Colchicine: Difference between revisions

No edit summary
 
(20 intermediate revisions by 6 users not shown)
Line 1: Line 1:
==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
===[[Gout]]===
**Flare treatment: Initial: 1.2 mg and then  0.6 mg in an hour (maximum 1.8 mg 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)
*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: 0.6 mg twice daily (maximum 1.2 mg/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>
*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 (FMF): 1.2 mg to 2.4 mg per day in 1-2 decided dose. Titrate (increase or decrease) 0.3 mg daily increment based on efficacy and adverse effects.
 
===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 (FMF):
===Familial Mediterranean Fever===
**Children 4 to 6 years: 0.3 to 1.8 mg daily in 1-2 divided doses
*Children 4 to 6 years: 0.3 to 1.8mg daily in 1-2 divided doses
**Children 6 to 12 years: 0.9 to 1.8 mg 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
*Adolescents >12 years: Adult dosing
*Gout prophylaxis/treatment: Adult dosing
 
===Gout===
*Prophylaxis/treatment: Adult dosing


==Special Populations==
==Special Populations==
Line 27: Line 31:
***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 0.6 mg, 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:  
**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: 0.3 mg daily, titrate with caution, monitor closely for adverse effects.
***CrCl <30 mL/minute: nitial dose: 0.3mg daily, titrate with caution, monitor closely for adverse effects.
***Dialysis: 0.3 mg twice weekly, monitor closely for adverse effects.
***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: 0.3 mg daily, titrate with caution, monitor closely for adverse effects.
***CrCl <30mL/minute: Initial dose: 0.3mg daily, titrate with caution, monitor closely for adverse effects.
***Dialysis: a single dose of 0.3 mg, titrate with caution, monitor closely for adverse effects.
***Dialysis: a single dose of 0.3mg, titrate with caution, monitor closely for adverse effects.


*Pediatric: Not defined
*Pediatric: Not defined
Line 41: Line 45:
===Hepatic Dosing===
===Hepatic Dosing===
*Adult:
*Adult:
*Pediatric:
**Mild to moderate impairment: use with caution, closely monitor for adverse effects.
**Severe impairment: consider dosage adjustment.
*Pediatric: Not defined


==Contraindications==
==Contraindications==
*Allergy to class/drug
*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==
==Adverse Reactions==
===Serious===
===Serious (<1%)===
*Bone marrow suppression
*Disseminated intravascular coagulation
*Toxic neuromuscular disease
*Rhabdomyolysis
*Hepatotoxicity
*Hypersensitivity reaction


===Common===
===Common===
*Diarrhoea
*Nausea
*Vomiting
*Abdominal cramp/abdominal pain
*Gout
*Pharyngolaryngeal pain
*Fatigue
*Headache


==Pharmacology==
==Pharmacology==
*Half-life:  
*Half-life: 27 to 31 hours (multiple dose; young, healthy volunteers)
*Metabolism:  
*Metabolism: Hepatic (CYP3A4)
*Excretion:  
*Excretion: Urine


==Mechanism of Action==
==Mechanism of Action==
*Disrupts cytoskeleton function: inhibit beta-tubulin polymerization into microtubules.
*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

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.
  • 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

  1. 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.