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Diseases of Uveal Tract
UVEA
• Constitutes- middle vascular coat of the eyeball
• 3 parts-
a)Iris
b)Ciliary body
c)Choroid
• Developmentally,structurally and functionally-
indivisible
• Color varies from light blue to dark brown
IRIS
• Anterior most part
• Avg diameter- 12mm, thickness- 0.5mm
• In centre an aperture of 3-4mm- PUPIL
• Thinnest at its root- tears away easily on blunt
trauma- IRIDODIALYSIS
• Divides space into anterior and posterior
chamber
MACROSCOPIC
APPEARANCE
 CILIARY ZONE-
 Radial streaks
 Crypts- peripheral-
near the iris
 central- near
collarette
 Contraction furrows-
faints lines outside
collarette
 PUPILLARY ZONE-
 Between collarette
and pigmented frill
 Pigmented frill-
black pigment at
pupillary margin
 -represents ant end
of optic cup
MICROSCOPIC STRUCTURE
1.)Anterior limiting layer
2.)Iris stroma
3.)Anterior epithelial layer
4.)Posterior pigmented epithelial layer
FUNCTIONS OF IRIS
• CONTROLS AMOUNT OF LIGHT
ENTERING THE EYE THROUGH PUPIL
• DEFINES EYE COLOUR
• CONTROL DEPTH OF FIELD
• SOURCE OF BLOOD OCULAR TISSUES
CILIARY BODY
• Forward continuation of
choroid at ora serrata
• Two parts-
a) Anterior part- ciliary
processes (pars
plicata) 2-2.5mm
b) Posterior part- smooth
(pars plana) 5mm
wide temporally &
3mm nasally
MICROSCOPIC STRUCTURE
1.)Supraciliary lamina
2.)Stroma of the ciliary body
3.)Layer of pigmented epithelium
4.)Layer of non-pigmented epithelium
5.)Internal limiting membrane
FUNCTIONS OF CILIARY
BODY
• Site of aqueous humour production
• Maintenance of IOP
• Constitutes blood aqueous barrier
• Accommodation
• Eicosanoids are synthesised in ciliary
body
CHOROID
• Posterior most part
• Extension- optic disc to ora serrata
• Inner surface- smooth, brown and in
contact with RPE
• Outer surface-rough and in contact with
sclera
• Thickness- posteriorly 0.22mm
- anteriorly 0.10mm
MICROSCOPIC STRUCTURE
1) Suprachoroidal lamina
2) Stroma of the choroid
3) Basal lamina
FUNCTIONS OF CHOROID
• BLOOD SUPPLY TO OUTER FOUR LAYERS OF
RETINA
• MODULATION OF VASCULARISATION
• REGULATE RETINAL HEAT
• ASSIST IN THE CONTROL OF INTRAOCULAR
PRESSURE
• PIGMENT ABSORBS EXCESS LIGHT SO
AVOIDING REFLECTION
BLOOD SUPPLY UVEAL
TRACT
1.SHORT POSTERIOR CILIARY ARTERIES
• Branches of ophthalmic artery
• Divides into 10-20 branches, pierce sclera around optic nerve
• Supply choroid in segmental manner
2) LONG POSTERIOR CILIARY ARTERIES
• Anastomose with anterior ciliary arteries- form major arterial circle supply
ciliary body
3)ANTERIOR CILIARY ARTERIES
• From muscular arteries
• 2 each SR,IR, MR and 1 from LR
Anastomse with LPCA
• Circulous arterious major and minor
VENOUS DRAINAGE
1. Anterior ciliary veins- tributaries of
muscular veins
2. Smaller veins from sclera- carry blood
only from sclera and not from choroid
3. Vena verticosae- 4 in no.
 Drain whole of choroid
UVEITIS
The inflammation of uveal tract
Classification-
I. ANATOMICAL CLASSIFICATION
II. CLINICAL CLASSIFICATION
III. ETIOLOGICAL CLASSIFICATION
IV. PATHOLOGICAL CLASSIFICATION
A. Anatomical Classification –
(IUSG) International Uveitis Study
Group
1) Anterior Uveitis – Inflammation of iris and
anterior part of ciliary body
2) Intermediate Uveitis – Involvement of posterior
part of ciliary body and extreme periphery of retina.
