A Systematic Review and Meta-analysis of Externally Validated Epic Clinical Decision Support Tools
Open accessAbstract
Background: Clinical Decision Support (CDS) tools integrated with Electronic Health Records increasingly guide clinical practice. Epic Systems, storing more than 325 million patient records, offers various proprietary predictive models to healthcare systems. Despite widespread adoption, no systematic review has examined these tools’ real-world performance compared to vendor-reported metrics. Methods: This study was prospectively registered on PROSPERO (CRD420251148571). We systematically searched PubMed, Scopus, and Embase (January 2018 to August 2025) for external validations of Epic’s CDS tools. We pooled Area Under the Receiver Operating Characteristic Curve (AUROC) values using random-effects models and assessed heterogeneity using Higgins’ I 2 . Results: We included 22 studies in our systematic review, validating Epic CDS tools on a total of over 2.3 million patients and 34 sites. The Epic Deterioration Index (EDI, 7 studies, 542,983 patients) achieved pooled AUROC 0.79 [95% CI 0.76–0.80]; Epic Sepsis Model (ESM, 3 studies, 922,754 patients) 0.65 [0.61–0.70]; Epic Unplanned Readmission Model (EURM, 5 studies, 145,595 patients) 0.70 [0.68–0.73]; Epic End-of-Life Care Index (EEOL-CI, 3 studies, 217,885 patients) 0.76 [0.67–0.83]; and Epic Risk of Patient No-Show (ERPNS, 2 studies, 93,863 patients) 0.62 [0.54–0.68]. All models showed high heterogeneity (I 2 ≥ 93%, p < 0.001). For ESM, EURM, and EEOL-CI, Epic’s reported confidence intervals did not overlap with our pooled estimates, with Epic reporting consistently higher performance. Two additional models (ED-to-Inpatients and ICU Mortality) had one study each. Conclusion: Epic’s CDS tools demonstrated modest real-world performance, with none exceeding AUROC 0.79. Three models (ESM, EURM, EEOL-CI) underperformed Epic’s reported ranges. High heterogeneity across sites emphasizes the need for local validation before clinical deployment.
AI snapshot
Written from the paper’s full text.
TL;DR
This systematic review and meta-analysis found that externally validated Epic clinical decision support tools had modest real-world discrimination, with no pooled AUROC exceeding 0.79. For several models, Epic’s vendor-reported performance was higher than pooled external validation estimates, and heterogeneity was high across sites.
Key findings
- Across 22 studies and over 2.3 million patients, pooled AUROCs were: Epic Deterioration Index (EDI) 0.79 (7 studies; 542,983 patients; abstract 95% CI 0.76–0.80, results 0.77–0.80); Epic Sepsis Model (ESM) 0.65 (3 studies; 922,754 patients; 0.61–0.70); Epic Unplanned Readmission Model (EURM) 0.70 (5 studies; 145,595 patients; 0.68–0.73); Epic End-of-Life Care Index (EEOL-CI) 0.76 (3 studies; 217,885 patients; 0.67–0.83); and Epic Risk of Patient No-Show (ERPNS) 0.62 (2 studies; 93,863 patients; abstract 0.54–0.68, results 0.61 [0.55–0.68]).
- All five meta-analyzed models showed high heterogeneity (I² ≥ 93%, p < 0.001).
- For ESM, EURM, and EEOL-CI, Epic’s reported confidence intervals did not overlap the pooled estimates, with Epic reporting consistently higher performance. Epic-reported values included ESM 95% CI 0.76–0.83, EURM 0.73 (0.73–0.74), EEOL-CI 0.89 (0.89–0.90), EDI 0.80 (0.75–0.84), and ERPNS 0.77 without a CI.
- Two additional models had one study each: ED-to-Inpatients AUROC 0.84 (329,194 patients) and ICU Mortality AUROC 0.89 (63,775 patients).
Methods
- Prospectively registered on PROSPERO (CRD420251148571); searched PubMed, Scopus, and Embase from January 2018 to August 2025 for external validations of Epic CDS tools, limited to English, following PRISMA and using Covidence.
- Included peer-reviewed external validation studies of Epic proprietary predictive models; excluded duplicates, abstracts, articles without full text, preprints, editorials, locally developed models, studies without AUROC, and studies focused on downstream interventions.
- Data were extracted in duplicate; risk of bias assessed with PROBAST; random-effects meta-analysis performed in R 4.3.3 with metafor 4.8.0, pooling AUROC and 95% CI, testing heterogeneity with Cochran’s Q and quantifying with Higgins’ I²; meta-analysis conducted for models with more than one article.
Limitations
- The authors state significant heterogeneity across studies, meaning the average AUROC is not necessarily reflective of performance at a particular site; they also note AUROC does not account for operating threshold, calibration metrics were not included because most studies did not report them, publication bias is possible, and excluding abstracts or papers without AUROC could inflate pooled estimates.
- The authors note risk-of-bias concerns in some included studies, including high selection bias in Singh 2021 and Cummings 2021 (COVID) for EDI, and significant concerns in Hwang 2021, Hwang 2023, and Drew 2023 for EURM.
- Evident from the text: the abstract and results report different site counts (34 vs. 40) and different confidence intervals for EDI and ERPNS, though the authors do not discuss these discrepancies as limitations.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
22 of 32 cited sources checked · 9 supported · 1 flagged · accuracy not yet measured
- Study design and conductreasoning
Cummings 2021 (COVID) only included patients with COVID-19.
“Similarly, Cummings 2021 3 (COVID) only included patients with COVID-19.”
Quote in the paperSubstantial claim1 of 1 sources checked- cites [3] Cummings BC, Ansari S, Motyka JR, et al. Predicting intensive care transfers and other unforeseen events: Analytic model validation study and comparison to existing methods. JMIR Med Inform. 2021;9(4). https://doi.org/10.2196/25066. source
The Introduction states that the study trained and tuned PICTURE on a large non–COVID-19 cohort and validated it in both non–COVID-19 patients and patients with COVID-19. The Methods > Setting and Study Population section identifies the COVID-19 patients as one of four cohorts, not the only patients included. Page numbers are not available in the supplied copy. (LLM, conf=0.91)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
- Interpretationreasoning
Hwang 2021, conducted at Swiss Hospitals with differences in demographic populations and disease prevalence, may not reflect performance in the United States.
