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CompletedNCT03892551EMERGE IVUpdated May 25, 2022

Triage - Symptoms and Other Predictors in an All-comer Emergency Department Population; (EKBB 236/13)

An observational study in Triage Risk Stratification, sponsored by University Hospital, Basel, Switzerland. Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2022-05-25.

Sponsored by University Hospital, Basel, Switzerland · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
7,309
Ages
18 Years and older
Sex
All
01

Study summary

This study is to develop a tool capable of improved risk prediction regarding the 30-day mortality. Based on vital signs, impaired mobility on presentation (IMOP), Clinical Frailty Scale (CFS) and patients' symptomatology three risk categories (low, intermediate, high risk) will be established.

Read the detailed description

Most Emergency Departments (EDs) perform an initial risk stratification of patients, called Triage. Establishing a diagnosis is key for the administration of the appropriate treatment and the following disposition decision. The earlier and the more accurate the final diagnosis is established, the shorter the time to treatment and time to disposition, and thus, the more efficient the patient flow. New ways to improve diagnosis accuracy early on in patients' ED visits are needed. Although a great number of well validated and widely used triage systems exists, to this date no gold standard in triage risk stratification has been established. Most of the existing triage systems rely on the measurement of vital signs and a list of chief complaints.

This study is to develop a tool capable of improved risk prediction regarding the 30-day mortality. Based on vital signs, impaired mobility on presentation (IMOP), Clinical Frailty Scale (CFS) and patients' symptomatology three risk categories (low, intermediate, high risk) will be established.

According to acuity patients undergo triage or directly proceed to the treatment unit. Patients awaiting triage will be approached by a member of the study personnel and will be verbally informed about the study. Afterwards, patients will be interviewed asking about their symptoms and their reason for presentation. Patients in need of immediate therapy will receive therapy before start of the interview. Following the interview, patients undergo routine triage.The physician performing initial triage will be asked to rate how ill patients appear to be using a numeric scale ranging from 0 (perfect condition) to 10 (extremely ill). Treating physician's will be asked to state their suspected diagnosis as well as differential diagnoses. Follow-up to assess 30-day and 1-year mortality rate and date of death will start one year after the end of the inclusion period.

02

Conditions studied

  • Triage Risk Stratification

Keywords

  • risk prediction
  • Electronic triage systems (ETS)
  • undertriage
  • overtriage
03

In context

Lead sponsor

University Hospital, Basel, Switzerland is the lead sponsor of 989 studies on the registry; 189 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients presenting to the ED of the University Hospital Basel over a time-course of 9 weeks from 25.03.2019 to 27.05.2019.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • patients presenting to the ED of the University Hospital Basel and awaiting triage

Exclusion criteria

Exclusion Criteria:

  • unwillingness to participate
  • insufficient ability to communicate with the study personnel.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
7,309 participants (actual)
Patient registry
No

Groups and cohorts

  • patients admitted to emergency ward

    all patients admitted to the emergency ward and awaiting triage are observed

    Other: Assessment of symptoms patients presenting when admitted to ED · Other: Reason for patient presentation at ED · Other: physicians rating of severity of illness · Diagnostic Test: Assessment of vital signs · Other: Clinical Frailty Scale · Other: Impaired mobility on presentation (IMOP) · Other: Assessment of suspected diagnosis and differential diagnoses

Interventions

  • OtherAssessment of symptoms patients presenting when admitted to ED

    Questionnaire with a predefined list of 35 symptoms

  • OtherReason for patient presentation at ED

    Exploratory interview assessing reason for patient presentation at ED

  • Otherphysicians rating of severity of illness

    numeric scale ranging from 0 (perfect condition) to 10 (extremely ill)

  • Diagnostic testAssessment of vital signs

    Assessment of vital signs (heart rate, blood pressure, body temperature, respiration rate, peripheral capillary haemoglobin oxygen saturation)

  • OtherClinical Frailty Scale

    Assessment of frailty by Clinical Frailty Scale (CFS): assess patients' frailty level from 1, very fit, to 9, terminally ill

  • OtherImpaired mobility on presentation (IMOP)

    Assessment of IMOP: defined as being unable to stand unaided or walk without help

  • OtherAssessment of suspected diagnosis and differential diagnoses

    Assessment of treating physician's suspected diagnosis and differential diagnoses. Answers will be recorded in free text form.

06

What researchers measure

Primary outcomes

  1. 30-day mortality

    30-day mortality is defined as death within 30 days of the day of presentation to the ED

    Time frame: within 30 days of the day of presentation to the ED

Secondary outcomes

  1. Number of hospitalizations

    Hospitalization is defined as the direct admission from the ED to any hospital in-patient department with a stay of over 24 hours

    Time frame: day of presentation to the ED

  2. Number of ICU-admissions

    ICU-admission is defined as any direct admission to the ICU of the University Hospital of Basel

    Time frame: day of presentation to the ED

  3. Death rate (In-hospital mortality)

    In-hospital mortality is defined as death occurring during presentation to the ED and hospital discharge

    Time frame: from day of presentation to the ED to day of hospital discharge (assessed within 365 days of the day of presentation to the ED)

  4. Number of institutionalisations

    Institutionalisation is defined as no time spent at home during 365 days following presentation

    Time frame: within 365 days of the day of presentation to the ED

07

Study locations

1 site
  • Department of Emergency Medicine, University Hospital Basel
    Basel, 4031, Switzerland
08

References and documents

Publications

  • Rueegg M, Nissen SK, Brabrand M, Kaeppeli T, Dreher T, Carpenter CR, Bingisser R, Nickel CH. The clinical frailty scale predicts 1-year mortality in emergency department patients aged 65 years and older. Acad Emerg Med. 2022 May;29(5):572-580. doi: 10.1111/acem.14460. Epub 2022 Apr 23. PubMed 35138670 ↗
  • Kaeppeli T, Rueegg M, Dreher-Hummel T, Brabrand M, Kabell-Nissen S, Carpenter CR, Bingisser R, Nickel CH. Validation of the Clinical Frailty Scale for Prediction of Thirty-Day Mortality in the Emergency Department. Ann Emerg Med. 2020 Sep;76(3):291-300. doi: 10.1016/j.annemergmed.2020.03.028. Epub 2020 Apr 24. PubMed 32336486 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 25, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03892551
Responsible party
Sponsor
First posted
Mar 27, 2019
Start date
Mar 18, 2019
Primary completion
Nov 30, 2020
Completion
Nov 30, 2020
Last update
May 25, 2022

Study contacts

Roland Bingisser, Prof. Dr.
principal investigator · Department of Emergency Medicine, University Hospital Basel

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2022. You cannot join it, but the record below documents what was studied.

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