What is the management of ST-Elevation Myocardial Infarction (STEMI)?

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Management of ST-Elevation Myocardial Infarction (STEMI)

Immediate Actions Upon First Medical Contact

Administer 162-325 mg of non-enteric coated aspirin (chewed) immediately to all STEMI patients without contraindications 1, 2. This should occur at first medical contact, not delayed until hospital arrival.

  • Obtain a 12-lead ECG within 10 minutes of first medical contact or emergency department arrival 1, 2
  • STEMI is defined as ST-segment elevation >0.1 mV in at least two contiguous precordial or adjacent limb leads, new left bundle branch block, or true posterior MI 2
  • If initial ECG is non-diagnostic but suspicion remains high, repeat ECGs at 5-10 minute intervals 2
  • Initiate continuous ECG monitoring with defibrillator capacity 3
  • Avoid routine oxygen therapy unless oxygen saturation is <90% 3

Reperfusion Strategy: The Critical Time-Based Decision

Primary PCI is the preferred reperfusion strategy if first medical contact-to-device time can be achieved within 90-120 minutes 1, 2. This is the single most important decision point in STEMI management.

When to Choose Primary PCI:

  • First medical contact-to-device time ≤90 minutes at PCI-capable centers 3
  • First medical contact-to-device time ≤120 minutes with transfer 1, 2
  • Patients should bypass the emergency department and go directly to the catheterization laboratory 1
  • Use radial access and drug-eluting stents as standard of care 3

When to Choose Fibrinolytic Therapy:

If primary PCI cannot be performed within 120 minutes of STEMI diagnosis, initiate fibrinolytic therapy immediately, preferably in the pre-hospital setting 1, 2.

  • Fibrinolysis is indicated for patients with symptoms <12 hours duration and persistent ST-segment elevation 1
  • Use fibrin-specific agents: tenecteplase, alteplase, or reteplase 1
  • For patients 12-24 hours after symptom onset with ongoing ischemia, large area of myocardium at risk, or hemodynamic instability, fibrinolysis is reasonable 1

Critical contraindications to fibrinolysis:

  • Active pathological bleeding 1
  • History of transient ischemic attack or stroke 1, 4
  • ST depression (except true posterior MI or ST elevation in aVR) 1

Antithrombotic Therapy for Primary PCI

Administer dual antiplatelet therapy with aspirin plus a potent P2Y12 inhibitor before or at the time of PCI 1, 2, 3.

P2Y12 Inhibitor Selection:

  • Prasugrel 60 mg loading dose or ticagrelor are strongly preferred over clopidogrel 1, 2, 3
  • Prasugrel is contraindicated in patients with prior TIA/stroke 4
  • For patients ≥75 years old, prasugrel is generally not recommended except in high-risk situations (diabetes or prior MI) 4
  • Consider prasugrel 5 mg maintenance dose (instead of 10 mg) for patients <60 kg due to increased bleeding risk 4
  • Clopidogrel is acceptable if prasugrel or ticagrelor are unavailable or contraindicated 1, 2

Anticoagulation:

  • Unfractionated heparin IV bolus at 100 U/kg (60 U/kg if glycoprotein IIb/IIIa inhibitors are used) 3
  • Fondaparinux is not recommended for primary PCI 1

Antithrombotic Therapy for Fibrinolytic Strategy

For patients receiving fibrinolysis, administer aspirin plus clopidogrel with anticoagulation 1, 2.

Antiplatelet Therapy:

  • Aspirin 162-325 mg loading dose, then 81-325 mg daily (81 mg preferred for maintenance) 1
  • Clopidogrel 300 mg loading dose for patients <75 years; 75 mg loading dose for patients ≥75 years 1
  • Continue clopidogrel 75 mg daily for at least 14 days, up to 1 year 1

Anticoagulation (choose one):

  • Enoxaparin (preferred over UFH): IV bolus followed by subcutaneous injection for duration of hospitalization up to 8 days or until revascularization 1
  • UFH: weight-adjusted IV bolus and infusion to achieve aPTT 1.5-2.0 times control for 48 hours or until revascularization 1
  • Fondaparinux: initial IV dose, then daily subcutaneous injections if creatinine clearance >30 mL/min, for up to 8 days or until revascularization 1

Post-Fibrinolysis Management: The Pharmaco-Invasive Approach

All patients receiving fibrinolysis must be transferred to a PCI-capable center immediately after fibrinolysis 1.

