Gout Treatment
For acute gout attacks, initiate treatment within 24 hours using NSAIDs, oral corticosteroids, or low-dose colchicine as first-line monotherapy options, selecting based on comorbidities and contraindications. 1
Acute Gout Attack Management
Treatment Initiation and General Principles
- Start pharmacologic therapy within 24 hours of symptom onset for optimal outcomes, as delayed treatment significantly reduces effectiveness 1
- Continue established urate-lowering therapy (ULT) without interruption during acute attacks—do not stop ULT during a flare 1
- Educate patients to self-initiate treatment at first warning symptoms without needing to contact their provider for each attack 1
First-Line Monotherapy Options (for mild-moderate attacks involving 1-3 small joints or 1-2 large joints)
NSAIDs:
- Use full FDA/EMA-approved anti-inflammatory doses and continue until the attack completely resolves 1
- FDA-approved options include naproxen (Evidence A), indomethacin (Evidence A), and sulindac (Evidence B) 1
- No single NSAID is superior—select based on patient factors 1
- Avoid in patients with chronic kidney disease, congestive heart failure, peptic ulcer disease, cirrhosis, or on anticoagulation 1, 2, 3
Oral Colchicine:
- Dosing: 1.2 mg at onset, followed by 0.6 mg one hour later (maximum 1.8 mg in first 12 hours) 1, 2, 3
- Most effective when started within 12 hours of symptom onset, but can be used up to 36 hours 1, 2
- For patients already on prophylactic colchicine, choose alternative therapy (NSAID or corticosteroid) 1
- Adjust dose for renal impairment: In severe renal impairment (CrCl <30 mL/min) or dialysis patients, use single dose of 0.6 mg and do not repeat more than once every two weeks 4
- Adjust for drug interactions: Reduce dose or avoid with strong CYP3A4 and P-glycoprotein inhibitors (e.g., clarithromycin, cyclosporine) 1, 5, 4
Oral Corticosteroids:
- Prednisone 0.5 mg/kg per day for 5-10 days at full dose then stop, OR taper over 7-10 days 1, 2, 3
- Alternative: Prednisone 30-35 mg/day for 3-5 days 2
- Particularly useful for patients with contraindications to NSAIDs or colchicine 1, 2
- Avoid in patients with diabetes, active infection, or high infection risk 2
Combination Therapy (for severe pain ≥7/10 or polyarticular attacks involving ≥4 joints)
- Appropriate combinations include: 1
- Colchicine + NSAIDs (full doses)
- Oral corticosteroids + colchicine
- Intra-articular steroids + any other modality
- Do not combine NSAIDs with systemic corticosteroids due to synergistic gastrointestinal toxicity 1
Special Populations
NPO (Nil Per Os) Patients:
- Intra-articular corticosteroid injection for 1-2 accessible joints (dose depends on joint size) 1, 2
- Intravenous/intramuscular methylprednisolone 0.5-2.0 mg/kg as alternative 1
- Subcutaneous ACTH 25-40 IU as alternative 1
Renal Impairment:
- Corticosteroids are the safest option in severe renal impairment 5
- Avoid NSAIDs and adjust colchicine dosing as above 1, 5, 4
Adjunctive Measures
- Topical ice application to affected joint is appropriate adjunctive therapy 1, 2, 3
- Rest the inflamed joint 6
Inadequate Response Definition and Management
- Inadequate response = <20% improvement in pain within 24 hours OR <50% improvement after 24 hours 1, 3
- For inadequate response: Switch to another monotherapy or add a second appropriate agent 1
Long-Term Urate-Lowering Therapy (ULT)
Indications for ULT
- Initiate ULT in patients with: 2, 3, 5
- Recurrent acute attacks (≥2 per year)
- Tophaceous gout
- Chronic gouty arthropathy
- Radiographic changes of gout
- History of nephrolithiasis
Target and First-Line Agents
- Target serum urate level: <6 mg/dL (357 μmol/L) 1, 2, 3, 5
- Xanthine oxidase inhibitors (allopurinol or febuxostat) are first-line options 1, 2, 5
- Allopurinol starting dose: ≤100 mg/day (50 mg/day in stage 4 or worse CKD), then titrate every 2-5 weeks to reach target 2, 5
Anti-Inflammatory Prophylaxis During ULT Initiation
Rationale and Timing
- Mandatory prophylaxis when starting ULT to prevent acute flares 1, 2, 3
- Initiate prophylaxis with or just prior to starting ULT 1, 2
First-Line Prophylaxis Options
Low-dose Colchicine (First-line):
- Dosing: 0.6 mg once or twice daily (0.5 mg once or twice daily outside US) 1, 2, 3
- Adjust for renal impairment and drug interactions 1, 4
Low-dose NSAIDs (Second-line):
Low-dose Prednisone/Prednisolone:
- <10 mg/day if colchicine and NSAIDs are contraindicated, not tolerated, or ineffective 1, 2, 3
- Monitor carefully for corticosteroid-related adverse effects, especially in patients with diabetes or infection risk 1
Duration of Prophylaxis
Continue prophylaxis for the greater of: 1, 2, 3
- At least 6 months duration, OR
- 3 months after achieving target serum urate (for patients without tophi on physical exam), OR
- 6 months after achieving target serum urate (for patients with tophi detected on physical exam, continued until tophi resolution)
Lifestyle Modifications
- Weight loss for obese patients 1, 2, 5, 7
- Avoid alcohol (especially beer and spirits) 1, 2, 5, 7
- Avoid sugar-sweetened beverages and high-fructose corn syrup 2, 5, 7
- Reduce intake of purine-rich foods (organ meats, shellfish) 1, 5, 7
- Encourage consumption of vegetables and low-fat or nonfat dairy products 5, 7
- Discontinue diuretics if possible when gout is associated with diuretic use 1
Common Pitfalls and How to Avoid Them
- Delaying treatment beyond 24 hours significantly reduces effectiveness—educate patients on early self-treatment 1, 3, 5
- Stopping ULT during acute attacks worsens outcomes—always continue ULT without interruption 1, 3
- Failing to provide prophylaxis when initiating ULT leads to acute flares and poor medication adherence—mandatory prophylaxis for at least 6 months 1, 3
- Using high-dose colchicine regimens causes significant GI toxicity with no additional benefit—use low-dose regimen only 1, 5
- Inadequate duration of prophylaxis leads to breakthrough flares—continue for specified duration based on tophi presence and urate target achievement 1, 3
- Ignoring drug interactions with colchicine can cause serious toxicity—adjust dose with CYP3A4/P-glycoprotein inhibitors and in renal impairment 1, 5, 4