“Hwang 2021 27 is a validation study conducted at Swiss Hospitals with innate differences amongst demographic populations and disease prevalence, and as such, results of this validation study may not reflect performance in the United States.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [27] Hwang AB, Schuepfer G, Pietrini M, Boes S. External Validation of EPIC’s Risk of Unplanned Readmission Model, the LACE+ Index and SQLape as Predictors of Unplanned Hospital Readmissions: A Monocentric, Retrospective, Diagnostic Cohort Study in Switzerland. Vol 16. 2021. https://doi.org/10.1371/journal.pone.0258338. source
The Discussion (Limitations; page not available) describes a single-center Swiss validation study and warns that its findings may not generalize to organizations outside Switzerland, which supports the caution about U.S. performance. It does not establish differences in demographics or disease prevalence between its patients and U.S. patients; the claim also calls the setting 'Swiss Hospitals' although the validation was conducted at one hospital. (LLM, conf=0.86)
Experimental — accuracy not yet measured
- Study design and conductreasoning
Singh 2021 had a high risk of selection bias due to restricting validation to COVID-19 patients.
“Singh 2021 21 had a high risk of selection bias due to restricting validation to COVID-19 patients.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [21] Singh K, Valley TS, Tang S, et al. Evaluating a widely implemented proprietary deterioration index model among hospitalized patients with COVID-19. Ann Am Thorac Soc. 2021;18(7):1129-1137. https://doi.org/10.1513/AnnalsATS.202006-698OC. source
The Methods (Study Cohort) restrict the cohort to adults hospitalized with COVID-19. The Discussion says thresholds may differ for patients hospitalized with other conditions and calls for broader validation, but it does not assess this restriction as a high risk of selection bias. (LLM, conf=0.83)
Experimental — accuracy not yet measured
- Findingcitation
The Epic ICU Mortality model had an AUROC of 0.89 (95% CI 0.89-0.89).
“Tan 2020 47 Mayo Clinic Prospective ICU 63,775 3.5% 0.89 (0.89, 0.89)”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [47] Tan EM, Kashyap R, Olson IC, O’Horo JC. Validation of a Retrospective Computing Model for Mortality Risk in the Intensive Care Unit. Mayo Clin Proc Innov Qual Outcomes. 2020;4(5):575-582. https://doi.org/10.1016/j.mayocpiqo.2020.09.001 source
The Abstract Results report an AUROC of 89.7% (95% CI, 89.5%–89.9%) for Epic’s ICU mortality risk model, not the stated 0.89 (0.89–0.89). The Abstract Methods also describe a retrospective cohort study, whereas the citing row labels it prospective. (LLM, conf=0.90)
Experimental — accuracy not yet measured
- Study design and conductcitation
Drew 2023 had significant concerns with regard to patient selection because only patients receiving outpatient parenteral antibiotics were included.
“Similar to Hwang 2023, 28 Drew 2023 26 also had significant concerns with regard to patient selection; only patients receiving outpatient parenteral antibiotics were included.”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [28] Hwang S, Urbanowicz R, Lynch S, et al. Toward Predicting 30-Day Readmission Among Oncology Patients: Identifying Timely and Actionable Risk Factors. JCO Clin Cancer Inform. 2023;(7):1-10. https://doi.org/10.1200/cci.22.00097. source
Section 3.1 (page unavailable) describes a selected oncology cohort at one institute and excludes patients who moved away, died within 30 days, or were readmitted elsewhere. This supports the existence of patient-selection restrictions, but Hwang does not characterize them as significant concerns. The outpatient parenteral antibiotic restriction is attributed to Drew, not Hwang. (LLM, conf=0.78)
Experimental — accuracy not yet measured - cites [26] Drew R, Brenneman E, Funaro J, et al. Electronic health record-based readmission risk model performance for patients undergoing outpatient parenteral antibiotic therapy (OPAT). PLOS Digit Health. 2023;2(8):e0000323. https://doi.org/10.1371/journal.pdig.0000323. source
- Findingown data
The included studies validated Epic CDS tools across 34 sites.
“validating Epic CDS tools on a total of over 2.3 million patients and 34 sites.”
Quote in the paperNot a substantial claim - Findingown data
The EDI meta-analysis had a total cohort size of 542,983 unique encounters.
“With a total cohort size of 542,983 unique encounters”
Quote in the paperNot a substantial claim - Findingown data
The EDI had a pooled AUROC of 0.79 (95% CI 0.77-0.80).
“the EDI had a pooled AUROC of 0.79 [95% CI, 0.77-0.80]”
Quote in the paperSubstantial claim - Findingown data
The EDI meta-analysis had a heterogeneity index (I2) of 97.2%.
“with a heterogeneity index ( I 2 ) of 97.2%.”
Quote in the paperNot a substantial claim - Findingown data
Two studies were included in the meta-analysis of the Epic Risk of Patient No-Show (ERPNS) model.
“Two studies were included in the meta-analysis of the ERPNS model”
Quote in the paperSubstantial claim - Findingreasoning
Seven studies were included in the meta-analysis of the Epic Deterioration Index (EDI).
“Seven studies were included in the meta-analysis of the EDI.”
Quote in the paperSubstantial claim - Findingown data
The ERPNS meta-analysis had a heterogeneity index of 98.6%.
“with a heterogeneity index of 98.6%.”
Quote in the paperNot a substantial claim - Findingown data
The EURM meta-analysis had a heterogeneity index of 93.6%.
“with a heterogeneity index of 93.6%.”
Quote in the paperNot a substantial claim - Findingown data
Five studies were included in the meta-analysis of the Epic Unplanned Readmission Model (EURM).
“Five studies were included in the meta-analysis of the EURM”
Quote in the paperNot a substantial claim - Findingnone given
Three studies were included in the meta-analysis of the Epic Sepsis Model (ESM).
“Three studies were included in the meta-analysis of the ESM.”
Quote in the paperSubstantial claim - Findingown data
The ESM meta-analysis had a heterogeneity index of 99.7%.
“and a heterogeneity index of 99.7%.”
Quote in the paperNot a substantial claim - Findingown data
The EURM meta-analysis had a total cohort size of 145,595.
“with a total cohort size of 145,595.”
Quote in the paperNot a substantial claim - Findingreasoning
The meta-analysis included 40 sites.
“With some articles reporting data from multiple sites, this led to 40 sites for the meta-analysis”
Quote in the paperNot a substantial claim - Findingown data
The ESM meta-analysis had a total cohort size of 922,754.
“The total cohort size was 922,754”
Quote in the paperNot a substantial claim - Findingown data
The EEOL-CI meta-analysis had a total cohort size of 217,885.
“with a total cohort size of 217,885.”
Quote in the paperNot a substantial claim - Findingown data
The ESM had a pooled AUROC of 0.65 (95% CI 0.61-0.70).
“with a pooled AUROC of 0.65 [0.61-0.70]”
Quote in the paperSubstantial claim - Findingown data
The systematic review included 22 studies.
“We included 22 studies in our systematic review”
- Also stated in: § Study Characteristics · plain
“22 articles were chosen for a systematic review.”
