{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,4]],"date-time":"2026-08-04T20:44:58Z","timestamp":1785876298650,"version":"3.56.0"},"reference-count":42,"publisher":"JMIR Publications Inc.","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JMIR Med Inform"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec sec-type=\"background\">\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Transfusion thresholds in upper gastrointestinal bleeding are debated; hemoglobin cutoffs of 70\u201080 g\/L are widely cited yet inconsistently applied. Common risk scores offer limited individualized guidance and rarely provide calibrated, interpretable predictions for transfusion decisions.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"objective\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>This study aimed to develop and validate a two-stage, clinically constrained gradient-boosting framework (Medically Constrained Gradient Boosting [MCGB]) that predicts transfusion need and estimates transfusion dose with quantified uncertainty and to implement a prototype recommendation system for clinical use.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"methods\">\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We analyzed a retrospective multicenter cohort of 849 adults with endoscopically confirmed upper gastrointestinal bleeding admitted to 3 hospitals in Chongqing, China (January 2019 to August 2025). Predictors available before the transfusion decision included demographics, first recorded vital signs, initial laboratory indices, and clinician-adjudicated etiology. Stage 1 used a calibrated classifier with prespecified monotonic constraints and stability-screened, clinically justified interactions. Stage 2 modeled transfusion dose via quantile predictions with conformal adjustment to generate 95% prediction intervals. Performance was assessed using a cross-site hold-out design. Overall, 2 hospitals were used as the development cohort, within which stratified 5-fold cross-validation was performed for model development, hyperparameter tuning, interaction screening, and calibration. The remaining hospital was held out as an independent test cohort for final evaluation. Hospital-wise alternating external testing was further conducted as a supplementary robustness analysis to assess performance stability across institutions. Classification performance was evaluated using discrimination metrics (area under the receiver operating characteristic curve and area under the precision-recall curve), calibration metrics, and decision-curve analysis; regression performance was evaluated using\n                      <jats:italic>R<\/jats:italic>\n                      \u00b2, mean absolute error, and prediction-interval coverage. A graphical user interface was implemented to enable clinicians to input patient data and obtain calibrated predictions of transfusion probability and corresponding dose recommendations.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"results\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      MCGB achieved strong discrimination and good calibration across subgroups (area under the receiver operating characteristic curve=0.97 and area under the precision-recall curve=0.91). At a reference probability threshold of .50, sensitivity, specificity, and\n                      <jats:italic>F<\/jats:italic>\n                      <jats:sub>1<\/jats:sub>\n                      -scores were 0.99, 0.87, and 0.85, respectively, providing a representative operating point for comparison. For dose prediction among transfused patients, MCGB achieved\n                      <jats:italic>R<\/jats:italic>\n                      \u00b2 of 0.95 and mean absolute error 0.04; 95% prediction-interval coverage was 0.94, indicating accurate point estimates with reliable uncertainty quantification. The software prototype further demonstrated feasibility of real-time decision support at the bedside.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec sec-type=\"conclusions\">\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>MCGB provides calibrated, interpretable predictions of transfusion need and individualized dose in upper gastrointestinal bleeding and may support bedside decision-making and blood-bank planning, with a prototype interface demonstrating potential for clinical deployment. External validation in additional settings is warranted to confirm generalizability.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.2196\/83889","type":"journal-article","created":{"date-parts":[[2026,6,12]],"date-time":"2026-06-12T17:50:08Z","timestamp":1781286608000},"page":"e83889-e83889","source":"Crossref","is-referenced-by-count":0,"title":["Prediction of Blood Transfusion Need and Dose in Patients With Upper Gastrointestinal Bleeding: Retrospective Multicenter Prediction Model 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