(Pars planitis)
3) Posterior uveitis – Retinochoroiditis, choroiditis,
retinitis, chorioretinitis
4) Diffuse or pan uveitis – Involvement of entire
uveal tract
B. Clinical Classification -
1) Acute – sudden symptomatic onset.
Persists for 3 weeks or less
2) Chronic – Frequently insidious and
asymptomatic. Persists for months or years
3) Recurrent
C. Etiological Classification
1) Exogenous-
Introduction of organism into the eye through
a perforating wound or ulcer.
2) Secondary infection-
Due to direct spread from adjoining structures-
 Cornea
 Sclera
 Retina
3) Endogenous
4) Allergic inflammation: Result of an antigen-
antibody reaction occurring in the eye due to
previous sensitization of uveal tissue to some
allergen. The allergen is a foreign protein.
 Most of the cases of iridocyclitis do not have
any specific cause and are probably allergic in
nature.
5) Auto-immune -
Immune disorders
e.g. rheumatoid arthritis, SLE, ankylosing
spondylitis, Reiter’s syndrome, Behcet’s
Syndrome.
Granulomatous Non-
granulomatous
1. Aetiology Organismal
invasion
Antigen-antibody
reaction
2. Course
a) Onset Insidious Acute
b) Duration Chronic Short
c) Inflammation Moderate Severe
D. Pathological Classification
Granulomatous Non-
granulomatous
3. Pathology
a) Lesion Circumscribed Diffuse
b) Iris Focal reaction Diffuse reaction
c) Keratic
precipitates
Mutton fat Fine plenty
d) Iris adhesions Coarse, few,
thick
Fine, plenty, thin
4.
Investigations
May be positive Negative
PATHOLOGY AND
CLINICAL SIGNS-
Inflammation of iris and ciliary body
Dilatation of blood vessels
Iris stromal edema.
SIGNS - Iris pattern altered.Iris colour
altered. Iris thickened.Also
accompanied by, ciliary congestion,
conjunctival hyperaemia and chemosis
of conjunctiva.
SIGNS –
 Iris pattern and colour altered.
 Iris thickened accompanied by, ciliary
congestion, conjunctival hyperaemia
and chemosis of conjunctiva.
Exudation of fibrin-rich fluid and
inflammatory cells in the tissues
Exudates escape into anterior chamber
 Plasmoid aqueous
 SIGNS - Aqueous flare (like the beam
of projector in smokey theatre)
Nutrition of corneal endothelium is
affected due to toxins
Corneal endothelium becomes sticky
and edematous
Cells desquamated at places
SIGN – Keratic precipitates
Inflammatory cells stick to endothelial
layer as cellular deposits .
In very intense cases, polymorphs pour
out to sink to bottom of anterior
chamber
SIGN – Hypopyon
Exudates cover the iris as a thin film and
spread over pupillary area
SIGN – Irritation of iris musculature
constrictor being more powerful than
dilator, spasm results in miosis.
If exudate is profuse
SIGN – Plastic iritis
Blockage of pupil
SIGN – impairment of sight.
In early stages, there is adhesion of iris to lens capsule
(Atropine may free the iris)
SIGN – Spots of exudate or pigment derived from posterior
layer of iris left permanently upon anterior capsule of
lens (valuable evidence of previous iritis)
Later on, the organization of the adhesion leads to formation of
fibrous bands between pupillary margin of iris and lens capsule
(atropine cannot rupture them)
SIGN – Posterior synechiae (more in lower part of pupil
due to effect of gravity)
When adhesions are localized and a
mydriatic is instilled, it causes
intervening portions of circle of pupil to
dilate.
SIGN– Festooned pupil
(due to irregular dilatation
and is a sign of present or
past iritis.)
Pigment epithelium on
posterior surface is pulled
around pupillary margin so
that patches of pigment on
anterior surface of iris are
seen.
SIGN – Ectropion of
uveal pigment (due to
contraction of
organizing exudates
upon iris)
With recurrent attacks or severe cases, the
whole circle of pupillary margin gets tied
to lens capsule.
SIGNS – Annular or ring synechiae or
Seclusio pupillae
Collection of aqueous behind iris since
aqueous drainage is hampered.
Iris is hence bowed forwards like sail.
