Validation of an Early Warning Score Based Triage System in the Emergency Department

This study has been completed.
Sponsor:
Information provided by:
Bispebjerg Hospital
ClinicalTrials.gov Identifier:
NCT01243021
First received: November 17, 2010
Last updated: NA
Last verified: November 2010
History: No changes posted
  Purpose

At Bispebjerg Hospital we have introduced an Early Warning Score based triage system , called Bispebjerg Early Warning Score (BEWS), in order to identify critically ill patient on arrival at the emergency department. The purpose of this study is to validate our triage system.


Condition
Critical Illness

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Nurse Administered Early Warning Score System Can be Used for Emergency Department Triage

Further study details as provided by Bispebjerg Hospital:

Primary Outcome Measures:
  • Critical illness [ Time Frame: 48 hours ]
    The investigators have defined a critically ill patient as a patient who dies within 48 hours of arrival at the emergency department or who is admitted to ICU within 48 hours of arrival at the emergency department


Enrollment: 300
Study Start Date: April 2009
Study Completion Date: September 2009
Primary Completion Date: September 2009 (Final data collection date for primary outcome measure)
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

When arriving at the emergency department patients are divided into on of three groups (red, blue nd white) according to the severity of their condition based on common regional guidelines. Red patients are the most servelery ill or injured patients. A random sample of "red" patients are included in this study

Criteria

Inclusion Criteria:

  • "Red" patient
  • Seen in our emergency department between 1. april 2009 and 30. september 2009

Exclusion Criteria:

  • None
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01243021

Locations
Denmark
Bispebjerg Hospital
Copenhagen, Copenhagen NV, Denmark, 2400
Sponsors and Collaborators
Bispebjerg Hospital
Investigators
Principal Investigator: Dorthea Christensen, MD Bispebjerg Hospital
  More Information

No publications provided

Responsible Party: Dorthea Christensen, Bispebjerg Hospital, Anaestesiological Department
ClinicalTrials.gov Identifier: NCT01243021     History of Changes
Other Study ID Numbers: BBH98765
Study First Received: November 17, 2010
Last Updated: November 17, 2010
Health Authority: Denmark: National Board of Health

Additional relevant MeSH terms:
Critical Illness
Emergencies
Disease Attributes
Pathologic Processes

ClinicalTrials.gov processed this record on July 20, 2014