How to Use Colchicine
Acute Gout Flare Treatment
For acute gout attacks, administer colchicine 1.2 mg (two tablets) at the first sign of symptoms, followed by 0.6 mg (one tablet) one hour later, for a total of 1.8 mg over one hour. 1
- Timing is critical: Colchicine must be started within 12-36 hours of flare onset for maximum effectiveness 2, 3. After 36 hours, efficacy drops significantly 4.
- This low-dose regimen (1.8 mg total) is as effective as higher doses but with significantly fewer gastrointestinal side effects 3, 5.
- The maximum dose for treating an acute flare is 1.8 mg over one hour—higher doses provide no additional benefit 1.
- Do not repeat treatment courses more frequently than every 3 days in patients with normal renal function 1.
Special Populations for Acute Flares
Severe renal impairment (CrCl <30 mL/min): The dose does not need adjustment, but treatment courses should not be repeated more than once every two weeks 1.
Dialysis patients: Give a single 0.6 mg dose only, and do not repeat for at least two weeks 4, 1.
Mild-moderate renal impairment (CrCl 30-80 mL/min): No dose adjustment needed, but monitor closely for adverse effects 1.
Prophylaxis of Gout Flares
For prevention of gout flares, prescribe colchicine 0.6 mg once or twice daily (maximum 1.2 mg/day). 1
- Prophylaxis should be initiated when starting urate-lowering therapy (allopurinol, febuxostat, etc.) and continued for at least 6 months 2, 3.
- For patients without tophi, continue prophylaxis for 3 months after achieving target uric acid levels 4.
- For patients with tophi, extend prophylaxis to 6 months after achieving target uric acid 4.
Special Populations for Prophylaxis
Severe renal impairment (CrCl <30 mL/min): Start with 0.3 mg daily and increase cautiously with close monitoring 1.
Dialysis patients: Start with 0.3 mg twice weekly with close monitoring 1.
Mild-moderate hepatic impairment: No dose adjustment required, but monitor closely 1.
Severe hepatic impairment: Consider dose reduction 1.
Critical Drug Interactions
Absolutely avoid colchicine in patients taking strong CYP3A4 and/or P-glycoprotein inhibitors such as cyclosporine, clarithromycin, ritonavir, atazanavir, or other protease inhibitors 2, 1.
If these medications cannot be avoided and colchicine is essential:
- For acute flares: Reduce to 0.6 mg × 1 dose, followed by 0.3 mg one hour later; do not repeat for at least 3 days 1.
- For prophylaxis: Maximum 0.3 mg once daily or 0.3 mg every other day, depending on the specific interacting drug 1.
- Never use colchicine in patients with renal or hepatic impairment who are also taking these interacting medications 1.
Treating Acute Flares While on Prophylaxis
If a patient on prophylactic colchicine develops an acute flare:
- Give 1.2 mg (two tablets) at first sign, followed by 0.6 mg one hour later 1.
- Wait 12 hours, then resume the prophylactic dose 1.
- However, do not treat acute flares with colchicine in patients on prophylaxis who are also taking CYP3A4 inhibitors 1.
- Do not treat acute flares with colchicine in patients with renal impairment who are receiving prophylactic colchicine—consider alternative therapy 1.
Alternative Treatments When Colchicine is Contraindicated
When colchicine cannot be used:
- NSAIDs at full approved doses until complete resolution (with proton pump inhibitors if appropriate) 2, 4.
- Oral corticosteroids: Prednisone 30-35 mg/day (or equivalent) for 3-5 days, then stop or taper over 7-10 days 2, 4.
- Intra-articular corticosteroid injection after joint aspiration 2, 4.
- IL-1 blockers for patients with frequent flares and contraindications to all other options 2.
Common Pitfalls to Avoid
- Starting too late: Colchicine loses effectiveness after 36 hours from symptom onset 4, 3.
- Using high doses: The old regimen of continuing colchicine every 1-2 hours until diarrhea occurs is obsolete and dangerous—it causes severe gastrointestinal toxicity without additional benefit 5.
- Ignoring drug interactions: Combining colchicine with CYP3A4/P-gp inhibitors can cause life-threatening toxicity, especially in patients with renal or hepatic impairment 2, 1.
- Inadequate prophylaxis duration: Stopping prophylaxis too early when initiating urate-lowering therapy leads to rebound flares 2, 3.
- Neuromuscular toxicity: Be vigilant for myopathy and neuropathy, especially in patients on statins, with renal impairment, or on long-term therapy 2.