Association of Use of an Intravascular Microaxial Left Ventricular Assist Device vs Intra-aortic Balloon Pump With In-Hospital Mortality and Major Bleeding Among Patients With Acute Myocardial Infarction Complicated by Cardiogenic Shock.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
25 02 2020
Historique:
pubmed: 11 2 2020
medline: 9 10 2020
entrez: 11 2 2020
Statut: ppublish

Résumé

Acute myocardial infarction (AMI) complicated by cardiogenic shock is associated with substantial morbidity and mortality. Although intravascular microaxial left ventricular assist devices (LVADs) provide greater hemodynamic support as compared with intra-aortic balloon pumps (IABPs), little is known about clinical outcomes associated with intravascular microaxial LVAD use in clinical practice. To examine outcomes among patients undergoing percutaneous coronary intervention (PCI) for AMI complicated by cardiogenic shock treated with mechanical circulatory support (MCS) devices. A propensity-matched registry-based retrospective cohort study of patients with AMI complicated by cardiogenic shock undergoing PCI between October 1, 2015, and December 31, 2017, who were included in data from hospitals participating in the CathPCI and the Chest Pain-MI registries, both part of the American College of Cardiology's National Cardiovascular Data Registry. Patients receiving an intravascular microaxial LVAD were matched with those receiving IABP on demographics, clinical history, presentation, infarct location, coronary anatomy, and clinical laboratory data, with final follow-up through December 31, 2017. Hemodynamic support, categorized as intravascular microaxial LVAD use only, IABP only, other (such as use of a percutaneous extracorporeal ventricular assist system, extracorporeal membrane oxygenation, or a combination of MCS device use), or medical therapy only. The primary outcomes were in-hospital mortality and in-hospital major bleeding. Among 28 304 patients undergoing PCI for AMI complicated by cardiogenic shock, the mean (SD) age was 65.0 (12.6) years, 67.0% were men, 81.3% had an ST-elevation myocardial infarction, and 43.3% had cardiac arrest. Over the study period among patients with AMI, an intravascular microaxial LVAD was used in 6.2% of patients, and IABP was used in 29.9%. Among 1680 propensity-matched pairs, there was a significantly higher risk of in-hospital death associated with use of an intravascular microaxial LVAD (45.0%) vs with an IABP (34.1% [absolute risk difference, 10.9 percentage points {95% CI, 7.6-14.2}; P < .001) and also higher risk of in-hospital major bleeding (intravascular microaxial LVAD [31.3%] vs IABP [16.0%]; absolute risk difference, 15.4 percentage points [95% CI, 12.5-18.2]; P < .001). These associations were consistent regardless of whether patients received a device before or after initiation of PCI. Among patients undergoing PCI for AMI complicated by cardiogenic shock from 2015 to 2017, use of an intravascular microaxial LVAD compared with IABP was associated with higher adjusted risk of in-hospital death and major bleeding complications, although study interpretation is limited by the observational design. Further research may be needed to understand optimal device choice for these patients.

Identifiants

pubmed: 32040163
pii: 2761003
doi: 10.1001/jama.2020.0254
pmc: PMC7042879
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

734-745

Subventions

Organisme : AHRQ HHS
ID : R03 HS025517
Pays : United States
Organisme : NHLBI NIH HHS
ID : K12 HL138046
Pays : United States
Organisme : NHLBI NIH HHS
ID : R56 HL130496
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL131535
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : FDA HHS
ID : U01 FD005938
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR000450
Pays : United States
Organisme : NCI NIH HHS
ID : KM1 CA156708
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000448
Pays : United States
Organisme : AHRQ HHS
ID : R01 HS025164
Pays : United States
Organisme : AHRQ HHS
ID : R01 HS025402
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States
Organisme : AHRQ HHS
ID : R01 HS022882
Pays : United States
Organisme : NCATS NIH HHS
ID : TL1 TR000449
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002346
Pays : United States
Organisme : AHRQ HHS
ID : K12 HS026379
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

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Auteurs

Sanket S Dhruva (SS)

University of California, San Francisco School of Medicine, San Francisco.
Section of Cardiology, Department of Medicine, San Francisco Veterans Affairs Medical Center, San Francisco, California.

Joseph S Ross (JS)

Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, Connecticut.
Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.
Department of Health Policy and Management, Yale School of Public Health, New Haven, Connecticut.

Bobak J Mortazavi (BJ)

Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, Connecticut.
Department of Computer Science and Engineering, Texas A&M University, College Station.
Center for Remote Health Technologies and Systems, Texas A&M University, College Station.
Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.

Nathan C Hurley (NC)

Department of Computer Science and Engineering, Texas A&M University, College Station.

Harlan M Krumholz (HM)

Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, Connecticut.
Department of Health Policy and Management, Yale School of Public Health, New Haven, Connecticut.
Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.

Jeptha P Curtis (JP)

Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, Connecticut.
Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.

Alyssa Berkowitz (A)

Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, Connecticut.

Frederick A Masoudi (FA)

Division of Cardiology, Department of Medicine, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora.

John C Messenger (JC)

Division of Cardiology, Department of Medicine, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora.

Craig S Parzynski (CS)

Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, Connecticut.

Che Ngufor (C)

Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota.
Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.

Saket Girotra (S)

Division of Cardiovascular Diseases, Department of Internal Medicine, Carver College of Medicine, University of Iowa, Iowa City.

Amit P Amin (AP)

Cardiovascular Division, Washington University School of Medicine in St Louis, St Louis, Missouri.

Nilay D Shah (ND)

Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota.
Division of Health Care Policy Research, Mayo Clinic, Rochester, Minnesota.

Nihar R Desai (NR)

Center for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, Connecticut.
Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut.

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