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What is Opthalmoscopy?
Ophthalmoscopy (funduscopy or 
fundoscopy) is a test that allows a health 
professional to see inside the fundus of the 
eye and other structures using an 
ophthalmoscope (or funduscope).
It is done as part of an eye examination and 
may be done as part of a routine physical 
examination. It is crucial in determining the 
health of the retina and the vitreous humor.
History of Ophthalmoscopy
• Ophthalmoscope was 
first invented by 
Hermann von 
Helmholtz(1821-1894), 
a professor of physics 
from Germany in 1851. 
• He called it an 
Augenspiegel (eye 
mirror)
• In 1915, Josh Zele and Jon Palumbo 
invented the world's first hand-held direct 
illuminating ophthalmoscope 
• Precursor to the device now used by 
clinicians around the world 
• The company started as a result of this 
invention is Welch Allyn.
Commonly used brands in 
our country 
• Keeler 
• Heine 
•Welch allyn
Types of Ophthalmoscope
Direct: 
This type of ophthalmoscope is most 
commonly used during a routine physical 
examination. 
Indirect: 
Indirect ophthalmoscopy provides a wider 
view of the inside of the eye and allows a better 
view of the fundus even if the lens is clouded 
by cataracts. Used by opthalmologist.
Parts of an ophthalmoscope
How to hold an ophthalmoscope?
Aperture settings
Wide angle view: 
Illuminates the largest 
area of fundus for the 
best possible general 
diagnosis through a 
large dilated pupil 
Intermediate angle view: 
Permits easier access 
through an undilated pupil 
and in peripheral 
examination. Particularly 
useful in pediatric 
examination. 
Macula view: Designed 
specifically for examination of 
the macula region of the 
fundus where a larger beam 
would create excessive 
pupillary reaction or patient 
discomfort. 
Glaucoma: Projects a 
graticule onto the retina 
to assess the optic 
cup/disc ratio as an aid 
to glaucoma diagnosis. 
Slit: Used primarily to 
determine retinal 
elevations and 
depressions, but may 
also be used to assess 
anterior chamber depth 
Fixation Star or Cross: 
Projects a graticule onto the 
retina to assess the degree 
and direction of eccentric 
fixation, eg, as a result of 
macula degeneration
Beam filter 
Red free: The red-free 
filter is used to examine 
the blood vessels in fine 
detail. By filtering out the 
red rays, blood vessels 
are silhouetted black 
against a dark green 
background. 
Cobalt blue: Used in 
conjunction with fluorescein 
dye for the detection and 
examination of corneal scars 
and abrasions. 
Safety: The unique Keeler 
safety filter cuts out the ultra 
violet, visible blue and 
infrared wavelengths said to 
cause phototoxic retinal 
damage with prolonged 
exposure.
Procedure of Opthalmoscopy
Pre-requisite: 
• It should be done in a dark room. 
• Explain whole of the procedure to the patient. 
• Pupil is dilated or moderately dilated, but be 
careful about mydriatic in Glaucoma or Intra 
ocular implanted lens (IOL). Dilating the pupil 
with 1% tropicamide or 1% cyclopentolate. 
This blurs the near vision for 2-3 hrs.
• Proper positioning: Lying or sitting in chair 
(better). If lying, move to opposite side 
when need to examine left eye. 
• Appropriate direction. 
• Proper positioning of the examiner. 
• Both the eye should be seen
Examination sequence
• At first check your 
ophthalmoscope’s 
battery. 
• Adjust the 
ophthalmoscope light 
to a comfortable 
brightness.
• Set the 
ophthalmoscope 
lens wheel to zero 
diopters (D) or 
correct your visual 
error by glass or 
ophthalmoscope 
lens. 
• Adjust the focus 
ring & focus filter.
• Stand 1 hand or half meter apart from the 
patient in same horizontal plane as 
patient’s eye. 
• Ask the patient to look straight ahead at 
a distant object – patient should continue 
to look in this direction even if the 
examiner’s head obscures the target.
• Patient’s right eye/ your right eye / your right 
hand /patient’s right side & vice versa.
A distance of about 10-30 cm from the 
patient try to see through the viewing hole 
of the ophthalmoscope and focus the light 
around the patient’s eye. Direction of light 
should be toward the nose, about 15 
degrees from the line of fixation. Instruct the 
patient to see the distal fixation point with 
the opposite eye.
