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Clinical Trials/NCT02663505
NCT02663505
Completed
Not Applicable

I See You Risk Your ICU Capacity - Development Of An ICU Risk Score

University Hospital Schleswig-Holstein1 site in 1 country6,918 target enrollmentFebruary 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Development of a Risk Score for ICU Admission
Sponsor
University Hospital Schleswig-Holstein
Enrollment
6918
Locations
1
Primary Endpoint
The necessity of an ICU stay
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Intensive care units are inevitable for high risk surgery and/or high risk patients i.e. patients with severe preconditions. However, usually the capacity of these units is limited such that at times elective surgery has to be postponed if there is no ICU capacity.

The aim of this study is to investigate potential influence/risk factors important for ICU admission in a university hospital in Germany and develop a risk score. In a second phase the risk score for ICU admission will be validated.

Detailed Description

It is one of the core duties of anesthesiologists in our hospital to identify patients with high risk for a post-surgery ICU stay upon hospital admission. We do know that there are two types of factors influencing the possibility of an ICU admission: The patient centered risk e.g. severe preconditions and the surgery centered risk depending on the type of surgery with sometimes high possibility for perioperative complications i.e. bleeding, hemodynamic instability, pulmonary complications etc. However, we do not know the effect size of these factors and, equally important, how they are correlated with one another. The aim of this study is to model the risk of an ICU stay by patient centered and surgery centered influence factors. If a good model is obtained, this can be utilized for allocating ICU capacities in an objective fashion. The study consists of two phases. In the first phase model selection is performed. In the second phase the developed model will be validated on independent data. Data will be gathered by a data collection sheet completed by the responsible anesthesiologists in all elective and emergency surgery during a specific period of time.

Registry
clinicaltrials.gov
Start Date
February 2016
End Date
July 2017
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital Schleswig-Holstein
Responsible Party
Principal Investigator
Principal Investigator

Timo Iden

MD

University Hospital Schleswig-Holstein

Eligibility Criteria

Inclusion Criteria

  • All patients ≥ 18 years receiving surgery in the time frame of data collection with ASA classification status I-IV

Exclusion Criteria

  • Patients \< 18 years
  • ASA classification status \> IV

Outcomes

Primary Outcomes

The necessity of an ICU stay

Time Frame: Immediately after surgery

This is recorded by the responsible anesthesiologist after the completion of surgery.

Study Sites (1)

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