Quote in the paperSubstantial claim - Also stated in: § Study Characteristics · plain
- Findingown data
The EEOL-CI meta-analysis had a heterogeneity index of 96.9%.
“with a heterogeneity index of 96.9%.”
Quote in the paperNot a substantial claim - Findingown data
The included studies validated Epic CDS tools on a total of over 2.3 million patients.
“validating Epic CDS tools on a total of over 2.3 million patients and 34 sites.”
Quote in the paperNot a substantial claim - Findingown data
The EURM had a pooled AUROC of 0.70 (95% CI 0.68-0.73).
“The pooled AUROC was 0.70 [0.68-0.73]”
Quote in the paperSubstantial claim - Findingown data
The ERPNS had a pooled AUROC of 0.61 (95% CI 0.55-0.68).
“The pooled AUROC was 0.61 [0.55-0.68]”
Quote in the paperSubstantial claim - Findingown data
Three studies were included in the meta-analysis of the Epic End-of-Life Care Index (EEOL-CI).
“Three studies were included in the meta-analysis of the EEOL-CI”
Quote in the paperNot a substantial claim - Findingown data
The EEOL-CI had a pooled AUROC of 0.76 (95% CI 0.67-0.83).
“The pooled AUROC was 0.76 [0.67-0.83]”
Quote in the paperSubstantial claim - Findingown data
The ERPNS meta-analysis had a total cohort size of 93,863.
“with a total cohort size of 93,863.”
Quote in the paperNot a substantial claim - Findingcitation
The Epic ED to Inpatient model had an AUROC of 0.84 (95% CI 0.84-0.85).
“Dadabhoy 2023 46 Brigham and Women's Hospital Prospective Inpatient Admissions 329,194 25.4% 0.84 (0.84, 0.85)”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [46] Dadabhoy FZ, Driver L, McEvoy DS, Stevens R, Rubins D, Dutta S. Prospective External Validation of a Commercial Model Predicting the Likelihood of Inpatient Admission From the Emergency Department. Ann Emerg Med. 2023;81(6):738-748. https://doi.org/10.1016/j.annemergmed.2022.11.012. source
- Findingnone given
Despite widespread implementation of Epic's CDS tools, no systematic evaluation of their real-world performance exists.
“Despite widespread implementation of Epic's CDS tools, no systematic evaluation of their real-world performance exists”
Quote in the paperNot a substantial claim - Findingnone given
There was significant heterogeneity across the studies in the meta-analysis.
“First, there was significant heterogeneity across the studies.”
Quote in the paperSubstantial claim - Findingown data
All models showed high heterogeneity (I2 ≥ 93%, p < 0.001).
“All models showed high heterogeneity (I 2 ≥ 93%, p < 0.001).”
- Also stated in: § DISCUSSION · plain
“The meta-analyses for all five CDS models exhibited marked heterogeneity (I 2 ) of at least 93%.”
Quote in the paperSubstantial claim - Also stated in: § DISCUSSION · plain
- Findingown data
There was one study for the Epic ICU In-Hospital Mortality Risk model.
“There was one study for each of the following: ICU In-Hospital Mortality Risk and ED Patient Likelihood to occupy an Inpatient Bed”
Quote in the paperNot a substantial claim - Findingown data
There was one study for the Epic ED Patient Likelihood to occupy an Inpatient Bed model.
“There was one study for each of the following: ICU In-Hospital Mortality Risk and ED Patient Likelihood to occupy an Inpatient Bed”
Quote in the paperNot a substantial claim - Findingown data
Epic's CDS models showed lower and highly variable AUROC performance in real-world validation studies than their own reported metrics.
“In summary, Epic's CDS models showed lower and highly variable AUROC performance in real-world validation studies than their own reported metrics, emphasizing the need for local validation and customization to specific populations.”
Quote in the paperSubstantial claim - Interpretationreasoning
AUROC does not provide a complete picture of the clinical performance of the model as it is used in practice, because it does not take the operating threshold into account.
“However, AUROC does not provide a complete picture of the clinical performance of the model as it is used in practice, precisely because it does not take the operating threshold into account.”
Quote in the paperSubstantial claim - Interpretationown data
The mean AUROC across studies is consistently lower than the numbers reported by Epic.
“We also found that the mean AUROC across studies is consistently lower than the numbers reported by Epic.”
Quote in the paperSubstantial claim - Interpretationreasoning
The pooled mean reported AUROC will not characterize the actual performance of the model when deployed across different patient populations, medical systems, and geographical locations.
“This means the pooled mean reported AUROC will not characterize the actual performance of the model when deployed across different patient populations, medical systems, and geographical locations.”
Quote in the paperSubstantial claim - Study design and conductreasoning
Data were synthesized using a random-effects model due to clinical heterogeneity of population studies within each Epic CDS tool.
“We synthesized data utilizing a random-effects model as opposed to a fixed-effects model due to the clinical heterogeneity of population studies within each Epic CDS tool.”
Quote in the paperSubstantial claim - Study design and conductnone given
None of the studies included in the ESM meta-analysis had a significant risk of bias.
“None of the studies included in the meta-analysis had a significant risk of bias.”
Quote in the paperNot a substantial claim - Interpretationreasoning
Publication bias is a possible issue in this meta-analysis.
“Publication bias is also a possible issue.”
Quote in the paperNot a substantial claim - Interpretationreasoning
Reported metrics of the Singh 2021 and Cummings 2021 COVID external validations should be taken with caution.
“Therefore, reported metrics of these two external validations should be taken with caution.”
Quote in the paperSubstantial claim - Interpretationown data
In the meta-analysis, none of the models achieved a mean AUROC greater than 0.79.
“In our meta-analysis, none of the models achieved a mean AUROC greater than 0.79.”
Quote in the paperSubstantial claim - Interpretationreasoning
Across externally validated studies, Epic's vendor-reported performance metrics appear to overestimate the discriminatory performance observed in real-world settings.
“Across externally validated studies, Epic's vendor-reported performance metrics appear to overestimate the discriminatory performance observed in real-world settings.”
Quote in the paperSubstantial claim - Interpretationcitation
The same threshold can lead to different performance metrics at different sites, even if the AUROC is the same.
“However, the same threshold can lead to different performance metrics at different sites, even if the AUROC is the same.”
Quote in the paperSubstantial claim - Interpretationreasoning
A model that developers train once and deploy everywhere will significantly underperform the mean advertised performance at some sites.
“Consequently, a model that developers train once and deploy everywhere will significantly underperform the mean advertised performance at some sites.”
Quote in the paperSubstantial claim - Study design and conductreasoning
Three studies in the EURM meta-analysis had significant concerns regarding risk of bias.
“Three studies had significant concerns regarding the risk of bias.”
