Key result
Real-world infliximab therapy in RA is linked to adverse events in ~28% of patients.
Why the study?
The safety of infliximab therapy in patients with rheumatoid arthritis in real clinical practice required evaluation.
Is infliximab safe for use in patients with rheumatoid arthritis in real clinical practice?
Observational (n=135)
Is infliximab safe for use in patients with rheumatoid arthritis in real clinical practice?
Infliximab is generally safe in real-world practice for rheumatoid arthritis, though serious side effects requiring discontinuation occur in about 14% of patients.
Reinforces adverse-event monitoring with infliximab in RA; leaves comparative safety versus alternatives unresolved.
A wide range of highly effective genetically engineered biological preparations introduced into clinical rheumatology in recent years causes a special interest in their safety. Purpose of the study. Evaluation of the safety of infliximab therapy in patients with rheumatoid arthritis. Materials and methods. The authors' own data, which analyzed the undesirable effects of infliximab in 135 patients with rheumatoid arthritis in actual clinical practice, are presented. A case report of the adverse reaction of combination therapy with leflunomide and infliximab is presented. Results and its discussion. The overall tolerability of infliximab was satisfactory. Adverse events were observed in 28.1 % of cases, including 19.1 % of patients (14.1 %) had serious side effects that required discontinuation of the drug. Findings. In most cases, infliximab is safe for use in actual clinical practice. Patients should be informed about the risks of undesirable effects and the need for a rheumatologist's examination before each infliximab administration before prescribing therapy.
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Aronova et al. (2019) conducted an observational in Rheumatoid arthritis (n=135). Infliximab was evaluated on Adverse events. In real clinical practice, infliximab therapy in patients with rheumatoid arthritis was associated with adverse events in 28.1% of cases, with 14.1% requiring drug discontinuation.
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