Ophthalmology
Ophthalmology
Neuro-ophthalmology 12
Squint 23
Lens 32
Glaucoma 42
om
Retina 58
l.c
ai
gm
Eyelids and Orbit 69
@
60
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Blow out fracture
l.c
ai
gm
Orbital Anatomy :
@
60
Base
23
(Quadrangular)
ik
hv
rit
|
Lateral wall
w
Medial
ro
wall
ar
Cone of muscle
M
©
Annulus of Zinn :
• Common tendinous ring
• Origin of EOM 45˚
Outermost :
1. Cornea :
• Transparent.
• Anterior 1/6th.
• Convex (Refracts light).
2. Sclera :
• Opaque (White).
• Posterior 5/6th.
• Covered by conjunctiva.
3. Limbus :
• Corneoscleral junction.
• Contains stem cells :
om
- Specific marker : ABCG2.
l.c
- Universal marker : CD34.
ai
gm
Middle : Uvea (Vascular).
@
60
1. Iris :
23
ik
2. Ciliary body :
w
ro
Limbus
Sclera
Iris
Seen posterior
to cornea Pupil
Pars plana
Choroid
Sclera (Uvea)
Ciliary body (Uvea) Retina Fovea :
Pars plicata • Max. no. of cones
(Centre of visual field)
Zonules • Best image
• Foveal fixation develops
Cornea by 3-4 months.
Iris (Uvea)
Pupil Optic nerve Neuroretinal rim
(Peripheral)
Optic cup (Central)
Aqueous (Anterior
segment)
Lens
om
Central artery & vein of retina
l.c
Vitreous
ai
(Posterior segment) Optic disc
gm
(Blind spot, no photoreceptors)
@
60
23
Limbal Pathologies :
w
ro
1. Limbal dermoid :
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M
2. Pterygium :
- Limbal stem cell deficiency.
- Conjunctiva grows over cornea Limbal dermoid
(Normally, conjunctiva only covers the sclera).
Can
regenerate
Thickest
om
l.c
ai
gm
Strongest
@
60
23
Can
ik
regenerate Posterior
hv
Most metabolically
rit
active (Innermost)
Layers of cornea
|
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ro
1. Epithelium :
ar
M
• Layers :
- Superficial : Squamous (Microvili + Adhesion of tear film).
- Basal : Columnar (Mitosis + Regeneration).
2. Bowman’s layer :
• False basement membrane (PAS -ve).
• Acellular
(No regeneration Heals by scar formation Corneal opacity LOV).
Corneal opacities :
Pupillary margin Iris details Depth of involvement
Nebular (Faintest) Visible Visible Bowman’s & superficial stroma
Macular Visible ≤ 1/2 stroma
Not seen
Leucoma (Most opaque) Not seen Not seen ≥ 1/2 stroma
Nebular opacity : Maximum discomfort (Induces irregular astigmatism).
Leucoma : Maximum visual loss.
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Cornea and Sclera 5
3. Stroma : Made of collagen (M/c Type 1) & GAGs (M/c keratan sulphate). ----- Active space -----
6. Endothelium :
• Metabolism + .
• Maintains corneal transparency.
No. of endothelial cells (Cells/mm2) Significance
2400-3000 Normal
<2400 Corneal compensation
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<500 (Critical point) Corneal decompensation Edema Hazy cornea
l.c
ai
gm
Note : Counted using specular microscopy
@
60
Orbicularis oculi
©
Blink No blinking
----- Active space ----- Special Investigations for the Cornea 00:15:59
1. Pachymetry :
• Measures corneal thickness (CT).
• Normal CT ~ 540 microns/0.54 mm.
2. Keratometry :
• Measures corneal curvature.
• Astigmatism : Vertical curvature ≠ Horizontal curvature.
Positioning of
keratometric
mires
Keratometer Incorrect Incorrect Correct
om
l.c
ai
3. Topography : gm
Examination of corneal surface using Placido disc.
@
60
23
4. Staining :
ik
hv
a. Fluorescein dye :
rit
tonometry.
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©
Abrasion. Stroma
(Regenerates)
Corneal ulcer
om
l.c
Nocardia :
ai
gm
• Seen in traumatic cases.
@
Note :
hv
rit
Pseudomonas :
|
w
M/c cause of corneal ulcer in contact lens users. Wreath/Pin head pattern ulcer
ro
ar
M
om
• DOC : 5% Natamycin eye drops.
l.c
ai
• Rest of the management is similar to bacterial corneal ulcers.
gm
@
HERPETIC KERATITIS
60
23
Disease Progression :
ik
hv
rit
|
w
ro
If If
ar
M
untreated untreated
©
Note :
1. Neuroparalytic ulcer (Not d/t herpes) : CN VII palsy Loss of blinking
(Lagophthalmos) Exposure keratitis Neuroparalytic ulcer.
2. Lagophthalmos seen in Leprosy & Bell’s palsy.
Signs :
• Radial keratoneuritis. Pseudo dendrites
• Ring abscess.
• Pseudodendrites. Ring abscess
Culture :
Non-nutrient agar enriched with E.coli.
