Frailty tied to Adverse Events in RA Patients on Biologic and Targeted Synthetic DMARDs, finds study
Written By : Aditi
Medically Reviewed By : Dr. Kamal Kant Kohli
Published On 2024-06-06 15:30 GMT | Update On 2024-06-07 06:49 GMT
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It remains unknown whether frailty status portends an increased risk of adverse outcomes in patients with rheumatoid arthritis (RA) initiating biologic (b) or targeted synthetic disease-modifying anti-rheumatic drugs (tsDMARDs).
In an Original Article published in Arthritis Care & Research, Singh et al. and colleagues concluded that Patients with a history of rheumatoid arthritis who are treated with biologic (b) or targeted synthetic disease-modifying anti-rheumatic drugs (tsDMARDs) have an increased risk of adverse outcomes, with Frailty being a significant predictor.
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