• The pupil should 
appear pink from 10 
cm distance. This is 
the Red reflex. 
• Any opacity in the 
media appear black 
upon the red reflex. 
• If total red reflex is 
lost, it is due to 
Medial opacity ( 
cataract, vitreous 
haemorrhage) or 
Retinal problem. 
Pupillary red reflex 
opacity
If patient doesn’t 
cooperate, fix the head 
by placing your other 
hand on the patient’s 
forehead & gently retract 
the upper eyelid.
Now come close to the 
patient’s head ,bring the 
ophthalmoscope to within 
1-2cm of the eye . Not to 
touch the eye lash of the 
patient. Now you can see 
inside the eye. At first try 
to see any vessel, then 
follow it medially to find 
out the optic disc.
• Follow the blood vessels as they extend 
from the optic disc in four directions: 
superotemporally, inferotemporally, 
superonasally& inferonasally 
• Ask the patient to look up to see superior 
retina, look down to see inferior retina, 
look temporally to examine temporal retina 
,look nasally to examine the nasal retina
• Finally locate the centre of the macula 
by asking the patient to look directly 
at the light .Macula present two disc 
temporal from the optic disc
SOME COMMON MISTAKES that we can 
do, must be corrected by the following way: 
1.Examine at the same level 
2. Never obstruct the opposite eye 
3.Never examine the right eye by left eye 
and left hand & vice versa 
4.Never give too much pressure to the head 
and shoulder
Common misinterpretations 
1.Temporal pallor : Normally paler than nasal, 
often misinterpreted as abnormal 
2.Myopic fundus: Myopic eye is large, so disc 
appears paler ,may be mistaken for optic 
atrophy. 
3.Hypermetropic fundus: Small eye ,disc 
appears crowded, mistaken for papilledema
4.Drusen: Colloid bodies that may occcur on 
disc, mistaken for papilloedema 
5.Pigmentation on the disc edge :Normal-may 
make disc seem pale 
6.Tortuous vessels: normal
Purpose of Fundoscopy
• Detection of any haziness 
(opacity) in media, 
• Detection of any optical error. 
• To look inside of the eye.
Haziness in media 
• Corneal opacity, 
• Lens opacity, 
• Vitreous opacity. 
• It can be detected while observing the red reflex by 
moving the ophthalmoscope; Right/Left or up/down. 
• If opacity moves opposite to the light:- Corneal opacity. 
• If opacity moves towards the light :- Vitreous opacity. 
• If opacity is fixed :- Lens opacity
Various opacities in media 
Normal red reflex 
Corneal opacity cataract
Optical Error 
• If focus is hazy, adjust the lens of the 
ophthalmoscope to (-) or (+) and denote 
myopia or hypermetropia of the patient, but 
make sure that your eye is error free. 
• If operator's eye power is normal or if he/she 
using glasses and Still the focus is hazy, it is 
due to optical error of the patient.
• At first you will have to turn the focus dial 
clockwise (plus or black lens), if error is 
corrected – Patient is Hypermetropic. 
• If no improvement, then turn the focus dial 
anticlockwise (minus or red lens), if error is 
corrected – Patient is Myopic
What will see in fundus?
Retinal field
Disc
Macula
Blood Vessels 
Vein 
Artery
Optic Disc 
• The optic disc or optic nerve head is 
the location where ganglion cell 
axons exit the eye to form the optic 
nerve 
• The optic disc represents the 
beginning of the optic nerve
• There are no light sensitive rods or 
cones to respond to a light stimulus at 
this point. This causes a break in the 
visual field called "the blind spot" or 
the "physiological blind spot".
Things to be seen: 3c 
• Contour(Margin): 
– The borders of the optic disc should be clear and 
well defined 
• Color: 
– Typically the optic disc looks like an orange-pink 
area with a pale centre. The orange-pink 
appearance represents healthy, well perfused 
neuro-retinal tissue
Cup: 
As mentioned above 
the disc has an 
orange-pink rim with 
a pale centre. This 
pale centre is devoid 
of neuroretinal tissue 
and is called the cup
Blood vessels 
Arteries: 
They are superficial, tortuous & 
brighter. Normally arterial walls are 
invisible, seen as streak, when light is 
focused bright streak light reflexion is 
seen.
