Prospective Evaluation of Computerized Physician Order Entry in the Emergency Department
CPOE
1 other identifier
observational
N/A
1 country
1
Brief Summary
This study will evaluate various performance metrics of emergency department operations after the implementation of computerized physician order entry in an academic emergency department.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Mar 2012
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 29, 2011
CompletedFirst Posted
Study publicly available on registry
October 3, 2011
CompletedStudy Start
First participant enrolled
March 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2013
CompletedApril 5, 2017
April 1, 2017
9 months
September 29, 2011
April 4, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Time to Antibiotics
Primary outcome measure is time to antibiotics. This is defined as the time patients are registered to the time they receive their first antibiotics for patients with an ED diagnosis of pneumonia.
6 months
Secondary Outcomes (3)
Emergency Department Length of Stay
6 months
Lab turnaround time
6 months
Resource Utilization
6 months
Interventions
Computer ordering system allowing emergency department physicians to order medications, laboratory tests, radiology studies, and nursing interventions
Eligibility Criteria
All patients who are registered in the emergency department \> 18 years of age who do not elope, left without being seen, or leave AMA.
You may qualify if:
- All consecutive adult patients (Age \>=18) presenting to the Emergency Department during the study period will be included in the study.
You may not qualify if:
- Patients who eloped, left without being seen, or signed out against medical advice will be excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Steven Horng, MD
Beth Israel Deaconess Medical Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Instructor in Emergency Medicine
Study Record Dates
First Submitted
September 29, 2011
First Posted
October 3, 2011
Study Start
March 1, 2012
Primary Completion
December 1, 2012
Study Completion
December 1, 2013
Last Updated
April 5, 2017
Record last verified: 2017-04