(Pseudopods seen)
Treatment :
• PHMB 0.02% (DOC)
om
l.c
• Chlorhexidine 0.1.%
Accessible
ai
gm
• Propamidine
@
60
23
• Autosomal dominant.
w
ro
ar
Types :
M
©
Keratoconus 00:54:45
Cone-shaped cornea.
Signs :
om
l.c
ai
gm
@
60
23
ik
V-shaped lower lid Light thrown from one side refracts to form
|
Note :
©
Treatment :
• INTACS’s surgery : Intracorneal stromal ring
segments.
• Rigid contact lens.
• Keratoplasty : Corneal transplantation (Cadaveric
donor). INTACS Sx :
• Corneal collagen cross linking with riboflavin & UVA Ring stretches the cornea
radiation
(C3R) : Best initial treatment.
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Cornea and Sclera 11
Sclera 00:59:45
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Hue Reddish Bluish/violaceous
l.c
ai
Pain Mild gm Deep seated, chronic
Response to phenylephrine Redness disappears Redness persists
@
60
Before After
Episcleritis : Phenylephrine test
Retina :
• Covers posterior part of eye till ora serrata.
• Deficient anteriorly.
Left Right
Nasal (N)
visual field
om
Temporal Temporal (T) Nasal visual field → Temporal fibers
l.c
visual visual field Temporal visual field → Nasal fibers
ai
field
gm
@
60
Temporal
23
Temporal
fibers
ik
fibers Nasal
hv
5
ro
8
M
©
Lateral geniculate
6 body (LGB)
Relay centre I/L Temporal & C/L Nasal fibers
9
Superior fibres 7
Inferior fibres Optic radiations
(OR)
Note : FOF
Field loss is opposite to loss of fibres. (Temporal fibres injured Nasal field lost.)
T N N T
L R
om
Optic chiasm
l.c
under ACA Bitemporal/Heteronymous
ai
gm Hemianopia
@
L R
|
w
ro
ar
L T N N T R
M
©
Junctional scotoma
T : Temporal
SN : Superonasal
IN : Inferonasal
M/c cause : Meningioma
L T N N T R
4. Lateral optic chiasma :
- B/L temporal (Always B/L)
- Very rare
Binasal hemianopia
P C/L homonymous
F 9 superior quadrantanopia,
LGB AKA “Pie in the sky.”
Mnemonic : TIPS
VC
om
(Temporal inferior pie in the sky)
T 8
l.c
L R
ai
gm T N N T
9. Superior OR : Baum’s loop
@
quadrantanopia,
|
T N N T
©
C/L homonymous
macular defect
T N N T
L R
Causes for bitemporal hemianopia : 3PC & AC ----- Active space -----
1. 3rd ventricular CSF blockage Ventricular dilatation O ptic chiasma
glioma compression.
2. Pituitary macroadenoma (>10 mm/1 cm).
3. Craniopharyngioma.
4. Anterior communicating artery aneurysm.
5. Caverous sinus thrombosis.
om
Optic
Present bilaterally Present (Optic radiations are
l.c
atrophy
ai
gm post ganglionic : 4th order)
@
Pupillary Reflex
hv
00:34:04
rit
|
Light stimulus
(L) (R)
B/L short
ciliary nerve
1. Optic nerve
6. B/L ciliary
ganglion
om
5. B/L CN III
l.c
2. Optic tract
(Inferior fibres of
ai
gm
inferior oblique Pupillomotor fibres exit from optic
@
Note :
©
AAPD RAPD
Light stimulus on
Light stimulus on N eye :
B/L pupils constrict
N eye :
B/L pupils constrict
om
Paradoxical dilatation Nerve fatigue
l.c
of pupils
ai
gm
Pupils size Isocoria : Both pupils equal in size
@
60
• Cause : Neurosyphilis.
w
ro
ar
Loss of accomodation.
Constricts d/t denervation hypersensitivity
MOA : Sphincter pupillae denervated
Diluted
Does not constrict
Pilocarpine
Over-expression of receptors (Even with 1% pilocarpine)
(0.125%)
Hyperreactive to stimuli.
om
Muscles of Iris 00:51:36
l.c
ai
gm
Sphincter pupillae Dilator pupillae
@
via (Excitatory)
|
Via
w
ro
1˚neuron
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©
Course and Lesions of Sympathetic Supply to the Iris : ----- Active space -----
Ophthalmic division of
trigeminal nerve
Hypothalamus
Long ciliary nerve
om
Causes : ganglion • Cluster headache
l.c
• Brain stem lesions T1 • Internal carotid artery dissection
ai
(Tumor, etc)
gm • Otitis media
Second order neuron • Cavernous sinus mass
@
• Syringomyelia
60
Spinal cord
hv
Causes :
w
• Pancoast tumor
ro
ar
• Neck lesions
©
1 % amphetamine test
om
Pupil dilates Pupil does not dilate
l.c
ai
gm Post ganglionic lesion.
Pre ganglionic lesion.
@
60
Optic atrophy without antecedent Optic atrophy after optic disc Optic atrophy due to disease of
ar
Definition
optic disc swelling swelling inner retina and its blood supply
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©
Optic cup -
Treatment :
• Steroids : Anti-inflammatory for Rx of multiple sclerosis IV f/b oral.
