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Area of Science:

  • Health Informatics
  • Human Factors Engineering
  • Patient Safety

Background:

  • Medication-related clinical decision support (CDS) alerts are crucial for patient safety.
  • Integrating human factors principles into CDS design is essential for effective alert management.
  • Existing tools like the Instrument for Evaluating Human Factors Principles in Medication-Related Decision Support Alerts (I-MeDeSA) provide a foundation for assessment.

Purpose of the Study:

  • To develop and pilot a human factors assessment for medication-related CDS alerts.
  • To evaluate the integration of human factors principles in drug-drug interaction (DDI) alerts within outpatient electronic health record (EHR) systems.
  • To identify areas for improvement in CDS alert design and implementation.

Main Methods:

  • A human factors assessment was developed based on the validated I-MeDeSA tool, with modifications to questions and answer formats.
  • The assessment was piloted in 10 outpatient clinics across the US, each using a different commercial EHR system.
  • Clinics triggered high-severity DDI alerts and subsequently completed the human factors assessment.

Main Results:

  • The final assessment comprised five sections and twelve questions covering alert timing, visual aspects, severity, content, and actions.
  • The mean overall score across clinics was 62%, indicating substantial variability in human factors integration.
  • While timing and visual aspects scored well, 40% of clinics lacked safeguards to prevent bypassing high-severity alerts in the 'actions' section.

Conclusions:

  • There is significant variability in how outpatient clinics integrate human factors principles into DDI alerts.
  • Some EHR systems lack essential medication safeguards, posing a risk to patient safety.
  • The developed human factors assessment can be utilized by outpatient clinics for targeted safety improvement initiatives.