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The analysis of Medical Emergency Teams in the Netherlands, a multi center approach. The COMET study.

Analysis of effectiveness and associated costs of implementing a Rapid Response System (RRS).

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23531
Enrollment
27720
Registered
2011-01-19
Start date
2009-04-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Deteriorating patient Medical Emergency Team Rapid Response System Rapid Response Team Modified Early Warning Score MEWS Situation-Background-Assessment-Recommendation SBAR

Interventions

Following a baseline measurements phase of five months, the MEWS and SBAR instruments are implemented and primary endpoints are measured for seven months. Measurements of vital parameters is protocoli

Sponsors

Funding is provided by the participating centers and primarily from the Academic Medical Center in Amsterdam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All adult patients admitted to the study wards and all primary outcomes are included if transpired on nursing wards.

Exclusion criteria

Exclusion criteria: Outcomes on higher care wards like Medium Care, Intensive Care etc. are excluded from analysis.

Design outcomes

Primary

MeasureTime frame
1. Cardiac arrest rate; 2. Unplanned ICU admission rate (following the NICE registry); 3. Unexpected death rate. These endpoints will be analyzed as a composite endpoint and as separate outcomes. Rate is defined as number of outcomes per 1000 admitted patients.

Secondary

MeasureTime frame
1. Total mortality (irrespective of code); 2. Hospital Length of Stay (LOS); 3. ICU length of stay; 4. Number of RRT calls per 1000 admitted; 5. Costs from a hospital perspective.

Contacts

Public ContactJeroen Ludikhuize

PO Box 22660

J.Ludikhuize@amc.uva.nl+31 (0)20 5665991

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)