IV Heparin in Myocardial Infarction Without PCI
For STEMI patients not undergoing PCI, start IV unfractionated heparin immediately upon diagnosis with a weight-based bolus of 60 U/kg (maximum 4,000 U) followed by continuous infusion at 12 U/kg/hour (maximum 1,000 U/hour), targeting an aPTT of 1.5-2.0 times control (50-70 seconds). 1, 2, 3
Timing of Initiation
- Begin IV heparin as soon as the diagnosis of myocardial infarction is established, regardless of whether fibrinolytic therapy is planned 4, 2
- For patients receiving fibrinolytic therapy, administer heparin concurrently with or immediately after the fibrinolytic agent 4, 3
- Do not delay heparin administration while awaiting laboratory confirmation if clinical and ECG findings strongly suggest MI 2
Dosing Regimen
Initial Bolus Dose
- 60 U/kg IV bolus (maximum 4,000 U) for patients receiving fibrinolytic therapy 4, 3, 5
- 60-70 U/kg IV bolus (maximum 5,000 U) for patients with NSTE-ACS or those not receiving reperfusion therapy 4, 2, 5
Continuous Infusion
- 12 U/kg/hour (maximum 1,000 U/hour) adjusted to maintain therapeutic aPTT 4, 3, 5
- Target aPTT: 50-70 seconds (1.5-2.0 times control) 4, 1, 3
Monitoring Protocol
- Check aPTT at 3,6,12, and 24 hours after initiation 4, 2, 3
- Recheck aPTT 4-6 hours after any dose adjustment 3
- Monitor daily platelet counts to detect heparin-induced thrombocytopenia 2, 3
- aPTT values >70 seconds are associated with increased mortality, bleeding, and reinfarction risk—adjust infusion downward immediately 4
Duration of Therapy
- Continue heparin for minimum 48 hours after fibrinolytic therapy 4, 2, 3
- Preferably extend through duration of hospitalization, up to 8 days 2, 3
- May discontinue earlier if revascularization (delayed PCI) is performed 2, 3
- For patients at high risk for systemic or venous thromboembolism, continuation beyond 48 hours is reasonable 1
Rationale for Heparin Use
With Fibrinolytic Therapy
- Improves coronary artery patency when used with tissue plasminogen activators (alteplase, reteplase, tenecteplase) 4, 1
- Prevents reocclusion after successful fibrinolysis, though benefit must be balanced against bleeding risk 4, 1
- Particularly important with fibrin-specific agents (t-PA, r-PA, TNK-tPA) which have shorter half-lives 2
Without Reperfusion Therapy
- Prevents left ventricular thrombus formation, especially in anterior wall MI 4, 2
- Reduces risk of systemic embolization and stroke 4, 2
- Prevents deep vein thrombosis and pulmonary embolism during prolonged bed rest 4
- Acts as antithrombotic therapy to prevent infarct extension 4
Alternative Anticoagulant Options
Enoxaparin (LMWH)
- For patients <75 years without renal dysfunction: 30 mg IV bolus followed by 1.0 mg/kg subcutaneous every 12 hours 4, 2, 3
- For patients ≥75 years: Omit IV bolus, start with 0.75 mg/kg subcutaneous every 12 hours 4, 2
- Contraindicated if creatinine clearance <30 mL/min 4
- Enoxaparin showed reduced death and reinfarction compared to UFH in the ExTRACT trial, though with increased non-cerebral bleeding 4
Fondaparinux
- 2.5 mg subcutaneous daily for patients not undergoing PCI 4
- Must add additional anticoagulant with anti-IIa activity if patient subsequently undergoes PCI 4
- Not recommended as sole anticoagulant for primary PCI due to catheter thrombosis risk 4
Critical Pitfalls to Avoid
- Never exceed maximum bolus doses (4,000-5,000 U depending on indication) even in obese patients—overdosing increases bleeding risk without improving efficacy 3, 5
- Do not use fixed-dose regimens—weight-based dosing significantly improves outcomes 1, 5
- Avoid aPTT >70 seconds—supratherapeutic anticoagulation paradoxically increases mortality and reinfarction rates 4
- Do not switch between UFH and LMWH—this increases bleeding complications 3
- Never discontinue heparin abruptly in high-risk patients (large anterior MI, atrial fibrillation, severe LV dysfunction)—taper or transition to oral anticoagulation 1, 3
- Do not use LMWH in elderly patients (≥75 years) receiving fibrinolytics without dose adjustment—this significantly increases intracranial hemorrhage risk 4, 2