Management of Uveitis
Topical corticosteroids are the first-line treatment for anterior uveitis, while systemic immunosuppression with methotrexate followed by anti-TNF biologics (adalimumab preferred) is recommended for refractory cases or posterior segment involvement. 1
Initial Treatment Approach
Anterior Uveitis
- First-line therapy: Topical corticosteroids (preferably prednisolone acetate 1% or dexamethasone) 1
- Initial dosing: Every 1-2 hours, then taper as inflammation subsides
- Goal: Complete resolution of anterior chamber cells
- Monitor: IOP, cataract formation
Poor Prognostic Factors Requiring Early Systemic Therapy
- Male gender
- Posterior synechiae
- Band keratopathy, glaucoma, or cataract
- Poor initial vision
- Macular edema 1
- Uveitis antedating arthritis 2
Systemic Therapy Algorithm
Initiate systemic immunosuppression if:
First-line systemic therapy: Methotrexate 2, 1
- Dosing: 15-25 mg weekly (subcutaneous preferred over oral) 1
- Monitor: Liver function, complete blood count
Second-line therapy (if methotrexate ineffective or not tolerated):
For refractory cases:
Treatment Monitoring
- Goal of treatment: No cells in anterior chamber 2
- Monitoring frequency:
- Within 1 month after each change in topical therapy
- At least every 3 months while on stable therapy 1
- Collaborative care: Regular communication between ophthalmologist and rheumatologist 2, 1
Duration of Therapy and Tapering
- Maintenance of therapy: Minimum 2 years of inactive disease off topical steroids before reducing systemic immunosuppression 2, 1
- Tapering sequence: Reduce topical steroids first, then systemic therapy 1
Special Considerations
Posterior/Panuveitis
- Requires more aggressive systemic therapy from the outset 3
- Higher risk of sight-threatening complications 3
Pediatric Patients (JIA-associated uveitis)
- Higher risk of steroid-induced IOP elevation 1
- More aggressive monitoring required
- Same treatment algorithm applies, with careful attention to growth and development
Common Pitfalls to Avoid
Prolonged topical steroid monotherapy (>3 months) without systemic immunomodulatory therapy increases risk of cataract and glaucoma 1
Overreliance on systemic corticosteroids instead of steroid-sparing immunomodulatory agents 1, 4
Using etanercept for uveitis management (ineffective and associated with high relapse rates) 2, 1
Inadequate monitoring for treatment response and complications
Premature discontinuation of systemic therapy (maintain for at least 2 years of inactive disease) 2, 1