Is atropine indicated in the management of Pulseless Electrical Activity (PEA) and asystole?

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Last updated: January 30, 2026View editorial policy

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Atropine is NOT Indicated for PEA and Asystole

Atropine is no longer recommended for routine use in the management of pulseless electrical activity (PEA) and asystole, as current evidence demonstrates it is unlikely to provide therapeutic benefit and has been removed from cardiac arrest algorithms since 2010. 1

Current Guideline Recommendations

The American Heart Association made a definitive change in their 2010 guidelines that remains unchanged:

  • Atropine was explicitly removed from the cardiac arrest algorithm for PEA and asystole management 1
  • Available evidence suggests routine use of atropine during PEA or asystole is unlikely to have therapeutic benefit (Class IIb, LOE B) 1
  • This recommendation was maintained without revision in the 2015 AHA guidelines update 1

Why Atropine Was Removed

The rationale for removing atropine from cardiac arrest protocols is based on several key factors:

  • No prospective controlled clinical trials have demonstrated benefit of atropine in asystole or bradycardic PEA cardiac arrest 1
  • Lower-level clinical studies provide conflicting evidence with no consistent therapeutic benefit 1
  • While atropine has no proven detrimental effects during cardiac arrest, the lack of efficacy led to its removal from standard protocols 1

Historical Context and Evidence Quality

Older guidelines (1997 European Resuscitation Council) previously considered atropine use based on theoretical vagal tone mechanisms, but acknowledged that evidence was limited to small case series and case reports only 1. The recommended dose at that time was 3 mg IV to achieve complete vagal blockade 1.

Current Management of PEA/Asystole

Instead of atropine, focus should be on:

  • High-quality CPR with adequate chest compression rate, depth, and minimal interruptions 1
  • Vasopressor therapy (epinephrine) as soon as feasible to increase myocardial and cerebral blood flow (Class IIb, LOE A) 1
  • Identifying and treating reversible causes (H's and T's: hypoxia, hypovolemia, hydrogen ion/acidosis, hypo/hyperkalemia, hypothermia, tension pneumothorax, tamponade, toxins, thrombosis pulmonary/coronary) 1
  • Advanced airway management for adequate oxygenation, particularly important in PEA where hypoxemia may be causative 1

Important Distinction: Atropine Still Has Other Indications

While atropine is not indicated for PEA/asystole, it remains the first-line drug for symptomatic bradycardia with hemodynamic instability (Class IIa, LOE B) 1. The FDA label also indicates atropine for "bradyasystolic cardiac arrest," but this reflects older labeling that predates current evidence-based guidelines 2.

Common Pitfall to Avoid

Do not confuse symptomatic bradycardia (where atropine IS indicated) with PEA/asystole cardiac arrest (where it is NOT indicated). The key distinction is the presence or absence of a pulse and perfusion 1.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 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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