A National Study of Intravenous Medication Errors
NCT02359734 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 900
Last updated 2016-08-24
Summary
To identify the key issues around use of computerized patient infusion devices (called "smart pumps").
To develop strategies that will improve the prevention of intravenous errors that will be broadly applicable.
The investigators will conduct a national study using the general methodology developed by Husch et al. to allow a rapid assessment of the frequency and types of medication errors at an institution.
The key questions the investigators will address are:
1. What are the frequency and types of intravenous medication errors?
2. How much variability is there by frequency and type among settings?
3. After review of the initial data, what strategies appear to have the greatest potential for reducing intravenous medication error frequency?
4. How effective is an intervention including a bundle of these strategies at multiple sites?
Conditions
- Medication Administered in Error
Interventions
- OTHER
-
Smart pump safety Intervention bundle for improving IV medication administration process with smart pump
Smart pump safety intervention bundle includes three components--1) eliminating unauthorized medications; implement standardized discontinuation policy of medications, implement standardized keep vein open rates and keep vein open rate order sets, and implement standardized verbal order practice. 2) Implement standardized intravenous(IV) labeling and IV tubing labels. 3) Implement standardized drug library lists and drug library use policies
Sponsors & Collaborators
- collaborator OTHER
-
Winchester Medical Center
collaborator OTHER -
Central DuPage Hospital
collaborator OTHER -
Vanderbilt University
collaborator OTHER -
Massachusetts General Hospital
collaborator OTHER -
University of California, San Diego
collaborator OTHER -
Valleywise Health
collaborator OTHER -
Danbury Hospital
collaborator OTHER -
Association for the Advancement of Medical Instrumentation
collaborator OTHER -
CareFusion foundation
collaborator UNKNOWN -
Candler Hospital
collaborator UNKNOWN -
Brigham and Women's Hospital
lead OTHER
Principal Investigators
-
David W Bates, MD, MSc · Brigham and Women's Hospital
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2012-04-30
- Primary Completion
- 2015-03-31
- Completion
- 2015-12-31
Countries
- United States
Study Locations
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