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Ophthalmology & Rheumatology & Family Medicine

Uvéite | Clinique Omicron Québec

Uveitis is an inflammation of the uvea - the vascular tunica of the eye consisting of the iris + ciliary body + and choroid - which can affect these structures in isolation or in combination + and represents the third leading cause of avoidable blindness in developed countries + after age-related macular degeneration and glaucoma. With an annual incidence of 17 to 52 per 100,000 inhabitants + and a prevalence of 38 to 714 per 100,000 depending on the population studied + uveitis represents a diagnostic and therapeutic challenge, as its etiological spectrum is extremely broad - encompassing infectious (toxoplasmosis + herpes + CMV + tuberculosis + syphilis + Lyme) + autoimmune and systemic (HLA-B27 spondylarthropathies + sarcoidosis + Behçet's disease + rheumatoid arthritis + lupus + IBD) + neoplastic (intraocular lymphoma - to be considered in any adult over 50 with treatment-refractory posterior uveitis) + and idiopathic (50 % of cases). The anatomical classification of uveitis according to the Standardization of Uveitis Nomenclature (SUN) group - universally adopted - divides uveitis into anterior uveitis (iris + anterior ciliary body - most frequent : 50-60 % of cases) + intermediate uveitis (vitreous body + pars plana) + posterior uveitis (choroid + retina) + and panuveitis (all structures) - this anatomical classification directly guides probable etiology + visual prognosis + and treatment. The diagnosis of uveitis is an ophthalmological emergency, as delays in treatment can lead to irreversible complications (iridial synechiae + cataract + glaucoma + macular edema + blindness).

Anatomical classification and main etiologies

Type Affected structures Clinical presentation Main causes
Anterior uveitis (iritis + iridocyclitis) Iris + anterior ciliary body Eye pain + photophobia + tearing + perilimbal flush + miosis + retrocorneal precipitates (RCP) on slit lamp + Tyndall effect (cells + flare in aqueous humor) + hypopyon if severe HLA-B27 +++ (spondyloarthropathies - SpA + RCUH + Crohn's disease + reactive arthritis + psoriatic arthritis) + idiopathic + herpes (HSV + VZV - fine + greasy KP precipitates) + sarcoidosis + JIA (juvenile idiopathic arthritis - silent non-granulomatous anterior uveitis in children)
Intermediate uveitis (pars planitis) Vitreous body + pars plana Floaters (myodesopsia) + progressive decrease in visual acuity + little pain + little redness + «snowbank» on the pars plana during fundus examination Sarcoidosis + multiple sclerosis + Lyme disease + idiopathic
Posterior uveitis (chorioretinitis) Choroid + retina Decreased vision + floaters + scotomas + metamorphopsias + little or no pain or external redness (inflammation is deep) → emergency due to threat to central vision Toxoplasmosis +++ (focal chorioretinitis «headlight in fog» - active white lesion adjacent to an old pigmented scar) + CMV (immunocompromised) + HSV + VZV + tuberculosis + syphilis + sarcoidosis + Behçet's disease + intraocular lymphoma
Do you have any? Entire uvea Combination of anterior and posterior signs Sarcoidosis + Behçet's disease + VKH (Vogt-Koyanagi-Harada) + syphilis + tuberculosis + intraocular lymphoma

Etiological assessment of uveitis

  • Baseline Assessment (all uveitis): Chest X-ray (sarcoidosis + tuberculosis) + CBC + ESR + CRP + ACE (angiotensin-converting enzyme — sarcoidosis) + syphilis serology (VDRL + TPHA) + QuantiFERON-TB Gold + blood glucose + HLA-B27 (anterior uveitis)
  • Targeted infectious disease assessment: Toxoplasmosis serology (IgG + IgM — posterior uveitis) + HSV PCR + VZV + CMV in aqueous or vitreous humor if doubt + Lyme serology if exposed in endemic area + HIV serology (atypical posterior uveitis)
  • Extended autoimmune panel: ANA + anti-dsDNA (lupus) + ANCA (Wegener's) + HLA-B27 (if not done) + rheumatoid factor + anti-CCP antibodies + spondyloarthritis workup as indicated
  • Imaging : Thoracic CT (occult sarcoidosis if X-ray normal) + brain MRI (multiple sclerosis if intermediate uveitis) + PET-CT if lymphoma suspected
  • Aqueous humor or vitreous humor analysis (biopsy): PCR for infectious agents + cytology (malignant cells - lymphoma) + intraocular antibody assay (local/serum ratio) → for refractory or atypical uveitis