Quote in the paperNot a substantial claim
- May combine two claims. 20
- Classified as probably not a substantial claim. 20
May combine two claims.
PremisecitationFor the EDI, using a threshold of 6, Wong 2021 reports a PPV of 12% while Kamran 2024 reports a PPV of 8%, despite similar AUROC values (0.63 and 0.62).
“For example, using a threshold of 6 for the EDI, Wong 2021 35 reports a PPV of 12% while Kamran 2024 36 reports a PPV of 8% despite having similar AUROC values (0.63 and 0.62).”
Quote in the paperSubstantial claim1 of 2 sources checked- cites Wong 2021 source
The Results (ESM Performance) report a positive predictive value of 12% at a score threshold of 6 and a hospitalization-level AUC of 0.63. However, Wong et al. evaluated the Epic Sepsis Model (ESM), not the EDI. The Kamran 2024 figures are not attributed to Wong and are outside this verdict. (LLM, conf=0.91)
Experimental — accuracy not yet measured - cites Kamran 2024 source
Probably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationEpic Systems stores more than 325 million patient records with a 41.3% inpatient market share as of 2025.
“Epic Systems, a leading provider in the EHR industry, stores more than 325 million patient records with a 41.3% inpatient market share as of 2025.[8][9][10]”
Quote in the paperNot a substantial claim1 of 3 sources checked- cites [8] About | Epic. https://www.epic.com/about/. Accessed 29 Dec 2025.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [9] Discover the Most Common EHR Systems in Hospitals. https://www.definitivehc.com/blog/most-common-inpatient-ehr-systems. Accessed 29 Dec 2025.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- cites [10] Waxler S, Blazek P, White D, et al. Generative Medical Event Models Improve with Scale. arXiv. Preprint posted online November 7, 2025:arXiv:2508.12104. https://doi.org/10.48550/arXiv.2508.12104. source
The Introduction (p. 1) says Epic Cosmos aggregates records for more than 300 million patients as of August 2025, supporting the general point that Epic-associated systems hold records at this scale. It does not establish more than 325 million records or a 41.3% inpatient market share; the inpatient percentage in Data Pre-Processing (p. 21) describes encounter types, not market share. (LLM, conf=0.88)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationCDS tool performance has been shown to drift when validated in hospitals and regions outside of the development sites and over time.
“Importantly, CDS tool performance has been shown to drift when validated in hospitals and regions outside of the development sites 14,15 and over time.16,17”
Quote in the paperSubstantial claim4 of 4 sources checked- cites [14] van Klaveren D, Zanos TP, Nelson J, et al. Prognostic models for COVID-19 needed updating to warrant transportability over time and space. BMC Med. 2022;20(1):1-11. https://doi.org/10.1186/s12916-022-02651-3. source
- cites [15] Wessler BS, Nelson J, Park JG, et al. External Validations of Cardiovascular Clinical Prediction Models: A Large-Scale Review of the Literature. Circ Cardiovasc Qual Outcomes. 2021;14(8):E007858. https://doi.org/10.1161/CIRCOUTCOMES.121.007858. source
- cites [16] Davis SE, Greevy RA, Lasko TA, Walsh CG, Matheny ME. Detection of calibration drift in clinical prediction models to inform model updating. J Biomed Inform. 2020;112:103611. https://doi.org/10.1016/J.JBI.2020.103611. source
- cites [17] Levy TJ, Coppa K, Cang J, et al. Development and validation of self-monitoring auto-updating prognostic models of survival for hospitalized COVID-19 patients. Nat Commun 2022 131. 2022;13(1):1–14. https://doi.org/10.1038/s41467-022-34646-2. source
May combine two claims.
PremisecitationFalse positive rates can contribute to unnecessary diagnostics and antimicrobial use, potentially avoidable ICU transfers, and alert fatigue.
“False positive rates, on the other hand, can contribute to unnecessary diagnostics and antimicrobial use, potentially avoidable intensive care unit (ICU) transfers, and alert fatigue.6,7”
Quote in the paperNot a substantial claim2 of 2 sources checked- cites [6] Bedoya AD, Clement ME, Phelan M, Steorts RC, O’Brien C, Goldstein BA. Minimal Impact of Implemented Early Warning Score and Best Practice Alert for Patient Deterioration. Crit Care Med. 2019;47(1):49-55. https://doi.org/10.1097/CCM.0000000000003439. source
The Discussion reports that alerts requiring no clinical intervention contributed to alert fatigue. It does not report that false positives caused unnecessary diagnostics, antimicrobial use, or avoidable ICU transfers; the Results report no change in ICU transfer rates after implementation. Page numbers are not available in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measured - cites [7] Fallon A, Haralambides K, Mazzillo J, Gleber C. Addressing Alert Fatigue by Replacing a Burdensome Interruptive Alert with Passive Clinical Decision Support. Appl Clin Inform. 2024;15(1):101-110. https://doi.org/10.1055/a-2226-8144. source
The Background and Significance section says unnecessary interruptive alerts pose a risk of alert fatigue, and the Abstract reports that redesigning a frequently firing COVID alert reduced alert burden. The paper does not link false-positive rates to unnecessary diagnostics, antimicrobial use, or avoidable ICU transfers. Page numbers were not available for these passages. (LLM, conf=0.85)
Experimental — accuracy not yet measured
May combine two claims.
Study design and conductreasoningHwang 2023 is a validation study only including oncology patients, introducing significant bias with regard to patient selection.
“Hwang 2023 28 is a validation study only including oncology patients, introducing significant bias with regard to patient selection.”
Quote in the paperNot a substantial claim1 of 1 sources checked- cites [28] Hwang S, Urbanowicz R, Lynch S, et al. Toward Predicting 30-Day Readmission Among Oncology Patients: Identifying Timely and Actionable Risk Factors. JCO Clin Cancer Inform. 2023;(7):1-10. https://doi.org/10.1200/cci.22.00097. source
The Cohort and Dataset section describes a cohort restricted to oncology patients, supporting that part of the claim. But the Conclusions say the authors developed and validated models, so this was not a validation-only study. The Limitations section notes that the models were not evaluated at another hospital; it does not establish significant patient-selection bias. Our copy provides no page numbers for these passages. (LLM, conf=0.89)
Experimental — accuracy not yet measured
May combine two claims.
PremisecitationFor the EEOL-CI, at a threshold of 45, Gensheimer 2025 reports sensitivity, specificity, and PPV of 0.63, 0.70, and 0.38, while Frechman 2025 reports 0.23, 0.98, and 0.22.
“In the EEOL-CI, for a threshold of 45, Gensheimer 2025 37 reports a sensitivity, specificity, and PPV of 0.63, 0.70, and 0.38, respectively, while Frechman 2025 38 reports 0.23, 0.98, and 0.22, respectively.”
