A Trial of Automated Safety Alerts for Inpatient Digoxin Use with Computerized Physician Order Entry
- Affiliations of the authors: Section of General Internal Medicine, College of Medicine, University of Illinois at Chicago, Chicago, IL (WLG); University of Illinois Hospital, Chicago, IL (AP); Department of Pharmacy Practice, College of Pharmacy, University of Illinois at Chicago, Chicago, IL (RJD)
- Correspondence and reprints: William L. Galanter, MD, PhD, Department of Medicine, Section of General Internal Medicine (M/C 718), University of Illinois at Chicago, 840 South Wood Street, Chicago, IL 60612; e-mail: <billg{at}uic.edu>
- Received 15 November 2003
- Accepted 4 March 2004
Abstract
Objective Automated clinical decision support (CDS) has shown promise in improving safe medication use. The authors performed a trial of CDS, given both during computerized physician order entry (CPOE) and in response to new laboratory results, comparing the time courses of clinician behaviors related to digoxin use before and after implementation of the alerts.
Design Alerts were implemented to notify of the potential risk from low electrolyte concentrations or unknown digoxin or electrolyte concentrations during CPOE. Alerts were also generated in response to newly reported hypokalemia and hypomagnesemia in patients given digoxin.
Measurements Clinician responses to the alerts for six months were compared with responses to similar situations for six months prior to implementation.
Results During CPOE, checking for unknown serum values increased after implementation compared with control at one hour: 19% vs. 6% for digoxin, 57% vs. 9% for potassium, and 40% vs. 12% for magnesium as well as at 24 hours (p < 0.01 for all comparisons). Electrolyte supplementation increased with newly reported hypokalemia and hypomagnesemia after implementation at one hour: 35% vs. 6% and 49% vs. 5% for potassium and magnesium, respectively, as well as at 24 hours (p < 0.01 for all comparisons). During CPOE, supplementation for hypokalemia was not improved, whereas supplementation for hypomagnesemia improved at one hour (p < 0.05).
Conclusion Overall, the alerts improved the safe use of digoxin. During CPOE, alerts associated with missing levels were effective. For hypokalemia and hypomagnesemia, the alerts given during CPOE were not as effective as those given at the time of newly reported low electrolytes.
Footnotes
-
Special thanks to Amy Looi, RN, for technical assistance in the CDS alert development. Portions of this work were presented at the annual meeting of the Society of General Internal Medicine, Atlanta, GA, May 2002.
-
Dr. Polikaitis was an employee of Cerner Corporation at the time that the research was performed.
