What is the standard dosing regimen for Unfractionated Heparin (UFH)?

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Last updated: December 8, 2025View editorial policy

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Unfractionated Heparin Dosing

For therapeutic anticoagulation, administer UFH as an 80 units/kg IV bolus (maximum 4000 units) followed by 18 units/kg/hour continuous infusion (maximum 1000 units/hour), targeting an aPTT of 1.5-2.0 times control (approximately 50-70 seconds). 1, 2

Standard Weight-Based Dosing Regimen

Initial Dosing

  • Bolus dose: 80 units/kg IV (maximum 4000 units for patients >50 kg) 1
  • Infusion rate: 18 units/kg/hour (maximum 1000 units/hour for patients >55 kg) 1, 2
  • This represents the highest quality evidence from the American College of Chest Physicians and FDA labeling 3, 2

Alternative Fixed-Dose Approach

  • Bolus: 5,000 units IV 2
  • Infusion: 1,000 units/hour continuous 2
  • The American College of Chest Physicians suggests this fixed-dose approach is equivalent to weight-based dosing, though weight-based dosing is preferred 3

Context-Specific Modifications

STEMI with Fibrinolytic Therapy

Use reduced dosing to minimize bleeding risk: 3

  • Bolus: 60 units/kg IV (maximum 4000 units) 3
  • Infusion: 12 units/kg/hour (maximum 1000 units/hour) 3
  • This lower dose is specifically recommended by ACC/AHA when combining UFH with fibrin-specific agents (alteplase, reteplase, tenecteplase) 3

Unstable Angina/NSTEMI

  • Bolus: 60-70 units/kg IV 3
  • Infusion: 12-15 units/kg/hour 3
  • If glycoprotein IIb/IIIa inhibitors are planned during PCI, target ACT of 200 seconds rather than standard aPTT monitoring 3

Cardiovascular Surgery

  • Minimum dose: 150 units/kg IV bolus 2
  • For procedures <60 minutes: 300 units/kg 2
  • For procedures >60 minutes: 400 units/kg 2

VTE Prophylaxis (Subcutaneous)

  • 5,000 units subcutaneously 2 hours before surgery, then every 8-12 hours for 7 days or until fully ambulatory 2

Monitoring Protocol

aPTT Monitoring Schedule

  • First check: 6 hours after bolus dose 2
  • Subsequent checks: Every 4-6 hours until therapeutic, then daily once stable 2
  • Target aPTT: 1.5-2.0 times control (approximately 50-70 seconds) 3, 1, 2

Additional Monitoring Requirements

  • Platelet counts: Daily throughout therapy to detect heparin-induced thrombocytopenia 3, 2
  • Hematocrit: Periodically 2
  • Occult blood in stool: Periodically 2

Critical Dosing Pitfalls to Avoid

Excess Dosing Errors

Do not exceed maximum doses, as this significantly increases bleeding risk: 1, 4

  • Maximum bolus: 70-80 units/kg or 4000 units total 1
  • Maximum infusion: 18 units/kg/hour or 1000 units/hour total 1
  • Research demonstrates that excess weight-adjusted dosing (>70 U/kg bolus or >15 U/kg/hour infusion) is associated with proportionally increased major bleeding 4

High-Risk Populations for Overdosing

Elderly patients and women are at highest risk for receiving excess weight-adjusted doses: 4

  • Patients with lower body weight frequently receive fixed doses (e.g., 5,000 unit bolus, 1,000 units/hour infusion) that exceed weight-based recommendations 4
  • Age (per 10-year increase) and female sex are strongly associated with excess dosing 4

Morbidly Obese Patients

Use adjusted body weight formulas rather than actual body weight in morbidly obese patients (BMI ≥40): 5, 6

  • Standard weight-based protocols with maximum dose caps can cause significant delays in achieving therapeutic anticoagulation 5
  • Consider: Dosing weight = IBW + 0.3(ABW - IBW) or IBW + 0.4(ABW - IBW) 5
  • Morbidly obese patients require smaller infusion rates per kilogram actual body weight (approximately 11.5 units/kg/hour vs 13.5 units/kg/hour in normal weight patients) 6

Special Populations

Pediatric Dosing

Use preservative-free formulations in neonates and infants: 2

  • Initial bolus: 75-100 units/kg IV over 10 minutes 2
  • Infusion for infants: 25-30 units/kg/hour (infants <2 months require highest doses, averaging 28 units/kg/hour) 2
  • Infusion for children >1 year: 18-20 units/kg/hour 2
  • Target aPTT: 60-85 seconds (reflecting anti-Factor Xa level of 0.35-0.70) 2

Chronic Kidney Disease

UFH is the preferred anticoagulant in severe renal insufficiency (CrCl <30 mL/min): 7

  • Use standard weight-based dosing without dose reduction 7
  • UFH undergoes hepatic metabolism rather than renal excretion, making it safer than LMWH in advanced CKD 7
  • LMWH is contraindicated when CrCl <30 mL/min due to drug accumulation 7

Absolute Contraindications

Do not administer UFH in the following situations: 2

  • Active or history of heparin-induced thrombocytopenia (HIT) 7, 2
  • Known hypersensitivity to heparin or pork products 2
  • Uncontrolled active bleeding (except in disseminated intravascular coagulation) 2
  • Recent neuraxial anesthesia (risk of spinal hematoma) 7

Duration of Therapy

With Fibrinolytic Therapy

  • Minimum duration: 48 hours 3
  • Preferred duration: Up to 8 days or duration of hospitalization 3
  • Prolonged UFH infusions beyond 48 hours increase risk of heparin-induced thrombocytopenia without clear benefit unless ongoing indication exists 3

Transition to Oral Anticoagulation

For warfarin: Continue full-dose UFH for several days until INR reaches stable therapeutic range, then discontinue without tapering 2

For direct oral anticoagulants: Stop IV UFH immediately after first dose of oral anticoagulant, or start oral agent 0-2 hours before next scheduled intermittent UFH dose 2

References

Guideline

Unfractionated Heparin Dosing for Therapeutic Anticoagulation

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

UFH Dosing in Chronic Kidney Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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