Warfarin: Difference between revisions

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==Dosing==
==General==
*Type: [[anticoagulant]]
*Dosage Forms: oral
*Common Trade Names: Coumadin


==Adult Dosing==
*Day 1: 5 - 7.5mg oral at bedtime (to ensure absorption on empty stomach)
*Day 2 and beyond: 2.5 - 7.5mg daily (usually 5mg)
*INR increase of >0.3 - 0.4 per day requires dose reduction
*Response also influenced by congestive heart failure, liver disease, Vitamin K deficiency, many drugs


Day 1: 5 to 7.5 mg po at night (to ensure absorption on an empty stomach),
===Target Range of INR===
*2.5 - 3.5: Mechanical prosthetic valves or recurrent thromboembolism
*2.0 - 3.0: All other indications


Day 2, 3, 4...: 2.5 to 7.5 mg po qhs (most often 5 mg)
==Pediatric Dosing==
''Safety and efficacy not well-established, though it is sometimes used in pediatrics for VTE treatment''


*An increase in INR of >0.3-0.4 units per day necessitates dose reduction
==Special Populations==
*[[Drug Ratings in Pregnancy|Pregnancy Rating]]: Contraindicated (Category D)
*[[Lactation risk categories|Lactation risk]]: infant risk minimal
*Renal Dosing: caution advised
*Hepatic Dosing: consider decreased dose


*CHF, liver disease, Vitamin K def, drugs may influence warfarin response
==Contraindications==
*Allergy to class/drug
*Active bleeding or tendency to bleed


==Adverse Reactions==
 
*Bleeding
==Range (INR)==
**Risk increased when INR >3
 
**Exponential increase when INR >5
 
**Avoid giving NSAIDs, sulfas, macrolidies (azithromycin ok), fluoroquinolones
2.5 to 3.5: mechanical prosthetic valves or recurrent thromboembolism
*Skin necrosis
 
**Usually in patient with protein C deficiency
2.0-3.0: all other indications
**Occurs 3 - 8 days after starting treatment
 
*Treatment: see [[Warfarin (Coumadin) Reversal]]
 
==Reversal==
 
 
FFP (10-20/kg) to decr INR to 1.5 (should occur in 6-24 hr)
 
+/- Vitamin K (10 mg IM) (takes 24hrs to affect & 2wk to wear off)
 
 
==Potentiators==
 
 
 
 
 
 
 
 
==Source ==
 
 
1/26/06 DONALDSON (addapted from Lampe), EMP 1/11


==Pharmacology==
*Half-life: 20-60h (anticoagulant effect)
**Of note, half-life highly variable based on rate of clotting factor catabolism
*Metabolism: Liver
*Excretion: Urine 92%, bile
*Mechanism of Action:
**Blocks activation of vitamin K dependent prothrombotic factors II, VII, IX, X
**Blocks synthesis of vitamin K dependent antithrombotic proteins C and S
*Albumin bound


==Comments==
*Because of differing factor half-lives, can cause transient (24-36 hour) prothrombosis at start of therapy
**Bridge with [[heparin]] for 1-2 days until INR is in desired range


==See Also==
*[[Warfarin (Coumadin) Reversal]]
*[[Coagulopathy (Main)]]


==References==
<references/>
[[Category:Pharmacology]]
[[Category:Heme/Onc]]
[[Category:Heme/Onc]]

Latest revision as of 13:58, 25 February 2021

General

  • Type: anticoagulant
  • Dosage Forms: oral
  • Common Trade Names: Coumadin

Adult Dosing

  • Day 1: 5 - 7.5mg oral at bedtime (to ensure absorption on empty stomach)
  • Day 2 and beyond: 2.5 - 7.5mg daily (usually 5mg)
  • INR increase of >0.3 - 0.4 per day requires dose reduction
  • Response also influenced by congestive heart failure, liver disease, Vitamin K deficiency, many drugs

Target Range of INR

  • 2.5 - 3.5: Mechanical prosthetic valves or recurrent thromboembolism
  • 2.0 - 3.0: All other indications

Pediatric Dosing

Safety and efficacy not well-established, though it is sometimes used in pediatrics for VTE treatment

Special Populations

  • Pregnancy Rating: Contraindicated (Category D)
  • Lactation risk: infant risk minimal
  • Renal Dosing: caution advised
  • Hepatic Dosing: consider decreased dose

Contraindications

  • Allergy to class/drug
  • Active bleeding or tendency to bleed

Adverse Reactions

  • Bleeding
    • Risk increased when INR >3
    • Exponential increase when INR >5
    • Avoid giving NSAIDs, sulfas, macrolidies (azithromycin ok), fluoroquinolones
  • Skin necrosis
    • Usually in patient with protein C deficiency
    • Occurs 3 - 8 days after starting treatment
  • Treatment: see Warfarin (Coumadin) Reversal

Pharmacology

  • Half-life: 20-60h (anticoagulant effect)
    • Of note, half-life highly variable based on rate of clotting factor catabolism
  • Metabolism: Liver
  • Excretion: Urine 92%, bile
  • Mechanism of Action:
    • Blocks activation of vitamin K dependent prothrombotic factors II, VII, IX, X
    • Blocks synthesis of vitamin K dependent antithrombotic proteins C and S
  • Albumin bound

Comments

  • Because of differing factor half-lives, can cause transient (24-36 hour) prothrombosis at start of therapy
    • Bridge with heparin for 1-2 days until INR is in desired range

See Also

References