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Overriding of Drug Safety Alerts in Computerized Physician Order Entry
Affiliation:1. Expert Center Clinical Chemistry Eindhoven, Eindhoven, the Netherlands;2. Clinical Laboratory, Catharina Hospital, Eindhoven, the Netherlands;3. Laboratory of Chemical Biology and Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, the Netherlands;4. Clinical Laboratory, Máxima Medical Center, Veldhoven, the Netherlands;5. Department of Clinical Pharmacy and Pharmacology, Máxima Medical Center, Veldhoven, the Netherlands;1. Pulmonary/Critical Care Medicine, Fletcher Allen Health Care, Burlington, VT;2. School of Engineering, University of Vermont, Burlington, VT;3. Department of Medicine, University of Vermont, Burlington, VT
Abstract:
Many computerized physician order entry (CPOE) systems have integrated drug safety alerts. The authors reviewed the literature on physician response to drug safety alerts and interpreted the results using Reason's framework of accident causation. In total, 17 papers met the inclusion criteria. Drug safety alerts are overridden by clinicians in 49% to 96% of cases. Alert overriding may often be justified and adverse drug events due to overridden alerts are not always preventable. A distinction between appropriate and useful alerts should be made. The alerting system may contain error-producing conditions like low specificity, low sensitivity, unclear information content, unnecessary workflow disruptions, and unsafe and inefficient handling. These may result in active failures of the physician, like ignoring alerts, misinterpretation, and incorrect handling. Efforts to improve patient safety by increasing correct handling of drug safety alerts should focus on the error-producing conditions in software and organization. Studies on cognitive processes playing a role in overriding drug safety alerts are lacking.
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