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Heterogenous effect of automated alerts on mortality
Benjamin D Wissel1,2, Zana Percy3, Tanner J Zachem2
1Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, United States.
Electronic alerts for acute kidney injury (AKI) have varied effects on patient mortality. Personalizing alert delivery to patients predicted to benefit can improve outcomes and reduce deaths.
Area of Science:
- Nephrology
- Medical Informatics
- Clinical Decision Support
Background:
- Electronic alerts aim to improve patient outcomes by flagging potential health issues like acute kidney injury (AKI).
- The effectiveness of these alerts can vary significantly among different patient populations.
- Understanding this heterogeneity is crucial for optimizing alert systems.
Purpose of the Study:
- To investigate the diverse treatment effects of electronic alerts for acute kidney injury (AKI).
- To identify patient subgroups that benefit from or are potentially harmed by AKI alerts.
- To explore how alert-triggered provider actions influence patient mortality.
Main Methods:
- Secondary analysis of individual patient data from three randomized controlled trials.
- Utilized machine learning to predict individualized alert effects on 14-day all-cause mortality.
- Performed internal and external validation, including a meta-analysis of individual patient data.
Main Results:
- Patients predicted to benefit from alerts showed a lower risk of death compared to those predicted to be harmed.
- Machine learning identified reduced mortality with alerts in patients with higher blood pressure and lower predicted risk.
- Increased mortality was observed with alerts in non-urban and non-teaching hospitals, with varied provider responses.
Conclusions:
- Significant heterogeneity exists in the impact of AKI alerts on patient mortality.
- Tailoring alert delivery based on predicted benefit may reduce harm and improve clinical outcomes.
- Individualized alerts hold potential for reducing all-cause mortality, warranting prospective trials.
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