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ANTERIOR UVEITIS
Uveitis
• Inflammation of the uveal
tissue
CLASSIFICATION
Anatomical
Anterior
Intermediate
Posterior
Panuveitis
Pathological
1.Suppurative
2.Non suppurative
a) Granulomatous
b) Non
Uveitis
• It is inflammation of the uveal tissue from iris up
to pars plicata of ciliary body
Anterior Uveitis
• Iritis
• Iridocyclitis
• Cyclitis
CLASSIFICATION
• Infectious, traumatic, neoplastic, autoimmune, idiopathic
• Inflammation of the uvea
• Inflammatory response: chemical mediators result in
vasodilation, increased vascular permeability, and chemotaxis of
inflammatory cells in eye.
PATHOPHYSIOLOGY
• Infectious uveitis
• Non-infectious uveitis
ETIOLOGY
BACTERIA
Syphilis
Tuberculosis
Chronic post-operative
endophthalmitis from
propiono-bacterium acnes
PROTOZOA
Toxoplasmosis
Toxocariasis
VIRUSES
Herpes simplex
Varicella zoster
FUNGI
Candida
INFECTIOUS UVEITIS
• Associated with systemic
disease
• Sarcoidosis
• Behcets disease
• Juvenile idiopathic arthritis
• Collagen vascular disease
• Wegener’s granulomatosis
• Polyarteritis nodosa
• HLA-B27 associated
Psoriatic arthropathy, Crohns
disease, ulcerative colitis,
ankylosing spondylitis, Reiters
syndrome
Idiopathic
Autoimmune
CLINICAL FEATURES
• Acute: Symptoms more severe
• Chronic: Signs more severe than signs
• PAIN:
Acute Severe dull aching throbbing
Radiates along V1 nerve distribution
Worst at night
• REDNESS
Due to circumcorneal congestion,
• PHOTOPHOBIA & BLEPHEROSPASAM
.
SYMPTOMS
• DEFECTIVE VISION
• TURBID AQUEOUS
• Sec. glaucoma
• Vitreous exudates
• Ciliary spasm
• Exudates in pupillary
area
• Complicated Cataract
• Cystoid Macular Edema
• LACRIMATION
lacrimatory reflex mediated by fifth nerve (afferent) &
secretomotor fibres of the seventh nerve (efferent)
1) Lid Edema
2) Circumcorneal congestion
SIGNS
3. CORNEAL SIGNS:
a) Corneal edema
d/t toxic endothelitis & increased IOP
a) Keratitis precipitates
• Cellular deposits on the corneal endothelium
• Arlt’s triangle
• Small & medium:
− pathognomic of nongranulomatous uveitis
− composed of lymphocyte
− Small KPs may be hundreds in number
endothelial dusting.
• large (mutton fat)
− occur in granulomatous iridocyclitis
− composed of epithelioid cells & macrophages.
• Red KP:
− Inflammatory cells & RBCs
− Haemorrhagic uveitis.
• Old KP:
− Sign of healed uveitis
− Ground glass appearance due to hyalinization.
C) Posterior corneal opacities
1. Aqueous cells
− Early feature of iridocyclitis
− The cells should be counted in
an oblique slit-lamp beam, 3-
mm long and 1-mm wide, with
maximal light intensity and
magnification
ANTERIOR CHAMBER SIGNS
2) AQUEOUS FLARE
− leakage of protein
particles into the
aqueous humour
− point of beam projected
on the iris plane
− Protein particles seen
floating the beam of
light:
3) HYPOPYON
4) HYPHAEMA
5) IRREGULAR AC DEPTH D/T
SYNECHIA
6) DEPOSITS OF DEBRIS IN
ANTERIOR CHAMBER ANGLE
7) ANTERIOR SYNECHIA
• Loss of normal pattern
• Changes in iris colour
−Muddy in color in active stage & hyper/
hypopigmented
• Iris nodules
− Aggregations of lymphyocytes and
epitheloid cells.
