Best Treatment for Suspected Acute Gout
For an otherwise healthy adult with a suspected acute gout flare, initiate treatment immediately with colchicine (1.2 mg followed by 0.6 mg one hour later), NSAIDs at full anti-inflammatory doses, or oral corticosteroids (prednisone 30-35 mg daily for 5 days)—all three are equally effective first-line options with the choice driven by patient-specific contraindications and access. 1, 2
First-Line Treatment Options
The 2020 American College of Rheumatology guidelines provide Level A evidence (the highest quality) that three medication classes are equally effective for acute gout flares, with no single agent prioritized over the others 1:
Colchicine: FDA-approved dosing is 1.2 mg (two 0.6 mg tablets) at the first sign of flare, followed by 0.6 mg one hour later (total 1.8 mg over one hour). Higher doses provide no additional benefit but significantly increase gastrointestinal side effects. 3, 1
NSAIDs: Any potent NSAID at full anti-inflammatory doses (e.g., naproxen 500 mg twice daily, indomethacin 50 mg three times daily). The key to success is early initiation within 24 hours of symptom onset, not which specific NSAID is chosen. 1, 4
Oral corticosteroids: Prednisone 0.5 mg/kg/day (approximately 30-35 mg for average adults) for 5-10 days at full dose then stopped abruptly, OR 2-5 days at full dose followed by a 7-10 day taper. Both regimens are equally effective. 2, 1
Treatment Selection Algorithm
Step 1: Assess Contraindications
Choose corticosteroids as first-line if the patient has: 2, 5
- Severe renal impairment (eGFR <30 mL/min)—NSAIDs can precipitate acute kidney injury and colchicine carries fatal toxicity risk
- Cardiovascular disease or heart failure—NSAIDs increase cardiovascular events
- Active peptic ulcer disease or recent GI bleeding—NSAIDs pose hemorrhage risk
- Cirrhosis or hepatic impairment—NSAIDs are contraindicated
- Current anticoagulation therapy—NSAIDs increase bleeding risk
Avoid corticosteroids if: 2
- Active systemic infection (absolute contraindication due to immune suppression)
- Poorly controlled diabetes (though short courses cause only transient, manageable hyperglycemia)
- Patient has cardiovascular disease (colchicine may reduce MI risk)
- NSAIDs and corticosteroids are contraindicated
- Severe renal insufficiency (CrCl <30 mL/min)—requires dose reduction to 0.6 mg × 1 dose, then 0.3 mg one hour later
- Combined hepatic-renal insufficiency
- Patient is taking strong CYP3A4 inhibitors (clarithromycin, ketoconazole, ritonavir)—fatal toxicity reported
Step 2: Initiate Treatment Within 24 Hours
Early treatment is critical—pharmacologic therapy should begin within 24 hours of symptom onset for optimal efficacy. 1, 4 Educate patients to self-initiate treatment at the first warning signs without waiting for provider contact ("pill-in-pocket" strategy). 1
Step 3: Consider Combination Therapy for Severe Attacks
For severe pain (>6/10 on pain scale) or polyarticular involvement (>3 small joints or >2 large joints), initiate combination therapy with two agents simultaneously: 1, 2
- Colchicine plus NSAIDs
- Oral corticosteroids plus colchicine
- Intra-articular corticosteroid injection (for 1-2 accessible large joints) plus any oral agent
Step 4: Monitor Response and Adjust
Define inadequate response as: 1, 2
- <20% improvement in pain within 24 hours, OR
- <50% improvement at ≥24 hours after initiating therapy
If inadequate response occurs, switch to an alternative monotherapy or add a second agent. Consider alternative diagnoses (especially septic arthritis). 1
Alternative Routes When Oral Therapy Not Possible
For patients unable to take oral medications (NPO status, surgery, severe nausea): 1, 2
- Intramuscular triamcinolone acetonide 60 mg (single injection)
- IV/IM methylprednisolone 0.5-2.0 mg/kg (approximately 40-140 mg for most adults)
- Intra-articular corticosteroid injection for monoarticular or oligoarticular involvement of accessible large joints
Critical Management Principles
Do NOT stop urate-lowering therapy (allopurinol, febuxostat) during an acute flare—continue it without interruption. 1
Topical ice can be used as adjuvant therapy but should not replace pharmacologic treatment. 1
IL-1 inhibitors (canakinumab, anakinra) are reserved only for patients who have failed, cannot tolerate, or have contraindications to all conventional therapies due to high cost and modest benefit relative to first-line agents. 1, 6
Common Pitfalls to Avoid
Delaying treatment beyond 24 hours significantly reduces effectiveness of all agents. 1, 4
Using high-dose colchicine regimens (hourly dosing until diarrhea)—this outdated approach causes severe GI toxicity without additional benefit compared to the low-dose FDA-approved regimen. 3, 6
Prescribing NSAIDs to patients with renal impairment or cardiovascular disease—this substantially increases risk of acute kidney injury and cardiovascular events. 2, 5
Failing to provide patient education about self-initiating treatment at first symptom onset—early intervention is the most important determinant of therapeutic success. 1