{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,15]],"date-time":"2026-09-15T13:53:56Z","timestamp":1789480436689,"version":"build-2803163510"},"reference-count":27,"publisher":"JMIR Publications Inc.","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JMIR Cardio"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec sec-type=\"background\">\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Mortality prediction in intensive care unit (ICU) patients with ischemic stroke complicated by intracranial artery stenosis or occlusion remains difficult. Conventional scoring systems often lack discriminatory power and fail to provide individualized risk estimates. Machine learning approaches have been increasingly explored to integrate diverse clinical features for prognostic modeling.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"objective\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>This study aims to develop and evaluate machine learning models for individualized mortality prediction in ICU patients with ischemic stroke associated with intracranial artery stenosis or occlusion.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"methods\">\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Using the Medical Information Mart for Intensive Care IV (MIMIC-IV) database, we conducted a retrospective cohort study including 5280 adult ICU patients identified through\n                      <jats:italic>International Classification of Diseases, Ninth and Tenth Revision<\/jats:italic>\n                      (\n                      <jats:italic>ICD-9\/10<\/jats:italic>\n                      ) codes. Mortality status was determined based on the presence of a recorded date of death (dod) in the MIMIC-IV database. Patients with a documented dod were classified as deceased, whereas those without a recorded dod were classified as nondeceased. The primary outcome was all-cause mortality as recorded in the MIMIC-IV database, defined by the presence of a documented dod. Patients were randomly split into training (n=3696, 70%) and testing (n=1584, 30%) cohorts. Missing value imputation, correlation reduction, and multistep supervised feature selection (gradient boosting, BorutaShap, recursive feature elimination with cross-validation, LassoCV, and chi-square analysis) were performed exclusively within the training set and subsequently applied to the test set, resulting in 35 retained predictive features. Eight machine learning models\u2014including light gradient boosting machine (LightGBM), Bagging (bootstrap aggregating), random forest, logistic regression, support vector machine, gradient boosting, adaptive boosting, and k-nearest neighbors\u2014were trained with hyperparameter optimization using RandomizedSearchCV. Model performance was evaluated using area under the curve, accuracy, recall, precision,\n                      <jats:italic>F<\/jats:italic>\n                      <jats:sub>1<\/jats:sub>\n                      -score, and calibration curves. Shapley additive explanations were used for global and individual-level interpretability.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"results\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>LightGBM, Bagging, and logistic regression demonstrated comparable discrimination, achieving an area under the curve of approximately 0.82\u20100.83 and accuracy above 73% on the independent test set. LightGBM demonstrated balanced performance (recall 0.70; precision 0.72) and good calibration. Shapley additive explanations analysis identified acute physiology score III, suspected infection, Charlson comorbidity index, age, weight on admission, and red cell distribution width as the most influential predictors. Overall, higher physiological severity, greater comorbidity burden, and older age were consistently associated with increased observed mortality risk.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"conclusions\">\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>Machine learning models\u2014including LightGBM and Bagging\u2014provide interpretable predictions of all-cause mortality in ICU patients with ischemic stroke and intracranial arterial disease. These models highlight key prognostic features and may support mortality risk stratification. External validation and evaluation of workflow integration are warranted before clinical implementation.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.2196\/82042","type":"journal-article","created":{"date-parts":[[2026,2,24]],"date-time":"2026-02-24T20:53:01Z","timestamp":1771966381000},"page":"e82042-e82042","source":"Crossref","is-referenced-by-count":4,"title":["Machine Learning Models for Mortality Prediction in Intensive Care Unit Patients With Ischemic Stroke Associated With Intracranial Artery Stenosis: Retrospective Cohort 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