Treatment of Uveitis
The treatment of uveitis begins with topical corticosteroids for anterior uveitis, while moderate to severe cases involving posterior segments require systemic immunosuppression with methotrexate as first-line therapy, followed by monoclonal antibody TNF inhibitors like adalimumab if needed. 1
Initial Treatment Approach
Anterior Uveitis
- First-line therapy: Prednisolone acetate 1% topical drops
- Initial dosing: Frequent administration (every 1-2 hours)
- Taper as inflammation comes under control 1
- Goal: Rapid control to prevent permanent tissue damage
- Regular ophthalmologist monitoring required
Intermediate, Posterior, and Panuveitis
- Urgent ophthalmology referral required before initiating treatment 1
- Systemic corticosteroids in addition to topical treatment
- Starting dose: 1-2 mg/kg/day methylprednisolone equivalents IV for severe cases 1
- Topical steroid monotherapy should be limited to ≤3 months 1
- Prolonged use increases risk of cataracts and glaucoma
Systemic Immunosuppressive Therapy
When to Initiate
- If topical steroids are insufficient after 3 months
- If inflammation reactivates during steroid taper
- If patient requires ongoing topical steroids to maintain control 1
First-Line Immunosuppressive Agent
- Methotrexate (subcutaneous preferred over oral)
Second-Line Therapy (If Methotrexate Fails)
- Anti-TNF biologics:
For Severe Cases with Sight-Threatening Complications
- Combination therapy with methotrexate and a monoclonal antibody TNFi immediately is recommended over methotrexate monotherapy 2
Treatment Algorithm
- Initial therapy: Topical steroids + methotrexate
- If inadequate response: Add adalimumab
- If adalimumab fails: Switch to infliximab 1
Monitoring and Follow-up
- Monitoring should occur no less frequently than every 3 months while on stable therapy 1
- Ophthalmologic evaluation within 1 month after each change in topical therapy 1
- Regular monitoring for complications:
- Cataracts
- Glaucoma
- Increased intraocular pressure
- Posterior synechiae
- Band keratopathy
- Cystoid macular edema 1
Important Considerations and Pitfalls
Steroid-Related Complications
- Risk of IOP elevation increases with dosing of ≥4 drops daily and prolonged use beyond 3 months 1
- Children have a higher risk of steroid-induced IOP elevation 1
- Long-term topical steroid use (>3 months) increases risk of cataracts and glaucoma 1
Duration of Therapy
- Maintenance of therapy should be for a minimum of 2 years of inactive disease off topical steroids before reducing systemic immunosuppression 1
- The induction treatment must be aggressive to overcome inflammation rapidly and avoid permanent tissue damage 4
Collaborative Care
- Regular communication between ophthalmologist and rheumatologist is essential 1
- Comprehensive autoimmune workup is strongly recommended for patients with episcleritis or scleritis who only respond to prednisolone acetate 1% ophthalmic drops 1
Poor Prognostic Factors
Factors that may warrant earlier systemic therapy include:
- Male gender
- Posterior synechiae
- Band keratopathy
- Glaucoma or cataract
- Poor initial vision
- Macular edema 1
The addition of immunosuppressive therapy is effective in allowing reduction of systemic prednisolone to 10 mg/day or less, controlling inflammation, reducing relapses, and maintaining vision 5.