Timing of Angiography After Fibrinolysis:

  • Immediate emergency angiography and PCI for cardiogenic shock or heart failure 1
  • Rescue PCI immediately if fibrinolysis fails (<50% ST-segment resolution at 60-90 minutes) or hemodynamic/electrical instability develops 1
  • Routine angiography 2-24 hours after successful fibrinolysis 1, 5
  • Emergency angiography for recurrent ischemia or evidence of reocclusion 1

Management of Cardiogenic Shock

Emergency revascularization (PCI or CABG) is recommended regardless of time delay from MI onset for patients with cardiogenic shock 1, 2, 3.

  • Immediate transfer to PCI-capable hospital for patients developing cardiogenic shock or acute severe heart failure 1
  • CABG is indicated for patients <75 years with shock within 36 hours of STEMI who have severe multivessel or left main disease, if revascularization can be performed within 18 hours of shock 3
  • Intra-aortic balloon counterpulsation for patients not quickly stabilized with pharmacological therapy 2

Long-Term Medical Management Post-STEMI

Continue dual antiplatelet therapy for 12 months after PCI unless contraindications exist 1, 3.

Maintenance Antiplatelet Therapy:

  • Aspirin 75-100 mg daily indefinitely 1, 3
  • P2Y12 inhibitor (ticagrelor, prasugrel, or clopidogrel) for 12 months 1, 3

Additional Medical Therapy:

  • Initiate ACE inhibitors within 24 hours in all patients, particularly those with anterior MI, heart failure, or ejection fraction ≤0.40 2
  • Continue oral beta-blockers indefinitely in all eligible patients, especially those with heart failure or LVEF <40% 2, 3
  • High-intensity statin therapy as early as possible 3

Surgical Considerations

If CABG is required, discontinue prasugrel at least 7 days prior to surgery when possible 4.

  • Do not start prasugrel in patients likely to undergo urgent CABG 4
  • The risk of CABG-related bleeding is substantial in patients recently treated with antiplatelet agents 1

Post-Discharge Assessment and Follow-Up

Routine echocardiography during hospital stay is recommended to assess LV and RV function, detect mechanical complications, and exclude LV thrombus 1, 2.

  • Follow-up ECGs at 24 hours and hospital discharge to assess reperfusion success and infarct extent 2
  • Participation in cardiac rehabilitation program is strongly recommended 1
  • Identify smokers and provide repeated cessation advice with pharmacotherapy support 1

Critical Pitfalls to Avoid

Never delay reperfusion therapy beyond guideline-recommended time windows 1, 2. The effectiveness of all treatments declines rapidly with time, and patient outcomes worsen 6.

  • Do not miss STEMI equivalents: hyperacute T-waves, true posterior MI (ST depression in V1-V4), or multilead ST depression with ST elevation in aVR suggesting left main disease 3
  • Atypical presentations are common in women, elderly, and diabetic patients who may present without chest pain 3
  • Do not discontinue antiplatelet therapy prematurely, particularly in the first few weeks after ACS, as this increases the risk of stent thrombosis, MI, and death 4
  • Suspect bleeding in any hypotensive patient who has recently undergone coronary angiography, PCI, CABG, or other surgical procedures while on prasugrel 4
  • If possible, manage bleeding without discontinuing antiplatelet therapy 4

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of ST-Elevation Myocardial Infarction (STEMI)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Acute Coronary Syndromes

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Management of ST-elevation myocardial infarction: an update on pharmacoinvasive recanalization.

American journal of cardiovascular drugs : drugs, devices, and other interventions, 2008

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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