Future research agenda: propositions developed through three Delphi rounds
No | Proposition |
---|---|
NSAID, non-steroidal anti-inflammatory drug; SUA, serum uric acid. | |
1 | The optimal drug (colchicine or NSAID), dose, and duration for prophylaxis of acute attacks when starting urate lowering treatment, and whether this should vary in different clinical settings (for example, in the presence of tophi) needs to be determined |
2 | Studies are required to determine the optimal dose and frequency of oral colchicine for treatment of an acute attack |
3 | Further studies are required to determine the target SUA for urate lowering treatment that ensures crystal dissolution and eventual cure |
4 | Direct comparison (efficacy, side effects, cost utility) between allopurinol and alternative urate lowering treatments are needed |
5 | The efficacy and safety of combined urate lowering treatment (for example, allopurinol plus a uricosuric drug) should be determined and compared with monotherapy in patients with severe gout |
6 | The efficacy of educational programmes for lifestyle modification (weight loss, reduced alcohol intake, restriction of dietary purines) in patients with gout needs to be assessed |
7 | The indications for initiating urate lowering treatment (for example, recurrent acute attacks, tophi, polyarticular acute attacks, radiographic joint damage) need further evaluation |
8 | Whether initiation of urate lowering treatment during an acute attack is disadvantageous and should be avoided, and if so for how long, requires investigation |
9 | The possible benefits on cardiovascular disease of lowering SUA merit investigation |