Prediction of Blood Lactate Values in Critically Ill Patients: A Retrospective Multi-center Cohort Study
Authors: Behrooz Mamandipoor, Wesley Yeung, Louis Agha-Mir-Salim, David J. Stone, Venet Osmani, Leo Anthony Celi
AI-generated Key Points
- Mamandipoor et al. conducted a retrospective multi-center cohort study on predicting blood lactate values in critically ill patients to assess mortality risk.
- Elevated serum lactate levels upon initial testing are known predictors of poor outcomes in critical care settings.
- The study aimed to determine if machine learning models could accurately predict subsequent changes in serum lactate levels to help clinicians adjust patient care accordingly.
- Three distinct subgroups were established based on initial lactate levels: normal (<2 mmol/L), mild (2-4 mmol/L), and severe (>4 mmol/L).
- LSTM models successfully predicted deterioration in serum lactate values among MIMIC-III patients, achieving AUC of 0.77 for the normal group, 0.77 for the mild group, and 0.85 for the severe group.
- While slightly lower performance was observed during external validation, the LSTM models still showed promising discrimination capabilities.
- The research suggests that machine learning models can effectively forecast changes in serum lactate levels among critically ill patients, potentially aiding clinicians in early intervention strategies and optimizing patient care decisions.
Abstract: Purpose. Elevations in initially obtained serum lactate levels are strong predictors of mortality in critically ill patients. Identifying patients whose serum lactate levels are more likely to increase can alert physicians to intensify care and guide them in the frequency of tending the blood test. We investigate whether machine learning models can predict subsequent serum lactate changes. Methods. We investigated serum lactate change prediction using the MIMIC-III and eICU-CRD datasets in internal as well as external validation of the eICU cohort on the MIMIC-III cohort. Three subgroups were defined based on the initial lactate levels: i) normal group (<2 mmol/L), ii) mild group (2-4 mmol/L), and iii) severe group (>4 mmol/L). Outcomes were defined based on increase or decrease of serum lactate levels between the groups. We also performed sensitivity analysis by defining the outcome as lactate change of >10% and furthermore investigated the influence of the time interval between subsequent lactate measurements on predictive performance. Results. The LSTM models were able to predict deterioration of serum lactate values of MIMIC-III patients with an AUC of 0.77 (95% CI 0.762-0.771) for the normal group, 0.77 (95% CI 0.768-0.772) for the mild group, and 0.85 (95% CI 0.840-0.851) for the severe group, with a slightly lower performance in the external validation. Conclusion. The LSTM demonstrated good discrimination of patients who had deterioration in serum lactate levels. Clinical studies are needed to evaluate whether utilization of a clinical decision support tool based on these results could positively impact decision-making and patient outcomes.
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