This document discusses anterior uveitis, which is inflammation of the iris, ciliary body, and anterior chamber of the eye. It can be caused by infection, autoimmune disorders, trauma, or idiopathic factors. Symptoms include eye pain, redness, photophobia, and blurred vision. Signs include cells in the anterior chamber, flare, hypopyon, keratic precipitates, iris nodules, and synechiae. Treatment involves cycloplegic eye drops, topical corticosteroids, and sometimes systemic corticosteroids or immunosuppressants depending on the severity and cause of inflammation. Complications like glaucoma and cataracts may require additional treatment.
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
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
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)
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
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)
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
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
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.
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.