What is the appropriate heparin (unfractionated heparin) dosing regimen for a typical adult patient with deep vein thrombosis or pulmonary embolism and no significant impaired renal function?

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Unfractionated Heparin Dosing for DVT/PE in Adults

For treatment of deep vein thrombosis or pulmonary embolism in adults with normal renal function, administer an initial IV bolus of 80 units/kg (or 5,000 units) followed by continuous IV infusion of 18 units/kg/hour (or 32,000-40,000 units per 24 hours), adjusted to maintain aPTT at 1.5-2.5 times control. 1, 2

Initial Dosing Regimen

Weight-based dosing is superior to fixed dosing and should be the preferred approach:

  • IV bolus: 80 units/kg (maximum 5,000 units) 1, 2
  • Continuous infusion: 18 units/kg/hour 1, 2

Alternative fixed-dose regimen (if weight-based unavailable):

  • IV bolus: 5,000 units 1, 2
  • Continuous infusion: 32,000-40,000 units per 24 hours 1, 2

The weight-based nomogram approach reduces recurrent thromboembolism rates compared to fixed dosing, as patients achieve therapeutic aPTT levels more rapidly. 1

Monitoring Requirements

Check aPTT 4 hours after initiation and 4 hours after any dose adjustment, then at appropriate intervals once therapeutic. 2

Target aPTT: 1.5-2.5 times control value 1, 2

  • This corresponds to heparin levels of 0.2-0.4 U/mL by protamine titration 1
  • Or anti-factor Xa levels of 0.30-0.7 U/mL 1

Additional monitoring throughout therapy (regardless of route):

  • Platelet counts periodically to detect heparin-induced thrombocytopenia 2
  • Hematocrit 2
  • Occult blood in stool 2

Duration and Overlap with Oral Anticoagulation

Continue heparin for at least 5 days AND until INR is therapeutic (2.0-3.0) for at least 24 hours on two consecutive measurements. 1, 2

  • Start warfarin within 24 hours of initiating heparin 3
  • Overlap heparin and warfarin for minimum 4-5 days 1, 3
  • Do not discontinue heparin until INR is stable in therapeutic range 2

Alternative Routes (When IV Access Limited)

Subcutaneous administration is an acceptable alternative:

  • Initial: 5,000 units IV bolus, followed by 17,500 units (or 250 units/kg) subcutaneously every 12 hours 1, 2
  • Adjust dose to maintain aPTT in therapeutic range 1
  • Check aPTT 4-6 hours after injection 2

Critical Pitfalls to Avoid

Failure to achieve therapeutic aPTT within 24 hours is associated with 25% recurrence rate of venous thromboembolism. 1 This is the most common and dangerous error.

Do not use prophylactic doses for established thrombosis. Prophylactic dosing (5,000 units every 8-12 hours subcutaneously) is only for prevention, not treatment. 1, 2

Confirm vial strength before administration - fatal medication errors have occurred from confusion between treatment-dose vials and catheter lock flush vials. 2

Avoid intramuscular administration due to high risk of hematoma formation. 2

When to Use Unfractionated Heparin Over LMWH

While LMWH is generally preferred for DVT treatment 1, unfractionated heparin is specifically indicated when:

  • Severe renal dysfunction (creatinine clearance <30 mL/min) 1
  • High bleeding risk requiring rapid reversibility 1
  • Hemodynamic instability 4
  • Morbid obesity 4
  • High-risk pulmonary embolism with cardiogenic shock 1

For pulmonary embolism, either unfractionated heparin or LMWH is appropriate for initial treatment. 1

Dose Adjustment Algorithm

If aPTT is below therapeutic range (<1.5 times control):

  • Increase infusion rate and recheck aPTT in 4 hours 2

If aPTT is above therapeutic range (>2.5 times control):

  • Decrease infusion rate and recheck aPTT in 4 hours 2
  • Consider holding infusion temporarily if significantly elevated 2

The therapeutic window is narrow, requiring vigilant monitoring to balance efficacy against bleeding risk. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Current management of acute symptomatic deep vein thrombosis.

American journal of cardiovascular drugs : drugs, devices, and other interventions, 2001

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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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