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Rheumatology · ACR

Gout

ACR
A
Source:American College of Rheumatology Guideline for the Management of Gout (2020)EULAR 2017 (still active)BSR 2017
Verified Apr 2026
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Red Flags

  • Acute hot swollen joint with fever, prior prosthesis, or rapid worsening — exclude septic arthritis (joint aspiration with Gram stain, culture); empirical antibiotic until ruled out[1]
  • Tophaceous deposits with skin breakdown, secondary infection, or compressive neuropathy — surgical / multidisciplinary referral[1]
  • Tumour lysis syndrome or chronic kidney disease with hyperuricaemia — nephrology and oncology; rasburicase for prevention/treatment[1]
  • Severe drug reaction on allopurinol (SCAR/SJS) — stop drug, supportive care, dermatology; HLA-B*5801 association in Han Chinese, Korean, Thai, South Asian[1]

First-line treatment

Interventions

  • Acute attack — early treatment[1]
    Treat at first symptoms; the earlier started, the more effective; combination therapy in severe or polyarticular attack
  • Treat-to-target urate-lowering therapy[1]
    Indications: ≥2 attacks/year, tophaceous deposits, radiographic damage, gouty nephropathy. Target serum urate <6.0 mg/dL (<5.0 in tophaceous or severe). Continue indefinitely
  • Lifestyle and dietary measures[1]
    Reduce purine-rich red meat, organ meats, seafood, alcohol (especially beer), sugar-sweetened beverages; weight reduction; moderate dairy and coffee may protect; address sleep apnoea
  • Comorbidity management[1]
    Treat hypertension preferentially with losartan (uricosuric), avoid thiazide and loop diuretics where possible; SGLT2 inhibitors lower urate; statins and metformin neutral; review aspirin role

