Treatment of Acute Gout
For acute gout, initiate treatment within 24 hours of symptom onset with NSAIDs, oral colchicine, or corticosteroids as first-line monotherapy, selecting based on patient comorbidities and contraindications. 1, 2
First-Line Treatment Options
NSAIDs
- Use full FDA-approved anti-inflammatory doses until the acute attack completely resolves 3, 1
- FDA-approved NSAIDs include naproxen (500mg twice daily), indomethacin, and sulindac 1
- No single NSAID is superior to another; the key is early initiation rather than agent selection 3, 4
- Contraindicated in patients with renal disease, heart failure, cirrhosis, or peptic ulcer disease 1, 5
Colchicine
- Most effective when started within 36 hours of symptom onset 3, 1
- Recommended low-dose regimen: 1.2 mg loading dose followed by 0.6 mg one hour later (total 1.8 mg over one hour) 1, 2
- This low-dose regimen is as effective as higher doses with significantly fewer gastrointestinal side effects 1, 2, 5
- After the loading dose, continue 0.6 mg once or twice daily (prophylactic dosing) 12 hours later until the attack resolves 3
- Requires dose reduction in moderate to severe chronic kidney disease and with strong CYP3A4/P-glycoprotein inhibitors (cyclosporine, clarithromycin) 3, 5
Corticosteroids
- Considered first-line therapy due to safety profile and low cost, particularly when NSAIDs and colchicine are contraindicated 1, 2
- 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 2
- Alternative: prednisolone 35 mg daily for 5 days 2
- Intra-articular corticosteroid injection is highly effective for single joint involvement 2, 5
- For NPO patients with polyarticular involvement: intravenous/intramuscular methylprednisolone (0.5-2.0 mg/kg) 5
- Use with caution in diabetic patients due to hyperglycemia risk 1
Treatment Selection Algorithm Based on Comorbidities
Renal Impairment
- Corticosteroids are the safest option 2, 5
- Avoid NSAIDs 1
- Reduce colchicine dose or avoid entirely depending on severity 3
Cardiovascular Disease
- Prefer colchicine or corticosteroids over NSAIDs 1
Gastrointestinal Risk Factors
- Prefer corticosteroids or low-dose colchicine over NSAIDs 2
- If NSAIDs are used, add gastroprotection 1
Diabetes
- Prefer NSAIDs or colchicine over corticosteroids 2
Combination Therapy for Severe Disease
- For severe pain (≥7/10) or polyarticular involvement, use combination therapy 2, 5
- Effective combinations include:
Critical Management Principles
- Initiate treatment within 24 hours of symptom onset for optimal outcomes 1, 2, 5
- Continue treatment at full dose until the gouty attack has completely resolved 3, 1
- Continue established urate-lowering therapy (if already prescribed) without interruption during the acute attack 1, 2, 5
- Educate patients to self-medicate at first warning symptoms ("pill in the pocket" approach) 5
Management of Inadequate Response
- Define inadequate response as <20% improvement in pain within 24 hours or <50% improvement after 24 hours 5
- Switch to another monotherapy or add a second recommended agent 1, 5
- For severe refractory attacks, IL-1 inhibitors (anakinra or canakinumab) may be considered, though off-label 5, 6
Prophylaxis After Acute Attack
- Strongly recommended when starting urate-lowering therapy 1, 5
- Options include low-dose colchicine (0.6 mg once or twice daily), low-dose NSAIDs with gastroprotection, or low-dose prednisone 1, 5
- Continue prophylaxis for at least 6 months, or 3 months after achieving target serum urate (<6 mg/dL) if no tophi present, or 6 months after achieving target if tophi present 1, 5
Common Pitfalls to Avoid
- Delaying treatment beyond 24 hours significantly reduces effectiveness 5, 4
- Avoid high-dose colchicine regimens (previously used dosing of repeated doses until diarrhea) as they cause severe gastrointestinal toxicity without additional benefit 5
- Never discontinue urate-lowering therapy during acute flares 2, 5
- Inadequate duration of prophylaxis when initiating urate-lowering therapy leads to breakthrough flares and poor adherence 5
- Monitor for colchicine drug interactions, particularly with strong P-glycoprotein/CYP3A4 inhibitors, which can cause life-threatening toxicity 3, 5