• Interferons
Papilledema
om
01:04:52
l.c
Signs :
ai
gm
• Blurring of disc margins : Earliest.
@
60
• Normal vision.
23
↑ICP
rit
Edematous OD :
|
w
D/t ↑ICP
ro
Transient blindness
• Visual field defects : Enlargement of blind spot.
• Paton’s lines : Retinochoroidal folds around OD d/t
fluid accumulation.
Treatment : Control ICP. Paton’s lines
1° colors :
• Red : Prota. • Green : Deutra. • Blue : Trita.
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• Perception of 2 Only rod + One type of
• Perception of all 3 colors + cone +
l.c
colors
ai
Features • Perception is defective
• Blindness for 1 gm Total color blind
(Anomalous)
color (Anopia)
@
• Protanopia • Protanomaly
23
Clinical Hemaralopia
ik
• Deuteranopia • Deuteranomaly -
hv
Tests :
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ro
Chart
Numbers
Shapes
• M/c used
Features Used to test pediatric age group
• Disadv. : Cannot detect tritan defects
Chart
6 EOMs act on eyeball & I EOM acts on eyelid (Levator palpabrae superioris).
om
Actions
l.c
Muscle
ai
1˚ (Predominates in abduction) 2˚ (Predominates in adduction)
gm 3˚
Superior Rectus (SR) Elevation Intorsion
@
Adduction
60
Abduction
Inferior Oblique (IO) Extorsion Elevation
rit
|
w
ro
Nerve supply :
ar
M
Adduction Abduction
Intorsion Extorsion
Depression
Anatomical action of EOM Clinical action of EOM
Note : Superior oblique function can be confirmed by asking the pt. to look at the
tip of their nose.
1˚ gaze
2˚ gaze
3˚ gaze
om
l.c
ai
gm
@
60
Upward/Hyperdeviation Downward/Hypodeviation
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5. Incyclotropia 6. Excyclotropia
l.c
ai
gm
@
60
23
ik
Note :
|
w
Incyclotropia and excyclotropia are clinically not visible. Dx : Double Maddox rod
ro
ar
test.
M
©
Investigations 00:19:06
1. Normal : 0˚
Reflection 2. At pupillary margin : 15˚
Reflection nasal at centre
to centre 1 2 3 4 4. At limbus : 45˚
3. B/w 2 & 4 : 30˚
DOOR : Deviation
Opposite Of Reflection Position of corneal reflection
Note :
Temporal deviation. • 1 prism dioptre = 0.5 degree.
(AKA : Exotropia) • 1 mm deviation = 7˚ of squint.
om
l.c
ai
gm
2. Cover & Uncover Test :
@
At presentation :
At presentation :
RE Exophoria
om
l.c
Concave lines
ai
gm Note :
Amsler’s grid has straight lines,
@
60
not concave.
23
ik
hv
rit
|
w
Equipment :
M
4 dots :
©
Interpretation :
om
6 CN
th
• Uncrossed diplopia.
Lateral rectus Abduction Esotropia -
l.c
Palsy • I/L face turn.
ai
gm
@
out pupil
ar
M
©
LE hypertropia
↑↑Hypertropia
(Worse on opposile gazes)
Improved hypertropia
(Better on opposite tilt)
MR LR
Afferent
Efferent
om
l.c
ai
gm
3rd
@
60
23
ik
hv
rit
Internuclear
|
X
w
X
M
RE LE RE LE
C/L abduction +
Left gaze palsy : Left gaze defect :
Lt. PPRF/Rt. FEF lesions Rt. MLF lesion
Esotropia/Crossed-eyes :
M/c presentation of concomitant squint.
1. Accomodative : (Role of accomodation + )
om
Refractive Non-refractive
l.c
ai
Hypermetropia D/t high accomodative
Cause gm
(SO HYPER) convergence/accomodation ratio
@
60
Bifocal spectacles
ik
Rx Convex spectacles
hv
Miotics : Echothiophate
rit
Clinical Features :
• Ptosis :
- B/L
- Worsens as day progresses (D/t ↓ ACh Fatigue)
• Diplopia
• Cogan lid twitch sign : Upper eyelid shoots up on switching from downward
gaze to upward gaze.
Diagnosis :
Tensilon test : Definitive test.
om
l.c
ai
gm
Inj Edrophonium
@
60
23
Anatomy :
om
l.c
ai
gm
@
Metabolic Pathways :
• Anaerobic glycolysis (>80%).
• Kreb’s cycle & HMP shunt (~ 15%). Polyol
• Sorbitol pathway (<5%) : Glucose Aldose Sorbitol Fructose.
Reductase dehydrogenase
Accumulate in lens
- Normally inactive.
Cataract
- Activated by hyperglycemia (DM & galactosemia).
Cataract :
• Gradual & painless loss of vision.
