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. Author manuscript; available in PMC: 2023 Oct 10.
Published in final edited form as: Arthritis Care Res (Hoboken). 2020 May 11;72(6):744–760. doi: 10.1002/acr.24180

Table 2.

Recommendations for choice of initial urate-lowering therapy (ULT) in patients with gout*

Recommendation PICO question Certainty of evidence
For patients starting any ULT, we strongly recommend allopurinol over all other ULT as the preferred first-line agent for all patients, including in those with CKD stage ≥3. 10 Moderate
We strongly recommend a xanthine oxidase inhibitor over probenecid for those with CKD stage ≥3.
For allopurinol and febuxostat, we strongly recommend starting at a low dose with subsequent dose titration to target over starting at a higher dose (e.g., ≤100 mg/day [and lower in patients with CKD] for allopurinol or ≤40 mg/day for febuxostat). 7 Moderate
For probenecid, we conditionally recommend starting at a low dose (500 mg once or twice daily) with dose titration over starting at a higher dose.
We strongly recommend initiating concomitant antiinflammatory prophylaxis therapy (e.g., colchicine, NSAIDs, prednisone/prednisolone) over no antiinflammatory prophylaxis.
The choice of specific antiinflammatory prophylaxis should be based upon patient factors.
9 Moderate
We strongly recommend continuing prophylaxis for 3–6 months rather than <3 months, with ongoing evaluation and continued prophylaxis as needed if the patient continues to experience flares. 9 Moderate
When the decision is made that ULT is indicated while the patient is experiencing a gout flare, we conditionally recommend starting ULT during the gout flare over starting ULT after the gout flare has resolved. 6 Moderate
We strongly recommend against pegloticase as first-line therapy.. 10 Moderate

Strongly recommend Conditionally recommend Strongly recommend against Conditionally recommend against
*

PICO = population, intervention, comparator, outcomes; CKD = chronic kidney disease; NSAIDs = nonsteroidal antiinflammatory drugs.

Moderate evidence is in support of the efficacy of pegloticase, but due to cost, safety concerns, and favorable benefit-to-harm ratios of other untried treatment options, the recommendation is against using pegloticase as first-line agent.