ArticleBiomedical engineering online2026
Development and validation of a machine learning model for predicting 6-month mortality in patients with infective endocarditis.
Article in Biomedical engineering online, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
objectiveThis study aimed to develop and validate a machine learning (ML)-based model for predicting 6-month all-cause mortality in patients diagnosed with infective endocarditis (IE), using retrospective data from a single tertiary care center. Additionally, key prognostic features were identified through model interpretability analysis.
methodsA cohort of 444 patients with IE was retrospectively assessed and randomly divided into a training set (n = 310) and a test set (n = 134). Following feature selection, a Cox proportional hazards model and four ML-based survival models: Random Survival Forest, Extremely Randomized Survival Trees (EST), eXtreme Gradient Boosting, and Support Vector Machine were established. Model performance was assessed using the concordance index (C-index), time-dependent area under the curve (AUC), and Kaplan-Meier survival analysis. The model demonstrating optimal performance underwent interpretability analysis using Shapley additive explanations and an exploratory online tool was developed to demonstrate its functionality.
resultsNine predictors were selected for model construction: hemoglobin concentration, presence of severe valvular regurgitation, occurrence of septic shock, New York Heart Association (NYHA) classification, serum albumin level, intracerebral hemorrhage, neutrophil percentage, history of coronary heart disease, and receipt of surgical intervention. The EST model demonstrated the highest predictive performance in the test set (C-index: 0.852), with the smallest discrepancy in performance between the training and test datasets, indicating favorable generalizability. Time-dependent AUCs at 30, 90, and 180 days were 0.957, 0.925, and 0.855, respectively. Surgical intervention was modeled as a protective factor, associated with lower mortality risk, while intracerebral hemorrhage, higher NYHA class, severe valvular regurgitation, and septic shock were associated with increased risk.
conclusionsThe EST model demonstrated a high predictive accuracy for 6-month mortality in patients with IE, outperforming both conventional and other ML models. Its robust performance and interpretability suggest that, following rigorous external and multicenter validation, it may serve as a hypothesis-generating tool for risk stratification. It is not yet validated for direct clinical application and should currently be considered exploratory.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.