• Veins : 
They are thick, deeper & darker. Normally 
venous pulsation is visible near the disc. 
• Total vessels count in disc : 7-10, which 
include vein & artery. Count only the main 
vessels not the branches. 
• Normal vein : artery = 3:2.
Common retinal abnormalities
White/yellow lesions: 
Cotton wool spots (soft 
exudates): White fluffy 
spots with indistinct margin 
caused by retinal ischemia 
due to accumulation of 
axonal proteins in the nerve 
fiber layer. 
Causes: Severe HTN, DM, 
retinal vein occlusion 
,SLE,AIDS. 
Cotton wool
Hard exudates: Bright 
yellowish sharp-edged 
lesions consist of lipid 
deposition that result from 
leakage of plasma from 
abnormal retinal 
capillaries. 
Causes: DM, HTN. 
Chorioretinal atrophy: 
Well defined punched out 
lesion. 
Cause: Previous retinal 
inflammation, injury 
Hard exudate 
Hard exudate
Black lesion: 
Retinal pigment 
hypertrophy: Black 
lesion like bony spicules 
in periphery. Causes: 
Retinitis pigmentosa 
due to any cause, 
previous injury/laser. 
Retinitis pigmentosa
Laser burns: black 
edged round lesion. 
Usually in regular 
pattern. 
Moles: flat, usually 
round. Normal 
findings. 
Melanoma: raised 
irregular malignant 
tumour. 
Laser burns 
Malignant melanoma
Red lesion 
Dot haemorrhage: Thin 
vertical haemorrhage that 
may be difficult to 
differentiate from 
microaneurysms seen 
adjacent to blood vessels. 
Cause: DM. 
Blot haemorrhage: Larger 
full thickness 
haemorrhages in the 
deeper layer of retina 
.Rounded, localized. 
Causes: DM 
Dot haemorrhage 
Blot haemorrhage
Flame haemorrhage: 
Superficial bleed, 
shaped by nerve fibres 
into a fan with point 
towards the disc. 
Cause: HTN, retinal 
vein oclusion.
Deep large 
haemorrhage: 
Retinal/pre-retinal. 
Causes: Bleeding 
diathesis.
Subhyaloid 
haemorrhage: 
Irregular superficial 
with flat top. 
Causes: 
Subarachnoid 
haemorrhage.
Pathology in Optic Disc 
Common abnormality in optic disc: 
• Optic disc swelling (Papilloedema/ Papillitis) 
• Optic atrophy. 
• Glaucomatous cupping. 
• Abnormal vessels.
Optic disc swelling 
Optic nerve head 
swelling can be 
inflammatory or non-inflammatory 
. 
If non-inflammatory: 
Papilloedema 
If Inflammatory: 
Papillitis.
Papilledema 
• Caused by raised intracranial pressure. 
• Loss of venous pulsation (normally absent 
in 15% people.) 
• Disc is abnormally red. 
• Margins are blurred, upper nasal quadrant 
first, then lower nasal, then temporal 
margin.
• Physiological cup becomes obliterated. 
• Retinal veins are slightly distended. 
• If papilloedema develops rapidly, there 
will be marked engorgement of the retinal 
veins with haemorrhages & exudates on & 
arround the disc. 
• If develops slowly, may be little or no 
vascular change.
PAPILLITIS 
Ophthalmoscopy 
• Ophthalmoscopy may show no 
abnormalities on retrobulbar optic neuritis. 
• Dilatation of retinal arteries and veins on 
optic nerve disc . 
• Possible petty splinter hemorrhages on the 
optic nerve disc .
• Retinal edema 
around the optic disc. 
• Optic nerve disc has 
blurred margins 
• Reddish (hyperemic) 
optic nerve disc due 
to dilatation of blood 
vessels . 
• Possible white 
exudates on the optic 
nerve disc .
PAPILLITIS PAPILLOEDEMA 
Usually unilateral Usually bilateral 
Marked dimness of vision. May be slight dimness of vision. 
Not loss. 
Loss of afferent pupillary reflex Not loss. 
Visual field defect is usually central, 
particularly for red & green. 
Peripheral constriction or enlargement of 
blind spot. 
Eye ball is painful & tender. Not painful/tender.