IRIS SIGNS
KOEPPE’S NODULE BUSSACCA’S
NODULE
• POSTERIOR SYNECHIAE
Adhesion of post. Surf. Of iris to ant. Surf of lens
• Segmental
• Annular
− 360 degree adhesions
− Seclusio pupillae –block aq flow
from post to ant chamber
− Iris bomb
• Total
Plastering of total posterior
surface of iris with the anterior
capsule of lens
• SLUGGISH PUPILLARY REACTION& MIOSIS
Irritation of sphincter pupillae by toxin
• IRREGULAR PUPIL
festooned pupil
Pupillary signs
• OCCULSIO PUPIL
Pupil is completely occluded due to
organisation of the exudates across the
entire pupillary area.
• ECTROPION PUPILLAE
− Evertion of pupillary margin
−It may develop due to contraction of
fibrinous exudate on the anterior surface
of the iris.
• Pigment dispersion on lens surface
• Fibrin exudates on lens surface
• Complicated cataract
−Polychromatic lusture Bread crumb
appearance
−Early posterior subcapsular opacities
Changes in the lens
• Exudates and inflammatory cells
Change in the vitreous
COMPLICATIONS AND SEQUELAE
Secondary glaucoma
Early glaucoma
− In active phase of disease
− Due to exudates & inflammatory cells in
Ant Chamber angle blocking the
Trabecular meshwork
− Decreased aqueous flow leading to
increased IOP (Hypertensive Glaucoma)
Late Glaucoma
−Post Inflammatory Glaucoma
−D/t pupillary block (Seclusio
Pupil/Occlusio pupil)
−Causes Iris Bombe then occlusion
Trabecular Meshwork
−Decreased aqueous outflow
CYCLITIC MEMBRANE
− Retrolental, fibrovascular
membrane which stretches across
the back of the lens
CHOROIDITIS
RETINAL SIGNS
− Cystoid Macular Degeneration
− Macular Degeneration
− Serous Retinal Detachment
− Secondary periphlebitis retinae.
− PAPILLITIS -inflammation of the optic disc.
− Band-shaped KERATOPATHY.
It occurs as a complication of long-standing chronic uveitis
• Phthisis bulbi
− It is the final stage end result of any form of chronic
uveitis
− ciliary body is disorganised
− aqueous production is hampered.
− Eye becomes soft, shrinks and eventually becomes a
small atrophic globe
INVESTIGATION
Hematological Examination
−TLC/DC: Gross idea of inflammatory response of body
−ESR: r/o Chronic infection
−Blood sugar: r/o DM
−Blood Uric Acid: r/o Gout
−Seological Test: Syphilis, toxoplasmosis & histoplasmosis
−Test : Antinuclear Antibodies, CRP, Rh factor Anti-streptolysin
O
Urine Examination
• For WBC, Pus cells, RBS
• Culture : r/o Urinary tract infection
Stool Examination
• For Cysts & ova to r/o parasitic infestations.
Radiological Investigation
• Skin Tests:Tuberculin test, & Toxoplasmin test.
RADIOLOGICAL EXAMINATION
• CXR, Paranasal sinus, Sacroiliac joints,Lumbar spine.
• CT scan high resolution thorax for suspecting sarcoidosis
• MRI of head for suspecting sarcoidosis,demyelination &
lymphomas
TREATMENT
Non- specific treatment
Local therapy
Systemic therapy
Specific Treatment
T/t of Complications
NON-SPECIFIC TREATMENT:LOCAL
THERAPY
1. Cycloplegics
2. Corticosteroids
3. Broad spectrum antibiotics
CYCLOPLEGICS
Short acting cycloplegics
Tropicamide 1% e/d (3hrs)
Cyclopentolate 1% e/d (24hrs) – 3-4 times a day
Long acting cycloplegics
Homatropine 2% e/d (4days) – 3-4 times a day
Atropine sulphate 1% e/d (7- 14days) – 2-3 times a day
0.25 ml mydricain -mixture of atropine, adrenaline and procaine
cycloplegics should be continued for at least 2-3
weeks after the eye becomes quiet, otherwise relapse
may occur.
MODE OF ACTIONS OF CYCLOPLEGICS
• Relieves pain: Relieves spasm of iris sphincter & ciliary
muscle
• Prevents posterior synechiae formation
• Breaks posterior synechiae
• Reduces hyperemia & vascular permeability which reduces
exudation
Corticosteroids
LONG ACTING
Dexamethasone
Betamethasone
Hydrocortisone
Prednisolone
Triamcinolone
SHORT ACTING
Fluoromethalone
Loteprednol
Fluocinolone
MOA : Antifibrotic activity, they reduce fibrosis and thus prevent disorganisation and destruction of
the tissues
ROUTE OF ADMINISTRATION
• Topical Eye drops 6 times a day
• Eye ointments at bed time,
• Anterior subtenon injection For severe cases
BROAD SPECTRUM ANTIBIOTIC
• Doesn’t have much role in anterior uveitis
• Prescribed with topical steroid preparations to provide an
umbrella cover for them.
