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Predicting multiple organ dysfunction syndrome in trauma-induced sepsis: Nomogram and machine learning approaches
Jinyu Peng1,2, Yun Li1,2, Chao Liu2
1Medical School of Chinese PLA, Beijing, China.
Background:
Multiple organ dysfunction syndrome (MODS) is a critical complication in trauma-induced sepsis patients and is associated with a high mortality rate. This study aimed to develop and validate predictive models for MODS in this patient population using a nomogram and machine learning approaches.
Methods:
This retrospective cohort study utilized data from the Medical Information Mart for Intensive Care-IV 2.2 database, focusing on trauma patients diagnosed with sepsis within the first day of intensive care unit (ICU) admission. Predictive variables were extracted from the initial 24 h of ICU data. The dataset (2008-2019) was divided into a training set (2008-2016) and a temporal validation set (2017-2019). Feature selection was conducted using the Boruta algorithm. Predictive models were developed and validated using a nomogram and various machine learning techniques. Model performance was evaluated based on discrimination, calibration, and decision curve analysis.
Results:
Among 1295 trauma patients with sepsis, 349 (26.95%) developed MODS. The 28-day mortality rates were 11.21% for non-MODS patients and 23.82% for MODS patients. Key predictors of MODS included the simplified acute physiology score II score, use of mechanical ventilation, and vasopressor administration. In temporal validation, all models significantly outperformed traditional scoring systems (all P <0.05). The nomogram achieved an area under the curve (AUC) of 0.757 (95% confidence interval [CI]: 0.700 to 0.814), while the random forest model demonstrated the highest performance with an AUC of 0.769 (95% CI: 0.712 to 0.826). Calibration plots showed excellent agreement between predicted and observed probabilities, and decision curve analysis indicated a consistently higher net benefit for the newly developed models.
Conclusion:
The nomogram and machine learning models provide enhanced predictive accuracy for MODS in trauma-induced sepsis patients compared to traditional scoring systems. These tools, accessible via web-based applications, have the potential to improve early risk stratification and guide clinical decision-making, ultimately enhancing outcomes for trauma patients. Further external validation is recommended to confirm their generalizability.
Insights
New nomogram and machine learning models accurately predict multiple organ dysfunction syndrome (MODS) in trauma sepsis patients. These tools improve early risk stratification, aiding clinical decisions and potentially enhancing patient outcomes.
Area of Science:
- Critical care medicine
- Trauma surgery
- Sepsis research
Background:
- Multiple organ dysfunction syndrome (MODS) is a severe complication in trauma patients with sepsis, leading to high mortality rates.
- Early and accurate prediction of MODS is crucial for timely intervention and improved patient outcomes.
Purpose of the Study:
- To develop and validate predictive models for MODS in trauma-induced sepsis patients.
- To compare the performance of nomogram and machine learning models against traditional scoring systems.
Main Methods:
- Retrospective cohort study using the MIMIC-IV database (2008-2019).
- Development and validation of nomogram and machine learning models using initial 24-hour ICU data.
- Feature selection via Boruta algorithm; performance evaluation using discrimination, calibration, and decision curve analysis.
Main Results:
- 349 out of 1295 trauma sepsis patients (26.95%) developed MODS, with higher mortality in MODS patients (23.82% vs 11.21%).
- Key predictors included SAPS II score, mechanical ventilation, and vasopressor use.
- Nomogram (AUC 0.757) and Random Forest (AUC 0.769) models showed superior performance to traditional systems in temporal validation.
Conclusions:
- Nomogram and machine learning models offer enhanced predictive accuracy for MODS in trauma sepsis.
- These models can aid in early risk stratification and clinical decision-making.
- Further external validation is recommended to confirm generalizability.