• M/c cause of blindness in India.
om
l.c
Classification :
ai
gm
@
Acquired Congenital
60
23
Metabolic Infantile
ik
Traumatic
hv
Developmental
rit
Complicated
|
w
Senile/age related
ro
ar
Metabolic Cataract
M
00:11:37
©
1. Parathyroid tetany :
Children : Lamellar cataract.
Hypocalcemia
Adults : Anterior & posterior subcapsular cataract.
Snowflake cataract
2. Snowflake cataract :
DM (Type 1 > Type 2) Carbamylation of crystallins Cortical cataract.
Note :
----- Active space -----
1. Kayser Fleischer ring : A/w Wilson’s disease
- Golden-brown Cu2+ deposition in the Descemet’s membrane near the limbus.
- Progression : Superior Inferior Lateral Circumferential.
- All cases with neurological manifestation and 50% cases with only hepatic
manifestation.
2. Fleischer’s ring : A/w keratoconus.
Kayser Fleischer ring 3. Pseudo-fleischer’s ring : A/w hypermetropia.
om
BLUNT TRAUMA
l.c
Contusion injury Posterior subcapsular cataract.
ai
gm
(Tennis ball/Fist injury) (Rosette shaped cataract)
@
60
23
Signs :
ik
hv
Chamber (AC).
ar
M
2. Iris signs :
©
• Retinal Detachment (RD) : M/c rhegmatogenous RD. ----- Active space -----
• Commotio retinae : Pale fundus.
• Traumatic optic neuropathy : Causes 1° optic atrophy.
• Vitreous hemorrhage : M/c cause in young adults.
5. 2° open angle glaucoma:
• Angle recession glaucoma. • Ghost cell glaucoma.
Note :
Cherry red spot at macula
Mnemonic : Cherry Trees Never Grow Tall in Sand, Mud & Grime
• Central retinal artery occlusion (CRAO)
• Trauma (Blunt)
• Niemann-Pick disease
• GM1 gangliosidoses
• Tay-Sachs disease
om
• Sandhoff’s disease
l.c
• Metachromatic leukodystrophy
ai
• Multiple sulfatase deficiency gm
• Gaucher’s disease (Type 2 only) : Least common
@
60
23
Blowout fracture
Complicated Cataract 00:30:15
Opacified nucleus
Nucleus
Cataract +
Clinical Features :
• Induced myopia (Near-sightedness).
• Second sight phenomenon : Improved near vision.
• LOV : Day > Night (D/t central location; Pupil dilates in low light).
om
• Xanthopsia : Yellow colored vision d/t discolored lens.
l.c
ai
gm
Cortical Cataract :
@
60
Pathogenesis :
23
ik
hv
Hydration of lens
rit
|
w
(Earliest change)
M
Intumescent cataract
©
Wedge-shaped opacities
Liquified cortex
(Cuneiform cataract) Sunken Nucleus
Persistent hydration
Swollen lens
(Intumescent cataract)
Morgagnian/Hypermature cataract Argentinian flag sign
M/c complication : d/t puncturing of
Cortex liquefied. Phacolytic glaucoma swollen lens during CCC
(Morgagnian cataract) (2° OA glaucoma)
Clinical Features :
• Glare Difficulty in driving at night (M/c).
• Max. LOV (Near > Far; Day > Night).
om
Causes : AACG
l.c
• Amiodarone • Chlorpromazine
ai
gm
• Atopic dermatitis • Gold deposits
@
60
23
Surgical Methods:
|
Techniques of ECCE :
Site of Incision Size of Incision
1. Conventional ECCE Limbus 8–10 mm
2. Small Incision Cataract Surgery (SICS) Sclera (Sclera-corneal tunnel) 5–7 mm
3. Phacoemulsification Clear corneal 2.2–3.2 mm
Nd : Glass Laser
Principle Photodisruption
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
38 Ophthalmology
om
l.c
ai
gm
@
60
Types of IOL :
M
©
C shaped haptic
Optic
S shaped haptic
PCIOL ACIOL
(Posterior chamber IOL) (Anterior chamber IOL)
• Implanted in the capsular bag.
• Better choice.
2. A-scan USG : Axial length/AP diameter of eye ( N AL ~ 24 mm). ----- Active space -----
Axial Length
Operative :
• Posterior Capsular Rupture (PCR).
om
• Uveitis-Glaucoma-Hyphema (UGH) Syndrome d/t ACIOL.
l.c
• Vitreous loss.
ai
gm
• Expulsive choroidal hemorrhage : Bleeding from choroidal artery.
@
60
or gas in AC Descemetopexy.
ik
hv
rit
Postoperative :
|
w
- Types
©
om
better vision
l.c
Evisceration Immediate pars plana
ai
(Removal of all vitrectomy
gm Vitreous tap
structures but sclera) +
@
60
+
ik
Congenital Cataract
ar
01:03:00
M
©
Types :
Blue dot/punctate
m/c type Riders cataract
Opacity
(Spoke like (A/w Downs syndrome)
in fetal
opacities)
nucleus
Rx Immediate surgery -
Cornea
Cortex
Aqueous Opacity at the centre
of posterior capsule
Anterior capsule
Miscellaneous 01:05:50
om
l.c
of zonules.
ai
gm
Inferiorly displaced lens
Causes :
@
60
Lenticonus :
Cornea
Aqueous
Anterior lens surface
PATHOPHYSIOLOGY
Optic neuropathy :
• Optic disc changes : Progressive, characteristic.
