Management of Pulseless Electrical Activity with Sinus Bradycardia During CPR
Epinephrine is the first-line drug for a patient with pulseless electrical activity (PEA) showing sinus bradycardia on the rhythm strip during cardiopulmonary resuscitation. 1
Primary Management Algorithm
Initial drug administration:
- Administer epinephrine 1 mg IV/IO every 3-5 minutes
- Continue high-quality CPR without interruption
Secondary considerations:
- Identify and treat potential reversible causes of PEA (H's and T's)
- Avoid routine administration of atropine for PEA
Rationale for Epinephrine as First-Line Treatment
Epinephrine remains the cornerstone vasopressor for all forms of cardiac arrest, including PEA with bradycardia. The 2015 American Heart Association guidelines clearly indicate that epinephrine should be administered for cardiac arrest, including PEA, regardless of the underlying rhythm 1. This recommendation is based on epinephrine's alpha-adrenergic effects that increase coronary and cerebral perfusion pressure during CPR.
Role of Atropine in PEA
The 2015 AHA guidelines specifically state: "Available evidence suggests that routine use of atropine during PEA or asystole is unlikely to have a therapeutic benefit" (Class IIb, LOE B) 1. This represents a significant shift from earlier practices where atropine was commonly used for all bradycardic rhythms.
Research evidence supports this recommendation. A large study of 7,448 adults with non-shockable rhythms found that administration of atropine had no long-term neurological benefit in adults with out-of-hospital cardiac arrest due to non-shockable rhythm, and specifically concluded that "atropine is not useful for adults with PEA" 2.
Important Clinical Distinctions
It's crucial to distinguish between:
- PEA with bradycardia - Requires epinephrine as first-line treatment
- Symptomatic bradycardia with pulse - May benefit from atropine (Class IIa, LOE B) 1
The key difference is the presence or absence of a pulse. In PEA, despite electrical activity on the monitor showing sinus bradycardia, there is no effective mechanical cardiac output, making atropine ineffective as the primary intervention.
Addressing Reversible Causes
While administering epinephrine, simultaneously search for and treat potential reversible causes of PEA:
- Hypovolemia
- Hypoxia
- Hydrogen ion (acidosis)
- Hypo/hyperkalemia
- Hypothermia
- Tension pneumothorax
- Tamponade (cardiac)
- Toxins
- Thrombosis (pulmonary or coronary)
Special Considerations
- If the patient regains pulse but remains bradycardic, then atropine may be considered (0.5 mg IV every 3-5 minutes, maximum total 3 mg) 3
- For patients with cardiac transplantation, atropine is ineffective due to lack of vagal innervation 3
- If bradycardia persists after return of spontaneous circulation, consider epinephrine infusion (2-10 μg/min) or dopamine (2-10 μg/kg/min) 3
Monitoring During Resuscitation
- Continuous cardiac monitoring to assess response to interventions
- Consider point-of-care ultrasound if available to assess for cardiac activity and identify potential reversible causes
- Monitor end-tidal CO2 as a surrogate marker for cardiac output during CPR
By following this evidence-based approach with epinephrine as the first-line medication for PEA with sinus bradycardia, you optimize the chances for return of spontaneous circulation and improved patient outcomes.