Optic Atrophy 
Features of optic atrophy 
• Disc is small. 
• Pale. 
• Loss of function. 
Added may be 
• Reduced number of 
vessels (< 7). 
• Margin may be sharp / 
blurred.
Types 
1. primary 
2. secondary
Primary optic atrophy 
• Due to disease of the optic 
nerve. 
• Disc is flat, pale/white. 
• Clear-cut, sharp margins. 
• Decreased / loss of vision 
Secondary optic atrophy 
• Due to long standing 
papilloedema. 
• Disc is greyish-white. 
• Indistinct margins. 
• Decreased / loss of 
vision.
Papilloedema Optic atrophy 
In both picture disc margins are blurred/indistinct & vessels 
count decreased, but in secondary optic atrophy disc colour 
is pale & in papilloedema disc colour is abnormally red.
Optic cup and Cup Disc ratio(CDR) 
• The optic cup is the white, 
cup-like area in the center of 
the optic disc. 
• The ratio of the size of the 
optic cup to the optic disc 
(or cup-to-disc ratio) is the 
cup disc ratio. 
• Normally the cup should 
take up less than 50% of the 
disc,i.e. CDR is <.5 
• The CDR is measured to 
diagnose Glaucoma
Glaucoma 
CDR= .4 
CDR= .77
Progression of 
glucomatous 
Optic nerve 
Damage
Hypertensive retinopathy 
Grade 1 : 
Arteriolar thickening, tortuosity, increased reflectiveness 
(‘Silver wiring’). 
Grade 2: 
Grade 1 plus constriction of veins at arterial crossings 
(‘Arteriovenous nipping/nicking’). 
Grade 3: 
Grade 2 plus evidence of retinal ischaemia (‘Flame shaped 
or blot hemorrhage and cotton wool exudate’). 
Grade 4: 
Grade 3 plus papilloedema.
Grade 1
Grade 1
Grade 1 
Silver wiring: 
– It’s the appearance of blood vessels in 
which the arterial wall becomes so 
completely opaque that the blood 
column is not seen and the central light 
reflex occupies all of the width of the 
arteriole. 
– The light is completely reflected, yielding 
a white ‘line,’ likened to a silver wire,
Grade 2 
Normal AV nipping
Grade 2 
• AV nicking: A vascular abnormality in the 
retina of the eye, visible on ophthalmologic 
examination, in which a vein is 
compressed by an arteriovenous crossing 
• The vein appears "nicked" as a result of 
constriction or spasm
Grade 3 
Cotton wool 
exudate 
Blot Haemorrhage 
Flame shaped
Grade 4
Hypertensive Retinopathy
Diabetec Retinopathy 
Classification of Diabetic Retinopathy 
–Non-proliferative ‘background’ 
retinopathy without maculopathy, 
–Maculopathy, 
– Pre-proliferative retinopathy, 
– Proliferative retinopathy
Non-proliferative ‘background 
retinopathy without maculopathy 
Blot hemorrhage 
Dot hemorrhage 
Hard Exudate
Maculopathy 
Hard exudate 
Dot and blot 
Haemorrhage 
Macular oedema Macular oedema, exudates, dot & blot 
hemorrhage
Pre proliferative retinopathy 
Features of pre-proliferative retinopathy: 
–Venous loops & beading, dot-blot 
haemorrhage, large retinal hemorrhage, 
cotton wool exudates, macular oedema with 
reduced visual acuity, perimacular exudates, 
retinal hemorrhages of any size. But no 
proliferative changes.
