Uveitis

 

Types of Uveitis
CommonInfrequentRare

Painful

Red

Rapid Onset

Painless

Rarely Red

Gradual Onset

Painless

Not Red

Gradual Onset

 

Onset ageAny
Onset speedRapid or gradual 
PatternSingle episode or recurrent
DurationShort or long (<3/12)
SeverityMild or severe

 

 

Acute Anterior Uveitis

Sudden onset over a few days

Unknown pathophysiology

>95% non-infectious

 

Symptoms
PainIncreasing over hours
RednessIncreasing over hours
MistinessIncreasing over hours
PhotophobiaIncreasing over hours
WateryMaybe

 

There will be NO foreign body sensation.  If there is then it is NOT uveitis

 

Symptoms
RedCircumcorneal injection 'ciliary blush'

Cells in the anterior chamber

  - causes flare

Tyndall effect, light scattering

Crucial for diagnosis

FibrinPlasmoid aqueous

Synachiae, posterior

Can progress to

 ~ seclusion pupillae

 ~ Iris bombé

Keratic precipitatesendothelial deposition
Hypopyon
Raised intra-ocular pressure (IOP)associate signs

 

 

Possible symptoms
Photophobia
Reduced VA
Tearing
Lid puffiness
Some drooping of the eyelid
Usually unilateral, but can be bilateral

 

 

Signs

  • White blood cell accumulation (and must be present for diagnosis)
  • Anterior chamber cells
  • Keratic precipitates
  • Flare
  • Hypopyon
  • Iris Nodules
  • Posterior Synechiae
  • Fibrin
  • Pupillary Miosis
  • Bank Keratopathy
  • Look for iris bombe

 

Most commonly linked to HLA-B27 genotype & ankylosing spondylitis

May be linked to localised infection  ie herpes simplex virus

May not be associated with illness or inflammation elsewhere

 

 

Immediate Action:

  • Drops to enlarge the pupil ASAP
  • Take 400mg Ibuprufen (per 8 hours)
  •    It's safe to take ibuprofen with paracetamol or codeine.
  •    Do not take ibuprofen with similar painkillers like aspirin or naproxen without talking to a                pharmacist or doctor.
  •    Not to be taken during preganancy, especially after 30 weeks
  •    It is safe to take during pregnancy
  • Heat pad on eyes
  • Refer to HES

 

Differencial Diagnosis

  • Conjunctivitis
  • Keratitis
  • Scleritis

Infectious

  • Syphilis
  • TB
  • HSV (genital herpes)
  • CMV
  • Toxoplasmosis
  • Rubela
  • VZV  (chicken pox, zoster)

Inflammatory

Malignancy

  • Lymphoma (lymphatic cancer)
  • Retinoblastoma

Other

  • Idiopathic
  • Medication-induced

 

Treatment

The mainstay of therapy for AAU is topical drops. These usually include a topical corticosteroid drop such as prednisolone acetate 1% and often a dilating drop such as cyclopentolate. The corticosteroid drop treats the underlying inflammation. The dilating drop reduces pain and helps to prevent the complication of the pupil sticking to the adjacent lens. The frequency of the drops depends primarily on the intensity of the inflammation. Some forms of AAU are associated with an infection such as herpes and will also require therapy directed at the known infectious cause. Other patients may have an illness of other organs that will also impact the treatment recommendations. On occasion AAU is severe enough to warrant treatment by the local injection (shot) of corticosteroid near the eye itself or by oral therapy such as prednisone. Any treatment, including eye drops, may result in adverse effects; these must be balanced with potential benefits in recommending therapies. Complications of inflammation such as an elevated intraocular pressure and cystoid macular edema may also affect treatment choices.

For recurrent or chronic disease and flares that are vision threatening despite local therapy, systemic immunosuppression therapy may be indicated that sometimes requires the expertise of a rheumatologist or uveitis specialist.