SIGN – Iris Bombe (anterior chamber is
funnel shaped i.e. deepest in centre,
shallowest at periphery)
As iris bulges forward and comes into contact with
cornea
Adhesions of iris to cornea at periphery develop
SIGNS – Peripheral anterior synechiae
Obliteration of filtration angle (Hypertensive
iridocyclitis)
SIGNS – Rise in IOP (secondary glaucoma)
When exudate is more extensive
Organization of exudate across entire pupillary
area
Film of opaque fibrous tissue in pupillary area
SIGNS – Occlusio pupillae or Blocked
pupil
Exudates fill up posterior chamber if there is
much of cyclitis
When these adhesions organize, the iris
adheres to lens capsule.
SIGNS – Total posterior synechiae
When these adhesions organize, the iris
adheres to lens capsule.
SIGNS – Total posterior synechiae
Retraction of peripheral part of iris
Anterior chamber is abnormally deep at
periphery
In worst cases of plastic iridocyclitis
Cyclitic membrane formed
behind lens
Finally, degenerative
changes in ciliary body
Vitreous becomes fluid
Nutrition of lens impaired
SIGNS – Complicated
cataract
Phthisis bulbi will be the
eventuality.
In final stages, there is
interference with
secretion of aqueous
Fall in IOP
Eye shrinks (development
of soft eye is an
ominous sign)
SIGNS – Phthisis bulbi
Clinical Features
SYMPTOMS
 Pain
 Diminished vision
 Redness of eye
 lacrimation
 photophobia
SIGNS
 Signs of vascular
congestion
 Signs of exudation
 Signs of pupillary
changes
Clinical Features
SIGNS
 Lid oedema
 Circumcorneal congestion
 Corneal signs
 Anterior chamber signs
 Iris signs
 Pupillary signs
 Lenticular changes
 Changes in the vitreous
Clinical Features
SIGNS
 Corneal signs
Corneal oedema
Keratic precipitates (KPs)
Mutton fat, granular, red & old KPs
Posterior corneal opacity
Clinical Features
SIGNS
 Anterior chamber signs
 1. Aqueous cells. It is an early feature of
iridocyclitis.
 – = 0 cells,
 ± = 1–5 cells,
 +1 = 6–10 cells,
 +2 = 11-20 cells,
 +3 = 21–50 cells, and
 +4 = over 50 cells
Clinical Features
 2. Aqueous flare. It is due to leakage of protein
particles into the aqueous humour from damaged
blood vessels. It is demonstrated on the slit lamp
examination by a point beam of light passed obliquely to
the plane of iris.
 Grade :
 0 = no aqueous flare,
 +1 = just detectable;
 +2 = moderate flare with clear iris details;
 +3 = marked flare (iris details not clear);
 +4 = intense flare (fixed coagulated aqueous
with considerable fibrin).
 Aqueous Flare
Clinical Features
SIGNS
 Anterior chamber signs
3. Hypopyon. When exudates are heavy and thick,
they settle down in lower part of the anterior chamber
as hypopyon (sterile pus in the anterior chamber)
4. Hyphaema (blood in the anterior chamber): It may
be seen in haemorrhagic type of uveitis.
 Hypopyon in anterior uveitis
Clinical Features
SIGNS
 Iris signs
1. Loss of normal pattern.
2. Changes in iris colour.
3. Iris nodules
4. Posterior synechiae.
5. Neovascularsation of iris
Clinical Features
SIGNS
 Pupillary signs
1. Narrow pupil.
2. Irregular pupil shape.
3. Ectropion pupillae
4. Sluggish pupillary reaction
5. Occlusio pupillae
Clinical Features
SIGNS
 Lenticular signs
1. Pigment dispersal over anterior lens capsule
2. Exudates
3. Complicated cataract
 Change in the vitreous
Anterior vitreous may show exudates and
inflammatory cells after an attack of acute
iridocyclitis.
Differential Diagnosis
Character Conjunctivitis Iridocyclitis Glaucoma
Infection Superficial Deep ----
Secretion Mucopurulent Watery Watery
Pupil Normal Small,
irregular
Large, Oval
Character Conjunctivitis Iridocyclitis Glaucoma
Media Clear Sometimes
pupil
opaque
Corneal
oedema
Tension Normal Usually
normal
High
Pain Mild Moderate
with first
division of
trigeminal
Severe and
entire
trigeminal
Character Conjunctivitis Iridocyclitis Glaucoma
Tenderness Absent Marked Marked
Vision Good Fair Poor
Onset Gradual Usually
gradual
Sudden
Systemic
complications
Absent Little Prostration
and
vomiting
Complications of Uveitis
 Hypertensive uveitis – Secondary glaucoma
 Endothelial opacities in cornea due to formation of keratic
precipitates
 Hypopyon and hyphaema
 Suppurative uveitis may progress to end-ophthalmitis or
pan-ophthalmitis
 Toxic matter goes into lens – complicated cataract.