Pre-proliferative retinopathy
Proliferative diabetec retinopathy 
Abnormal blood 
vessels
HTN with DM
Fundoscopy findings in 
different conditions
Retinitis pigmentosa 
1.Retinal 
pigmentation 
2.Thin Blood 
vessels 
3.Pale optic disc
Central retinal vein occlusion 
1.Dilated and 
tortuous retinal 
veins 
2.Diffuse intraretinal 
haemorrhage in all 
4 quadrants 
3.Cotton wool spots 
4.Swollen optic disk 
5. Retinal oedema
Central retinal artery occlusion 
1. Retina appears 
pale due to Retinal 
edema 
2. Optic disc 
swelling 
3. Macula with 
cherry-red spot on 
white-yellow 
background
Acute Leukaemia 
Acute leukemia: 
Intra-retinal 
white-centered 
hge. (Roth spot) 
Cotton-wool 
spots
Aplastic anaemia 
Disc edema 
Retinal hge
Vitreous haemorrhage 
preretinal- unclotted 
blood with 
boatshaped 
configuration, 
moving towards 
gravity
Sub arachnoid Haemorrhage 
Disc swelling 
Retinal hge 
Subhyaloid hge 
Vitreous hge
Photocoagulation scar mark
Retinal detachment 
Mobile 
Convex 
Corrugated 
retina
Retinoblastoma 
Leukocoria 
Direct 
visualization of 
tumor 
(Multi globulat- 
-ed white mass with 
overlying retinal 
detachment)
Roth’s spot 
Bacterial endocarditis 
DM , Leukemia 
Pernicious anemia 
HTN,AIDS
Cytoid body 
Systemic lupus erythematosus.
IOL (intra ocular lens) 
Anterior chamber IOL Posterior chamber IOL
Thank You

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Opthalmoscopy Uploaded by Parash

  • 1.
  • 3. Ophthalmoscopy (funduscopy or fundoscopy) is a test that allows a health professional to see inside the fundus of the eye and other structures using an ophthalmoscope (or funduscope).
  • 4. It is done as part of an eye examination and may be done as part of a routine physical examination. It is crucial in determining the health of the retina and the vitreous humor.
  • 6. • Ophthalmoscope was first invented by Hermann von Helmholtz(1821-1894), a professor of physics from Germany in 1851. • He called it an Augenspiegel (eye mirror)
  • 7. • In 1915, Josh Zele and Jon Palumbo invented the world's first hand-held direct illuminating ophthalmoscope • Precursor to the device now used by clinicians around the world • The company started as a result of this invention is Welch Allyn.
  • 8. Commonly used brands in our country • Keeler • Heine •Welch allyn
  • 10. Direct: This type of ophthalmoscope is most commonly used during a routine physical examination. Indirect: Indirect ophthalmoscopy provides a wider view of the inside of the eye and allows a better view of the fundus even if the lens is clouded by cataracts. Used by opthalmologist.
  • 11. Parts of an ophthalmoscope
  • 12.
  • 13. How to hold an ophthalmoscope?
  • 14.
  • 16. Wide angle view: Illuminates the largest area of fundus for the best possible general diagnosis through a large dilated pupil Intermediate angle view: Permits easier access through an undilated pupil and in peripheral examination. Particularly useful in pediatric examination. Macula view: Designed specifically for examination of the macula region of the fundus where a larger beam would create excessive pupillary reaction or patient discomfort. Glaucoma: Projects a graticule onto the retina to assess the optic cup/disc ratio as an aid to glaucoma diagnosis. Slit: Used primarily to determine retinal elevations and depressions, but may also be used to assess anterior chamber depth Fixation Star or Cross: Projects a graticule onto the retina to assess the degree and direction of eccentric fixation, eg, as a result of macula degeneration
  • 17. Beam filter Red free: The red-free filter is used to examine the blood vessels in fine detail. By filtering out the red rays, blood vessels are silhouetted black against a dark green background. Cobalt blue: Used in conjunction with fluorescein dye for the detection and examination of corneal scars and abrasions. Safety: The unique Keeler safety filter cuts out the ultra violet, visible blue and infrared wavelengths said to cause phototoxic retinal damage with prolonged exposure.
  • 19. Pre-requisite: • It should be done in a dark room. • Explain whole of the procedure to the patient. • Pupil is dilated or moderately dilated, but be careful about mydriatic in Glaucoma or Intra ocular implanted lens (IOL). Dilating the pupil with 1% tropicamide or 1% cyclopentolate. This blurs the near vision for 2-3 hrs.
  • 20. • Proper positioning: Lying or sitting in chair (better). If lying, move to opposite side when need to examine left eye. • Appropriate direction. • Proper positioning of the examiner. • Both the eye should be seen
  • 22. • At first check your ophthalmoscope’s battery. • Adjust the ophthalmoscope light to a comfortable brightness.
  • 23. • Set the ophthalmoscope lens wheel to zero diopters (D) or correct your visual error by glass or ophthalmoscope lens. • Adjust the focus ring & focus filter.
