Australian recommendations on tapering of biologic and targeted synthetic disease-modifying anti-rheumatic drugs in inflammatory arthritis.
Samuel Lawrance WhittleVanessa GlennonRenea V JohnstonJodie C AveryJ Simon BellSue E BrennanChristopher FongPravin HissariaBen HorganSean O'NeillHuai Leng PisanielloLyndal TrevenaGlen A WhittakerAnita WlukaRachelle BuchbinderPublished in: Internal medicine journal (2022)
Biological and targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARD) have been an important advance in the management of inflammatory arthritis, but are expensive medications, carry a risk of infection and other adverse effects, and are often perceived as a burden by patients. We used GRADE methodology to develop recommendations for dose reduction and discontinuation of b/tsDMARD in people with rheumatoid arthritis (RA), axial spondyloarthritis (AxSpA) and psoriatic arthritis (PsA) who have achieved a low disease activity state or remission. The recommendations form part of the Australian Living Guideline for the Pharmacological Management of Inflammatory Arthritis, an NHMRC-endorsed 'living' guideline, in which recommendations are updated in near real-time as new evidence emerges. Conditional recommendations were made in favour of dose reduction in RA and AxSpA but not in PsA. Abrupt discontinuation of b/tsDMARD is not recommended in any of the three diseases.
Keyphrases
- rheumatoid arthritis
- disease activity
- ankylosing spondylitis
- rheumatoid arthritis patients
- clinical practice
- juvenile idiopathic arthritis
- prostate cancer
- interstitial lung disease
- end stage renal disease
- oxidative stress
- systemic lupus erythematosus
- chronic kidney disease
- depressive symptoms
- cancer therapy
- mental health
- physical activity
- radical prostatectomy
- patient reported