A National Study of Intravenous Medication Errors

NCT02359734 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 900

Last updated 2016-08-24

No results posted yet for this study

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

  • Johns Hopkins University

    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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02359734 on ClinicalTrials.gov