ArticleResearch square2026
Cardiovascular and Autonomic Phenotypes Reveal Distinct Mechanisms of Sepsis Decompensation via Deep Learning.
Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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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.
The trial behind it
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Who cites it
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Authors and funding
12 authors.
Funding
Abstract
Sepsis heterogeneity reflects diverse etiologies and patient-specific physiological responses, motivating phenotype identification to enable precision therapeutics. However, most phenotyping approaches rely on intermittently sampled clinical variables, whereas continuously recorded physiological waveforms remain underutilized. We developed a deep-learning framework to derive physiological phenotypes from five-minute pre-onset electrocardiogram, photoplethysmogram and respiratory-impedance waveforms in 2,174 ICU patients meeting Sepsis-3 criteria. From these signals, 192 cardiorespiratory physiomarkers were extracted and embedded using a Feature Tokenizer Transformer encoder, which outperformed alternative representation methods. Consensus clustering identified four stable sepsis physio-phenotypes (SP-1-SP-4) associated with distinct autonomic and peripheral vascular signatures. Despite similar baseline severity and demographics, phenotypes differed significantly in mortality (19-29%), septic shock, vasopressor use and mechanical ventilation, with divergent 28-day survival trajectories (P<0.01). Explainable AI provided clinically interpretable characterizations, and a trained classifier enabled real-time bedside phenotyping. This framework establishes waveform-based phenotyping as a foundation for precision medicine in sepsis care.
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Registered trials
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.