{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,5]],"date-time":"2026-11-05T08:41:12Z","timestamp":1793868072141,"version":"4.6.1"},"reference-count":31,"publisher":"American Medical Association (AMA)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi260015-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>The Epic Sepsis Model version 2 (ESM v2) is a widely implemented proprietary sepsis prediction model, but no multicenter, external validation of its performance has been reported to guide adoption and use.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260015-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To conduct a multicenter validation of the ESM v2 to compare performance against the original ESM v1, outline differences across heterogenous clinical sites, and compare model performance against clinician recognition of sepsis.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260015-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>This prognostic study included adult inpatient encounters at 4 large US health systems between August 31, 2023, and March 11, 2025. At each site, data were collected for a consecutive period immediately following new model implementation. Data were analyzed from July 23 to August 19, 2025.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260015-7\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Sepsis was defined using Sepsis-3 clinical consensus criteria. Model discrimination was assessed using area under the receiver operating characteristic curve (AUROC) at the encounter level and prediction level with 4-hour, 12-hour, and hospitalization-wide time horizons. Performance against clinician recognition of sepsis was measured using antibiotics, lactate, and body culture orders.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260015-8\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>Of 227\u202f091 inpatient encounters, 7401 (3.3%; median [IQR] age, 65 [54-75] years; 3359 [45.4%] female; 2.7% Asian; 24.6% Black; 64.6% White; 7.1% Hispanic ethnicity) met sepsis criteria and 219\u202f690 (96.7%; median [IQR] age, 48 [33-65] years; 123\u202f563 [56.2%] female; 2.5% Asian; 38.8% Black; 49.6% White; 9.6% Hispanic ethnicity) did not. At the encounter level, the AUROC ranged from 0.82 (95% CI, 0.81-0.83) to 0.92 (95% CI, 0.92-0.93) across study sites. At the prediction level with a 12-hour time horizon, the AUROC ranged from 0.75 (95% CI, 0.74-0.75) to 0.85 (95% CI, 0.85-0.85). Comparison against clinician recognition of sepsis yielded a minor decrease in performance, with the resulting encounter-level AUROC ranging from 0.80 (95% CI, 0.79-0.81) to 0.90 (95% CI, 0.89-0.90) across sites. Positive predictive values remained low, from 0.13 (95% CI, 0.13-0.14) to 0.26 (95% CI, 0.25-0.27), with a high number needed to evaluate and high alert burden.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260015-9\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this prognostic study of a new sepsis prediction model, a multicenter prospective validation performed across 4 major US health systems found improved discrimination for the early prediction of sepsis but noted high institutional variability, low positive predictive value, and high alert burden.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2026.0181","type":"journal-article","created":{"date-parts":[[2026,2,27]],"date-time":"2026-02-27T16:30:27Z","timestamp":1772209827000},"page":"e260181","source":"Crossref","is-referenced-by-count":25,"title":["Multicenter Prospective Validation of an Updated 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