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February 8, 2026Scientific Reports2 citationsOpen Access

A randomized controlled trial of artificial intelligence-based analytics for clinical deterioration

JKJessica Keim‐MalpassSRSarah J. RatcliffeMCMatthew T. Clark

Key Points

  • This trial aimed to evaluate the impact of AI-based predictive analytics on clinical deterioration in hospitalized patients.
  • Randomized controlled trial design with 10,422 inpatient visits assigned by cluster to intervention or control groups.
  • Intervention group received passive display of AI risk trajectories; control group received standard care.
  • Comparison of clinical deterioration events and mortality after 21 days post-admission was the primary analysis.
  • No significant difference in primary outcome of clinical deterioration between intervention and control groups.
  • Patients with increased risk scores had longer hospital stays (6.8 days vs. 3.4 days).
  • Event-free hours were higher in the intervention group, but not statistically significant.

Abstract

This pragmatic randomized controlled trial aimed to assess the effect of a passive display of artificial intelligence (AI)-based predictive analytics on hours free of clinical deterioration events among medical and surgical patients in an acute care cardiology medical-surgical ward. 10,422 inpatient visits were randomly assigned by cluster to the intervention group of a display of risk trajectories or to a control group of usual medical care. The trial was undertaken on an 85-bed inpatient cardiology and cardiac surgery ward of an academic hospital with a substantial implementation and education plan. This was a passive display with no specific response mandated. The primary analysis compared events of clinical deterioration (death, emergent ICU transfer, emergent endotracheal intubation, cardiac arrest, or emergent surgery) and compared mortality 21 days after admission. Patients with a large spike in risk score had, on average, twice the length of hospital stay (6.8 compared to 3.4 days). There was no change in the primary outcome between groups. Among those who had a clinical event, there were more event-free hours in the intervention/display-on group compared to the standard-of-care/display-off, but this did not reach statistical significance. Clinicians chose to transfer 11% of patients into or out of display beds, a censoring event removing them from the analysis, thereby undermining aspects of the randomized nature of the study. Predictive analytics monitoring incorporating continuous cardiorespiratory monitoring and displays of risk trajectories coupled with an education plan did not improve patient outcomes. While necessary to conduct the study, the pragmatic design allowed for significant movement towards intervention/displayed beds for sicker patients. Design considerations in the future must focus on understanding clinicians' interpretation, care processes, and communication practices.Clinical trial registration number: NCT04359641 Registered 4/24/20.

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Cite This Study

Keim‐Malpass et al. (2026) studied this question.

synapsesocial.com/papers/698827c90fc35cd7a8846c3chttps://doi.org/10.1038/s41598-026-39051-z
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