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ACR 2020 gout management guideline: key recommendations

This guideline from the American College of Rheumatology addresses the pharmacologic management of hyperuricemia in gout, including when to start urate-lowering therapy, treatment targets, drug choice, and management of flares. It emphasizes a treat-to-target strategy using serum urate levels and strongly favors allopurinol as first-line therapy across most patient groups.

ACR2020 editionSummary
Official guideline2020 American College of Rheumatology Guideline for the Management of Gout. ACR, 2020.
Read the official guideline · Checked for a newer edition on 2026-10-20
We do not reproduce the guideline text — this page is an independent summary.

Who it applies to

Adults with gout, including those with comorbid chronic kidney disease, in primary care and rheumatology settings.

Key recommendations

  • Urate-lowering therapy is strongly recommended for patients with frequent flares (two or more annually), tophi, or evidence of radiographic joint damage from gout, rather than reserving it only for severe disease.
    strong
  • Allopurinol is recommended as the preferred first-line urate-lowering agent for all patients, including those with chronic kidney disease, over febuxostat and other alternatives.
    strong
  • A treat-to-target approach is favored, starting urate-lowering drugs at a low dose and titrating upward (with monitoring of serum urate) rather than using a fixed-dose strategy without titration.
    strong
  • A serum urate target below 6 mg/dL is recommended over no target or a higher target, to reduce flare frequency and tophus burden.
    strong
  • HLA-B*5801 testing is conditionally recommended before starting allopurinol in patients of Southeast Asian (e.g., Korean, Han Chinese, Thai) or African American descent, given higher risk of severe hypersensitivity reactions.
    conditional
  • Routine use of anti-inflammatory prophylaxis (such as low-dose colchicine or NSAIDs) is recommended when starting urate-lowering therapy, to reduce the risk of treatment-associated flares, continued for several months.
    strong
  • For acute gout flares, colchicine, NSAIDs, and corticosteroids are all considered acceptable first-line options, with choice guided by comorbidities and patient preference rather than one agent being universally preferred.
    strong
  • Low-dose colchicine is favored over high-dose colchicine for treating flares, given similar efficacy with fewer gastrointestinal side effects.
    strong
  • Continuing urate-lowering therapy during an acute flare is recommended rather than interrupting it, since stopping treatment does not improve flare resolution and may complicate long-term management.
    conditional
  • Lifestyle and dietary counseling (such as limiting alcohol and purine-rich foods) is suggested as an adjunct but is not considered a substitute for pharmacologic urate-lowering therapy in patients with indications for it.
    conditional

Practice points for students

  • Allopurinol remains first-line even in CKD; dose should be started low and titrated rather than avoided or capped arbitrarily.
  • Treat-to-target with serial serum urate monitoring is central to gout management, analogous to treat-to-target strategies in other chronic diseases.
  • Do not stop urate-lowering therapy during an acute flare; manage the flare symptomatically while continuing the urate-lowering drug.
  • Consider HLA-B*5801 screening before allopurinol in at-risk ethnic groups to reduce risk of severe hypersensitivity syndrome.
  • ULT initiation in patients with tophi, radiographic damage, or frequent flares, the choice of first-line flare therapy, and the sub-6 mg/dL urate target are strong recommendations, while several other aspects of management remain conditional due to limited high-quality trial data.

Condition

Gout

Other guidelines on this topic

Independent educational summary written by the WhiteCoat Pro editorial team with AI assistance and checked by a second AI model. It does not reproduce the guideline text, tables or figures, and it is not affiliated with or endorsed by ACR. It is not medical advice: always read the original guideline before applying it to patients.