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Published on: June 11, 2012
A computerized physician order entry set designed to improve safety of intravenous haloperidol utilization: a
Andrew J Muzyk1, Sarah K Rivelli, Wei Jiang
1Campbell University College of Pharmacy and Health Sciences, Buies Creek, NC 27710, USA. Andrew.Muzyk@duke.edu
Insights
Computerized physician order entry sets improved safety for intravenous haloperidol use by increasing adherence to monitoring and reducing doses. This enhanced patient care and mitigated risks for QTc prolongation.
Area of Science:
- Clinical Pharmacy
- Health Informatics
- Cardiology
Background:
- Intravenous haloperidol administration is associated with risks of corrected QT (QTc) interval prolongation, torsades de pointes (TdP), and sudden cardiac death.
- Effective monitoring and risk factor mitigation are crucial for safe haloperidol use in hospitalized patients.
Purpose of the Study:
- To evaluate the impact of a computerized physician order entry (CPOE) set on the safe administration of intravenous haloperidol.
- To assess adherence to monitoring parameters, dose limitations, and risk factor management for QTc prolongation.
Main Methods:
- Retrospective cohort study comparing two 1-year periods before and after CPOE set implementation (October 1, 2008).
- Included medically ill inpatients prescribed intravenous haloperidol.
- Analyzed data on dosing, electrocardiogram (ECG) monitoring, and magnesium levels.
Main Results:
- Post-CPOE set implementation, patients were more likely to receive lower cumulative haloperidol doses (<2 mg/24h).
- Increased adherence to baseline ECGs, 24-hour follow-up ECGs, and magnesium level assessments was observed.
- These improvements were statistically significant (p < 0.05).
Conclusions:
- Successful implementation of a CPOE set significantly enhanced the safety of intravenous haloperidol administration.
- The CPOE set improved adherence to critical safety monitoring parameters and dose management in medically ill patients.
Background:
Intravenous haloperidol can increase the risk for corrected QT (QTc) interval prolongation, torsades de pointes (TdP) and sudden death.
Objective:
The purpose of this study was to examine the effects of implementation of a computerized physician order entry (CPOE) set on adherence to monitoring parameters, maximum and cumulative doses, and identification or mitigation of risk factors for QTc prolongation in patients prescribed intravenous haloperidol.
Methods:
A retrospective cohort study of medically ill hospitalized inpatients prescribed intravenous haloperidol was conducted. Data were collected for two distinct 1-year time periods: the pre-CPOE set period (30 June 2007 through 30 June 2008) and the post-CPOE set period (1 January 2009 through 1 January 2010). The CPOE set was implemented on 1 October 2008.
Results:
A total of 151 subjects were included; 84 subjects were in the pre-CPOE set group and 67 subjects were in the post-CPOE set group. Following CPOE set implementation, subjects in the post-CPOE group, compared with the pre-CPOE group, were more likely to receive a 24-hour cumulative dose of intravenous haloperidol <2 mg (Fisher's exact test; p < 0.048), have a baseline ECG (Fisher's exact test; p = 0.045), have a follow-up ECG within 24 hours of intravenous haloperidol administration (Fisher's exact test; p = 0.009) and have a magnesium value assessed at the time of intravenous haloperidol administration (Fisher's exact test; p = 0.004).
Conclusion:
This study reports on the successful implementation of a CPOE set designed to improve the safety of intravenous haloperidol administration in medically ill patients.
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