What are the recommendations for heparin (unfractionated heparin) drip in patients with myocardial infarction (MI)?

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Last updated: October 16, 2025View editorial policy

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Recommendations for Heparin Drip in Myocardial Infarction

For patients with ST-elevation myocardial infarction (STEMI), unfractionated heparin (UFH) should be administered as a weight-adjusted IV bolus of 60 U/kg (maximum 4000 U) followed by an initial infusion of 12 U/kg/hour (maximum 1000 U/hour), with dose adjustments to maintain activated partial thromboplastin time (aPTT) at 1.5 to 2.0 times control (approximately 50 to 70 seconds). 1, 2

Dosing Recommendations by Treatment Strategy

For Patients Receiving Fibrin-Specific Thrombolytics (alteplase, reteplase, tenecteplase)

  • Initial bolus: 60 U/kg (maximum 4000 U) 1
  • Initial infusion: 12 U/kg/hour (maximum 1000 U/hour) 1
  • Target aPTT: 1.5-2.0 times control (approximately 50-70 seconds) 1, 2
  • Duration: Continue anticoagulation until revascularization (if performed) or for the duration of hospital stay up to 8 days 1

For Patients Undergoing Primary PCI

  • Initial bolus: 60-70 U/kg IV 1
  • Initial infusion: 12-15 U/kg/hour 1
  • Additional boluses may be needed during PCI to maintain therapeutic anticoagulation 1
  • Monitor ACT during procedure (target 250-300 seconds with HemoTec device or 300-350 seconds with Hemochron device if no GP IIb/IIIa inhibitors are used) 1

For Patients Not Receiving Reperfusion Therapy

  • Weight-adjusted dosing as above: 60-70 U/kg IV bolus followed by 12-15 U/kg/hour infusion 1
  • Consider subcutaneous heparin (7500 U twice daily) for patients not at high risk for systemic embolism 1

Monitoring and Adjustment

  • Check aPTT 4-6 hours after initiation of therapy and after any dose change 1, 2
  • Monitor platelet counts daily in patients receiving UFH 1, 3
  • Monitor for signs of bleeding and hematoma formation 2
  • Adjust dosing based on aPTT results to maintain therapeutic range (50-70 seconds) 1, 2

Alternative Anticoagulants

  • Enoxaparin is superior to UFH for patients receiving fibrinolytic therapy (30 mg IV bolus followed by 1 mg/kg SC every 12 hours) 4
  • For patients ≥75 years old receiving enoxaparin: omit initial bolus and start with 0.75 mg/kg SC every 12 hours 1
  • For patients with renal dysfunction (CrCl <30 mL/min): reduce enoxaparin to 1 mg/kg once daily 1
  • Fondaparinux (2.5 mg IV followed by 2.5 mg SC daily) may be considered for patients with serum creatinine <3.0 mg/dL 1
  • Bivalirudin may be considered for patients with heparin-induced thrombocytopenia 1

Important Considerations and Caveats

  • UFH has a short half-life (approximately 1.5 hours) and immediate anticoagulant effect when given intravenously 3
  • Weight-based dosing is critical as the effect of a given dose of heparin is primarily mediated by patient weight 1
  • Risk of heparin-induced thrombocytopenia increases with duration of therapy; monitor platelet counts regularly 3
  • When transitioning from heparin to warfarin, continue full heparin therapy until INR reaches therapeutic range 2
  • For patients undergoing CABG, heparin should not be discontinued prior to surgery 1
  • Avoid intramuscular injections during heparin therapy to prevent hematoma formation 2

Special Populations

Pediatric Patients

  • Initial dose: 75-100 U/kg IV bolus over 10 minutes 2
  • Maintenance:
    • Infants: 25-30 U/kg/hour (infants <2 months have highest requirements) 2
    • Children >1 year: 18-20 U/kg/hour 2
  • Target aPTT: 60-85 seconds 2

Elderly Patients

  • Consider lower initial doses and more frequent monitoring due to increased bleeding risk 1
  • LMWHs should not be used as an alternative to UFH in patients over 75 years receiving fibrinolytic therapy 1

The evidence strongly supports the use of anticoagulation with heparin in patients with STEMI, with dosing regimens tailored to the reperfusion strategy. The most recent guidelines emphasize weight-adjusted dosing to achieve optimal anticoagulation while minimizing bleeding complications.

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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