 Post inflammatory atrophy of zonules – subluxation of
lens
 Vitreous – opacification of vitreous, liquification of gel,
shrinkage of gel, retinal detachment
Contd..
…
 macular edema
 optic neuritis – undergoes atrophy – optic nerve
atrophy
 occlusive pupillae
 seclusion pupillae
 Ectropion of uveal pigment
 Hypotony – atrophic bulbi
 Secondary squint
 Iris atrophy
Investigations
 Local
 Vision, refraction, fundus examination
 IOP by Schiotz Tonometer
 Slit Lamp examination
 Focal –
 ENT, Dental, Genito-urinatory
examination for septic focus.
 For associated systemic disorders –
 CBC, ESR, MT, X-ray chest – Tuberculosis
 Urine, Blood examination-Diabetes
 VDRL, Kahn Test – syphilis
 Urethral smear – gonorrhoeae
 Urine culture – for UTI
 Blood culture – Septicemia
 ASLO Titre, C-reactive protein – for
rheumatic disorders
 Screening test for auto immune disorders
Treatment
1. Of iridocyclitis
2. Of complications and sequelae.
Treatment of Iridocyclitis
 LOCAL THERAPHY –
 Cycloplegics
 Corticosteroids
 Broad spectrum antibiotics (no role)
Cycloplegics
 Short acting
-Tropicamide 1% e/d
(3 hrs)
-Cyclopentolate 1%
e/d (24 hrs)
 Long acting
-Homatropine 2% e/d
(4 days)
-Atropine sulphate 1%
e/d (7-14 days)
 Acts in following ways
 By keeping the iris and ciliary body at rest
 By diminishing hyperaemia -reduces exudation
 By preventing formation of posterior
synechiae and breaking down any already
formed.
 Increases blood supply to anterior uvea
Mydriasis -the sub-conjunctival injection of 0.3
ml. of mydricaine, a mixture of atropine,
procaine and adrenaline
To avoid relapse-Atropine, or its equivalent -
continued for at least 10 days to a fortnight
after the eye appears to be quiet.
Corticosteroids
 Short acting-
-Fluoromethalone
-Loteprednol
-Fluocinolone
 Long acting-
-Dexamethasone
-Betamethasone
-Hydrocortisone
-Prednisolone
-Triamcinolone
 Routes-
1.)Topical-e/d or e/o 4-6 times a day
2.)Anterior subtenon injection-for severe
cases
 SYSTEMIC THERAPHY-
 Corticosteroids
 NSAIDS
 Immunosuppressives
Corticosteroids
 Indication- intractable anterior uveitis
 Prednisolone-1 mg/kg body wt and
taper gradually according to response
 Side effects- glaucoma & cataract
Aspirin (NSAIDS)
 Used when steroids are C/I
 Is very useful in relieving pain but if it
is intense, stronger preparation are
required.
Immunosuppressives
 Cyclosporin
-T-cell immunosuppressive drug. Used in resistant
cases.
In specific inflammations-Behcet’s
syndrome,sympathetic ophthalmitis,VKH,pars planitis
 Broad spectrum antibiotic
- In case of suppurative uveitis.
 Specific Chemotherapy for
Tuberculosis, syphilis, gonorrhoea.
 Increasing body resistance by multi-
vitamins.
Treatment of complications
and sequelae-
 Inflammatory glaucoma- timolol 0.5%
BD & tab acetazolamide 250mg BD
C/I-latanoprost and pilocarpine
 Post-inflammatory glaucoma (d/t ring
synechiae)- Laser iridotomy
 Complicated cataract-cataract sx after 3
months of quiet period
 Retinal detachment- anterior vitrectomy
 Phthisis bulbi- enucleation
 Hypopyon and Hyphaema may need
evacuation and A.C. Wash.
 End-ophthalmitis – intravitreal injection of
Decadron and Gentamicin
 Pan ophthalmitis – Evisceration
 Iris Bombe
Medical – 1. Atropine 2. Diamox
Surgical – 4-dot Iridotomy
 using von Graefe’s knife
 YAG Laser for breaking posterior synechiae
THANK YOU!

