Completed

Triage of Children at the Emergency Department: Manchester Triage System or Pediatric Early Warning Score?

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Emergencies+1

+ Pathologic Processes

+ Pathological Conditions, Signs and Symptoms

Until 18 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Observational
Study Start: December 2013
See protocol details

Summary

Principal SponsorE.P. de Groot
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 2013

Actual date on which the first participant was enrolled.

Background: Triage systems are used at EDs to prioritize patients to make sure that those who need it, receive immediate care. The MTS is used for children at EDs by many hospitals worldwide, also at the ED of the Isala, the Netherlands. This triage system has been proven safe, but many patients are classified as too urgent. This is a disadvantage because accurate triage is needed to provide access for immediate ill patients and for sufficient flow at the ED. Currently, adult patients at the ED of the Isala are classified by the early warning score. This is a score based on vital signs and it is easily calculated. It originally has been developed to determine clinical deterioration. For children normal values are different for each age. Therefore there has been developed the PEWS, which is now only used to evaluate clinical patients. Ideally for the continuity in this hospital, there would be one system which can be used for triage as well as for clinical patients. The investigators hypothesize that the PEWS is a safe alternative for the triage of children at the ED. Design: A form will be attached on the file of all children presenting at the ED, for recording data. These forms will be collected afterwards. The emergency department nurses will record the vital signs, which the investigators need to calculate the PEWS as well as the urgency determined by the MTS for each patient. The expert opinion will also be recorded. This is de urgency according to the doctor who has seen the patient, maximal acceptable door-to-doctor time: very urgent (immediate), urgent (<15minutes) or normal (<1hour). At the end of the consultation at the ED, the reference standard will be determined for each patient independent of MTS urgency or PEWS, with data available from the patient file. (1) For secondary outcome measures may or may not hospital admission or intensive care admission will be recorded. No interventions are made and this study is of no influence on the treatment of the patients.

Official TitleTriage of Children at the Emergency Department: Manchester Triage System or Pediatric Early Warning Score?
Principal SponsorE.P. de Groot
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

727 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Until 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

EmergenciesPathologic ProcessesPathological Conditions, Signs and SymptomsDisease Attributes

Criteria

1 inclusion criteria required to participate
All children presenting at the Emergency Department of the Isala.

1 exclusion criteria prevent from participating
Children seen in room 17, the plaster and little trauma room (because of practical reasons).

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Isala

Zwolle, NetherlandsOpen Isala in Google Maps
CompletedOne Study Center