
Options in Tough-To-Treat Uveitis
Reports in a pediatric ophthalmology journal reveal risk factors and best treatments for refractory/recurrent uveitis in JIA.
Last week's articles on rheumatology topics in the major non-rheumatology journals.
More than half of children with refractory uveitis responded to treatment with adalimumab (Humira), according to a small study. Most of the patients had juvenile idiopathic arthritis (JIA).
The drug controlled initial acute inflammatory activity in 60% of the 15 patients, according to the Standardization of Uveitis Nomenclature (SUN) Working group criteria. However, the drug was less effective long-term.
These patients had failed to respond to systemic steroids, methotrexate, cyclosporine, azathioprine, etanercept (Enbrel), and infliximab (Remicade).
Immunomodulatory therapy (IMT) at an earlier age was associated with longer remission of uveitis in JIA.
This study reviewed the records of 30 patients with JIA who were successfully treated with IMT during 1990-2011, with corticosteroid-free remission of uveitis for at least one year.
A little more than half (57%) of the patients remained in remission, and almost half (43%) relapsed. Patients who had received IMT at an earlier age were more likely to go into remission.
Methotrexate monotherapy was sufficient to induce remission in 13 of 30 patients. Other drugs included mycophenolate mofetil, azathioprine, etanercept, infliximab, and chlorambucil.
Also new last week:
Among 766 patients with cutaneous vasculitis, 16 had an underlying malignancy in this case review. There were nine hematologic and seven solid underlying malignancies.
Skin cells were the initial presentation, usually palpable purpura. Hematologic cytopenias and immature peripheral blood cells were frequently observed in the full blood count.
Three to ten percent of patients with osteonecrosis have involvement of ≥3 anatomic sites.
In a retrospective study of 29 patients, 24% had high factor VIII levels, and 20% were positive for antiphospholipid antibody.