  • 24. • Stand 1 hand or half meter apart from the patient in same horizontal plane as patient’s eye. • Ask the patient to look straight ahead at a distant object – patient should continue to look in this direction even if the examiner’s head obscures the target.
  • 25. • Patient’s right eye/ your right eye / your right hand /patient’s right side & vice versa.
  • 26. A distance of about 10-30 cm from the patient try to see through the viewing hole of the ophthalmoscope and focus the light around the patient’s eye. Direction of light should be toward the nose, about 15 degrees from the line of fixation. Instruct the patient to see the distal fixation point with the opposite eye.
  • 27. • The pupil should appear pink from 10 cm distance. This is the Red reflex. • Any opacity in the media appear black upon the red reflex. • If total red reflex is lost, it is due to Medial opacity ( cataract, vitreous haemorrhage) or Retinal problem. Pupillary red reflex opacity
  • 28. If patient doesn’t cooperate, fix the head by placing your other hand on the patient’s forehead & gently retract the upper eyelid.
  • 29. Now come close to the patient’s head ,bring the ophthalmoscope to within 1-2cm of the eye . Not to touch the eye lash of the patient. Now you can see inside the eye. At first try to see any vessel, then follow it medially to find out the optic disc.
  • 30. • Follow the blood vessels as they extend from the optic disc in four directions: superotemporally, inferotemporally, superonasally& inferonasally • Ask the patient to look up to see superior retina, look down to see inferior retina, look temporally to examine temporal retina ,look nasally to examine the nasal retina
  • 31. • Finally locate the centre of the macula by asking the patient to look directly at the light .Macula present two disc temporal from the optic disc
  • 32. SOME COMMON MISTAKES that we can do, must be corrected by the following way: 1.Examine at the same level 2. Never obstruct the opposite eye 3.Never examine the right eye by left eye and left hand & vice versa 4.Never give too much pressure to the head and shoulder
  • 33. Common misinterpretations 1.Temporal pallor : Normally paler than nasal, often misinterpreted as abnormal 2.Myopic fundus: Myopic eye is large, so disc appears paler ,may be mistaken for optic atrophy. 3.Hypermetropic fundus: Small eye ,disc appears crowded, mistaken for papilledema
  • 34. 4.Drusen: Colloid bodies that may occcur on disc, mistaken for papilloedema 5.Pigmentation on the disc edge :Normal-may make disc seem pale 6.Tortuous vessels: normal
  • 36. • Detection of any haziness (opacity) in media, • Detection of any optical error. • To look inside of the eye.
  • 37. Haziness in media • Corneal opacity, • Lens opacity, • Vitreous opacity. • It can be detected while observing the red reflex by moving the ophthalmoscope; Right/Left or up/down. • If opacity moves opposite to the light:- Corneal opacity. • If opacity moves towards the light :- Vitreous opacity. • If opacity is fixed :- Lens opacity
  • 38. Various opacities in media Normal red reflex Corneal opacity cataract
  • 39. Optical Error • If focus is hazy, adjust the lens of the ophthalmoscope to (-) or (+) and denote myopia or hypermetropia of the patient, but make sure that your eye is error free. • If operator's eye power is normal or if he/she using glasses and Still the focus is hazy, it is due to optical error of the patient.
  • 40. • At first you will have to turn the focus dial clockwise (plus or black lens), if error is corrected – Patient is Hypermetropic. • If no improvement, then turn the focus dial anticlockwise (minus or red lens), if error is corrected – Patient is Myopic
  • 41. What will see in fundus?
  • 43. Disc
  • 46. Optic Disc • The optic disc or optic nerve head is the location where ganglion cell axons exit the eye to form the optic nerve • The optic disc represents the beginning of the optic nerve
  • 47. • There are no light sensitive rods or cones to respond to a light stimulus at this point. This causes a break in the visual field called "the blind spot" or the "physiological blind spot".
  • 48. Things to be seen: 3c • Contour(Margin): – The borders of the optic disc should be clear and well defined • Color: – Typically the optic disc looks like an orange-pink area with a pale centre. The orange-pink appearance represents healthy, well perfused neuro-retinal tissue
  • 49. Cup: As mentioned above the disc has an orange-pink rim with a pale centre. This pale centre is devoid of neuroretinal tissue and is called the cup
  • 50. Blood vessels Arteries: They are superficial, tortuous & brighter. Normally arterial walls are invisible, seen as streak, when light is focused bright streak light reflexion is seen.