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1167_Anterior-Uveitis 2.pptx

  • 2.
  • 3. UVEA • Constitutes- middle vascular coat of the eyeball • 3 parts- a)Iris b)Ciliary body c)Choroid • Developmentally,structurally and functionally- indivisible • Color varies from light blue to dark brown
  • 4. IRIS • Anterior most part • Avg diameter- 12mm, thickness- 0.5mm • In centre an aperture of 3-4mm- PUPIL • Thinnest at its root- tears away easily on blunt trauma- IRIDODIALYSIS • Divides space into anterior and posterior chamber
  • 5. MACROSCOPIC APPEARANCE  CILIARY ZONE-  Radial streaks  Crypts- peripheral- near the iris  central- near collarette  Contraction furrows- faints lines outside collarette  PUPILLARY ZONE-  Between collarette and pigmented frill  Pigmented frill- black pigment at pupillary margin  -represents ant end of optic cup
  • 6.
  • 7. MICROSCOPIC STRUCTURE 1.)Anterior limiting layer 2.)Iris stroma 3.)Anterior epithelial layer 4.)Posterior pigmented epithelial layer
  • 8. FUNCTIONS OF IRIS • CONTROLS AMOUNT OF LIGHT ENTERING THE EYE THROUGH PUPIL • DEFINES EYE COLOUR • CONTROL DEPTH OF FIELD • SOURCE OF BLOOD OCULAR TISSUES
  • 9. CILIARY BODY • Forward continuation of choroid at ora serrata • Two parts- a) Anterior part- ciliary processes (pars plicata) 2-2.5mm b) Posterior part- smooth (pars plana) 5mm wide temporally & 3mm nasally
  • 10. MICROSCOPIC STRUCTURE 1.)Supraciliary lamina 2.)Stroma of the ciliary body 3.)Layer of pigmented epithelium 4.)Layer of non-pigmented epithelium 5.)Internal limiting membrane
  • 11. FUNCTIONS OF CILIARY BODY • Site of aqueous humour production • Maintenance of IOP • Constitutes blood aqueous barrier • Accommodation • Eicosanoids are synthesised in ciliary body
  • 12. CHOROID • Posterior most part • Extension- optic disc to ora serrata • Inner surface- smooth, brown and in contact with RPE • Outer surface-rough and in contact with sclera • Thickness- posteriorly 0.22mm - anteriorly 0.10mm
  • 13.
  • 14. MICROSCOPIC STRUCTURE 1) Suprachoroidal lamina 2) Stroma of the choroid 3) Basal lamina
  • 15. FUNCTIONS OF CHOROID • BLOOD SUPPLY TO OUTER FOUR LAYERS OF RETINA • MODULATION OF VASCULARISATION • REGULATE RETINAL HEAT • ASSIST IN THE CONTROL OF INTRAOCULAR PRESSURE • PIGMENT ABSORBS EXCESS LIGHT SO AVOIDING REFLECTION
  • 16. BLOOD SUPPLY UVEAL TRACT 1.SHORT POSTERIOR CILIARY ARTERIES • Branches of ophthalmic artery • Divides into 10-20 branches, pierce sclera around optic nerve • Supply choroid in segmental manner 2) LONG POSTERIOR CILIARY ARTERIES • Anastomose with anterior ciliary arteries- form major arterial circle supply ciliary body 3)ANTERIOR CILIARY ARTERIES • From muscular arteries • 2 each SR,IR, MR and 1 from LR Anastomse with LPCA • Circulous arterious major and minor
  • 17.
