Pulseless Electrical Activity as the Initial Cardiac Arrest Rhythm: Importance of Preexisting Left Ventricular Function.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
06 07 2021
Historique:
pubmed: 15 6 2021
medline: 3 11 2021
entrez: 14 6 2021
Statut: ppublish

Résumé

Background Pulseless electrical activity (PEA) is a common initial rhythm in cardiac arrest. A substantial number of PEA arrests are caused by coronary ischemia in the setting of acute coronary occlusion, but the underlying mechanism is not well understood. We hypothesized that the initial rhythm in patients with acute coronary occlusion is more likely to be PEA than ventricular fibrillation in those with prearrest severe left ventricular dysfunction. Methods and Results We studied the initial cardiac arrest rhythm induced by acute left anterior descending coronary occlusion in swine without and with preexisting severe left ventricular dysfunction induced by prior infarcts in non-left anterior descending coronary territories. Balloon occlusion resulted in ventricular fibrillation in 18 of 34 naïve animals, occurring 23.5±9.0 minutes following occlusion, and PEA in 1 animal. However, all 18 animals with severe prearrest left ventricular dysfunction (ejection fraction 15±5%) developed PEA 1.7±1.1 minutes after occlusion. Conclusions Acute coronary ischemia in the setting of severe left ventricular dysfunction produces PEA because of acute pump failure, which occurs almost immediately after coronary occlusion. After the onset of coronary ischemia, PEA occurred significantly earlier than ventricular fibrillation (<2 minutes versus 20 minutes). These findings support the notion that patients with baseline left ventricular dysfunction and suspected coronary disease who develop PEA should be evaluated for acute coronary occlusion.

Identifiants

pubmed: 34121419
doi: 10.1161/JAHA.119.018671
pmc: PMC8403333
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e018671

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL126092
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Daniel I Ambinder (DI)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.

Kaustubha D Patil (KD)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.

Hikmet Kadioglu (H)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.

Pace S Wetstein (PS)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.

Richard S Tunin (RS)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.

Sarah J Fink (SJ)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.

Susumu Tao (S)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.

Giulio Agnetti (G)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.
DIBINEM University of Bologna Bologna Italy.

Henry R Halperin (HR)

Division of Cardiology Department of Medicine Johns Hopkins University Baltimore MD.
Departments of Biomedical Engineering and Radiology Johns Hopkins University Baltimore MD.

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Classifications MeSH