Colchicine Dosing for Pericarditis: Once Daily vs Twice Daily
Use weight-based dosing: 0.5 mg twice daily for patients ≥70 kg or 0.5 mg once daily for patients <70 kg, continued for at least 6 months in recurrent pericarditis and 3 months in acute pericarditis. 1, 2, 3
Weight-Based Dosing Algorithm
The dosing regimen is straightforward and based solely on body weight:
- Patients ≥70 kg: Colchicine 0.5 mg twice daily 1, 2, 4, 5
- Patients <70 kg: Colchicine 0.5 mg once daily 1, 2, 4, 5
- Patients intolerant to higher doses: 0.5 mg once daily regardless of weight 1
This weight-adjusted approach was validated in multiple randomized controlled trials (COPE, CORE, CORP-2, ICAP) and consistently demonstrated efficacy with acceptable tolerability. 4, 6, 7, 5
Treatment Duration by Clinical Scenario
Acute Pericarditis (First Episode)
- Duration: 3 months 3, 5
- Outcome: Reduces recurrence from 37.5% to 16.7% (NNT=4) 5
- Evidence: The ICAP trial demonstrated that 3 months of colchicine added to NSAIDs significantly reduced incessant or recurrent pericarditis compared to placebo. 5
Recurrent Pericarditis
- Duration: Minimum 6 months 1, 2, 4, 7
- Extended therapy: Consider >6 months based on clinical response 1
- Outcome: Reduces recurrence from 42.5% to 21.6% (NNT=5) in patients with multiple recurrences 4
- Evidence: The CORP-2 trial specifically studied patients with multiple recurrences and found 6 months of therapy was effective and safe. 4
Dose Adjustments for Renal and Hepatic Impairment
Renal Impairment
- Severe renal impairment (CrCl <30 mL/min): Colchicine is contraindicated OR use 0.3 mg once daily with extreme caution 3
- Moderate impairment (CrCl 30-50 mL/min): Standard weight-based dosing with close monitoring for toxicity 3
- Dialysis patients: Maximum 0.3 mg twice weekly 3
Critical pitfall: Colchicine accumulates in renal dysfunction and can cause severe neuromyopathy, rhabdomyolysis, and bone marrow suppression. 3 Always verify renal function before initiating therapy.
Hepatic Impairment
- Dose reduction required in severe hepatic impairment 1
- Monitor closely for hepatotoxicity (occurred in 3 patients vs 1 in placebo in CORP-2) 4
Combination Therapy Requirements
Colchicine must always be added to NSAIDs or aspirin, never used as monotherapy. 2, 3
First-Line Combination
- Aspirin: 750-1000 mg every 8 hours 1, 3
- OR Ibuprofen: 600 mg every 8 hours 1, 3
- PLUS Colchicine: Weight-adjusted dosing as above 1, 2, 3
The combination reduces recurrence rates from 55% to 24% at 18 months (56% relative risk reduction). 2
Tapering Strategy
Only begin tapering after complete symptom resolution AND CRP normalization. 1, 3
- Taper one drug class at a time 2
- Stop NSAIDs/aspirin first, then gradually taper colchicine 2
- If symptoms recur during tapering, do NOT increase corticosteroids; instead maximize NSAID dosing and ensure colchicine adherence 1
Critical threshold: Premature tapering before CRP normalization leads to rebound inflammation and dramatically increases recurrence risk. 3
Safety and Tolerability
Common Adverse Effects
- Gastrointestinal intolerance: 5-10% of patients 8
- Management: Temporary dose reduction or brief discontinuation 8
- Discontinuation rate: 8.3% in COPE trial, primarily due to diarrhea 6
Serious Adverse Events
- No serious adverse events reported in major trials (COPE, CORE, CORP-2, ICAP) 4, 6, 7, 5
- Overall adverse effects similar between colchicine and placebo groups 4, 5
Critical Pitfalls to Avoid
Using corticosteroids first-line: Increases recurrence risk (OR 4.30) and should be avoided unless NSAIDs/colchicine are contraindicated. 1, 3, 6
Inadequate treatment duration: Shorter courses than recommended (3 months for acute, 6 months for recurrent) increase recurrence to 15-30% after first episode and up to 50% after first recurrence. 3
Ignoring renal function: Severe renal impairment is a contraindication; failure to adjust dosing can lead to life-threatening toxicity. 1, 3
Monotherapy with colchicine: Always combine with NSAIDs/aspirin for optimal efficacy. 2, 3
Starting tapering too early: Wait for complete symptom resolution AND CRP normalization before any dose reduction. 1, 3