What is the management of gouty arthritis?

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Management of Gouty Arthritis

Initiate pharmacologic therapy within 24 hours of acute gout attack onset using NSAIDs, corticosteroids, or colchicine as first-line monotherapy, with treatment selection based on contraindications and severity of joint involvement. 1, 2

Acute Attack Management

Timing and General Principles

  • Start treatment within 24 hours of symptom onset for optimal effectiveness—delaying beyond this window significantly reduces treatment efficacy. 1, 2, 3
  • Continue established urate-lowering therapy (ULT) without interruption during an acute attack; stopping ULT worsens and prolongs the attack. 1, 2, 3
  • Educate patients to self-initiate treatment at the first signs of an attack. 2

First-Line Treatment Options (Choose One Based on Contraindications)

NSAIDs:

  • Use full FDA-approved anti-inflammatory/analgesic doses until the attack completely resolves. 1, 2, 3
  • FDA-approved NSAIDs for acute gout include naproxen, indomethacin, and sulindac, though other NSAIDs are equally effective. 1, 2, 3
  • Avoid in patients with renal impairment as NSAIDs can exacerbate or cause acute kidney injury. 2, 4

Corticosteroids (Preferred in Renal Impairment):

  • Oral prednisone 0.5 mg/kg per day for 5-10 days at full dose then stop, OR 2-5 days at full dose followed by 7-10 day taper. 1, 2
  • Alternative: Prednisolone 35 mg for 5 days. 2
  • Intra-articular injection: Dose varies by joint size (can be combined with oral therapy). 1
  • Intramuscular: Triamcinolone acetonide 60 mg, then oral prednisone as above. 1
  • Preferred in patients with renal impairment or contraindications to NSAIDs/colchicine. 2, 4
  • Use caution in diabetic patients; consider NSAIDs or colchicine instead. 2

Colchicine:

  • Low-dose regimen: 1.2 mg followed by 0.6 mg one hour later (as effective as higher doses with fewer gastrointestinal side effects). 2, 3
  • Most effective when started within 36 hours of symptom onset. 1, 3
  • If patient is already on prophylactic colchicine, choose alternative therapy (NSAID or corticosteroid). 1
  • Requires dose adjustment in chronic kidney disease and for drug interactions—colchicine toxicity increases significantly in CKD. 1, 4
  • Avoid high-dose regimens due to significant gastrointestinal toxicity without additional benefit. 3

Treatment Algorithm Based on Severity

Mild to Moderate Pain (≤6/10) with Limited Joint Involvement:

  • Monotherapy with any first-line agent (NSAID, corticosteroid, or colchicine) is appropriate. 2, 3

Severe Pain or Polyarticular Involvement (≥4 joints):

  • Combination therapy is appropriate: 2, 3
    • Colchicine plus NSAIDs
    • Oral corticosteroids plus colchicine
    • Intra-articular steroids with any other modality
  • Avoid combining NSAIDs with systemic corticosteroids due to increased gastrointestinal toxicity risk. 3

Anti-Inflammatory Prophylaxis During ULT Initiation

When to Initiate Prophylaxis

  • Start prophylaxis with or just prior to initiating urate-lowering therapy to prevent acute flares triggered by crystal mobilization. 1, 5, 6
  • Continue prophylaxis for at least 6 months or until serum urate target (<6 mg/dL) is achieved and there is freedom from acute attacks for several months. 1, 3, 6

Prophylaxis Options

Low-dose Colchicine (First-Line):

  • 0.6 mg once or twice daily. 1, 5
  • Adjust dose in chronic kidney disease and for drug interactions. 1

Low-dose NSAIDs (Alternative First-Line):

  • Use with proton pump inhibitor when gastrointestinal risk factors present. 1, 5

Long-Term Urate-Lowering Therapy (ULT)

Indications for ULT

  • Recommended for patients with frequent attacks (≥2 per year), tophi, or chronic gouty arthritis. 2, 5
  • Not recommended for patients with single or infrequent attacks (<2 per year). 2

ULT Medications

Allopurinol (First-Line):

  • Start with 100 mg daily and increase at weekly intervals by 100 mg until serum uric acid ≤6 mg/dL is achieved (maximum 800 mg/day). 6
  • Target serum urate: <6 mg/dL (upper limit of normal is ~7 mg/dL for men and postmenopausal women, 6 mg/dL for premenopausal women). 6
  • Dose adjustment required in renal impairment: 6
    • Creatinine clearance 10-20 mL/min: 200 mg daily
    • Creatinine clearance <10 mL/min: ≤100 mg daily
    • Creatinine clearance <3 mL/min: may need to lengthen interval between doses
  • Maintain adequate hydration (≥2 liters daily urinary output) and neutral to slightly alkaline urine. 6

Febuxostat (Alternative First-Line):

  • Appropriate for patients with allopurinol intolerance or contraindications. 5
  • Not studied in patients with creatinine clearance <30 mL/min. 4

Critical Pitfalls to Avoid

  • Never stop ULT during an acute attack—this worsens and prolongs the attack. 2, 5, 3
  • Never delay treatment beyond 24 hours of symptom onset—effectiveness drops significantly. 3
  • Never fail to provide prophylaxis when initiating ULT—this leads to increased flare frequency. 5, 3
  • Never use high-dose colchicine regimens—they cause significant gastrointestinal side effects without additional benefit. 3
  • Never ignore drug interactions with colchicine—this can lead to serious toxicity. 3
  • Never combine NSAIDs with systemic corticosteroids—this increases gastrointestinal toxicity risk. 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Acute Gout Attack

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Acute Gout Attack Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Treatment for Increased Gouty Tophi in a Joint

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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