  • 18. VENOUS DRAINAGE 1. Anterior ciliary veins- tributaries of muscular veins 2. Smaller veins from sclera- carry blood only from sclera and not from choroid 3. Vena verticosae- 4 in no.  Drain whole of choroid
  • 20. Classification- I. ANATOMICAL CLASSIFICATION II. CLINICAL CLASSIFICATION III. ETIOLOGICAL CLASSIFICATION IV. PATHOLOGICAL CLASSIFICATION
  • 21. A. Anatomical Classification – (IUSG) International Uveitis Study Group 1) Anterior Uveitis – Inflammation of iris and anterior part of ciliary body 2) Intermediate Uveitis – Involvement of posterior part of ciliary body and extreme periphery of retina. (Pars planitis) 3) Posterior uveitis – Retinochoroiditis, choroiditis, retinitis, chorioretinitis 4) Diffuse or pan uveitis – Involvement of entire uveal tract
  • 22. B. Clinical Classification - 1) Acute – sudden symptomatic onset. Persists for 3 weeks or less 2) Chronic – Frequently insidious and asymptomatic. Persists for months or years 3) Recurrent
  • 23. C. Etiological Classification 1) Exogenous- Introduction of organism into the eye through a perforating wound or ulcer. 2) Secondary infection- Due to direct spread from adjoining structures-  Cornea  Sclera  Retina
  • 24. 3) Endogenous 4) Allergic inflammation: Result of an antigen- antibody reaction occurring in the eye due to previous sensitization of uveal tissue to some allergen. The allergen is a foreign protein.  Most of the cases of iridocyclitis do not have any specific cause and are probably allergic in nature.
  • 25. 5) Auto-immune - Immune disorders e.g. rheumatoid arthritis, SLE, ankylosing spondylitis, Reiter’s syndrome, Behcet’s Syndrome.
  • 26. Granulomatous Non- granulomatous 1. Aetiology Organismal invasion Antigen-antibody reaction 2. Course a) Onset Insidious Acute b) Duration Chronic Short c) Inflammation Moderate Severe D. Pathological Classification
  • 27. Granulomatous Non- granulomatous 3. Pathology a) Lesion Circumscribed Diffuse b) Iris Focal reaction Diffuse reaction c) Keratic precipitates Mutton fat Fine plenty d) Iris adhesions Coarse, few, thick Fine, plenty, thin 4. Investigations May be positive Negative
  • 28. PATHOLOGY AND CLINICAL SIGNS- Inflammation of iris and ciliary body Dilatation of blood vessels Iris stromal edema. SIGNS - Iris pattern altered.Iris colour altered. Iris thickened.Also accompanied by, ciliary congestion, conjunctival hyperaemia and chemosis of conjunctiva.
  • 29. SIGNS –  Iris pattern and colour altered.  Iris thickened accompanied by, ciliary congestion, conjunctival hyperaemia and chemosis of conjunctiva.
  • 30. Exudation of fibrin-rich fluid and inflammatory cells in the tissues Exudates escape into anterior chamber  Plasmoid aqueous  SIGNS - Aqueous flare (like the beam of projector in smokey theatre)
  • 31. Nutrition of corneal endothelium is affected due to toxins Corneal endothelium becomes sticky and edematous Cells desquamated at places
  • 32. SIGN – Keratic precipitates Inflammatory cells stick to endothelial layer as cellular deposits .
  • 33. In very intense cases, polymorphs pour out to sink to bottom of anterior chamber SIGN – Hypopyon
  • 34. Exudates cover the iris as a thin film and spread over pupillary area SIGN – Irritation of iris musculature constrictor being more powerful than dilator, spasm results in miosis. If exudate is profuse SIGN – Plastic iritis Blockage of pupil SIGN – impairment of sight.
  • 35. In early stages, there is adhesion of iris to lens capsule (Atropine may free the iris) SIGN – Spots of exudate or pigment derived from posterior layer of iris left permanently upon anterior capsule of lens (valuable evidence of previous iritis) Later on, the organization of the adhesion leads to formation of fibrous bands between pupillary margin of iris and lens capsule (atropine cannot rupture them) SIGN – Posterior synechiae (more in lower part of pupil due to effect of gravity)
  • 36. When adhesions are localized and a mydriatic is instilled, it causes intervening portions of circle of pupil to dilate. SIGN– Festooned pupil (due to irregular dilatation and is a sign of present or past iritis.)