SYSTEMIC THERAPY
• Corticosteroids
• Non-Steroidal Anti- inflammatory Drugs(NSAIDS)
• Immunosupressives
CORTICOSTEROIDS
• Indication: Intractable anterior uveitis
• Prednisolone: 1mg/kg bd wt & taper gradually according to
response
• Dosage schedule : prednisolone (60-100mg)
Daily therapy : marked inflammatory activity at least 2
week
Alternate day therapy : In absence of a/c disease
Dose is decreased by a week’s interval & taper completely in about 6-8 week
NON- STEROIDAL ANTI - INFLAMMATORY
DRUGS
• Used when steroid are contraindicated or not tolerated.
• Phenylbutazone & oxyphenylbutazone
IMMUNOSUPPRESSIVES
• In corticosteroid resistant or intolerant cases
• In specific inflammations:
Behcet’s syndrome
Sympathetic ophthalmitis
VKH(Vogt-Koyanagi-Harada)
Pars planitis
A few available cytotoxic immunosuppressive drugs include
cyclophosphamide, chlorambucil, azathioprine and methotrexate.
SPECIFIC TREATMENT
• Tuberculosis: ATT
• Parenteral Penicillin: Syphilis
• HSV: Acyclovir
PHYSICAL MEASURES
1. Hot fomentation
2. Dark goggles-Reducing photophobia, lacrimation and
blepharospasm
TREATMENT OF
COMPLICATION
• Inflammatory Glaucoma
Timolol 0.5% BD
T.Acetazolamide 250mg BD
Contraindicated are Latanoprost & Pilocarpine.
• Post-inflammatory Glaucoma(d/t
ring synechiea):
Laser iridotomy
• Complicated Cataract
Cataract sx. After 3 mths of
quiet period.
• Retinal Detachment
Anterior vitrectomy
• Phthisis bulbi
Enucleation
• Thank you

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Anterior UVEitis.pptx

  • 2. Uveitis • Inflammation of the uveal tissue CLASSIFICATION Anatomical Anterior Intermediate Posterior Panuveitis Pathological 1.Suppurative 2.Non suppurative a) Granulomatous b) Non Uveitis
  • 3. • It is inflammation of the uveal tissue from iris up to pars plicata of ciliary body Anterior Uveitis
  • 4. • Iritis • Iridocyclitis • Cyclitis CLASSIFICATION
  • 5. • Infectious, traumatic, neoplastic, autoimmune, idiopathic • Inflammation of the uvea • Inflammatory response: chemical mediators result in vasodilation, increased vascular permeability, and chemotaxis of inflammatory cells in eye. PATHOPHYSIOLOGY
  • 6. • Infectious uveitis • Non-infectious uveitis ETIOLOGY
  • 7. BACTERIA Syphilis Tuberculosis Chronic post-operative endophthalmitis from propiono-bacterium acnes PROTOZOA Toxoplasmosis Toxocariasis VIRUSES Herpes simplex Varicella zoster FUNGI Candida INFECTIOUS UVEITIS
  • 8. • Associated with systemic disease • Sarcoidosis • Behcets disease • Juvenile idiopathic arthritis • Collagen vascular disease • Wegener’s granulomatosis • Polyarteritis nodosa • HLA-B27 associated Psoriatic arthropathy, Crohns disease, ulcerative colitis, ankylosing spondylitis, Reiters syndrome Idiopathic Autoimmune
  • 9. CLINICAL FEATURES • Acute: Symptoms more severe • Chronic: Signs more severe than signs
  • 10. • PAIN: Acute Severe dull aching throbbing Radiates along V1 nerve distribution Worst at night • REDNESS Due to circumcorneal congestion, • PHOTOPHOBIA & BLEPHEROSPASAM . SYMPTOMS
  • 11. • DEFECTIVE VISION • TURBID AQUEOUS • Sec. glaucoma • Vitreous exudates • Ciliary spasm • Exudates in pupillary area • Complicated Cataract • Cystoid Macular Edema • LACRIMATION lacrimatory reflex mediated by fifth nerve (afferent) & secretomotor fibres of the seventh nerve (efferent)
  • 12. 1) Lid Edema 2) Circumcorneal congestion SIGNS
  • 13. 3. CORNEAL SIGNS: a) Corneal edema d/t toxic endothelitis & increased IOP a) Keratitis precipitates • Cellular deposits on the corneal endothelium • Arlt’s triangle
  • 14. • Small & medium: − pathognomic of nongranulomatous uveitis − composed of lymphocyte − Small KPs may be hundreds in number endothelial dusting. • large (mutton fat) − occur in granulomatous iridocyclitis − composed of epithelioid cells & macrophages.
