Evidence map›Paper›PMID 41814437›Full record

ArticleJournal of intensive care2026

Echocardiographic phenotypes in sepsis: identifying subgroups using latent profile analysis.

Tatyana Shvilkina, Gabriel Erion-Barner, Timothy P Downs, Ryan C Burke, Nadim Kattouf, Jordan B Strom, Robert E Gerszten, Tamar Sofer, Daniel B Kramer, Michael W Donnino and 2 more

Abstract read
In one paragraph

Article in Journal of intensive care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Tatyana ShvilkinaDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center, 1 Deaconess Rd, Boston, MA, 02115, USA. tshvilki@bidmc.harvard.edu.
Gabriel Erion-BarnerDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center, 1 Deaconess Rd, Boston, MA, 02115, USA.
Timothy P DownsDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center, 1 Deaconess Rd, Boston, MA, 02115, USA.
Ryan C BurkeDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center, 1 Deaconess Rd, Boston, MA, 02115, USA.
Nadim KattoufIcahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Jordan B StromRichard A. and Susan F. Smith Center for Outcomes Research in Cardiology, Beth Israel Deaconess Medical Center, Boston, MA, 02215, USA.
Robert E GersztenDepartment of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA, 02215, USA.
Tamar SoferDepartment of Medicine, Cardiovascular Institute, Boston, MA, 02215, USA.
Daniel B KramerRichard A. and Susan F. Smith Center for Outcomes Research in Cardiology, Beth Israel Deaconess Medical Center, Boston, MA, 02215, USA.
Michael W DonninoDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center, 1 Deaconess Rd, Boston, MA, 02115, USA.
Michael J LanspaDivision of Pulmonary and Critical Care, Intermountain Medical Center, Murray, UT, 84107, USA.
Nathan I ShapiroDepartment of Emergency Medicine, Beth Israel Deaconess Medical Center, 1 Deaconess Rd, Boston, MA, 02115, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSepsis remains a leading cause of mortality, and optimizing treatment is challenging due to patient heterogeneity. Identification of cardiac phenotypes may inform precision medicine approaches and guide resuscitation. We performed a clustering analysis of patients with sepsis using echocardiographic data without using any a priori definitions of cardiac dysfunction or outcomes to establish the subgroups.

methodsThis was a retrospective cohort study of patients admitted to the hospital with sepsis at a single academic center. Patients were identified using sepsis-related ICD codes, and those who had echocardiogram performed within 14 days of admission underwent chart review to ensure sepsis-3 criteria were met. Those with preexisting heart disease were excluded. Clustering by echocardiographic variables was performed using latent profile analysis. Clinical features such as patient characteristics, laboratory studies, sepsis source, and outcomes were compared across the clusters.

resultsThere were 2,071 patients included in the analysis. Our cluster analysis yielded five phenotypes: cluster 1, elevated mean E/e' 24.5 (SD 9.6); cluster 2, reduced ejection fraction, mean 33.1% (SD 10.6), and cardiac index 2.6 L/min/m

conclusionsUsing an unsupervised clustering analysis, we identified five phenotypes of cardiac function in sepsis based on commonly recorded echocardiographic data: diastolic dysfunction, left ventricular systolic dysfunction with low cardiac index, right ventricular dilation with elevated tricuspid regurgitation gradient, hyperdynamic cardiac function, and normal. The right ventricular dilation group had the highest mortality. Future research should explore mechanisms and potential treatment implications for these groups.

Indexed as

Cluster analysisEchocardiographySepsisVentricular dysfunction, leftVentricular dysfunction, right

Identifiers

PMID41814437
PMCPMC13072529

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.