  • 37. Pigment epithelium on posterior surface is pulled around pupillary margin so that patches of pigment on anterior surface of iris are seen. SIGN – Ectropion of uveal pigment (due to contraction of organizing exudates upon iris)
  • 38. With recurrent attacks or severe cases, the whole circle of pupillary margin gets tied to lens capsule. SIGNS – Annular or ring synechiae or Seclusio pupillae
  • 39. Collection of aqueous behind iris since aqueous drainage is hampered. Iris is hence bowed forwards like sail. SIGN – Iris Bombe (anterior chamber is funnel shaped i.e. deepest in centre, shallowest at periphery)
  • 40. As iris bulges forward and comes into contact with cornea Adhesions of iris to cornea at periphery develop SIGNS – Peripheral anterior synechiae Obliteration of filtration angle (Hypertensive iridocyclitis) SIGNS – Rise in IOP (secondary glaucoma)
  • 41. When exudate is more extensive Organization of exudate across entire pupillary area Film of opaque fibrous tissue in pupillary area SIGNS – Occlusio pupillae or Blocked pupil Exudates fill up posterior chamber if there is much of cyclitis When these adhesions organize, the iris adheres to lens capsule. SIGNS – Total posterior synechiae
  • 42. When these adhesions organize, the iris adheres to lens capsule. SIGNS – Total posterior synechiae Retraction of peripheral part of iris Anterior chamber is abnormally deep at periphery In worst cases of plastic iridocyclitis
  • 43. Cyclitic membrane formed behind lens Finally, degenerative changes in ciliary body Vitreous becomes fluid Nutrition of lens impaired SIGNS – Complicated cataract Phthisis bulbi will be the eventuality.
  • 44. In final stages, there is interference with secretion of aqueous Fall in IOP Eye shrinks (development of soft eye is an ominous sign) SIGNS – Phthisis bulbi
  • 45. Clinical Features SYMPTOMS  Pain  Diminished vision  Redness of eye  lacrimation  photophobia SIGNS  Signs of vascular congestion  Signs of exudation  Signs of pupillary changes
  • 46. Clinical Features SIGNS  Lid oedema  Circumcorneal congestion  Corneal signs  Anterior chamber signs  Iris signs  Pupillary signs  Lenticular changes  Changes in the vitreous
  • 47. Clinical Features SIGNS  Corneal signs Corneal oedema Keratic precipitates (KPs) Mutton fat, granular, red & old KPs Posterior corneal opacity
  • 48. Clinical Features SIGNS  Anterior chamber signs  1. Aqueous cells. It is an early feature of iridocyclitis.  – = 0 cells,  ± = 1–5 cells,  +1 = 6–10 cells,  +2 = 11-20 cells,  +3 = 21–50 cells, and  +4 = over 50 cells
  • 49. Clinical Features  2. Aqueous flare. It is due to leakage of protein particles into the aqueous humour from damaged blood vessels. It is demonstrated on the slit lamp examination by a point beam of light passed obliquely to the plane of iris.  Grade :  0 = no aqueous flare,  +1 = just detectable;  +2 = moderate flare with clear iris details;  +3 = marked flare (iris details not clear);  +4 = intense flare (fixed coagulated aqueous with considerable fibrin).
  • 51. Clinical Features SIGNS  Anterior chamber signs 3. Hypopyon. When exudates are heavy and thick, they settle down in lower part of the anterior chamber as hypopyon (sterile pus in the anterior chamber) 4. Hyphaema (blood in the anterior chamber): It may be seen in haemorrhagic type of uveitis.
  • 52.  Hypopyon in anterior uveitis
  • 53. Clinical Features SIGNS  Iris signs 1. Loss of normal pattern. 2. Changes in iris colour. 3. Iris nodules 4. Posterior synechiae. 5. Neovascularsation of iris
  • 54. Clinical Features SIGNS  Pupillary signs 1. Narrow pupil. 2. Irregular pupil shape. 3. Ectropion pupillae 4. Sluggish pupillary reaction 5. Occlusio pupillae
  • 55. Clinical Features SIGNS  Lenticular signs 1. Pigment dispersal over anterior lens capsule 2. Exudates 3. Complicated cataract  Change in the vitreous Anterior vitreous may show exudates and inflammatory cells after an attack of acute iridocyclitis.
  • 56. Differential Diagnosis Character Conjunctivitis Iridocyclitis Glaucoma Infection Superficial Deep ---- Secretion Mucopurulent Watery Watery Pupil Normal Small, irregular Large, Oval
  • 57. Character Conjunctivitis Iridocyclitis Glaucoma Media Clear Sometimes pupil opaque Corneal oedema Tension Normal Usually normal High Pain Mild Moderate with first division of trigeminal Severe and entire trigeminal
  • 58. Character Conjunctivitis Iridocyclitis Glaucoma Tenderness Absent Marked Marked Vision Good Fair Poor Onset Gradual Usually gradual Sudden Systemic complications Absent Little Prostration and vomiting
  • 59. Complications of Uveitis  Hypertensive uveitis – Secondary glaucoma  Endothelial opacities in cornea due to formation of keratic precipitates  Hypopyon and hyphaema  Suppurative uveitis may progress to end-ophthalmitis or pan-ophthalmitis  Toxic matter goes into lens – complicated cataract.  Post inflammatory atrophy of zonules – subluxation of lens  Vitreous – opacification of vitreous, liquification of gel, shrinkage of gel, retinal detachment Contd..