  • 15. • Red KP: − Inflammatory cells & RBCs − Haemorrhagic uveitis. • Old KP: − Sign of healed uveitis − Ground glass appearance due to hyalinization. C) Posterior corneal opacities
  • 16. 1. Aqueous cells − Early feature of iridocyclitis − The cells should be counted in an oblique slit-lamp beam, 3- mm long and 1-mm wide, with maximal light intensity and magnification ANTERIOR CHAMBER SIGNS
  • 17. 2) AQUEOUS FLARE − leakage of protein particles into the aqueous humour − point of beam projected on the iris plane − Protein particles seen floating the beam of light:
  • 18.
  • 19. 3) HYPOPYON 4) HYPHAEMA 5) IRREGULAR AC DEPTH D/T SYNECHIA 6) DEPOSITS OF DEBRIS IN ANTERIOR CHAMBER ANGLE 7) ANTERIOR SYNECHIA
  • 20. • Loss of normal pattern • Changes in iris colour −Muddy in color in active stage & hyper/ hypopigmented • Iris nodules − Aggregations of lymphyocytes and epitheloid cells. IRIS SIGNS
  • 22. • POSTERIOR SYNECHIAE Adhesion of post. Surf. Of iris to ant. Surf of lens
  • 23. • Segmental • Annular − 360 degree adhesions − Seclusio pupillae –block aq flow from post to ant chamber − Iris bomb • Total Plastering of total posterior surface of iris with the anterior capsule of lens
  • 24. • SLUGGISH PUPILLARY REACTION& MIOSIS Irritation of sphincter pupillae by toxin • IRREGULAR PUPIL festooned pupil Pupillary signs
  • 25. • OCCULSIO PUPIL Pupil is completely occluded due to organisation of the exudates across the entire pupillary area. • ECTROPION PUPILLAE − Evertion of pupillary margin −It may develop due to contraction of fibrinous exudate on the anterior surface of the iris.
  • 26. • Pigment dispersion on lens surface • Fibrin exudates on lens surface • Complicated cataract −Polychromatic lusture Bread crumb appearance −Early posterior subcapsular opacities Changes in the lens
  • 27. • Exudates and inflammatory cells Change in the vitreous
  • 29. Secondary glaucoma Early glaucoma − In active phase of disease − Due to exudates & inflammatory cells in Ant Chamber angle blocking the Trabecular meshwork − Decreased aqueous flow leading to increased IOP (Hypertensive Glaucoma)
  • 30. Late Glaucoma −Post Inflammatory Glaucoma −D/t pupillary block (Seclusio Pupil/Occlusio pupil) −Causes Iris Bombe then occlusion Trabecular Meshwork −Decreased aqueous outflow
  • 31. CYCLITIC MEMBRANE − Retrolental, fibrovascular membrane which stretches across the back of the lens
  • 33. RETINAL SIGNS − Cystoid Macular Degeneration − Macular Degeneration − Serous Retinal Detachment − Secondary periphlebitis retinae. − PAPILLITIS -inflammation of the optic disc. − Band-shaped KERATOPATHY. It occurs as a complication of long-standing chronic uveitis
  • 34. • Phthisis bulbi − It is the final stage end result of any form of chronic uveitis − ciliary body is disorganised − aqueous production is hampered. − Eye becomes soft, shrinks and eventually becomes a small atrophic globe
  • 35.
