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

Hillerod Hospital, Denmark

Status: Unknown

Conditions: Critical Illness

Treatments: Behavioral: Structured admission procedure

Study type: Interventional

Funder types: Other

Identifiers

NCT03268967

113581

Details and patient eligibility

About

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.

Full 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.

Enrollment: 1,800 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• ICU admissions

Exclusion criteria

• None
• Drop-out are deaths

Trial design

Primary purpose: Health Services Research

Allocation: Non-Randomized

Interventional model: Sequential Assignment

Masking: Single Blind

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1,800 participants in 2 patient groups

Structured Admission procedure

Active Comparator group

Description:

After 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

Treatment:

Behavioral: Structured admission procedure

Standard Care

No Intervention group

Description:

Randomly admission procedure to all ICU patients based on the clinicians' evaluation prior implementation of the intervention.