Colchicine: Difference between revisions
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==Administration== | ==Administration== | ||
*Type: Antigout | *Type: Antigout, anti-inflammatory | ||
*Dosage Forms: Capsules, Tablets | *Dosage Forms: Capsules, Tablets | ||
*Routes of Administration: Oral | *Routes of Administration: Oral | ||
| Line 6: | Line 6: | ||
==Adult Dosing== | ==Adult Dosing== | ||
===[[Gout]]=== | |||
*Flare treatment: Initial: 1.2mg and then 0.6mg in an hour (maximum 1.8mg within 1 hour). In patient receiving prophylaxis treatment wait for 12 h after flare dosing before resuming prophylaxis dose. Do not repeat treatment for at least 3 days (Canadian labelling recommendation) | |||
*Prophylaxis Treatment: 0.6mg twice daily (maximum 1.2mg/day) for 3 months (without tophi) to 6 months (≥1 tophi) after reaching target serum uric acid levels <ref>Khanna D. et al.2012 ACR Guidelines for Management of Gout Part I: Systemic Non-pharmacologic and Pharmacologic Therapeutic Approach to Hyperuricemia. Arthritis Care Res (Hoboken). 2012 Oct; 64(10): 1431–1446.</ref> | |||
===Familial Mediterranean Fever=== | |||
*1.2mg to 2.4mg per day in 1-2 decided dose. Titrate (increase or decrease) 0.3mg daily increment based on efficacy and adverse effects. | |||
==Pediatric Dosing== | ==Pediatric Dosing== | ||
===Familial Mediterranean Fever=== | |||
*Children 4 to 6 years: 0.3 to 1.8mg daily in 1-2 divided doses | |||
*Children 6 to 12 years: 0.9 to 1.8mg daily in 1-2 divided doses | |||
*Adolescents >12 years: Adult dosing | |||
* | |||
===Gout=== | |||
*Prophylaxis/treatment: Adult dosing | |||
==Special Populations== | ==Special Populations== | ||
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***CrCl 30-80 mL/minute: dose adjustment not required, monitor closely for adverse effects. | ***CrCl 30-80 mL/minute: dose adjustment not required, monitor closely for adverse effects. | ||
***CrCl <30 mL/minute: consider dose reduction, should not repeat dose more frequently that every 14 days. | ***CrCl <30 mL/minute: consider dose reduction, should not repeat dose more frequently that every 14 days. | ||
***Dialysis: A single dose of 0. | ***Dialysis: A single dose of 0.6mg, should not repeat dose more frequently that every 14 days. | ||
**Gout prophylaxis: | **Gout prophylaxis: | ||
***CrCl 30-80 mL/minute: dose adjustment not required, monitor closely for adverse effects. | ***CrCl 30-80 mL/minute: dose adjustment not required, monitor closely for adverse effects. | ||
***CrCl <30 mL/minute: nitial dose: 0. | ***CrCl <30 mL/minute: nitial dose: 0.3mg daily, titrate with caution, monitor closely for adverse effects. | ||
***Dialysis: 0. | ***Dialysis: 0.3mg twice weekly, monitor closely for adverse effects. | ||
**FMF: | **FMF: | ||
***CrCl 30-80 mL/minute: monitor closely for adverse effects, consider dosage reduction. | ***CrCl 30-80 mL/minute: monitor closely for adverse effects, consider dosage reduction. | ||
***CrCl <30mL/minute: Initial dose: 0. | ***CrCl <30mL/minute: Initial dose: 0.3mg daily, titrate with caution, monitor closely for adverse effects. | ||
***Dialysis: a single dose of 0. | ***Dialysis: a single dose of 0.3mg, titrate with caution, monitor closely for adverse effects. | ||
*Pediatric: Not defined | *Pediatric: Not defined | ||
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*Disrupts cytoskeleton function: inhibit beta-tubulin polymerization into microtubules. | *Disrupts cytoskeleton function: inhibit beta-tubulin polymerization into microtubules. | ||
*Prevent activation, migration and degranulation of neutrophils mediating some gout symptoms. | *Prevent activation, migration and degranulation of neutrophils mediating some gout symptoms. | ||
==[[Colchicine toxicity|Toxicity]]== | |||
*Rapidly absorbed and extensively distributed | |||
*Maximum therapeutic dose: 8-10 mg in 1 day | |||
*Nausea, vomiting, abdominal pain, bloody diarrhea | |||
*Bone marrow suppression, renal failure | |||
*Lactic Acidosis | |||
*Delirium, seizures, coma | |||
*Death within 8-36 hours caused by respiratory failure or arrhythmia | |||
*Aggressive supportive care (colchicine-specific antibodies are not available in U.S.) | |||
*If survival, can see rebound leukocytosis and transient alopecia | |||
==Comments== | ==Comments== | ||
==See Also== | ==See Also== | ||
*[[Colchicine toxicity]] | |||
==References== | ==References== | ||
<references/> | <references/> | ||
[[Category:Pharmacology]] | [[Category:Pharmacology]] [[Category:Rheumatology]] | ||
Latest revision as of 17:48, 20 September 2019
Administration
- Type: Antigout, anti-inflammatory
- Dosage Forms: Capsules, Tablets
- Routes of Administration: Oral
- Common Trade Names: Colcris; Mitigare (US), Jamp-Colchicine; PMS-Colchicine (Canadian)
Adult Dosing
Gout
- Flare treatment: Initial: 1.2mg and then 0.6mg in an hour (maximum 1.8mg within 1 hour). In patient receiving prophylaxis treatment wait for 12 h after flare dosing before resuming prophylaxis dose. Do not repeat treatment for at least 3 days (Canadian labelling recommendation)
- Prophylaxis Treatment: 0.6mg twice daily (maximum 1.2mg/day) for 3 months (without tophi) to 6 months (≥1 tophi) after reaching target serum uric acid levels [1]
Familial Mediterranean Fever
- 1.2mg to 2.4mg per day in 1-2 decided dose. Titrate (increase or decrease) 0.3mg daily increment based on efficacy and adverse effects.