Quote in the paperSubstantial claim2 of 2 sources checkedMay combine two claims.
PremisecitationCDS tools directly influence patient care, with sepsis alerts prompting earlier antibiotic administration and fluid resuscitation, and deterioration scores used to trigger rapid response evaluations, intensified monitoring, and escalation of care.
“These tools directly influence patient care, with sepsis alerts prompting earlier antibiotic administration and fluid resuscitation, and deterioration scores used to trigger rapid response evaluations, intensified monitoring, and escalation of care.[3][4][5]”
Quote in the paperSubstantial claim3 of 3 sources checked- cites [3] Cummings BC, Ansari S, Motyka JR, et al. Predicting intensive care transfers and other unforeseen events: Analytic model validation study and comparison to existing methods. JMIR Med Inform. 2021;9(4). https://doi.org/10.2196/25066. source
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured - cites [4] Cummings BC, Blackmer JM, Motyka JR, et al. External Validation and Comparison of a General Ward Deterioration Index between Diversely Different Health Systems. Crit Care Med. 2023;51(6):775-786. https://doi.org/10.1097/CCM.0000000000005837. source
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured - cites [5] Liu VX, Fielding-Singh V, Greene JD, et al. The Timing of Early Antibiotics and Hospital Mortality in Sepsis. Am J Respir Crit Care Med. 2017;196(7):856-863. https://doi.org/10.1164/rccm.201609-1848OC. source
Split into 2 atoms — 0 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 2 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measured
Classified as probably not a substantial claim. May combine two claims.
InterpretationreasoningIn a general patient population like Frechman 2025, high specificity (0.98) may be desirable to avoid false positives, while in a high-risk mortality population like Gensheimer 2025 (metastatic cancer), higher sensitivity (0.63) may be favored.
“In a general patient population like Frechman 2025, 38 a high specificity (0.98) may be desirable to avoid false positives, while Gensheimer 2025 37 was in a population with a high risk of mortality (metastatic cancer) and may favor a higher sensitivity (0.63).”
Quote in the paperSubstantial claim2 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataDatabase screening followed by deletion of duplicate results yielded 2348 studies.
“Database screening followed by deletion of duplicate results yielded 2348 studies.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown dataMost studies in our analysis did not report calibration metrics, so we were unable to include them.
“However, most studies in our analysis did not report these metrics, so we were unable to include them.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataFor ESM, EURM, and EEOL-CI, Epic's reported confidence intervals did not overlap with the pooled estimates, with Epic reporting consistently higher performance.
“For ESM, EURM, and EEOL-CI, Epic's reported confidence intervals did not overlap with our pooled estimates, with Epic reporting consistently higher performance.”
- Also stated in: § DISCUSSION · plain
“For three models (ESM, EURM, and EEOL-CI), Epic's reported CI does not overlap with ours, with Epic's intervals being consistently higher than our pooled estimates.”
Quote in the paperSubstantial claim- Also stated in: § DISCUSSION · plain
May combine two claims.
PremisecitationEpic reported an ERPNS AUROC of 0.77 without a CI.
“Epic reported an AUROC of 0.77 without a CI.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [30] Galaxy - Cognitive Computing Model Brief: Risk of Patient No-Show (Version 1). https://galaxy.epic.com/?#Browse/page=1!68!50!3530079&from=Galaxy-Redirect. (Requires institutional access). Accessed 29 Dec 2025.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
PremisecitationEpic reported EEOL-CI AUROC at three different sites with a pooled AUROC of 0.89 (95% CI 0.89-0.90).
“Epic reported AUROC at three different sites with a pooled AUROC of 0.89 [0.89-0.90].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [29] Galaxy - Cognitive Computing Model Brief: End of Life Care Index. https://galaxy.epic.com/?#Browse/page=1!68!95!100039705&from=Galaxy-Redirect. (Requires institutional access). Accessed 29 Dec 2025.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Classified as probably not a substantial claim.
Study design and conductown dataThe authors systematically searched PubMed, Scopus, and Embase from January 2018 to August 2025 for external validations of Epic's CDS tools.
“We systematically searched PubMed, Scopus, and Embase (January 2018 to August 2025) for external validations of Epic's CDS tools.”
- Also stated in: § Search Strategy · plain
“In collaboration with an information specialist, J.M., we developed a search strategy and queried the PubMed, Scopus, and Embase databases for articles related to validated proprietary Epic CDS tools from January 2018 to August 2025 (Supplementary Appendix A).”
Quote in the paperSubstantial claim- Also stated in: § Search Strategy · plain
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenThe review protocol was prospectively registered on PROSPERO (CRD420251148571).
“This study was prospectively registered on PROSPERO (CRD420251148571).”
- Also stated in: § Search Strategy · plain
“The review protocol was registered in PROSPERO (CRD420251148571).”
Quote in the paperNot a substantial claim- Also stated in: § Search Strategy · plain
May combine two claims.
PremisecitationEpic reported EDI AUROC at three different sites with a pooled AUROC of 0.80 (95% CI 0.75-0.84).
“Epic reported AUROC for the EDI at three different sites with a pooled AUROC of 0.80 [95% CI, 0.75-0.84].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [20] Galaxy - Cognitive Computing Model Brief: Deterioration Index. https://galaxy.epic.com/?#Browse/page=1!68!50!3883949&from=Galaxy-Redirect. (Requires. institutional access). Accessed 29 Dec 2025.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
May combine two claims.
InterpretationreasoningThe net benefit of two models with the same AUROC can differ significantly based on the ROC curve and operating threshold, and AUROC does not reflect differences in performance in patient populations with different prevalences.
“The net benefit of two models with the same AUROC can differ significantly based on the ROC curve and operating threshold, and AUROC does not reflect differences in performance in patient populations with different prevalences (e.g., a lower prevalence will yield more 9).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFour independent reviewers screened article titles and abstracts.
“Four independent reviewers (H.P., S.C., J.M., D.H.) screened article titles and abstracts.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable), S3 (load-bearing), S4 (based).
Interpretationnone givenModel calibration metrics (slope, Brier score) can provide a more holistic picture of a model's performance.
“Model calibration metrics (slope, Brier score) can provide a more holistic picture of a model's performance.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
Study design and conductown dataData collection was performed in duplicate by two reviewers, with a third reviewer adjudicating discrepancies.
“Data collection (coding/extraction of AUROC and secondary metrics) was performed in duplicate by two reviewers (H.P. and S.C.), with a third reviewer (D.H.) adjudicating discrepancies.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationEpic's version 2 development of the ESM recommends localizing the algorithm on at least 35,000 hospital or emergency department encounters.
“Notably, with Epic's version 2 development of the ESM, they recommend localizing the algorithm on at least 35,000 hospital or emergency department encounters.34”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [34] Galaxy - Cognitive Computing Model Brief: Early Detection of Sepsis (Version 2). https://galaxy.epic.com/?#Browse/page=1!68!50!100170819&from=Galaxy-Redirect. (Requires institutional access). Accessed 12 Sept 2025.
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningThe suitability of operating points depends on the benefit and risk trade-off.
“The suitability of these operating points also depends on the benefit and risk trade-off.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationreasoningFor many clinical use cases, especially high-stakes applications like sepsis detection or ICU transfer, this level of discrimination may result in excessive false positives or missed cases, potentially limiting clinical utility.
“For many clinical use cases, especially high-stakes applications like sepsis detection or ICU transfer, this level of discrimination may result in excessive false positives or missed cases, potentially limiting clinical utility.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductcitationThe authors used Covidence systematic review software to adhere to PRISMA guidelines throughout the systematic review and meta-analysis.
“We utilized the Covidence systematic review software to strictly adhere to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines 18 throughout the systematic review and meta-analysis.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [18] PRISMA 2020 checklist. PRISMA statement. https://www.prisma-statement.org/prisma-2020-checklist. Accessed 6 Jan 2026.
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataFull-text review was performed in duplicate by at least two reviewers.
“Full-text review was performed in duplicate by at least two reviewers (H.P., S.C., and D.H.).”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationEpic reported their Sepsis v1 model achieved an AUROC between 0.76 and 0.83.
“Epic reported their Sepsis v1 model achieved an AUROC between 0.76 and 0.83.12”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [12] Galaxy - Cognitive Computing Model Brief: Early Detection of Sepsis (Version 1). https://galaxy.epic.com/?#Browse/page=1!68!50!3289911&from=Galaxy-Redirect (Requires institutional access).
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Probably not a substantial claim: may not pass S2 (checkable). May combine two claims.
InterpretationreasoningHigh heterogeneity among studies and the impact of threshold selection mean hospitals must carefully tailor models and operating points for optimal patient care.
“High heterogeneity among studies and the impact of threshold selection mean hospitals must carefully tailor models and operating points for optimal patient care.”
Quote in the paperNot a substantial claim- Rests on an assumption: Epic provides general guidelines on how to set an operating threshold that a hospital system can be comfortable with.
Classified as probably not a substantial claim.
Study design and conductnone givenA study was considered low risk only when all four PROBAST domains showed low risk.
“We considered a study low risk only when all four domains showed low risk.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenTwo reviewers were required to agree for inclusion at each stage.
“Two reviewers were required to agree for inclusion at each stage.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductown dataRisk of bias was assessed using the PROBAST tool.
“We assessed risk of bias using the Prediction model Risk Of Bias ASsessment (PROBAST) tool”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S2 (checkable).
InterpretationreasoningLocal validation and customization to specific populations are needed for Epic's CDS models.
“In summary, Epic's CDS models showed lower and highly variable AUROC performance in real-world validation studies than their own reported metrics, emphasizing the need for local validation and customization to specific populations.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductown dataTwo reviewers independently evaluated each study and rated domains as low, high, or unclear risk.
“Two reviewers (H.P. and S.C.) independently evaluated each study and rated domains as low, high, or unclear risk.”
Quote in the paperSubstantial claimMay combine two claims.
Premisenone givenAUROC does not depend on the operating threshold, so it can be used to compare discriminative ability across many studies.
“We selected AUROC because it does not depend on the operating threshold, so it can be used to compare discriminative ability across many studies.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
InterpretationreasoningStudies with null or unfavorable performance may be less likely to be published or to report AUROC, and our exclusion of abstracts and papers that did not report AUROC could preferentially remove such studies, potentially inflating pooled estimates.
“Studies with null or unfavorable performance may be less likely to be published or to report AUROC, and our exclusion of abstracts and papers that did not report AUROC could preferentially remove such studies, potentially inflating pooled estimates.”
Quote in the paperNot a substantial claim
The paper relies on this without support.
AUROC performance can vary significantly when models are run on populations that differ from the groups they were trained on.
“However, performance metrics such as AUROC can vary significantly when the models are run on populations that differ from the groups they were trained on.”
The paper relies on this without support.
Epic trains these models on data from a small number of hospitals.
“Epic trains these models on data from a small number of hospitals.”
The paper relies on this without support.
Epic provides general guidelines on how to set an operating threshold that a hospital system can be comfortable with.
“Epic provides general guidelines on how to set an operating threshold that a hospital system can be comfortable with.”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
The review reports both 34 and 40 sites
MajorThe abstract reports 34 sites, while the study characteristics section reports 40 sites for the included studies.
“We included 22 studies in our systematic review, validating Epic CDS tools on a total of over 2.3 million patients and 34 sites.”
“With some articles reporting data from multiple sites, this led to 40 sites for the meta-analysis (Fig. 1).”
The EDI pooled confidence interval differs between sections
MinorThe abstract gives the EDI interval as 0.76-0.80, but the results give 0.77-0.80 for the same pooled estimate.
“The Epic Deterioration Index (EDI, 7 studies, 542,983 patients) achieved pooled AUROC 0.79 [95% CI 0.76-0.80];”
“With a total cohort size of 542,983 unique encounters, the EDI had a pooled AUROC of 0.79 [95% CI, 0.77-0.80]with a heterogeneity index ( I 2 ) of 97.2%.”
The no-show model's pooled estimate differs between sections
MinorThe abstract reports an AUROC of 0.62 with a lower confidence limit of 0.54; the results report 0.61 and 0.55, respectively.
“and Epic Risk of Patient No-Show (ERPNS, 2 studies, 93,863 patients) 0.62 [0.54-0.68].”
“The pooled AUROC was 0.61 [0.55-0.68]with a heterogeneity index of 98.6%.”
The threshold example names the wrong model
MinorThe discussion calls Wong 2021 and Kamran 2024 examples of EDI performance, whereas Table 9 lists both under Sepsis.
“For example, using a threshold of 6 for the EDI, Wong 2021 35 reports a PPV of 12% while Kamran 2024 36 reports a PPV of 8% despite having similar AUROC values (0.63 and 0.62).”
“Sepsis Kamran 2024 6 0.38 0.08 0.62 Wong 2021 6 0.33 0.83 0.12 1.94 1.24 0.63”
Two included models exceed the stated maximum AUROC
MinorThe conclusion says none of Epic's CDS tools exceeded an AUROC of 0.79, but the included single-study validations report 0.84 for ED-to-Inpatient and 0.89 for ICU Mortality.
“Epic's CDS tools demonstrated modest real-world performance, with none exceeding AUROC 0.79.”
