What is the appropriate workup and initial treatment for a patient with suspected acute anterolateral ST‑segment elevation myocardial infarction?

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Last updated: February 26, 2026View editorial policy

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Workup and Management of Anterolateral ST-Elevation

Obtain a 12-lead ECG within 10 minutes of first medical contact, give aspirin 150–325 mg immediately, and activate the catheterization laboratory for primary PCI if door-to-balloon time will be ≤120 minutes; otherwise, administer fibrinolytic therapy within 10 minutes of diagnosis. 1

Immediate Diagnostic Actions (First 10 Minutes)

  • Record and interpret a 12-lead ECG within 10 minutes of first medical contact to confirm ST-elevation in anterolateral leads (V3–V6, I, aVL) or identify STEMI equivalents such as new left bundle branch block, hyperacute T-waves, or isolated anterior ST-depression with ST-elevation in aVR. 1, 2

  • Initiate continuous ECG monitoring with defibrillator capability immediately, as life-threatening ventricular arrhythmias are common in acute STEMI. 1, 2

  • Administer aspirin 150–325 mg orally (or 250–500 mg IV if unable to swallow) as soon as STEMI is suspected; this is the single most important initial pharmacologic intervention. 1, 2

  • Avoid routine supplemental oxygen unless peripheral oxygen saturation is <90%; routine oxygen therapy does not improve outcomes and may be harmful. 1, 2

  • Draw blood for high-sensitivity cardiac troponin, complete blood count, creatinine, electrolytes, glucose, lipid profile, and coagulation studies on arrival, but do not delay reperfusion therapy while awaiting results. 3

Reperfusion Strategy Selection (The 120-Minute Rule)

Primary PCI Strategy (Preferred)

  • Primary PCI is the preferred reperfusion method when the anticipated first-medical-contact-to-device time is ≤120 minutes; for patients presenting directly to a PCI-capable hospital, the target is ≤90 minutes. 1, 2

  • Transfer the patient directly to the catheterization laboratory, bypassing the emergency department, to eliminate unnecessary delays; PCI-capable centers must provide 24/7 service without delay. 1, 2

  • Give a potent P2Y12 inhibitor before or at the time of PCI: prasugrel 60 mg loading dose (preferred) or ticagrelor 180 mg loading dose; use clopidogrel 600 mg only if the former are unavailable or contraindicated. 1, 2

  • Administer unfractionated heparin 100 U/kg IV bolus (reduce to 60 U/kg if a GPIIb/IIIa inhibitor is used); enoxaparin or bivalirudin are acceptable alternatives, but fondaparinux is contraindicated for primary PCI. 1, 2

  • Use radial arterial access and implant drug-eluting stents as the standard of care; routine thrombus aspiration and deferred stenting are contraindicated. 1

Fibrinolytic Strategy (When PCI Delay >120 Minutes)

  • If primary PCI cannot be achieved within 120 minutes, administer fibrinolytic therapy within 10 minutes of STEMI diagnosis, preferably in the pre-hospital setting; target door-to-needle time ≤30 minutes. 1, 2

  • Use a fibrin-specific thrombolytic agent: tenecteplase (preferred for single-bolus administration), alteplase, or reteplase; these reduce mortality by an additional 10 deaths per 1,000 patients compared with streptokinase. 4, 5

  • Add clopidogrel 75 mg daily to aspirin (prasugrel and ticagrelor are not recommended with fibrinolysis); this combination reduces death, reinfarction, and stroke by approximately 9 events per 1,000 treated. 4

  • Provide anticoagulation with enoxaparin (IV bolus followed by subcutaneous dosing, preferred) or unfractionated heparin (weight-adjusted IV bolus followed by 24–48 hour infusion targeting aPTT 50–70 seconds). 4

Post-Fibrinolysis Management

Reperfusion Assessment (60–90 Minutes)

  • Obtain a repeat ECG 60–90 minutes after fibrinolytic administration and measure ST-segment resolution in the lead with the greatest initial ST-elevation; ≥50% resolution indicates successful reperfusion, while <50% indicates failure. 4

Rescue PCI Indications

  • Perform immediate rescue PCI without delay if fibrinolysis fails (<50% ST-segment resolution at 60–90 minutes); rescue PCI reduces the composite of death or reinfarction from 16.8% to 10.8% and all-cause mortality from 10.7% to 6.9%. 4

  • Emergency angiography and PCI are also indicated for hemodynamic instability, cardiogenic shock, sustained ventricular arrhythmias, worsening ischemia, or development of acute heart failure at any time after fibrinolysis. 4

Routine Angiography After Successful Fibrinolysis

  • Transfer all patients immediately to a PCI-capable center after fibrinolysis and perform angiography with PCI of the infarct-related artery within 2–24 hours, even if reperfusion appears successful; approximately 30% will require rescue PCI. 4

Mandatory Primary PCI Regardless of Time Delay

  • Cardiogenic shock or acute severe heart failure at any time after symptom onset mandates primary PCI, regardless of the elapsed time from first medical contact. 1

  • Contraindications to fibrinolytic therapy (prior intracranial hemorrhage, active bleeding, recent stroke, severe uncontrolled hypertension >180/110 mmHg despite treatment) require primary PCI as the only reperfusion option. 1, 4

In-Hospital Management

Monitoring and Imaging

  • Monitor all reperfused patients for at least 24 hours after therapy in a unit with continuous ECG monitoring and defibrillation capability. 1, 2

  • Perform routine transthoracic echocardiography during hospitalization to assess left- and right-ventricular function, detect mechanical complications (ventricular septal rupture, papillary muscle rupture, free wall rupture), and exclude left-ventricular thrombus. 1

Pharmacotherapy

  • Continue dual antiplatelet therapy (aspirin 75–100 mg daily plus prasugrel 10 mg daily or ticagrelor 90 mg twice daily) for 12 months unless the patient has a high bleeding risk. 1, 2

  • Initiate high-intensity statin therapy (atorvastatin 80 mg or rosuvastatin 40 mg) as early as possible, targeting LDL-C <1.8 mmol/L (70 mg/dL) or a ≥50% reduction if baseline is 1.8–3.5 mmol/L. 1

  • Start oral beta-blockers in patients with heart failure and/or left-ventricular ejection fraction <40% unless contraindicated (avoid IV beta-blockers in the acute phase). 1

  • Initiate ACE inhibitors within 24 hours in patients with heart failure, left-ventricular systolic dysfunction, diabetes, or anterior infarction. 1

Critical Pitfalls to Avoid

  • Do not delay reperfusion therapy to "stabilize" the patient or await troponin results; the ECG diagnosis of STEMI is sufficient to proceed immediately. 1, 2

  • Do not confuse non-ischemic ST-elevation (hypercalcemia, early repolarization, pericarditis, left ventricular hypertrophy) with STEMI; correlate ECG findings with clinical presentation, but when in doubt, activate the catheterization laboratory. 6, 7

  • Do not perform routine PCI of an occluded infarct-related artery >48 hours after symptom onset in asymptomatic, hemodynamically stable patients; late PCI does not improve outcomes. 1

  • Do not combine fibrinolysis with immediate planned PCI (so-called "facilitated PCI"); this strategy increases mortality and bleeding without benefit. 4

  • Do not re-administer streptokinase if it was used previously (antibodies persist ≥10 years); use a fibrin-specific agent or proceed to rescue PCI instead. 4

References

Guideline

Management of ST-Elevation Myocardial Infarction (STEMI)

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Immediate Emergency Management of Acute STEMI

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Streptokinase Use in STEMI When Primary PCI Is Not Feasible

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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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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