Pediatric Dosing
Familial Mediterranean Fever
- Children 4 to 6 years: 0.3 to 1.8mg daily in 1-2 divided doses
- Children 6 to 12 years: 0.9 to 1.8mg daily in 1-2 divided doses
- Adolescents >12 years: Adult dosing
Gout
- Prophylaxis/treatment: Adult dosing
Special Populations
- Pregnancy Rating: C
- Lactation risk: Colchicine enters breast milk, caution should be used when administering in a nursing woman.
Renal Dosing
- Adult:
- Gout flare treatment:
- Use colchicine to treat acute route flare is contraindicated in patients with renal impairment who are receiving colchicine for prophylaxis.
- CrCl 30-80 mL/minute: dose adjustment not required, monitor closely for adverse effects.
- CrCl <30 mL/minute: consider dose reduction, should not repeat dose more frequently that every 14 days.
- Dialysis: A single dose of 0.6mg, should not repeat dose more frequently that every 14 days.
- Gout prophylaxis:
- CrCl 30-80 mL/minute: dose adjustment not required, monitor closely for adverse effects.
- CrCl <30 mL/minute: nitial dose: 0.3mg daily, titrate with caution, monitor closely for adverse effects.
- Dialysis: 0.3mg twice weekly, monitor closely for adverse effects.
- FMF:
- CrCl 30-80 mL/minute: monitor closely for adverse effects, consider dosage reduction.
- CrCl <30mL/minute: Initial dose: 0.3mg daily, titrate with caution, monitor closely for adverse effects.
- Dialysis: a single dose of 0.3mg, titrate with caution, monitor closely for adverse effects.
- Gout flare treatment:
- Pediatric: Not defined
Hepatic Dosing
- Adult:
- Mild to moderate impairment: use with caution, closely monitor for adverse effects.
- Severe impairment: consider dosage adjustment.
- Pediatric: Not defined
Contraindications
- Allergy to class/drug
- Concomitant use with P-glycoprotein or strong CYP3A4 inhibitor in patients with renal or hepatic impairment
- Patient with both renal and hepatic impairment
- Serious gastrointestinal or cardiac disease
Adverse Reactions
Serious (<1%)
- Bone marrow suppression
- Disseminated intravascular coagulation
- Toxic neuromuscular disease
- Rhabdomyolysis
- Hepatotoxicity
- Hypersensitivity reaction
Common
- Diarrhoea
- Nausea
- Vomiting
- Abdominal cramp/abdominal pain
- Gout
- Pharyngolaryngeal pain
- Fatigue
- Headache
Pharmacology
- Half-life: 27 to 31 hours (multiple dose; young, healthy volunteers)
- Metabolism: Hepatic (CYP3A4)
- Excretion: Urine
Mechanism of Action
- Disrupts cytoskeleton function: inhibit beta-tubulin polymerization into microtubules.
- Prevent activation, migration and degranulation of neutrophils mediating some gout symptoms.
Toxicity
- Rapidly absorbed and extensively distributed
- Maximum therapeutic dose: 8-10 mg in 1 day
- Nausea, vomiting, abdominal pain, bloody diarrhea
- Bone marrow suppression, renal failure
- Lactic Acidosis
- Delirium, seizures, coma
- Death within 8-36 hours caused by respiratory failure or arrhythmia
- Aggressive supportive care (colchicine-specific antibodies are not available in U.S.)
- If survival, can see rebound leukocytosis and transient alopecia
Comments
See Also
References
- ↑ Khanna D. et al.2012 ACR Guidelines for Management of Gout Part I: Systemic Non-pharmacologic and Pharmacologic Therapeutic Approach to Hyperuricemia. Arthritis Care Res (Hoboken). 2012 Oct; 64(10): 1431–1446.
