Your browser doesn't support javascript.
loading
Clinical Course of Patients in Cardiogenic Shock Stratified by Phenotype.
Zweck, Elric; Kanwar, Manreet; Li, Song; Sinha, Shashank S; Garan, A Reshad; Hernandez-Montfort, Jaime; Zhang, Yijing; Li, Borui; Baca, Paulina; Dieng, Fatou; Harwani, Neil M; Abraham, Jacob; Hickey, Gavin; Nathan, Sandeep; Wencker, Detlef; Hall, Shelley; Schwartzman, Andrew; Khalife, Wissam; Mahr, Claudius; Kim, Ju H; Vorovich, Esther; Whitehead, Evan H; Blumer, Vanessa; Westenfeld, Ralf; Burkhoff, Daniel; Kapur, Navin K.
Affiliation
  • Zweck E; The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA; Division of Cardiology, Pulmonology, and Vascular Medicine, University Hospital Dusseldorf, Dusseldorf, Germany.
  • Kanwar M; Cardiovascular Institute at Allegheny Health Network, Pittsburgh, Pennsylvania, USA.
  • Li S; University of Washington Medical Center, Seattle, Washington, USA.
  • Sinha SS; Inova Heart and Vascular Institute, Inova Fairfax Campus, Falls Church, Virginia, USA.
  • Garan AR; Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Hernandez-Montfort J; Baylor Scott and White Health, Advanced Heart Failure Program Clinic, Temple, Texas, USA.
  • Zhang Y; The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.
  • Li B; The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.
  • Baca P; The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.
  • Dieng F; The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.
  • Harwani NM; The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA.
  • Abraham J; Center for Cardiovascular Analytics, Research and Data Science, Providence Heart Institute, Providence Research Network, Portland, Oregon, USA.
  • Hickey G; University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
  • Nathan S; University of Chicago, Chicago, Illinois, USA.
  • Wencker D; Baylor Scott and White Advanced Heart Failure Clinic, Dallas, Texas, USA.
  • Hall S; Baylor Scott and White Advanced Heart Failure Clinic, Dallas, Texas, USA.
  • Schwartzman A; Maine Medical Center, Portland, Maine, USA.
  • Khalife W; University of Texas Medical Branch, Galveston, Texas, USA.
  • Mahr C; University of Washington Medical Center, Seattle, Washington, USA.
  • Kim JH; Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, Texas, USA.
  • Vorovich E; Northwestern Medicine, Chicago, Illinois, USA.
  • Whitehead EH; Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Blumer V; Duke University Medical Center, Durham, North Carolina, USA.
  • Westenfeld R; Division of Cardiology, Pulmonology, and Vascular Medicine, University Hospital Dusseldorf, Dusseldorf, Germany.
  • Burkhoff D; Cardiovascular Research Foundation, New York, New York, USA.
  • Kapur NK; The CardioVascular Center, Tufts Medical Center, Boston, Massachusetts, USA. Electronic address: Nkapur@tuftsmedicalcenter.org.
JACC Heart Fail ; 11(10): 1304-1315, 2023 10.
Article in En | MEDLINE | ID: mdl-37354148
ABSTRACT

BACKGROUND:

Cardiogenic shock (CS) patients remain at 30% to 60% in-hospital mortality despite therapeutic innovations. Heterogeneity of CS has complicated clinical trial design. Recently, 3 distinct CS phenotypes were identified in the CSWG (Cardiogenic Shock Working Group) registry version 1 (V1) and external cohorts I, "noncongested;" II, "cardiorenal;" and III, "cardiometabolic" shock.

OBJECTIVES:

The aim was to confirm the external reproducibility of machine learning-based CS phenotypes and to define their clinical course.

METHODS:

The authors included 1,890 all-cause CS patients from the CSWG registry version 2. CS phenotypes were identified using the nearest centroids of the initially reported clusters.

RESULTS:

Phenotypes were retrospectively identified in 796 patients in version 2. In-hospital mortality rates in phenotypes I, II, III were 23%, 41%, 52%, respectively, comparable to the initially reported 21%, 45%, and 55% in V1. Phenotype-related demographic, hemodynamic, and metabolic features resembled those in V1. In addition, 58.8%, 45.7%, and 51.9% of patients in phenotypes I, II, and III received mechanical circulatory support, respectively (P = 0.013). Receiving mechanical circulatory support was associated with increased mortality in cardiorenal (OR 1.82 [95% CI 1.16-2.84]; P = 0.008) but not in noncongested or cardiometabolic CS (OR 1.26 [95% CI 0.64-2.47]; P = 0.51 and OR 1.39 [95% CI 0.86-2.25]; P = 0.18, respectively). Admission phenotypes II and III and admission Society for Cardiovascular Angiography and Interventions stage E were independently associated with increased mortality in multivariable logistic regression compared to noncongested "stage C" CS (P < 0.001).

CONCLUSIONS:

The findings support the universal applicability of these phenotypes using supervised machine learning. CS phenotypes may inform the design of future clinical trials and enable management algorithms tailored to a specific CS phenotype.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shock, Cardiogenic / Heart Failure Type of study: Prognostic_studies Limits: Humans Language: En Journal: JACC Heart Fail Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Shock, Cardiogenic / Heart Failure Type of study: Prognostic_studies Limits: Humans Language: En Journal: JACC Heart Fail Year: 2023 Document type: Article Affiliation country: