# Cardiovascular and Autonomic Phenotypes Reveal Distinct Mechanisms of Sepsis Decompensation via Deep Learning

**Authors:** Tilendra Choudhary, Haoming Shi, Ayman Ali, Victor Moas, Omer T. Inan, Mihai V. Podgoreanu, Vijay Krishnamoorthy, Craig S. Jabaley, Craig M. Coopersmith, Michael R. Pinsky, Gilles Clermont, Rishikesan Kamaleswaran

PMC · DOI: 10.21203/rs.3.rs-9136766/v1 · Research Square · 2026-03-23

## TL;DR

This study uses deep learning on continuous physiological waveforms to identify distinct sepsis subtypes, revealing differences in outcomes and treatment needs.

## Contribution

A novel deep-learning framework for waveform-based sepsis phenotyping that enables real-time, interpretable bedside classification.

## Key findings

- Four stable sepsis physio-phenotypes were identified with distinct autonomic and vascular signatures.
- Phenotypes showed significant differences in mortality, vasopressor use, and mechanical ventilation requirements.
- The deep-learning model outperformed alternative methods in embedding physiomarkers for clustering.

## 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.

## Full-text entities

- **Genes:** SP1 (Sp1 transcription factor) [NCBI Gene 6667], SP4 (Sp4 transcription factor) [NCBI Gene 6671] {aka HF1B, SPR-1}
- **Diseases:** septic shock (MESH:D012772), Sepsis (MESH:D018805)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13042179/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC13042179/full.md

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Source: https://tomesphere.com/paper/PMC13042179