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Physiologic phenotypes in blunt thoracic aortic injury: implications for risk stratification and surgical
Phillip D Jenkins1, Michael R Kolesnikov1, Shelby Willis1
1Department of Surgery, Oregon Health & Science University, Portland, OR, United States.
Machine learning identified three distinct patient groups for blunt thoracic aortic injury (BTAI), revealing that physiologic status, not just injury severity, impacts outcomes and guides treatment decisions.
Area of Science:
- Trauma Surgery
- Cardiovascular Surgery
- Machine Learning in Medicine
Background:
- Blunt thoracic aortic injury (BTAI) is a rare but often fatal condition.
- Current management strategies face challenges due to diverse patient presentations.
- Injury severity alone may not fully predict patient risk and outcomes.
Purpose of the Study:
- To apply machine learning to identify distinct physiologic phenotypes in BTAI patients.
- To analyze the outcomes associated with each identified phenotype.
- To utilize explainable AI (XAI) to understand the physiologic drivers of these phenotypes.
Main Methods:
- Analysis of 1,375 patients from the Aortic Trauma Foundation registry.
- K-means clustering (k=3) to define three distinct physiologic phenotypes based on eleven variables.
- XGBoost classification with SHapley Additive exPlanations (SHAP) for feature importance and validation.
Main Results:
- Three phenotypes identified: 'Stable' (n=431), 'Shock' (n=398), and 'Neurologically Compromised' (n=254).
- Mortality rates were significantly higher in 'Shock' (18.9%) and 'Neurologically Compromised' (18.1%) compared to 'Stable' (7.2%).
- Physiologic markers like blood pressure, lactate, and heart rate were key discriminators, with similar treatment patterns across phenotypes.
Conclusions:
- Machine learning successfully identified distinct BTAI phenotypes with varying mortality risks.
- Physiologic status, particularly perfusion and metabolic markers, is crucial for BTAI phenotyping and prognostication.
- These findings support the use of physiologic phenotyping to improve BTAI risk stratification and clinical decision-making.
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