroidal and the retinal circulation  Staining of disc :- normal  After 30 seconds of injection first high concentration flush of fluoroscein begins to empty and Recirculation phase follows.  Vessels completely empty of fluoroscein in approx 10 minutes.
  • 21. PHASE TIME ( IN Secs) Injection 0 Choroidal phase 10 Arterial 10-12 Arterio venous 13 Early venous 14-15 Mid venous 16-17 Late venous 18-20 Late ( elimination) 5 MINS
  • 23.  HYPERFLUORESCENCE – an area of abnormally high fluorescence due to increase density of dye molecule  HYPOFLUORESCENCE - an area of abnormally poor fluorescence
  • 24.
  • 25.  PSEUDOFLUORESCE NCE - Non fluorescent light passes through entire filter system. - Decreased contrast and resolution Conditions: Any light colored fundus change e.g. Sclera Scar tissue Myelinated nerve fibre Foreign Body
  • 26.  innate property of fluorescence in certain ocular tissue  fluorescence without dye  Optic nerve head drusen & astrocytic hamartoma
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35.  Fluorosence of Disc margins from surrounding capillaries  Fluorosence of lamina cribrosa  Fluorosence of Sclera at disc margin if RPE terminates away from disc as in Optic crescent  Fluoresence of Sclera if RPE is lightly pigmented.
  • 36.
  • 37.
  • 38.
  • 39.
  • 40.
  • 41. POOLING –  accumulation of dye in closed space e.g. RPE detachment, CSR SUB-RETINAL SPACE SUB RPE SPACE Early hyperfluorescence early hyperfluorescence increase in size & intensity increase intensity only e.g. CSR,CNVM e.g. PED
  • 42.
  • 43.
  • 44.
  • 45.  Refers to leakage of fluoroscein into tissue or material  Must be contrasted from Pooling  Rule out which tissue involved: RPE Bruch’s Memb Choroid Sclera
  • 46.
  • 47.
  • 48.
  • 49.
  • 50.
  • 51.
  • 52.
  • 53.
  • 54.
  • 55.  Evaluation of vascular integrity of retinal & choroidal vessels  Disease process affecting macula  Integrity of the Blood Ocular Barrier. - outer blood retinal barrier breaks in :- CSR - inner blood retinal barrier breaks in:-NVD ,NVE
  • 56.  Determining the extent of damage  Formulating the treatment strategy for retinal & choroidal disease.  Monitoring the result of treatment.
  • 57. MILD MODERATE SEVERE Staining of skin, sclera and mucous membrane Nausea ,vomiting laryngeal edema bronchospasm Stained secretion Tear, saliva Vasovagal response Circulatory shock, MI, cardiac arrest Orange-yellow urine urticaria Generalized convulsion Skin flushing, tingling lips, pruritus fainting Skin necrosis periphlebitis
  • 58.
  • 59.
  • 60. ABSOLUTE 1) known allergy 2) H/O adverse reaction in past.
  • 61.  Asthma  Hay fever  Renal failure  Hepatic failure  Pregnancy ( especially 1st trimester)