MedPath

Optimized Admission to the Intensive Care Unit by Using Crisis Resource Management (CRM)

Not Applicable
Conditions
Critical Illness
Interventions
Behavioral: Structured admission procedure
Registration Number
NCT03268967
Lead Sponsor
Hillerod Hospital, Denmark
Brief Summary

Admission to the intensive care unit (ICU) is vital for surviving critical illness. An admission to ICU without having a consistent structure, structured review of the patient and a solid team organization lead to unclear communication and responsibility. Factors that correlate with patient acceptance and safety, morbidity and mortality. The hypothesize was that a structured admission can improve patients safety, reduce delays in treatment, reduce ICU length of stay, and improve mortality rate. The overall objective was to optimize patient safety, and effectively use available resources to reduce admission time, delays in treatment and procedures and mortality by using both quantitative and qualitative methods.

Detailed Description

The quantitative before-data is a one-year observational period prior to the intervention measured by different perspectives; patients and staff outcomes.

After the intervention, was qualititive data collected from participants, who received simulation training.

The quantitative after-data is a one-year observational period post-intervention with same outcomes as before starting the intervention.

Data is already collected registry data from hospital quality assurance board. Data will be compared before and after with assessor blinded analysis. Missing data will not be replaced but reported as missing.

The investigators will try to compare the results with data from an approximately comparative ICU in Denmark due to the implementation of a new patient management system called the Health Portal.

The statistical analysis plan is based on descriptive and comparative analyses of the group before and after the trial. The quantitative results are explained in in-depths description from participants.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
1800
Inclusion Criteria
  • ICU admissions
Exclusion Criteria
  • None
  • Drop-out are deaths

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Structured Admission procedureStructured admission procedureAfter implementation of a structured admission procedure to all ICU patients inspired by principles of Crisis Resource Management, Closed loop communication, action cards, and staff simulation training
Primary Outcome Measures
NameTimeMethod
ICU length of stay (LOS)through study completion, an average of 1 year

Days admitted at the ICU using registre data

Secondary Outcome Measures
NameTimeMethod
Ventilated associated pneumonia (VAP)through study completion, an average of 1 year

Number of VAP measured by registre data

90-days Mortality90 days through study completion, an average of 1 year

90-days mortality rates after ICU discharge measured by registre data

Hospital length of stay (LOS)At Hospital discharge within one-year before and after the intervention implementation

Days admitted to the hospital using registre data

Re-intubationsthrough study completion, an average of 1 year

Number of re-intubations measured by registre data

Staff turn-overthrough study completion, an average of 1 year

Staff turn-over before and after the intervention measured by registre data

Line Sepsisthrough study completion, an average of 1 year

Treatment package of number of the line sepsis after ICU admission covering the number of patients with line sepsis using registre data on Lactat \<1 hour, bacteria samples ≤1 hour taken, time between diagnosis of sepsis and taken bacteria samples, time between diagnosis and given antibiotics measured by registre data

30-days Mortality30 days through study completion, an average of 1 year

30-days mortality rates after ICU discharge measured by registre data

Sick Leavethrough study completion, an average of 1 year

Sick leave amongst staff members measured by registre data

Trial Locations

Locations (1)

Department of Anaestesiology

🇩🇰

Holbæk, Denmark

© Copyright 2025. All Rights Reserved by MedPath