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Kennedy, Jason

https://orcid.org/0000-0001-7604-899X

Mayo Clinic

University of Pittsburgh

Citations 2

Cardiac Function Before Sepsis and Clinical Outcomes
Iyer, Stuthi , Kennedy, Jason , Senussi, Mourad H. , Seymour, Christopher W. , Jentzer, Jacob C.

JAMA | April 8, 2024 | Volume: 331 | Issue: 17 | Pages: 1496

10.1001/jama.2024.3917 Get It

This cohort study characterizes heterogeneity in cardiac function prior to sepsis and describes associations with hospitalization outcomes and mortality.
Validation of cardiogenic shock phenotypes in a mixed cardiac intensive care unit population
Jentzer, Jacob C. , Soussi, Sabri , Lawler, Patrick R. , Kennedy, Jason , Jentzer, Jacob C , Lawler, Patrick , Kashani, Kianoush

Catheterization and Cardiovascular Interventions | January 25, 2022 | Volume: 99 | Issue: 4 | Pages: 1006-1014

10.1002/ccd.30103 Get It

AbstractBackgroundProposed phenotypes have recently been identified in cardiogenic shock (CS) populations using unsupervised machine learning clustering methods. We sought to validate these phenotypes in a mixed cardiac intensive care unit (CICU) population of patients with CS.MethodsWe included Mayo Clinic CICU patients admitted from 2007 to 2018 with CS. Agnostic K means clustering was used to assign patients to three clusters based on admission values of estimated glomerular filtration rate, bicarbonate, alanine aminotransferase, lactate, platelets, and white blood cell count. In‐hospital mortality and 1‐year mortality were analyzed using logistic regression and Cox proportional‐hazards models, respectively.ResultsWe included 1498 CS patients with a mean age of 67.8 ± 13.9 years, and 37.1% were females. The acute coronary syndrome was present in 57.3%, and cardiac arrest was present in 34.0%. Patients were assigned to clusters as follows: Cluster 1 (noncongested), 603 (40.2%); Cluster 2 (cardiorenal), 452 (30.2%); and Cluster 3 (hemometabolic), 443 (29.6%). Clinical, laboratory, and echocardiographic characteristics differed across clusters, with the greatest illness severity in Cluster 3. Cluster assignment was associated with in‐hospital mortality across subgroups. In‐hospital mortality was higher in Cluster 3 (adjusted odds ratio [OR]: 2.6 vs. Cluster 1 and adjusted OR: 2.0 vs. Cluster 2, both p < 0.001). Adjusted 1‐year mortality was incrementally higher in Cluster 3 versus Cluster 2 versus Cluster 1 (all p < 0.01).ConclusionsWe observed similar phenotypes in CICU patients with CS as previously reported, identifying a gradient in both in‐hospital and 1‐year mortality by cluster. Identifying these clinical phenotypes can improve mortality risk stratification for CS patients beyond standard measures.