Key result
Combining clinical text and lab data improves acute heart failure phenotype prediction to 0.80 AUROC.
Why the study?
Early diagnosis of specific heart failure phenotypes is crucial for timely therapeutic intervention.
Does a machine learning model integrating clinical text and laboratory data improve the prediction of acute heart failure phenotypes compared to single data types?
Observational (n=1,707)
No
Does a machine learning model integrating clinical text and laboratory data improve the prediction of acute heart failure phenotypes compared to single data types?
Absolute Event Rate: 0.8% vs 0.78%
A machine learning model combining clinical text and laboratory data can predict acute heart failure phenotypes with moderate accuracy without relying on LVEF.
Supports AHF phenotyping without LVEF via multimodal ML; hypothesis-generating and requires prospective validation.
Background: Heart failure (HF), with its distinct phenotypes, poses significant public health challenges. Early diagnosis of specific HF phenotypes is crucial for timely therapeutic intervention. Objectives: We employed random forests to predict acute HF (AHF) phenotypes (HFrEF, HFmrEF, and HFpEF) during admission, using structured and unstructured data types while blinded to left ventricular ejection fraction (LVEF) information. Methods: We investigated the predictive performance of integrated natural language processing (NLP) and machine learning (ML)-based models in AHF phenotype classification by random forests, leveraging clinical text and laboratory data from the MIMIC-III database. Feature selection for unstructured textual data and biochemical test data was performed using the LASSO method, with selected textual features converted into structured data using one-hot encoding. The areas under the ROC and PRC curves (AUROC and AUPRC) assessed overall performance. Results: Our final study cohort comprised 1,192 training datasets and 513 independent validating datasets with primary data types and LVEF information available. The overall model from the training dataset showed the best performance with combined datasets (accuracy: 0.70 ± 0.03, AUROC: 0.76 ± 0.02) compared to the textual or laboratory dataset alone, which was replicated in the independent validating dataset. Our model achieved optimal performance by selecting up to 100 combined features from both textual and laboratory data. Reducing features to 20 did not substantially attenuate the overall model performance until only 10 features were selected. Conclusion: Our study enhances HF phenotype classification and underscores the value of multifaceted data analysis in clinical informatics, enabling more personalized heart failure treatment. Early identification of AHF phenotypes may support timely, phenotype-specific management and inform treatment decisions.
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Chang et al. (2025) conducted an observational in Acute Heart Failure (n=1,707). Random forest model using combined clinical text and laboratory data vs. Random forest models using textual data alone or laboratory data alone was evaluated on Area under the ROC curve (AUROC) for acute heart failure phenotype classification in the independent test dataset. A random forest model integrating clinical text and laboratory data achieved an AUROC of 0.80 for predicting acute heart failure phenotypes, outperforming models using textual data alone (AUROC 0.78) or laboratory data alone (AUROC 0.55).
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