Treatment

  • Non-infectious anterior uveitis — topical corticosteroids (1st line): dexamethasone ophthalmic solution 0.1% (%) (Maxidex®) + or prednisolone acetate 1% (%) → every hour during acute phase → gradual taper over 4-8 weeks depending on response + cycloplegic mydriatics (atropine 1% (%) + or cyclopentolate 1% (%)) → prevention of posterior synechiae (iris-lens adhesions) + analgesic + reduction of ciliary spasms + never topical corticosteroids without etiological workup and ophthalmological follow-up (risk of worsened herpetic keratitis)
  • Posterior or intermediate uveitis — systemic corticosteroids: prednisone 1 mg/kg/day orally -> gradual taper based on response + periocular corticosteroids (subconjunctival or sub-Tenon's injection of triamcinolone) if localized form + intraocular implant of extended-release corticosteroids (fluocinolone - Iluvien®) for chronic recurrent posterior uveitis
  • Infectious etiological treatment: toxoplasmosis: pyrimethamine + sulfadiazine + folinic acid × 6 weeks (+ corticosteroids if macular involvement) + herpes: acyclovir or valacyclovir + CMV: IV ganciclovir or valganciclovir + tuberculosis: four-drug antituberculosis therapy × 6–9 months + syphilis: IV penicillin G × 14 days
  • Immunosuppressants (chronic, recurrent uveitis refractory to corticosteroids): methotrexate (sarcoid uveitis + JIA) + mycophenolate mofetil + azathioprine + cyclosporine + tacrolimus
  • Biotherapies (severe refractory uveitis): anti-TNF (adalimumab — Humira® — only FDA + Health Canada approved biologic for non-infectious uveitis) + infliximab + rituximab (ocular lymphoma) + tocilizumab (JIA uveitis)
  • Complications to treat: Secondary glaucoma (glaucoma eye drops + surgery) + secondary cataract (surgery once uveitis is controlled) + macular edema (intravitreal corticosteroid or anti-VEGF injections)
ℙ️ Primary intraocular lymphoma (PIOL)—diffuse large B-cell lymphoma presenting as posterior uveitis or panuveitis—is the most important diagnosis not to miss in an adult over 50 years old with posterior uveitis or panuveitis refractory to immunosuppressive treatment. It can perfectly mimic chronic autoimmune uveitis. Systematically consider PIOL in any patient over 50 years old with recurrent posterior uveitis + floaters + and incomplete response to corticosteroids → vitreous biopsy + PCR + cytology + brain MRI (60 % of primary ocular PIOLs have simultaneous or secondary brain involvement).
Ophthalmological emergency

Consult an ophthalmologist urgently (within 24 hours) if painful red eye + photophobia + blurred vision + or abundant floaters appear suddenly — these signs suggest uveitis requiring slit-lamp examination and prompt treatment to preserve vision. Never self-prescribe ocular corticosteroids without prior examination — corticosteroids can worsen herpetic keratitis or eye infections. For ophthalmology referrals and systemic etiological workup for uveitis, Clinique Omicron offers medical consultations at its service points in Quebec and via telemedicine. To book an appointment, visit cliniqueomicron.ca.

Consult at Clinique Omicron

Clinique Omicron's physicians and nurse practitioners (NPs) rapidly refer any suspected uveitis cases to ophthalmology, prescribe systemic etiological workups (HLA-B27 + ACE + QuantiFERON + syphilis serology + toxoplasmosis + chest X-ray), investigate associated systemic diseases (spondyloarthropathies + sarcoidosis + Behçet's disease + inflammatory bowel disease), and coordinate between the ophthalmologist and organ specialists based on the etiology. Consultations are available at several service locations in Quebec and via telemedicine. To make an appointment, visit cliniqueomicron.ca.

The content of this page is for informational purposes only and does not replace the advice of an ophthalmologist. Uveitis is an ophthalmological emergency — delayed treatment can lead to irreversible complications (synechiae + cataracts + glaucoma + blindness). Never prescribe or self-administer ocular corticosteroids without a prior ophthalmological examination — the risk of worsening herpetic keratitis is significant.

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