  • 37. Hematological Examination −TLC/DC: Gross idea of inflammatory response of body −ESR: r/o Chronic infection −Blood sugar: r/o DM −Blood Uric Acid: r/o Gout −Seological Test: Syphilis, toxoplasmosis & histoplasmosis −Test : Antinuclear Antibodies, CRP, Rh factor Anti-streptolysin O
  • 38. Urine Examination • For WBC, Pus cells, RBS • Culture : r/o Urinary tract infection Stool Examination • For Cysts & ova to r/o parasitic infestations. Radiological Investigation • Skin Tests:Tuberculin test, & Toxoplasmin test.
  • 39. RADIOLOGICAL EXAMINATION • CXR, Paranasal sinus, Sacroiliac joints,Lumbar spine. • CT scan high resolution thorax for suspecting sarcoidosis • MRI of head for suspecting sarcoidosis,demyelination & lymphomas
  • 40. TREATMENT Non- specific treatment Local therapy Systemic therapy Specific Treatment T/t of Complications
  • 41. NON-SPECIFIC TREATMENT:LOCAL THERAPY 1. Cycloplegics 2. Corticosteroids 3. Broad spectrum antibiotics
  • 42. CYCLOPLEGICS Short acting cycloplegics Tropicamide 1% e/d (3hrs) Cyclopentolate 1% e/d (24hrs) – 3-4 times a day Long acting cycloplegics Homatropine 2% e/d (4days) – 3-4 times a day Atropine sulphate 1% e/d (7- 14days) – 2-3 times a day 0.25 ml mydricain -mixture of atropine, adrenaline and procaine cycloplegics should be continued for at least 2-3 weeks after the eye becomes quiet, otherwise relapse may occur.
  • 43. MODE OF ACTIONS OF CYCLOPLEGICS • Relieves pain: Relieves spasm of iris sphincter & ciliary muscle • Prevents posterior synechiae formation • Breaks posterior synechiae • Reduces hyperemia & vascular permeability which reduces exudation
  • 44. Corticosteroids LONG ACTING Dexamethasone Betamethasone Hydrocortisone Prednisolone Triamcinolone SHORT ACTING Fluoromethalone Loteprednol Fluocinolone MOA : Antifibrotic activity, they reduce fibrosis and thus prevent disorganisation and destruction of the tissues
  • 45. ROUTE OF ADMINISTRATION • Topical Eye drops 6 times a day • Eye ointments at bed time, • Anterior subtenon injection For severe cases
  • 46. BROAD SPECTRUM ANTIBIOTIC • Doesn’t have much role in anterior uveitis • Prescribed with topical steroid preparations to provide an umbrella cover for them.
  • 47. SYSTEMIC THERAPY • Corticosteroids • Non-Steroidal Anti- inflammatory Drugs(NSAIDS) • Immunosupressives
  • 48. CORTICOSTEROIDS • Indication: Intractable anterior uveitis • Prednisolone: 1mg/kg bd wt & taper gradually according to response • Dosage schedule : prednisolone (60-100mg) Daily therapy : marked inflammatory activity at least 2 week Alternate day therapy : In absence of a/c disease Dose is decreased by a week’s interval & taper completely in about 6-8 week
  • 49. NON- STEROIDAL ANTI - INFLAMMATORY DRUGS • Used when steroid are contraindicated or not tolerated. • Phenylbutazone & oxyphenylbutazone
  • 50. IMMUNOSUPPRESSIVES • In corticosteroid resistant or intolerant cases • In specific inflammations: Behcet’s syndrome Sympathetic ophthalmitis VKH(Vogt-Koyanagi-Harada) Pars planitis A few available cytotoxic immunosuppressive drugs include cyclophosphamide, chlorambucil, azathioprine and methotrexate.
  • 51. SPECIFIC TREATMENT • Tuberculosis: ATT • Parenteral Penicillin: Syphilis • HSV: Acyclovir
  • 52. PHYSICAL MEASURES 1. Hot fomentation 2. Dark goggles-Reducing photophobia, lacrimation and blepharospasm
  • 53. TREATMENT OF COMPLICATION • Inflammatory Glaucoma Timolol 0.5% BD T.Acetazolamide 250mg BD Contraindicated are Latanoprost & Pilocarpine. • Post-inflammatory Glaucoma(d/t ring synechiea): Laser iridotomy • Complicated Cataract Cataract sx. After 3 mths of quiet period. • Retinal Detachment Anterior vitrectomy • Phthisis bulbi Enucleation