- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01654393
Triage Nurse Initiated Radiographs According to OAR
Can Triage Nurse Initiated Radiographs in Accordance With the Ottawa Ankle Rule Shorten Emergency Department Length of Stay At a Tertiary Care Center?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Overcrowding in the emergency department (ED) has been an ongoing issue for many hospitals in North America. Numerous strategies have been implemented and explored in hopes of reducing wait times and length of stay. The Ottawa ankle rules are one such strategy developed and proven to reduce cost and wait time without patient dissatisfaction and missed fractures. As a result, they have gained widespread acceptance from emergency physicians around the world.
Since the implementation of the Ottawa ankle rules (OAR), numerous studies have examined nurses' application and interpretation of these rules. It has been shown that nurses' application of the rule yield similar sensitivity and negative predictability for diagnosis of fractures as physicians. It is believed that emergency nurses can make accurate assessment in the determination of the patients who require radiographs. What is unclear, however, is whether or not triage nurse initiated radiographs shortens patients' length of stay in the emergency department, a factor inversely correlated to patient satisfaction. Only a couple of studies have looked at this issue in the context of the Ottawa ankle rules. One is a retrospective study conducted at an A&E department in a small city while the other, although randomized prospectively, was carried out in an urgent care center rather than in a busy academic tertiary care hospital.
Our primary objective for this study is to investigate the median length of stay of patients presenting to a tertiary care academic center with blunt ankle injuries and assess whether triage nurse initiated radiographs in accordance to the Ottawa ankle rules would shorten their stay versus current standard of care. Presently, the emergency physician orders the x-ray at the time of patient encounter.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Jan Buchanan, BSN
- Phone Number: 6048754205
- Email: Jan.Buchanan@vch.ca
Study Contact Backup
- Name: Lyne Filiatrault, MD
- Email: filiatra@mail.ubc.ca
Study Locations
-
-
British Columbia
-
Vancouver, British Columbia, Canada, V5Z 1M9
- Recruiting
- Vancouver General Hospital
-
Contact:
- Jan Buchanan, BSN
- Phone Number: 6048754205
- Email: Jan.Buchanan@vch.ca
-
Contact:
- Wailliam W Lee, MD
- Email: wailliamlee37@gmail.com
-
Principal Investigator:
- Wailliam Lee, MD
-
Principal Investigator:
- Lyne Filiatrault, MD, FRCPC
-
Principal Investigator:
- Ryiad Abu-Laban, MD, MHSc, FRCPC
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Patients aged ≥ 19 presenting with an isolated blunt ankle injury
Exclusion Criteria:
- Injury >10 days
- Isolated skin injury
- Referred patient with outside x-ray
- Obvious fracture or deformity
- Polytrauma
- Pregnancy
- Diminished sensation due to neurological deficit
- Uncooperative, intoxicated or patients with altered mental status
- Patients returning for reassessment of same injury
- Injury due to or suspicious for domestic violence
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: OAR group
Patients with ankle injuries who are assessed by OAR trained triage nurses applying the OAR.
|
Triage nurses applying the OAR during assessment and ordering foot/ankle x-rays as necessary.
|
No Intervention: Control for OAR Triage Nurses
Patients with ankle injuries that are seen by OAR triage nurses but not assessed in accordance with the OAR.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Median length of stay (LOS) of patients presenting to a tertiary care academic center with blunt ankle injuries
Time Frame: 6 months
|
Median LOS will be measured and compared among patients with ankle injuries that were assessed by OAR trained triage nurses who applied the OAR and ordered X-rays if necessary vs those patients who were triaged as per usual practice, with no OAR application.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Fracture missed by Triage Nurse:
Time Frame: Estimated at 6 months.
|
Assess if fractures were missed by triage nurse via + X-rays ordered by EP or via follow-up questionnaire 2 weeks later to determine if other investigations were performed after the pt's visit to the ED
|
Estimated at 6 months.
|
Triage nurses' satisfaction
Time Frame: estimated at 6 months
|
Assess triage nurse' feedback regarding comfortability in applying the OAR, training, and whether the OAR has increased workload.
|
estimated at 6 months
|
Percent agreement regarding necessity for X-ray between emergency nurse and physician
Time Frame: estimated at 6 months
|
estimated at 6 months
|
|
Emergency physician's compliance with OAR
Time Frame: estimated at 6 months
|
Determine if emergency physicians are applying OAR during this study period
|
estimated at 6 months
|
Patient satisfaction with triage nurse initiated imaging
Time Frame: Estimated at 6 months
|
Estimated at 6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lyne Filiatrault, MD, FRCPC, Vancouver Coastal Health Authorities
- Principal Investigator: Wailliam W Lee, MD, Vancouver Costal Health Authorities
- Principal Investigator: Ryiad Abu-Laban, MD, MHSc, FRCPC, Vancouver Costal Health Authorities
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- H12-01352
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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