• Visual field defects : Irreversible.
• IOP : Normal/raised (Normal : 11-21 mmHg).
Glaucoma can occur by either ↑production or ↓clearance of aqueous.
Flow of Aqueous :
om
Trabecular and uveoscleral outflow.
l.c
ai
Trabecular outflow : gm
@
Trabecular meshwork
60
23
(Secretes aqueous)
ik
hv
rit
Schlemm’s canal
|
w
ro
ar
Aqueous vein
M
©
om
l.c
1. Kinetic (Moving targets) : Not preferred.
ai
gm Superior
2. Static (Idle targets) :
@
Fovea
23
Nasal Temporal
ik
hv
Blind spot
• Horizontally oval with an infero-nasal notch.
|
w
• Superior : Minimum.
ro
Inferior
ar
• Temporal : Maximum.
M
©
Area of ↓sensitivity
Fovea
Output
Blind-spot
HFA Machine
om
commonly used).
l.c
4. Applanation tonometry : M/c done.
ai
gm
Principle : Imbert Fick law Pressure =
@
Force/Area.
60
23
area.
rit
|
: CT
: PACD
3. Gonioscopy : Best.
Principle : Overcomes total internal reflection.
om
C/I : Dilated pupil.
l.c
Structures seen :
ai
gm
Mnemonic : Can’t see this stuff.
@
• Scleral spur.
ik
4 mirror Gonioscope
hv
• Trabecular meshwork.
rit
Baring of blind-spot
Paracentral scotoma
(Earliest clinically visible manifestation)
Occur in Connects with blind spot
Bjerrum’s Seidel’s scotoma : Paracentral scotoma Seidel’s scotoma
area Comma shaped Roenne’s
affecting Arches to opposite side nasal
arcuate Bjerrum/Arcuate scotoma step
nerve fibres.
Ring/Double arcuate scotoma Central
vision
Roenne’s central/peripheral nasal step spared
( D/t unequal contraction of upper &
om
Bjerrum/Arcuate Ring/Double
lower hemispheres)
l.c
scotoma arcuate scotoma
ai
gm
Loss of central vision
@
60
(Last to be lost)
ik
hv
Treatment :
rit
|
↓Aqueous production
Rho kinase inhibitors :
Netarsudil + -
↑Trabecular outflow
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Glaucoma 47
om
Primary Angle Closure Glaucoma 00:29:00
l.c
ai
gm
Acute disease.
@
60
Pathogenesis :
23
ik
No flow of aqueous
ro
ar
PACG
Clinical Features :
• Headache.
• Severe eye pain : IOP >40 mmHg (Rock hard eye in digital tonometry).
• High IOP disrupts the endothelium Corneal edema.
• Distorted vision : D/t hazy cornea.
• Redness of eye.
• Vomiting.
• Halos around lights : Prismatic dispersion d/t corneal edema.
om
• Oral acetazolamide
l.c
• Pilocarpine eyedrops (Miotic) : Given after ↓IOP; Pulls iris to center and open
ai
gm
angle.
@
60
Definitive Rx :
23
ik
• Nd-YAG Laser.
|
Equalizes pressure.
ar
M
Laser iridotomy
©
Signs :
1. Buphthalmos :
Enlarged eyeballs:
• Deep AC.
• ↑Axial length Myopia.
• Corneal diameter >13 mm.
• Blue sclera. Blue sclera
2. Haab’s striae
3. Hazy cornea : Earliest sign.
Symptoms :
• Blepharospasm
• Photophobia
• Lacrimation Haab’s striae
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Glaucoma 49
TYPES
1. Lens Induced :
• Phacomorphic : Intumescent cataract.
• Phacolytic : Morgagnian cataract.
2. Pigmentary :
• Presents as 2° open angle glaucoma.
• Krukenberg spindles : Characteristic.
Target sign
om
3. Pseudoexfoliation :
l.c
M/c cause of 2° open angle glaucoma.
ai
gm
@
Characteristic Signs :
60
23
material on lens.
rit
on pupillary margin.
ro
ar
Fnocks
M
Causes :
• Proliferative Diabetic Retinopathy (PDR).
• Ischemic CRVO.
Progression :
Hyphema 2° OAG (AKA neovascular glaucoma).
om
light (PL) 9
6
l.c
ai
gm Snellen’s chart
Principle :
@
Each letter subtends an angle of 5 minutes of arc at nodal point of eye when
60
23
5 letters in
M
each row
©
4. Menace reflex :
• Any object brought close to the child’s
eye Child moves away.
• Develops at 4 to 6 months of age.
om
M/c used.
l.c
ai
gm
2. Jaeger’s Chart : Snellen’s near chart
@
J1 to J7 vision.