“0.84 (0.84, 0.85) Table 7 Summary of Epic ICU Mortality Study Institution Study Type Population Description N Prevalence of Target Outcome AUROC (95% CI) Tan 2020 47 Mayo Clinic Prospective ICU 63,775 3.5% 0.89 (0.89, 0.89)”
Cites
The meaning and use of the area under a receiver operating characteristic (ROC) curve.
Hanley, J. A., & McNeil, B. J. (1982) · Radiology · doi:10.1148/radiology.143.1.7063747 · Cited by 21,856 · see citing works
Wynants, L., Van Calster, B., Bonten, M. M., Collins, G. S., Debray, T. P., De Vos, M., Haller, M. C., Heinze, G., Moons, K. G., Riley, R. D., et al. (2020) · doi:10.1101/2020.03.24.20041020 · Cited by 3,070 · see citing works
An overview of clinical decision support systems: Benefits, risks, and strategies for success
Sutton, R. T., Pincock, D., Baumgart, D. C., Sadowski, D. C., Fedorak, R. N., & Kroeker, K. I. (2020) · npj Digital Medicine · doi:10.1038/s41746-020-0221-y · Cited by 3,019 · see citing works
Prediction models need appropriate internal, internal-external, and external validation
Steyerberg, E. W., & Harrell, F. E. (2016) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2015.04.005 · Cited by 1,304 · see citing works
The timing of early antibiotics and hospital mortality in sepsis.
Liu, V. X., Fielding-Singh, V., Greene, J. D., Baker, J. M., Iwashyna, T. J., Bhattacharya, J., & Escobar, G. J. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201609-1848oc · Cited by 1,006 · see citing works
Wong, A., Otles, E., Donnelly, J. P., Krumm, A., McCullough, J., DeTroyer-Cooley, O., Pestrue, J., Phillips, M., Konye, J., Penoza, C., et al. (2021) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2021.2626 · Cited by 995 · see citing works
Collins, G. S., de Groot, J. A., Dutton, S., Omar, O., Shanyinde, M., Tajar, A., Voysey, M., Wharton, R., Yu, L.-M., Moons, K. G., et al. (2014) · BMC Medical Research Methodology · doi:10.1186/1471-2288-14-40 · Cited by 729 · see citing works
Minimal Impact of Implemented Early Warning Score and Best Practice Alert for Patient Deterioration*
Bedoya, A. D., Clement, M. E., Phelan, M., Steorts, R. C., O’Brien, C., & Goldstein, B. A. (2019) · Critical Care Medicine · doi:10.1097/ccm.0000000000003439 · Cited by 162 · see citing works
Detection of calibration drift in clinical prediction models to inform model updating
Davis, S. E., Greevy, R. A., Lasko, T. A., Walsh, C. G., & Matheny, M. E. (2020) · Journal of Biomedical Informatics · doi:10.1016/j.jbi.2020.103611 · Cited by 160 · see citing works
Singh, K., Valley, T. S., Tang, S., Li, B. Y., Kamran, F., Sjoding, M. W., Wiens, J., Otles, E., Donnelly, J. P., Wei, M. Y., et al. (2021) · Annals of the American Thoracic Society · doi:10.1513/annalsats.202006-698oc · Cited by 111 · see citing works
Early Warning Scores With and Without Artificial Intelligence
Edelson, D. P., Churpek, M. M., Carey, K. A., Lin, Z., Huang, C., Siner, J. M., Johnson, J. K., Krumholz, H. M., & Rhodes, D. J. (2024) · JAMA Network Open · doi:10.1001/jamanetworkopen.2024.38986 · Cited by 99 · see citing works
Wessler, B. S., Nelson, J., Park, J. G., McGinnes, H., Gulati, G., Brazil, R., Van Calster, B., van Klaveren, D., Venema, E., Steyerberg, E., et al. (2021) · Circulation: Cardiovascular Quality and Outcomes · doi:10.1161/circoutcomes.121.007858 · Cited by 83 · see citing works
Evaluation of sepsis prediction models before onset of treatment
Kamran, F., Tjandra, D., Heiler, A., Virzi, J., Singh, K., King, J. E., Valley, T. S., & Wiens, J. (2024) · NEJM AI · doi:10.1056/aioa2300032 · Cited by 74 · see citing works
To warrant clinical adoption AI models require a multi-faceted implementation evaluation
van de Sande, D., Chung, E. F. F., Oosterhoff, J. H. F., van Bommel, J., Gommers, D. A. M. P. J., & van Genderen, M. E. (2024) · npj Digital Medicine · doi:10.1038/s41746-024-01064-1 · Cited by 73 · see citing works
Lyons, P. G., Hofford, M. R., Yu, S. C., Michelson, A. P., Payne, P. R. O., Hough, C. L., & Singh, K. (2023) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2022.7182 · Cited by 62 · see citing works
Cummings, B. C., Ansari, S., Motyka, J. R., Wang, G., Medlin Jr, R. P., Kronick, S. L., Singh, K., Park, P. K., Napolitano, L. M., Dickson, R. P., et al. (2021) · JMIR Medical Informatics · doi:10.2196/25066 · Cited by 35 · see citing works
Gallagher, D. M., Zhao, C., Brucker, A., Massengill, J., Kramer, P., Poon, E. G., & Goldstein, B. A. (2020) · Journal of Personalized Medicine · doi:10.3390/jpm10030103 · Cited by 28 · see citing works
Hwang, S., Urbanowicz, R., Lynch, S., Vernon, T., Bresz, K., Giraldo, C., Kennedy, E., Leabhart, M., Bleacher, T., Ripchinski, M. R., et al. (2023) · JCO Clinical Cancer Informatics · doi:10.1200/cci.22.00097 · Cited by 25 · see citing works
Fallon, A., Haralambides, K., Mazzillo, J., & Gleber, C. (2024) · Applied Clinical Informatics · doi:10.1055/a-2226-8144 · Cited by 22 · see citing works
Hwang, A. B., Schuepfer, G., Pietrini, M., & Boes, S. (2021) · PLOS ONE · doi:10.1371/journal.pone.0258338 · Cited by 19 · see citing works
Cummings, B. C., Blackmer, J. M., Motyka, J. R., Farzaneh, N., Cao, L., Bisco, E. L., Glassbrook, J. D., Roebuck, M. D., Gillies, C. E., Admon, A. J., et al. (2023) · Critical Care Medicine · doi:10.1097/ccm.0000000000005837 · Cited by 19 · see citing works
Steitz, B. D., McCoy, A. B., Reese, T. J., Liu, S., Weavind, L., Shipley, K., Russo, E. M., & Wright, A. T. (2023) · Journal of General Internal Medicine · doi:10.1007/s11606-023-08349-3 · Cited by 19 · see citing works
Levy, T. J., Coppa, K., Cang, J., Barnaby, D. P., Paradis, M. D., Cohen, S. L., Makhnevich, A., van Klaveren, D., Kent, D. M., Davidson, K. W., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34646-2 · Cited by 14 · see citing works
