Abstract
Biologic and targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) target a specific pathway of the immune system, and are usually prescribed after failure of conventional synthetic disease-modifying antirheumatic drug therapy. The choice of b/tsDMARD depends on the disease profile and comorbidities, patient preference, registered indications of the drugs, and risks associated with therapy. It is recommended that b/tsDMARDs for immune-mediated inflammatory rheumatic diseases are prescribed by a rheumatologist, and all patients must be included in the South African Rheumatism and Arthritis Association biologic registry. Knowledge of and vigilance for adverse events, particularly infections, associated with b/ts DMARD therapies are of paramount importance.
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CITATION STYLE
Van Duuren, E., Potts, J., Brijlal, U., Botha, S., Didi, S., Makan, K., … Hodkinson, B. (2024). South African Rheumatism and Arthritis Association 2024 guidelines for the use of biologic and targeted synthetic disease-modifying antirheumatic drugs. South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde, 114(9), e2599. https://doi.org/10.7196/SAMJ.2024.v114i10.2599
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