60
23
ik
Visual axis F
A E N R
a B Pupillary axis Optical axis
k
O
(Object)
Axes : Angles :
1. Anatomical axis : ANR. 1. Kappa (k) : B/w pupillary and
2. Visual axis : OENF. visual axes.
3. Pupillary axis : BE (Axis to the centre 2. Alpha (a) : B/w anatomical and
of the pupil). visual axes.
om
Principal point : Nodal point : Focal point :
• Curvature of anterior corneal
l.c
1.35 mm 7.08 mm 24.13 mm
ai
surface. gm
Distance from anterior corneal surface
@
• Length of eyeball.
60
23
ik
Refractory Error
hv
00:12:09
rit
|
Types :
w
ro
ar
M
©
Monocular Binocular
(Visual defect in 1 eye) (Visual defect in 2 eyes)
Correctable with
More Less
Power
(Image in front of retina) (Image behind the retina)
Corrective lens ‘-’/Concave (Diverging) ‘+’/Convex (Converging)
Axial length ↑(Buphthalmos) ↓
Curvature ↑ ↓
Refractory index ↑(Nuclear cataract) ↓
Anterior
Position of lens Posterior
(Weill Marchesani syndrome)
Note : 1 mm ↑ in axial length = 3D myopia.
Myopia 00:15:40
om
• Temporal myopic crescent : Choroidal & retinal atrophy.
l.c
• Posterior staphyloma.
ai
gm
• Lacquer cracks : Break in Bruch’s membrane.
@
• Vitreous hemorrhage.
ik
hv
retinal detachment.
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ro
ar
M
©
Posterior
staphyloma
(Gutter-like)
OD
Temporal myopic crescent Lacquer cracks Foster fuch spots
Regular Irregular
om
l.c
180° 90°
ai
gm
With the rule Concave (-) Convex (+)
@
60
Sturm’s conoid :
|
w
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Vc : Vertical curvature
©
Hc : Horizontal curvature
Vp : Vertical power
Hp : Horizontal power
Vc > Hc
Vp > Hp
A B C D E F G
Vertical rays Circle of least Horizontal
focused diffusion rays focused
Prescription of Spectacles :
Lens Use
- Spherical Myopia
+ Spherical Hypermetropia
- Cylinder Simple myopic astigmatism
+ Cylinder Simple hypermetropic astigmatism
- Spherical/ - Cylinder Compound myopic astigmatism
+ Spherical/ + Cylinder Compound hypermetropic astigmatism
- Spherical/ + Cylinder
OR Mixed astigmatism
+ Spherical/ - Cylinder
om
l.c
ai
gm
Objective (1st test) Subjective
@
60
23
• Refinement of refraction :
rit
- Cylinder
|
- Sphere
i. Duochrome test
ii. Pinhole test
Streak Retinoscope :
• M/c used. Trial & error method
• Light produced in vertical/horizontal beams.
• Distance of examination : 1 mt.
• Method : Comparing movement of red streak to movement of retinoscope.
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SUBJECTIVE ASSESSMENT :
l.c
Refinement for Cylindrical Lenses :
ai
gm
a. Jackson Cross Cylinder (JCC) test :
Jackson's Cross Cylinder
@
Combinations used
23
Astigmatic Fan
ar
1. Duochrome test :
2. Pinhole test :
Eliminates peripheral light rays,
allows central light rays
Placed in front of eye
Visual acuity Size of hole :
1 mm in diameter
Improves Decreases
Residual refractory Macular disease.
error.
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Optics and Refraction 57
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l.c
ai
gm
@
Presbyopia :
60
23
Spasm of Accommodation :
ar
M
• AKA Pseudomyopia.
©
Anatomy 00:00:42
Arc-like vessels
Macula (Appears avascular & temporal to optic discs)
Neuroretinal rim Optic disc
Optic cup
• Diameter : 1.5 mm
• Shape : Vertical oval
• c ratio : 0.3
d
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Fundus : Ora serrata :
l.c
• Vitreous • Anterior termination of retina.
ai
Transparent gm
• Retina • Site of intravitreal injection : Anterior to ora serrata
@
60
plana)
ik
hv
Note : Subretinal space Space b/w inner 9 layers & pigment epithelium.
Appearance
om
• +20 D lens : 3X
Magnification 15X
l.c
• + 14D lens : 5X
ai
Small : gm Large :
• Central fundus • Peripheral fundus
@
Area visualised
60
Area viewed 2 DD 8 DD
rit
|
w
ro
• Diagnoses :
Dark
- Vascular disorders. Macula
- Macular disorders :
Normal macula appears dark.
Normal FFA
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• RPE : Always red. • Fovea : Depressed contour.
l.c
ai
B (Brightness) Scan USG : gm
Structures observed :
@
60
• Vitreous (Black/hypoechoic).
23
ik
• Retina
hv
White/hyperechoic
rit
• Choroid
|
w
ro
ar
Pathologies on B-scan :
M
©
Collar stud/
mushroom
appearance
Electrooculography (EOG) :
• Records retinal standing potential from outer retina.
(Photoreceptors + Pigment epithelium)
• Measurement : Arden’s ratio = Light peak (Normal > 185%)
Dark trough
• Detects photoreceptor pathology.
