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A simulation framework for mapping risks in clinical processes: the case of in-patient transfers
Adam G Dunn1, Mei-Sing Ong, Johanna I Westbrook
1Centre for Health Informatics, Australian Institute of Health Innovation, University of New South Wales, Sydney, Australia. a.dunn@unsw.edu.au
This study used agent-based simulation to model how clinical process violations lead to adverse events. Results show significant risks for patient misidentification and infection control, highlighting the need to simplify processes.
Area of Science:
- Healthcare systems engineering
- Patient safety research
- Computational modeling in medicine
Background:
- Routine clinical processes are susceptible to individual violations.
- Cumulative effect of these violations can increase the risk of adverse events.
- Understanding this risk cascade is crucial for improving patient safety.
Purpose of the Study:
- To develop an agent-based simulation framework to model cumulative risks from process violations.
- To quantify the risk of adverse events in hospital clinical processes.
- To identify novel methods for prospective risk analysis.
Main Methods:
- Agent-based simulation modeling of clinicians and information systems.
- Calibration and validation using observed patient transfer data.
- Repeated simulations to generate outcome distributions and risk likelihoods.
Main Results:
- Simulations indicated end-of-chain risks of 8% (misidentification) and 24% (infection control).
- Over 95% of simulated patient transfer processes showed unique trajectories.
- This demonstrates significant divergence from prescribed work practices.
Conclusions:
- Agent-based simulation provides a novel prospective risk analysis method for clinical processes.
- The high variability in patient transfer suggests complexity reduction is key for risk mitigation.
- Augmenting processes with more rules may be less effective than simplifying them.
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