  • 51. • Veins : They are thick, deeper & darker. Normally venous pulsation is visible near the disc. • Total vessels count in disc : 7-10, which include vein & artery. Count only the main vessels not the branches. • Normal vein : artery = 3:2.
  • 53. White/yellow lesions: Cotton wool spots (soft exudates): White fluffy spots with indistinct margin caused by retinal ischemia due to accumulation of axonal proteins in the nerve fiber layer. Causes: Severe HTN, DM, retinal vein occlusion ,SLE,AIDS. Cotton wool
  • 54. Hard exudates: Bright yellowish sharp-edged lesions consist of lipid deposition that result from leakage of plasma from abnormal retinal capillaries. Causes: DM, HTN. Chorioretinal atrophy: Well defined punched out lesion. Cause: Previous retinal inflammation, injury Hard exudate Hard exudate
  • 55. Black lesion: Retinal pigment hypertrophy: Black lesion like bony spicules in periphery. Causes: Retinitis pigmentosa due to any cause, previous injury/laser. Retinitis pigmentosa
  • 56. Laser burns: black edged round lesion. Usually in regular pattern. Moles: flat, usually round. Normal findings. Melanoma: raised irregular malignant tumour. Laser burns Malignant melanoma
  • 57. Red lesion Dot haemorrhage: Thin vertical haemorrhage that may be difficult to differentiate from microaneurysms seen adjacent to blood vessels. Cause: DM. Blot haemorrhage: Larger full thickness haemorrhages in the deeper layer of retina .Rounded, localized. Causes: DM Dot haemorrhage Blot haemorrhage
  • 58. Flame haemorrhage: Superficial bleed, shaped by nerve fibres into a fan with point towards the disc. Cause: HTN, retinal vein oclusion.
  • 59. Deep large haemorrhage: Retinal/pre-retinal. Causes: Bleeding diathesis.
  • 60. Subhyaloid haemorrhage: Irregular superficial with flat top. Causes: Subarachnoid haemorrhage.
  • 61. Pathology in Optic Disc Common abnormality in optic disc: • Optic disc swelling (Papilloedema/ Papillitis) • Optic atrophy. • Glaucomatous cupping. • Abnormal vessels.
  • 62. Optic disc swelling Optic nerve head swelling can be inflammatory or non-inflammatory . If non-inflammatory: Papilloedema If Inflammatory: Papillitis.
  • 63. Papilledema • Caused by raised intracranial pressure. • Loss of venous pulsation (normally absent in 15% people.) • Disc is abnormally red. • Margins are blurred, upper nasal quadrant first, then lower nasal, then temporal margin.
  • 64. • Physiological cup becomes obliterated. • Retinal veins are slightly distended. • If papilloedema develops rapidly, there will be marked engorgement of the retinal veins with haemorrhages & exudates on & arround the disc. • If develops slowly, may be little or no vascular change.
  • 65.
  • 66. PAPILLITIS Ophthalmoscopy • Ophthalmoscopy may show no abnormalities on retrobulbar optic neuritis. • Dilatation of retinal arteries and veins on optic nerve disc . • Possible petty splinter hemorrhages on the optic nerve disc .
  • 67. • Retinal edema around the optic disc. • Optic nerve disc has blurred margins • Reddish (hyperemic) optic nerve disc due to dilatation of blood vessels . • Possible white exudates on the optic nerve disc .
  • 68. PAPILLITIS PAPILLOEDEMA Usually unilateral Usually bilateral Marked dimness of vision. May be slight dimness of vision. Not loss. Loss of afferent pupillary reflex Not loss. Visual field defect is usually central, particularly for red & green. Peripheral constriction or enlargement of blind spot. Eye ball is painful & tender. Not painful/tender.
  • 69. Optic Atrophy Features of optic atrophy • Disc is small. • Pale. • Loss of function. Added may be • Reduced number of vessels (< 7). • Margin may be sharp / blurred.
  • 70. Types 1. primary 2. secondary
  • 71. Primary optic atrophy • Due to disease of the optic nerve. • Disc is flat, pale/white. • Clear-cut, sharp margins. • Decreased / loss of vision Secondary optic atrophy • Due to long standing papilloedema. • Disc is greyish-white. • Indistinct margins. • Decreased / loss of vision.