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l.c
ai
Retinoblastoma gm 00:23:20
@
60
Types :
23
Genetics :
M
©
Malignancy :
• M/c malignancy : PNET/pineoblastoma.
• M/c 2o malignancy : Osteosarcoma.
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a. Homer wright rosettes (Pseudo-rosettes).
l.c
b. Fleurettes c. Flexner wintersteiner rosette
ai
gm
• Empty central lumen.
@
Treatment :
hv
rit
Macular Disorders
ar
00:29:25
M
©
Tests :
1. Amsler’s grid : Patient asked to look at the central dot.
Risk factors :
• Steroids • H. pylori infection.
• Cushing’s syndrome. • Type A personality.
Treatment :
• Self resolving, treat risk factor.
• Photodynamic therapy with Verteporfin. Not routinely done.
• Laser photocoagulation.
• Steroids C/I.
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Investigations :
l.c
ai
gm
@
60
23
ik
Subretinal
hv
rit
fluid
|
collection
w
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stack appearance
©
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• Late Geographic atrophy of RPE + . Rx : Intravitreal anti-VEGF drugs.
l.c
ai
Rx : Antioxidants @
gm
60
23
ik
hv
rit
|
w
ro
ar
M
©
Retinitis Pigmentosa :
• Rod-cone dystrophy (Rods > cones).
• M/c inheritance : Autosomal recessive.
(M/c hereditary fundus dystrophy)
Clinical Features :
• Nyctalopia, ring/donut scotoma/
tunnel vision (Rods affected).
• Bony spicule pigmentation.
• Waxy, pale optic disc. Bony spicule pigmentation
• Systemic association : Lawrence-Moon-Biedl syndrome
• Arteriolar attenuation.
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Retina 65
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Stargardt Disease :
l.c
ai
M/c cause of juvenile hereditary macular dystrophy. gm
@
60
23
ik
hv
rit
|
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ro
ar
M
©
Diabetic Retinopathy :
Risk factor : Duration of DM.
Screening : TI DM : 5 years after Dx.
T2 DM : Immediately on Dx.
----- Active space ----- Early Treatment Diabetic Retinopatly Study (ETDRS) classification :
Proliferative DR (PDR) Non-proliferative DR (NPDR)
Neovascularisation : a. Micro-aneurysms (Earliest).
• NVD : At disc. b. Hemorrhages (Flame shaped, dot & blot).
• NVE : Elsewhere c. Exudates : Lipid deposits.
d. Cotton wool spots : Neuronal debris.
Tuft of vessels
c.
(Neovascularisation) d.
Signs
Straight vessels
b.
NVD
• Requires treatment d/t leaky newly formed
vessels.
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Rx : Panretinal photocoagulation > Anti-VEGF drugs Glycemic control
l.c
Note : Lasers in ophthalmology
ai
gm
@
Photodisruption Nd-YAG/Nd-glass
rit
Photoablation Excimer
|
w
Hypertensive Retinopathy :
ro
ar
CRAO :
Causes : Atherosclerosis (M/c).
Symptoms : Sudden LOV (Emergency).
Fundus signs :
• Pale. (Retinal edema).
• Cattle tracking. (D/t blocked arteries). Cherry red spot at macula
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Retina 67
Non-ischemic Ischemic
Stasis
Complete loss of blood supply
Pathogenesis Vasodilation
Cell death
↑Vascular permeability
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Severe flame-shaped hemorrhages
l.c
C/F Macular edema (Tomato splash fundus)
ai
gm
Rubeosis iridis (Iris NV) 100 day glaucoma
@
60
BRVO :
ik
hv
Screening of infants :
• Born ≥28wks and ≥1200g : Screen after 4 wks of birth.
• Born <28wks or <1200g : Screen within 2-3 wks of birth.
Types :
Rhegmatogenous Tractional Exudative
M/c cause Pathological myopia Diabetic retinopathy Choroidal melanoma
Retinal break + - -
Syneresis (Vitreous liquefaction) + - -
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Vitreo-retinal traction + + -
l.c
ai
Photopsia + gm - -
@
+ - -
60
Floaters
23
+ + +
ik
• Retinal atrophy.
ar
M
• Intraretinal cysts.
Shaffer’s sign
Other signs - Shifting fluid
(Tobacco dust appearance)
RAPD/Marcus Gunn pupil + + +
Investigations :
10C : Indirect ophthalmoscopy.
Grey detached
retina
Normal attached
SRF retina
Eyelids
Divided by ‘Grey line’
om
- Zeis
l.c
- Moll : Sweat gland
ai
gm
Muscles of eyelid :
@
60
C/f
Appearance
om
Lid Margin Pathologies 00:08:06
l.c
ai
gm
Ectropion Entropion
@
60
23
Appearance
ar
M
©
Note :
Symblepharon (Conjunctival disorder) : Fusion of bulbar & palpebral conjunctiva.
Congenital Ptosis :
Pathology : LPS malinsertion.
Absent upper
eyelid crease
Proptosis/Exophthalmos :
Eyeball protrusion >21 mm from lateral orbital rim.