Self-citationDadabhoy, F. Z., Driver, L., McEvoy, D. S., Stevens, R., Rubins, D., & Dutta, S. (2023) · Annals of Emergency Medicine · doi:10.1016/j.annemergmed.2022.11.012 · Cited by 10 · see citing works
Currey, D., & Tarabichi, Y. (2025) · The American Journal of Emergency Medicine · doi:10.1016/j.ajem.2025.07.056 · Cited by 9 · see citing works
Design Considerations for MYCIN
Shortliffe, E. H. (1976) · Elsevier eBooks · doi:10.1016/b978-0-444-00179-5.50008-1 · Cited by 8 · see citing works
Kulkarni, N. S., Landler, M. P., Cohen, E. R., Wayne, D. B., & Szmuilowicz, E. (2025) · Journal of Hospital Medicine · doi:10.1002/jhm.70012 · Cited by 8 · see citing works
Ryan, P., Furniss, A., Breslin, K., Everhart, R. M., Hanratty, R. L., & Rice, J. (2021) · Medical Care · doi:10.1097/mlr.0000000000001653 · Cited by 7 · see citing works
Augmenting existing deterioration indices with chest radiographs to predict clinical deterioration
Mu, E., Jabbour, S., Dalca, A. V., Guttag, J. V., Wiens, J., & Sjoding, M. W. (2022) · PLoS ONE · doi:10.1371/journal.pone.0263922 · Cited by 7 · see citing works
Shashikumar, S. P., Le, J. P., Yung, N., Ford, J., Singh, K., Malhotra, A., Nemati, S., & Wardi, G. (2024) · Critical Care Explorations · doi:10.1097/cce.0000000000001151 · Cited by 7 · see citing works
Validation of a Retrospective Computing Model for Mortality Risk in the Intensive Care Unit
Tan, E. M., Kashyap, R., Olson, I. C., & O’Horo, J. C. (2020) · Mayo Clinic Proceedings: Innovations, Quality & Outcomes · doi:10.1016/j.mayocpiqo.2020.09.001 · Cited by 5 · see citing works
Prognostic models for COVID-19 needed updating to warrant transportability over time and space
van Klaveren, D., Zanos, T. P., Nelson, J., Levy, T. J., Park, J. G., Retel Helmrich, I. R. A., Rietjens, J. A. C., Basile, M. J., Hajizadeh, N., Lingsma, H. F., et al. (2022) · BMC Medicine · doi:10.1186/s12916-022-02651-3 · Cited by 5 · see citing works
Self-citationNo-show Prediction Model Performance Among People With HIV: External Validation Study
Mason, J. A., Friedman, E. E., Rojas, J. C., & Ridgway, J. P. (2023) · Journal of Medical Internet Research · doi:10.2196/43277 · Cited by 5 · see citing works
Drew, R., Brenneman, E., Funaro, J., Lee, H.-J., Yarrington, M., Dicks, K., & Gallagher, D. (2023) · PLOS Digital Health · doi:10.1371/journal.pdig.0000323 · Cited by 5 · see citing works
Gensheimer, M. F., Lu, J., & Ramchandran, K. (2025) · PeerJ · doi:10.7717/peerj.18958 · Cited by 5 · see citing works
Generative Medical Event Models Improve with Scale
Waxler, S., Blazek, P., White, D., Sneider, D., Chung, K., Nagarathnam, M., Williams, P., Voeller, H., Wong, K., Swanhorst, M., et al. (2025) · arXiv · doi:10.48550/arxiv.2508.12104 · Cited by 4 · see citing works
Frechman, E., Jaeger, B. C., Kowalkowski, M., Williamson, J. D., Lenoir, K. M., Palakshappa, J. A., Wells, B. J., Callahan, K. E., Pajewski, N. M., & Gabbard, J. L. (2025) · Journal of the American Medical Informatics Association · doi:10.1093/jamia/ocaf062 · Cited by 3 · see citing works
External Validation of an EHR-Based Model for Risk of Patient No-Show in Primary Care
Agovi, A. M., Serdarevic, M., Gehr, A. W., et al. (2025) · JAMA Network Open · doi:10.1001/jamanetworkopen.2025.21637 · Cited by 3 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Cracks in the AI Crystal Ball: Why Clinical Prediction Tools Fall Short in the Real World
GAMBLE, D., Wong, A. H., & Baduashvili, A. (2026) · Journal of General Internal Medicine · doi:10.1007/s11606-026-10601-5
Decoding Algorithmic Inequity: Reversing the Generative AI Racial Divide in Healthcare
Davidson, J., Fowe, I. E., Oderinde, A., & Fadeyi, S. A. (2026) · Clinical Therapeutics · doi:10.1016/j.clinthera.2026.06.015
Tang, F., Zhang, M., Shen, J., et al. (2026) · JMIR Formative Research · doi:10.2196/87017
“However, evidence suggests that the Epic CDSS tools demonstrate only modest real-world performance with high intersite heterogeneity, underscoring the need for local validation prior to deployment [34].”
How Repeal of the NTAP Alternative Pathway will Impact U.S. Clinical AI Innovation
Wong, A. H., Adler‐Milstein, J., Price, W. N., & Singh, K. (2026) · NEJM AI · doi:10.1056/aipc2600711
- Authors
- Patel, H., Crusco, S., Hansen, D., Morales, J., Patale, T., Chiuzan, C., Sands, M., Naidich, J., Myers, K., Davidson, K. W., Hirsch, J. S., & Zanos, T. P.
- Affiliations
- Northwell Health (US)
- Corresponding author
- Zanos, Theodoros P.
- ORCID
- Venue
- Journal of General Internal Medicine
- Published
- 2026-03-31
- ISSN
- 0884-8734 (ISSN-L)
- 1525-1497
- OpenAlex
- W7147754297
- Cited by
- 4
- References
- 38
- Citations by year
- 2026: 4
- FWCI
- 9.16
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Journal of General Internal Medicine (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institute of Nursing Research (R01NR020774)
- Topics
- Health Sciences › Health Professions › Health Information Management › Electronic Health Records Systems
- Physical Sciences › Computer Science › Artificial Intelligence › Machine Learning in Healthcare
- Health Sciences › Medicine › Health Informatics › Artificial Intelligence in Healthcare and Education
- Keywords
- clinical decision support, Epic Systems, external validation, electronic health records, prediction model, end-of-life care, real-world performance, area under the receiver operating characteristic, ICU mortality prediction, local validation
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-27.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-27.
Cited sources are checked by gpt-6-sol.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review