  • 72. Papilloedema Optic atrophy In both picture disc margins are blurred/indistinct & vessels count decreased, but in secondary optic atrophy disc colour is pale & in papilloedema disc colour is abnormally red.
  • 73. Optic cup and Cup Disc ratio(CDR) • The optic cup is the white, cup-like area in the center of the optic disc. • The ratio of the size of the optic cup to the optic disc (or cup-to-disc ratio) is the cup disc ratio. • Normally the cup should take up less than 50% of the disc,i.e. CDR is <.5 • The CDR is measured to diagnose Glaucoma
  • 74. Glaucoma CDR= .4 CDR= .77
  • 75. Progression of glucomatous Optic nerve Damage
  • 76. Hypertensive retinopathy Grade 1 : Arteriolar thickening, tortuosity, increased reflectiveness (‘Silver wiring’). Grade 2: Grade 1 plus constriction of veins at arterial crossings (‘Arteriovenous nipping/nicking’). Grade 3: Grade 2 plus evidence of retinal ischaemia (‘Flame shaped or blot hemorrhage and cotton wool exudate’). Grade 4: Grade 3 plus papilloedema.
  • 79. Grade 1 Silver wiring: – It’s the appearance of blood vessels in which the arterial wall becomes so completely opaque that the blood column is not seen and the central light reflex occupies all of the width of the arteriole. – The light is completely reflected, yielding a white ‘line,’ likened to a silver wire,
  • 80. Grade 2 Normal AV nipping
  • 81. Grade 2 • AV nicking: A vascular abnormality in the retina of the eye, visible on ophthalmologic examination, in which a vein is compressed by an arteriovenous crossing • The vein appears "nicked" as a result of constriction or spasm
  • 82. Grade 3 Cotton wool exudate Blot Haemorrhage Flame shaped
  • 85. Diabetec Retinopathy Classification of Diabetic Retinopathy –Non-proliferative ‘background’ retinopathy without maculopathy, –Maculopathy, – Pre-proliferative retinopathy, – Proliferative retinopathy
  • 86. Non-proliferative ‘background retinopathy without maculopathy Blot hemorrhage Dot hemorrhage Hard Exudate
  • 87. Maculopathy Hard exudate Dot and blot Haemorrhage Macular oedema Macular oedema, exudates, dot & blot hemorrhage
  • 88. Pre proliferative retinopathy Features of pre-proliferative retinopathy: –Venous loops & beading, dot-blot haemorrhage, large retinal hemorrhage, cotton wool exudates, macular oedema with reduced visual acuity, perimacular exudates, retinal hemorrhages of any size. But no proliferative changes.
  • 90. Proliferative diabetec retinopathy Abnormal blood vessels
  • 92. Fundoscopy findings in different conditions
  • 93. Retinitis pigmentosa 1.Retinal pigmentation 2.Thin Blood vessels 3.Pale optic disc
  • 94. Central retinal vein occlusion 1.Dilated and tortuous retinal veins 2.Diffuse intraretinal haemorrhage in all 4 quadrants 3.Cotton wool spots 4.Swollen optic disk 5. Retinal oedema
  • 95. Central retinal artery occlusion 1. Retina appears pale due to Retinal edema 2. Optic disc swelling 3. Macula with cherry-red spot on white-yellow background
  • 96. Acute Leukaemia Acute leukemia: Intra-retinal white-centered hge. (Roth spot) Cotton-wool spots
  • 97. Aplastic anaemia Disc edema Retinal hge
  • 98. Vitreous haemorrhage preretinal- unclotted blood with boatshaped configuration, moving towards gravity
  • 99. Sub arachnoid Haemorrhage Disc swelling Retinal hge Subhyaloid hge Vitreous hge
  • 101. Retinal detachment Mobile Convex Corrugated retina
  • 102. Retinoblastoma Leukocoria Direct visualization of tumor (Multi globulat- -ed white mass with overlying retinal detachment)
  • 103. Roth’s spot Bacterial endocarditis DM , Leukemia Pernicious anemia HTN,AIDS
  • 104. Cytoid body Systemic lupus erythematosus.
  • 105. IOL (intra ocular lens) Anterior chamber IOL Posterior chamber IOL