First-line drug therapy

DrugClassAdultPaediatricNotes
Colchicine (acute and prophylaxis)[1]Microtubule inhibitor / anti-inflammatoryAcute: 1.2 mg PO at first symptom, then 0.6 mg 1 hour later (low-dose protocol); subsequent days 0.6 mg BD until resolution. Prophylaxis: 0.5–0.6 mg PO BD for 3–6 months at start of urate-lowering therapy—Renal and hepatic dose adjustment; avoid with strong CYP3A4 inhibitors (clarithromycin, ritonavir); GI side effects common
NSAIDs (acute)[1]Cyclooxygenase inhibitorNaproxen 500 mg PO BD; indomethacin 50 mg TDS; ibuprofen 800 mg TDS — until 24–48 h after attack resolves—First-line acute treatment in non-CKD non-cardiac patients; avoid in CKD, peptic ulcer, severe heart failure, anticoagulation; co-prescribe PPI
Glucocorticoid (acute)[1]Systemic corticosteroidPrednisolone 30–40 mg PO daily × 5 days then taper; or intra-articular methylprednisolone 40 mg in single joint—Useful in CKD, anticoagulation, NSAID/colchicine intolerance; intra-articular if monoarticular and septic arthritis excluded; brief course preferred
Allopurinol (urate-lowering)[1]Xanthine oxidase inhibitorStart 100 mg PO daily (50 mg if eGFR <60); titrate by 100 mg every 2–4 weeks to target serum urate <6.0; usual 300–600 mg/day, max 800 mg10 mg/kg/dayFirst-line urate-lowering; HLA-B*5801 screen in Han Chinese, Thai, Korean, South Asian; renal dose adjustment; do not stop during acute attack
Febuxostat (allopurinol-intolerant)[1]Non-purine xanthine oxidase inhibitor40 mg PO daily start, increase to 80–120 mg if not at target—Allopurinol-intolerant or failure; cardiovascular event signal in CARES trial — caution in cardiovascular disease; LFT monitoring
Probenecid (uricosuric — selected)[1]Uricosuric250 mg PO BD start, titrate to 500 mg–1 g BD—Add-on to xanthine oxidase inhibitor in those still above target with normal renal function and no urolithiasis history; ensure good fluid intake
Pegloticase (refractory tophaceous)[1]Recombinant uricase8 mg IV every 2 weeks—Refractory tophaceous gout failing oral therapy; immunogenic — anti-drug antibodies; G6PD screen; co-prescribe immunomodulator (methotrexate) to reduce immunogenicity
Colchicine (acute and prophylaxis)[1]
Microtubule inhibitor / anti-inflammatory
Adult
Acute: 1.2 mg PO at first symptom, then 0.6 mg 1 hour later (low-dose protocol); subsequent days 0.6 mg BD until resolution. Prophylaxis: 0.5–0.6 mg PO BD for 3–6 months at start of urate-lowering therapy
Paediatric
—
Renal and hepatic dose adjustment; avoid with strong CYP3A4 inhibitors (clarithromycin, ritonavir); GI side effects common
NSAIDs (acute)[1]
Cyclooxygenase inhibitor
Adult
Naproxen 500 mg PO BD; indomethacin 50 mg TDS; ibuprofen 800 mg TDS — until 24–48 h after attack resolves
Paediatric
—
First-line acute treatment in non-CKD non-cardiac patients; avoid in CKD, peptic ulcer, severe heart failure, anticoagulation; co-prescribe PPI
Glucocorticoid (acute)[1]
Systemic corticosteroid
Adult
Prednisolone 30–40 mg PO daily × 5 days then taper; or intra-articular methylprednisolone 40 mg in single joint
Paediatric
—
Useful in CKD, anticoagulation, NSAID/colchicine intolerance; intra-articular if monoarticular and septic arthritis excluded; brief course preferred
Allopurinol (urate-lowering)[1]
Xanthine oxidase inhibitor
Adult
Start 100 mg PO daily (50 mg if eGFR <60); titrate by 100 mg every 2–4 weeks to target serum urate <6.0; usual 300–600 mg/day, max 800 mg
Paediatric
10 mg/kg/day
First-line urate-lowering; HLA-B*5801 screen in Han Chinese, Thai, Korean, South Asian; renal dose adjustment; do not stop during acute attack
Febuxostat (allopurinol-intolerant)[1]
Non-purine xanthine oxidase inhibitor
Adult
40 mg PO daily start, increase to 80–120 mg if not at target
Paediatric
—
Allopurinol-intolerant or failure; cardiovascular event signal in CARES trial — caution in cardiovascular disease; LFT monitoring
Probenecid (uricosuric — selected)[1]
Uricosuric
Adult
250 mg PO BD start, titrate to 500 mg–1 g BD
Paediatric
—
Add-on to xanthine oxidase inhibitor in those still above target with normal renal function and no urolithiasis history; ensure good fluid intake
Pegloticase (refractory tophaceous)[1]
Recombinant uricase
Adult
8 mg IV every 2 weeks
Paediatric
—
Refractory tophaceous gout failing oral therapy; immunogenic — anti-drug antibodies; G6PD screen; co-prescribe immunomodulator (methotrexate) to reduce immunogenicity

Safety-net

  1. Continue urate-lowering therapy lifelong; do not stop during a flare; treating to target prevents future attacks and tophaceous damage[1]
  2. Any new rash within 8 weeks of starting allopurinol — stop the drug and seek same-day medical review (severe cutaneous adverse reaction)[1]
  3. Reduce alcohol (especially beer), sugar-sweetened drinks, and high-purine foods; weight reduction by even 5% can lower urate[1]

Referral criteria

  • Septic arthritis suspicion (hot joint with fever, prosthesis, immunosuppression)Emergency department / orthopaedics[1]
  • Refractory or tophaceous gout failing oral urate-lowering therapyRheumatology — pegloticase or combination therapy[1]
  • Allopurinol-induced severe cutaneous adverse reaction or drug intoleranceDermatology and rheumatology; switch and avoid same agent indefinitely[1]
  • Gout with CKD G4–G5 or recurrent uric acid kidney stonesRheumatology and nephrology joint[1]

Clinical summary

Diagnosis, acute attack management, and treat-to-target urate-lowering therapy for adults with gout.

References

  1. 1.American College of Rheumatology Guideline for the Management of Gout (2020); EULAR 2017 (still active); BSR 2017 (2020)

On this page

  • Red flags
  • First-line treatment
  • Safety-net
  • Referral
  • References