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Prospective Evaluation of Computerized Physician Order Entry in the Emergency Department

Prospective Evaluation of Computerized Physician Order Entry in the Emergency Department

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01444768
Acronym
CPOE
Enrollment
0
Registered
2011-10-03
Start date
2012-03-31
Completion date
2013-12-31
Last updated
2017-04-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Operational Metrics of the Emergency Department

Keywords

Alert Systems, Medication, Computerized Physician Order Entry System, CPOE, Medication Alert Systems, Medical Order Entry Systems

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.

Detailed description

The study will be a prospective before-after study comparing various operational and performance metrics before and after the implementation of a computerized physician order entry system in the emergency department. The investigators will collect 6 month before, 6 month after of data along with a 2-4 week washout period. The investigators will also administer a computerized physician order entry survey after the study is completed. This confidential survey will be emailed to all ED nurses, residents, and attendings using RedCap. Consent will be implied if they choose to participate.

Interventions

Computer ordering system allowing emergency department physicians to order medications, laboratory tests, radiology studies, and nursing interventions

Sponsors

Beth Israel Deaconess Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All consecutive adult patients (Age \>=18) presenting to the Emergency Department during the study period will be included in the study.

Exclusion criteria

* Patients who eloped, left without being seen, or signed out against medical advice will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
Time to Antibiotics6 monthsPrimary 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.

Secondary

MeasureTime frameDescription
Emergency Department Length of Stay6 monthsSecondary outcome measure is length of stay defined as the time from patient registration to time the patients leave the emergency department.
Lab turnaround time6 monthsLab turnaround time is defined as the time it takes from when the sample is collected to when the results are entered.
Resource Utilization6 monthsResource utilization defined as the number of CBC, Chem7, and troponin tests ordered.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026