Early Utilization of Mechanical Circulatory Support in Acute Myocardial Infarction Complicated by Cardiogenic Shock: The National Cardiogenic Shock Initiative.

Impella acute myocardial infarction cardiogenic shock mechanical circulatory support percutaneous coronary intervention pulmonary artery catheter

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:
05 Dec 2023
Historique:
medline: 7 12 2023
pubmed: 28 11 2023
entrez: 28 11 2023
Statut: ppublish

Résumé

Acute myocardial infarction complicated by cardiogenic shock (AMI-CS) is associated with significant morbidity and mortality. Mechanical circulatory support (MCS) devices increase systemic blood pressure and end organ perfusion while reducing cardiac filling pressures. The National Cardiogenic Shock Initiative (NCT03677180) is a single-arm, multicenter study. The purpose of this study was to assess the feasibility and effectiveness of utilizing early MCS with Impella in patients presenting with AMI-CS. The primary end point was in-hospital mortality. A total of 406 patients were enrolled at 80 sites between 2016 and 2020. Average age was 64±12 years, 24% were female, 17% had a witnessed out-of-hospital cardiac arrest, 27% had in-hospital cardiac arrest, and 9% were under active cardiopulmonary resuscitation during MCS implantation. Patients presented with a mean systolic blood pressure of 77.2±19.2 mm Hg, 85% of patients were on vasopressors or inotropes, mean lactate was 4.8±3.9 mmol/L and cardiac power output was 0.67±0.29 watts. At 24 hours, mean systolic blood pressure improved to 103.9±17.8 mm Hg, lactate to 2.7±2.8 mmol/L, and cardiac power output to 1.0±1.3 watts. Procedural survival, survival to discharge, survival to 30 days, and survival to 1 year were 99%, 71%, 68%, and 53%, respectively. Early use of MCS in AMI-CS is feasible across varying health care settings and resulted in improvements to early hemodynamics and perfusion. Survival rates to hospital discharge were high. Given the encouraging results from our analysis, randomized clinical trials are warranted to assess the role of utilizing early MCS, using a standardized, multidisciplinary approach.

Sections du résumé

BACKGROUND BACKGROUND
Acute myocardial infarction complicated by cardiogenic shock (AMI-CS) is associated with significant morbidity and mortality. Mechanical circulatory support (MCS) devices increase systemic blood pressure and end organ perfusion while reducing cardiac filling pressures.
METHODS AND RESULTS RESULTS
The National Cardiogenic Shock Initiative (NCT03677180) is a single-arm, multicenter study. The purpose of this study was to assess the feasibility and effectiveness of utilizing early MCS with Impella in patients presenting with AMI-CS. The primary end point was in-hospital mortality. A total of 406 patients were enrolled at 80 sites between 2016 and 2020. Average age was 64±12 years, 24% were female, 17% had a witnessed out-of-hospital cardiac arrest, 27% had in-hospital cardiac arrest, and 9% were under active cardiopulmonary resuscitation during MCS implantation. Patients presented with a mean systolic blood pressure of 77.2±19.2 mm Hg, 85% of patients were on vasopressors or inotropes, mean lactate was 4.8±3.9 mmol/L and cardiac power output was 0.67±0.29 watts. At 24 hours, mean systolic blood pressure improved to 103.9±17.8 mm Hg, lactate to 2.7±2.8 mmol/L, and cardiac power output to 1.0±1.3 watts. Procedural survival, survival to discharge, survival to 30 days, and survival to 1 year were 99%, 71%, 68%, and 53%, respectively.
CONCLUSIONS CONCLUSIONS
Early use of MCS in AMI-CS is feasible across varying health care settings and resulted in improvements to early hemodynamics and perfusion. Survival rates to hospital discharge were high. Given the encouraging results from our analysis, randomized clinical trials are warranted to assess the role of utilizing early MCS, using a standardized, multidisciplinary approach.

Identifiants

pubmed: 38014676
doi: 10.1161/JAHA.123.031401
doi:

Substances chimiques

Lactic Acid 33X04XA5AT

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e031401

Auteurs

Mir B Basir (MB)

Henry Ford Hospital Detroit MI.

Alejandro Lemor (A)

University of Mississippi Jackson MS.

Sarah Gorgis (S)

Henry Ford Hospital Detroit MI.

Kirit C Patel (KC)

St. Joseph Mercy Oakland MI.

Brian C Kolski (BC)

St. Joseph Hospital Orange Orange CA.

Aditya S Bharadwaj (AS)

Loma Linda University Medical Center Loma Linda CA.

Joshua W Todd (JW)

Fort Sanders Regional Medical Center Fort Sanders TN.

Behnam N Tehrani (BN)

Inova Fairfax Hospital Fairfax VA.

Alexander G Truesdell (AG)

Inova Fairfax Hospital Fairfax VA.

David M Lasorda (DM)

Allegheny General Hospital Pittsburg PA.

Thomas A Lalonde (TA)

Ascension St. John Hospital Detroit MI.

Amir Kaki (A)

Ascension St. John Hospital Detroit MI.

Theodore L Schrieber (TL)

Ascension St. John Hospital Detroit MI.

Nainesh C Patel (NC)

Lehigh Valley Hospital Allentown PA.

Shaun R Senter (SR)

Washington Regional Medical Center Washington AK.

Steven P Marso (SP)

Overland Park Regional Medical Center Overland Park KS.

Ayaz M Rahman (AM)

Parkwest Medical Center Knoxville TN.

Robert E Federici (RE)

Presbyterian Hospital Albuquerque NM.

Charles E Wilkins (CE)

San Juan Regional Medical Center San Juan NM.

A Thomas McRae (A)

TriStar Centennial Medical Center Nashville TN.

Ali Nsair (A)

Ronald Reagan UCLA Medical Center Los Angeles CA.

Christopher P Caputo (CP)

North Florida Regional Medical Center Gainesville FL.

Matheen A Khuddus (MA)

North Florida Regional Medical Center Gainesville FL.

Juan J Chahin (JJ)

Excela Health Westmoreland Hospital Greensburg PA.

Allison G Dupont (AG)

Northside Cardiovascular Institute Atlanta GA.

Andrew M Goldsweig (AM)

Baystate Medical Center Springfield MA.

Michael J Lim (MJ)

Hackensack Medical Center Hackensack NJ.

Navin K Kapur (NK)

Tufts Medical Center Boston MA.

David H W Wohns (DHW)

Spectrum Health Butterworth Hospital Grand Rapids MI.

Yueren Zhou (Y)

Henry Ford Hospital Detroit MI.

Michael J Hacala (MJ)

Henry Ford Hospital Detroit MI.

William W O'Neill (WW)

Henry Ford Hospital Detroit MI.

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Classifications MeSH