  • 60. …  macular edema  optic neuritis – undergoes atrophy – optic nerve atrophy  occlusive pupillae  seclusion pupillae  Ectropion of uveal pigment  Hypotony – atrophic bulbi  Secondary squint  Iris atrophy
  • 61. Investigations  Local  Vision, refraction, fundus examination  IOP by Schiotz Tonometer  Slit Lamp examination  Focal –  ENT, Dental, Genito-urinatory examination for septic focus.
  • 62.  For associated systemic disorders –  CBC, ESR, MT, X-ray chest – Tuberculosis  Urine, Blood examination-Diabetes  VDRL, Kahn Test – syphilis  Urethral smear – gonorrhoeae  Urine culture – for UTI  Blood culture – Septicemia  ASLO Titre, C-reactive protein – for rheumatic disorders  Screening test for auto immune disorders
  • 63. Treatment 1. Of iridocyclitis 2. Of complications and sequelae.
  • 64. Treatment of Iridocyclitis  LOCAL THERAPHY –  Cycloplegics  Corticosteroids  Broad spectrum antibiotics (no role)
  • 65. Cycloplegics  Short acting -Tropicamide 1% e/d (3 hrs) -Cyclopentolate 1% e/d (24 hrs)  Long acting -Homatropine 2% e/d (4 days) -Atropine sulphate 1% e/d (7-14 days)
  • 66.  Acts in following ways  By keeping the iris and ciliary body at rest  By diminishing hyperaemia -reduces exudation  By preventing formation of posterior synechiae and breaking down any already formed.  Increases blood supply to anterior uvea
  • 67. Mydriasis -the sub-conjunctival injection of 0.3 ml. of mydricaine, a mixture of atropine, procaine and adrenaline To avoid relapse-Atropine, or its equivalent - continued for at least 10 days to a fortnight after the eye appears to be quiet.
  • 68. Corticosteroids  Short acting- -Fluoromethalone -Loteprednol -Fluocinolone  Long acting- -Dexamethasone -Betamethasone -Hydrocortisone -Prednisolone -Triamcinolone
  • 69.  Routes- 1.)Topical-e/d or e/o 4-6 times a day 2.)Anterior subtenon injection-for severe cases
  • 70.  SYSTEMIC THERAPHY-  Corticosteroids  NSAIDS  Immunosuppressives
  • 71. Corticosteroids  Indication- intractable anterior uveitis  Prednisolone-1 mg/kg body wt and taper gradually according to response  Side effects- glaucoma & cataract
  • 72. Aspirin (NSAIDS)  Used when steroids are C/I  Is very useful in relieving pain but if it is intense, stronger preparation are required.
  • 73. Immunosuppressives  Cyclosporin -T-cell immunosuppressive drug. Used in resistant cases. In specific inflammations-Behcet’s syndrome,sympathetic ophthalmitis,VKH,pars planitis
  • 74.  Broad spectrum antibiotic - In case of suppurative uveitis.  Specific Chemotherapy for Tuberculosis, syphilis, gonorrhoea.  Increasing body resistance by multi- vitamins.
  • 75. Treatment of complications and sequelae-  Inflammatory glaucoma- timolol 0.5% BD & tab acetazolamide 250mg BD C/I-latanoprost and pilocarpine  Post-inflammatory glaucoma (d/t ring synechiae)- Laser iridotomy  Complicated cataract-cataract sx after 3 months of quiet period  Retinal detachment- anterior vitrectomy  Phthisis bulbi- enucleation
  • 76.  Hypopyon and Hyphaema may need evacuation and A.C. Wash.  End-ophthalmitis – intravitreal injection of Decadron and Gentamicin  Pan ophthalmitis – Evisceration  Iris Bombe Medical – 1. Atropine 2. Diamox Surgical – 4-dot Iridotomy  using von Graefe’s knife  YAG Laser for breaking posterior synechiae