Clinical Presentation and In-Hospital Trajectory of Heart Failure and Cardiogenic Shock.


Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
02 2023
Historique:
received: 12 06 2022
revised: 04 10 2022
accepted: 11 10 2022
pubmed: 8 11 2022
medline: 11 2 2023
entrez: 7 11 2022
Statut: ppublish

Résumé

Heart failure-related cardiogenic shock (HF-CS) remains an understudied distinct clinical entity. The authors sought to profile a large cohort of patients with HF-CS focused on practical application of the SCAI (Society for Cardiovascular Angiography and Interventions) staging system to define baseline and maximal shock severity, in-hospital management with acute mechanical circulatory support (AMCS), and clinical outcomes. The Cardiogenic Shock Working Group registry includes patients with CS, regardless of etiology, from 17 clinical sites enrolled between 2016 and 2020. Patients with HF-CS (non-acute myocardial infarction) were analyzed and classified based on clinical presentation, outcomes at discharge, and shock severity defined by SCAI stages. A total of 1,767 patients with HF-CS were included, of whom 349 (19.8%) had de novo HF-CS (DNHF-CS). Patients were more likely to present in SCAI stage C or D and achieve maximum SCAI stage D. Patients with DNHF-CS were more likely to experience in-hospital death and in- and out-of-hospital cardiac arrest, and they escalated more rapidly to a maximum achieved SCAI stage, compared to patients with acute-on-chronic HF-CS. In-hospital cardiac arrest was associated with greater in-hospital death regardless of clinical presentation (de novo: 63% vs 21%; acute-on-chronic HF-CS: 65% vs 17%; both P < 0.001). Forty-five percent of HF-CS patients were exposed to at least 1 AMCS device throughout hospitalization. In a large contemporary HF-CS cohort, we identified a greater incidence of in-hospital death and cardiac arrest as well as a more rapid escalation to maximum SCAI stage severity among DNHF-CS. AMCS use in HF-CS was common, with significant heterogeneity among device types. (Cardiogenic Shock Working Group Registry [CSWG]; NCT04682483).

Sections du résumé

BACKGROUND
Heart failure-related cardiogenic shock (HF-CS) remains an understudied distinct clinical entity.
OBJECTIVES
The authors sought to profile a large cohort of patients with HF-CS focused on practical application of the SCAI (Society for Cardiovascular Angiography and Interventions) staging system to define baseline and maximal shock severity, in-hospital management with acute mechanical circulatory support (AMCS), and clinical outcomes.
METHODS
The Cardiogenic Shock Working Group registry includes patients with CS, regardless of etiology, from 17 clinical sites enrolled between 2016 and 2020. Patients with HF-CS (non-acute myocardial infarction) were analyzed and classified based on clinical presentation, outcomes at discharge, and shock severity defined by SCAI stages.
RESULTS
A total of 1,767 patients with HF-CS were included, of whom 349 (19.8%) had de novo HF-CS (DNHF-CS). Patients were more likely to present in SCAI stage C or D and achieve maximum SCAI stage D. Patients with DNHF-CS were more likely to experience in-hospital death and in- and out-of-hospital cardiac arrest, and they escalated more rapidly to a maximum achieved SCAI stage, compared to patients with acute-on-chronic HF-CS. In-hospital cardiac arrest was associated with greater in-hospital death regardless of clinical presentation (de novo: 63% vs 21%; acute-on-chronic HF-CS: 65% vs 17%; both P < 0.001). Forty-five percent of HF-CS patients were exposed to at least 1 AMCS device throughout hospitalization.
CONCLUSIONS
In a large contemporary HF-CS cohort, we identified a greater incidence of in-hospital death and cardiac arrest as well as a more rapid escalation to maximum SCAI stage severity among DNHF-CS. AMCS use in HF-CS was common, with significant heterogeneity among device types. (Cardiogenic Shock Working Group Registry [CSWG]; NCT04682483).

Identifiants

pubmed: 36342421
pii: S2213-1779(22)00590-X
doi: 10.1016/j.jchf.2022.10.002
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT04682483']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

176-187

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL139785
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL159089
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures This work was supported by National Institutes of Health RO1 grants to Dr Kapur (R01HL139785-01 and R01HL159089-01) and institutional grants from Abiomed Inc, Boston Scientific Inc, Abbott Laboratories, Getinge Inc, and LivaNova Inc to Tufts Medical Center. The sponsors had no input on the collection, analysis, and interpretation of the data or on the preparation, review, or approval of the manuscript. Dr Hernandez-Montfort is a consultant for Abiomed Inc and Abbott Laboratories. Dr Sinha is a consultant for Abiomed Inc. Dr Abraham is a consultant for Abbott Laboratories and Abiomed Inc. Dr Burkhoff has received an unrestricted educational grant from Abiomed Inc. Dr Kapur has received consulting honoraria and institutional grant support from Abbott Laboratories, Abiomed Inc, Boston Scientific, Medtronic, LivaNova, Getinge, and Zoll. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Jaime Hernandez-Montfort (J)

Baylor Scott and White Health, Advanced Heart Disease Program, Temple, Texas, USA.

Manreet Kanwar (M)

Cardiovascular Institute at Allegheny Health Network, Pittsburgh, Pennsylvania, USA.

Shashank S Sinha (SS)

Inova Heart and Vascular Institute, Inova Fairfax Medical Campus, Falls Church, Virginia, USA.

A Reshad Garan (AR)

Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

Vanessa Blumer (V)

Duke University Medical Center, Durham, North Carolina, USA.

Rachna Kataria (R)

Massachusetts General Hospital, Boston, Massachusetts, USA.

Evan H Whitehead (EH)

Massachusetts General Hospital, Boston, Massachusetts, USA.

Michael Yin (M)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.

Borui Li (B)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.

Yijing Zhang (Y)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.

Katherine L Thayer (KL)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.

Paulina Baca (P)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.

Fatou Dieng (F)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.

Neil M Harwani (NM)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.

Maya Guglin (M)

Indiana University Health Advanced Heart and Lung Care, Indianapolis, Indiana, USA.

Jacob Abraham (J)

Providence Heart Institute, Portland, Oregon, USA.

Gavin Hickey (G)

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Sandeep Nathan (S)

University of Chicago, Chicago, Illinois, USA.

Detlef Wencker (D)

Baylor Scott and White Health, Advanced Heart Disease Program, Temple, Texas, USA.

Shelley Hall (S)

Baylor Scott and White Advanced Heart Failure Clinic, Dallas, Texas, USA.

Andrew Schwartzman (A)

Maine Medical Center, Portland, Maine, USA.

Wissam Khalife (W)

University of Texas Medical Branch, Galveston, Texas, USA.

Song Li (S)

University of Washington Medical Center, Seattle, Washington, USA.

Claudius Mahr (C)

University of Washington Medical Center, Seattle, Washington, USA.

Ju Kim (J)

Houston Methodist Research Institute, Houston, Texas, USA.

Esther Vorovich (E)

Northwestern Medicine, Chicago, Illinois, USA.

Mohit Pahuja (M)

Medstar Heart and Vascular Institute, Georgetown University, Washington, DC, USA.

Daniel Burkhoff (D)

Cardiovascular Research Foundation, New York, New York, USA.

Navin K Kapur (NK)

The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA. Electronic address: Nkapur@tuftsmedicalcenter.org.

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Classifications MeSH