What is the treatment for Acute Coronary Syndrome (ACS)?

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Treatment of Acute Coronary Syndrome (ACS)

All patients with suspected ACS should receive immediate aspirin (150-300 mg loading dose, then 75-100 mg daily) and dual antiplatelet therapy with a P2Y12 inhibitor for at least 12 months, combined with parenteral anticoagulation and risk-stratified invasive management based on presentation type (STEMI vs NSTE-ACS) and timing. 1, 2

Immediate Medical Management

Antiplatelet Therapy

  • Aspirin should be administered immediately to all patients with suspected ACS at a loading dose of 150-300 mg, followed by 75-100 mg daily maintenance 1, 2
  • Add a P2Y12 inhibitor for dual antiplatelet therapy (DAPT) for 12 months unless contraindicated by high bleeding risk 1, 2
  • Ticagrelor (180 mg loading, 90 mg twice daily) is the preferred P2Y12 inhibitor for moderate to high-risk patients, including those with elevated troponins 1
  • Prasugrel (60 mg loading, 10 mg daily) is preferred over clopidogrel in patients undergoing PCI, but is contraindicated in patients with prior stroke/TIA and generally not recommended in patients ≥75 years due to increased bleeding risk 1, 3
  • Clopidogrel (300-600 mg loading, 75 mg daily) is an alternative when ticagrelor or prasugrel are contraindicated 1, 4

Anticoagulation

  • Parenteral anticoagulation is mandatory for all ACS patients with options including unfractionated heparin (UFH), low-molecular-weight heparin (LMWH), fondaparinux, or bivalirudin 2, 5, 4
  • Enoxaparin may be considered as an alternative to UFH in prehospital settings for STEMI patients being transferred for primary PCI 1

Symptom Management

  • Nitroglycerin (sublingual then IV) should be given for relief of ischemia and chest pain 2
  • Morphine is indicated for persistent severe chest pain or acute pulmonary congestion 2
  • Beta-blockers should be administered for symptom control and to reduce myocardial oxygen demand, particularly in patients with preserved left ventricular function 2, 6
  • Supplementary oxygen should be withheld in normoxic patients (Class IIb recommendation) 1

Risk Stratification and Invasive Strategy Timing

STEMI Management

  • Primary PCI within 120 minutes of first medical contact is the goal for all STEMI patients 1, 7
  • If PCI cannot be achieved within 120 minutes, fibrinolytic therapy should be administered (alteplase, reteplase, or tenecteplase at full dose for patients <75 years; half dose for ≥75 years), followed by transfer for PCI within 24 hours 1, 7
  • For STEMI presenting within 2 hours of symptom onset, immediate fibrinolysis may be considered if expected delay to PCI exceeds 60 minutes 1
  • Prehospital fibrinolysis is reasonable when transport times exceed 30 minutes and in-hospital fibrinolysis is the alternative 1
  • Combined fibrinolytic therapy followed by immediate PCI is not recommended (Class III: Harm) 1

NSTE-ACS Management

The timing of invasive strategy depends on risk stratification 1, 2:

Immediate invasive strategy (<2 hours) for very high-risk patients with: 1, 2

  • Hemodynamic instability or cardiogenic shock
  • Recurrent or refractory chest pain despite medical treatment
  • Life-threatening arrhythmias or cardiac arrest
  • Mechanical complications of MI
  • Acute heart failure with refractory angina or ST deviation

Early invasive strategy (<24 hours) for high-risk patients with: 1, 2

  • Rise or fall in cardiac troponin compatible with MI
  • Dynamic ST- or T-wave changes (symptomatic or silent)
  • GRACE score >140

Invasive strategy (<72 hours) for intermediate-risk patients with: 1, 2

  • Diabetes mellitus
  • Renal insufficiency (eGFR <60 mL/min/1.73 m²)
  • LVEF <40% or congestive heart failure
  • Early post-infarction angina
  • Recent PCI or prior CABG
  • GRACE score 109-140

Revascularization Strategy

  • Complete revascularization is recommended in patients with STEMI or NSTE-ACS 1
  • Radial approach is preferred over femoral approach to reduce bleeding, vascular complications, and death 1
  • Intracoronary imaging should guide PCI in patients with complex coronary lesions 1
  • For STEMI with multivessel disease, PCI of nonculprit lesions can be performed in a single procedure or staged, with preference toward single-procedure multivessel PCI 1
  • In cardiogenic shock, emergency revascularization of the culprit vessel is indicated, but routine PCI of non-infarct-related arteries at the same time is not recommended 1

Special Considerations

Bleeding Risk Management

  • Proton pump inhibitors are recommended for patients at risk of gastrointestinal bleeding 1, 6, 4
  • In patients weighing <60 kg, consider reducing prasugrel maintenance dose to 5 mg daily due to increased bleeding risk 3
  • DAPT de-escalation to ticagrelor monotherapy ≥1 month after PCI is recommended in patients who have tolerated DAPT with ticagrelor 1, 5
  • In patients requiring long-term anticoagulation, discontinue aspirin 1-4 weeks after PCI and continue P2Y12 inhibitor (preferably clopidogrel) 1

CABG Considerations

  • Discontinue prasugrel at least 7 days prior to CABG when possible 3
  • Do not start prasugrel in patients likely to undergo urgent CABG 3

Cardiogenic Shock

  • Microaxial flow pump use is reasonable in selected patients with cardiogenic shock related to acute MI to reduce death, though bleeding, limb ischemia, and renal failure risks are higher 1

Long-Term Secondary Prevention

Pharmacotherapy

  • High-intensity statin therapy should be initiated as early as possible (within 1-4 days) and continued long-term, targeting LDL-C reduction ≥50% and LDL-C <1.4 mmol/L (<55 mg/dL) 1, 2, 6
  • ACE inhibitors are recommended for patients with LVEF ≤40%, heart failure, hypertension, or diabetes 1, 2, 6
  • Angiotensin receptor blockers (ARBs) are alternatives for ACE inhibitor-intolerant patients 1, 2
  • Beta-blockers are recommended in patients with reduced LVEF (≤40%) or heart failure 1, 2, 6
  • Mineralocorticoid receptor antagonists (preferably eplerenone) are recommended for patients with LVEF ≤35% and either heart failure or diabetes 2

Lifestyle Modifications

  • Smoking cessation is highly effective to reduce morbidity and mortality 1, 8
  • Regular aerobic exercise training three or more times weekly for 30 minutes per session is recommended 1
  • Cardiac rehabilitation program enrollment should be offered to all ACS patients 1, 2, 6

Common Pitfalls

  • Avoid premature discontinuation of DAPT, particularly in the first few weeks after ACS, as this increases risk of subsequent cardiovascular events 3
  • Do not administer prasugrel to patients with prior stroke/TIA (absolute contraindication) 3
  • Monitor for thrombotic thrombocytopenic purpura (TTP) in patients on prasugrel, which can occur after brief exposure (<2 weeks) and requires urgent plasmapheresis 3
  • Avoid routine supplementary oxygen in normoxic patients, as its usefulness has not been established 1
  • Do not combine immediate fibrinolysis with immediate PCI in STEMI patients, as this increases harm without benefit 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Acute Coronary Syndrome Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Acute Coronary Syndrome: Management.

FP essentials, 2020

Guideline

Management of Acute Coronary Syndrome

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Management of Acute Coronary Syndrome in Patients with Elevated Liver Enzymes

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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