Assessment :
om
l.c
ai
gm
@
Hertel’s exophthalmometer : Better option Luedde’s exophthalmometer : Easier to use (Used in children)
60
23
Orbital varices
• U/L phleboliths on MRI
|
w
ro
Encephalocele (Infant)
• B/L, pulsatile
• 75% cases : Traumatic
Carotid cavernous fistula
• CN VI : Earliest affected nerve
• IOC : Digital Subtraction Carotid Angiography (DSCA)
Adults Children
U/L Thyroid associated ophthalmopathy Orbital cellulitis
B/L (Grave's disease) AML (Chloroma), neuroblastoma
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• M/c intrinsic lacrimal gland lesion/lacrimal gland epithelial neoplasm :
l.c
Pleomorphic adenoma.
ai
gm
• M/c orbital metastasis (Paediatric age) : Neuroblastoma.
@
60
- Breast : 42%.
rit
|
OPHTHALMOLOGY
Anatomy of Conjunctiva :
Types :
• Bulbar : Lines sclera. Bulbar
• Palpebral : Lines eyelids. Forniceal
• Forniceal : Between bulbar & palpebral conjunctiva. Palpebral
Histology :
Goblet cells :
• Present in conjunctival epithelium.
om
• Secretes mucin Forms innermost layer of tear film.
l.c
ai
Lymphatic drainage : gm
@
• Laterally
23
Conjunctivitis/Eye Flu
rit
00:02:27
|
w
Clinical Features :
ro
ar
• Redness, watering.
M
©
• Stickiness, irritation.
• Foreign body sensation.
• No loss of vision.
• No pain.
Signs :
1. Discharge :
• Sticking together of eyelids in the morning. Discharge
• Colored halos. Hypertrophied vascular cores
• Types :
- Watery : Allergies.
- Mucopurulent : Bacterial & chlamydial conditions.
2. Papillae :
Seen in allergies & bacterial infections.
Yellowish colored
lymphoid aggregates
om
l.c
ai
gm
@
60
23
Papillae Follicles
|
w
Bacterial conjunctivitis :
Type Characteristics
Acute mucopurulent Staph. aureus (M/c)
• Neisseria gonorrhoeae
Acute/hyperacute purulent/
• Overhanging eyelids + copious discharge
blennorrhea
• Pre-auricular lymphadenopathy
Acute membranous Bleeds on removal
Acute pseudomembranous Does not bleed on removal
Acute pseudomembranous type • Moraxella axenfeld
Angular/Diplobacillary • Affects lateral canthi
• Rx : Tetracyclin, zinc boric acid drops
Etiology :
Disease Chlamydia serovar
Adult inclusion conjunctivitis D-K
Trachoma A, B, Ba , C
Ophthalmia neonatorum D-K serovars, other causes
Trachoma/Egyptian Ophthalmia :
Spread : Finger, fly, fomites.
Signs :
1. Sago grain follicles + papillae.
2. Arlt’s line : Line of cicatrization (D/t concurrent inflammation & healing).
3. Herbert’s pits at limbus.
om
l.c
4. Pannus : Vascularization of cornea.
ai
gm
@
60
23
ik
hv
rit
|
w
ro
ar
Prevention :
• Erythromycin eye ointment : First 2 hrs.
• Crede’s method : Obsolete (Used silver nitrate).
Viral Conjunctivitis :
Etiology & types :
• Adenoviral.
om
l.c
- Epidemic keratoconjunctivitis (EKC).
ai
gm
- Pharyngoconjunctival fever (PCF).
@
- Picornavirus.
ik
hv
- Adenovirus.
rit
- Coxsackie A24.
|
w
• HSV.
M
©
Allergic Conjunctivitis :
Seasonal.
Types :
• Vernal keratoconjunctivitis (VKC)/Spring catarrh.
• Atopic keratoconjunctivitis : Like VKC in adults.
• Giant papillary conjunctivitis :
D/t mechanical irritation : Contact lens, protruding sutures,
ill-fitting prosthesis
• Phlyctenular conjunctivitis.
VKC/Spring catarrh :
• M/c in boys of 5–15 yrs.
• Hypersensitivity : Type 1 > 2.
• Ropy discharge : Maxwell-Lyon sign.
Ophthalmology Revision • v4.0 • Marrow 8.0 • 2024
Conjunctiva and Community Ophthalmology 77
White ring
around
the limbus
Rx :
Olopatadine (DOC) : Antihistamine + mast cell stabilizer.
+
Topical steroids : For immediate relief/acute exacerbations.
om
Pterygium 00:14:43
l.c
ai
gm
Triangular growth of conjunctiva over cornea.
@
60
Causes :
23
ik
Progression :
ro
ar
M
©
Treatment :
Excision.
Goal :
↓Prevalence of avoidable blindness to <0.25% by 2025
(National blindness & visual impairment survey : 2015-2019).
Causes :
Blindness Visual Impairment <6/18
• Cataract (M/c) • Cataract (M/c)
om
≥50 yrs
• Corneal opacity • Refractive error
l.c
ai
• Corneal opacity (M/c)
gm • Refractive error (M/c)
0-49 yrs
• Amblyopia • Cataract
@
60
23
Screening : 4Ds
w
ro