Impact of a Triage Liaison Physician
1 other identifier
observational
69,893
1 country
1
Brief Summary
Due to an increasing number of patients admitted in emergency departments, many patients cannot be evaluated immediately after their admission. The function of "triage liaison physician" was introduced in Spring 2015. The objective of this study is to evaluate the impact of this new function on patients' flow in the ED.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2016
Shorter than P25 for all trials
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
Study Start
First participant enrolled
November 1, 2016
CompletedFirst Submitted
Initial submission to the registry
November 24, 2016
CompletedFirst Posted
Study publicly available on registry
December 2, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2017
CompletedJuly 27, 2017
July 1, 2017
7 months
November 24, 2016
July 26, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Proportion of patients evaluated within SETS objectives
Proportion of patients evaluated within time objective as defined by SETS standards.
Within 120 minutes after ED triage
Secondary Outcomes (1)
Time to first medical contact
Within 24 hours after ED triage
Study Arms (2)
Before triage liaison physician
All patients admitted before the introduction of the function of triage liaison physician.
After triage liaison physician
All patients admitted after the introduction of the function of triage liaison physician.
Interventions
A triage liaison physician is present from 7:30 am to 10:30 pm, Monday to Friday, with the mission to evaluate quickly patients who cannot be immediately installed in an ED room
Eligibility Criteria
All patient admitted in GUH ED during 2 years.
You may qualify if:
- \>= 16 y
- admitted in GUH ED
You may not qualify if:
- patients triaged to outpatient clinics
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Geneva University Hospitals, ED
Geneva, 1211, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Olivier T Rutschmann, MD, MPH
University Hospital, Geneva
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Chief deputy
Study Record Dates
First Submitted
November 24, 2016
First Posted
December 2, 2016
Study Start
November 1, 2016
Primary Completion
June 1, 2017
Study Completion
June 1, 2017
Last Updated
July 27, 2017
Record last verified: 2017-07
Data Sharing
- IPD Sharing
- Will not share