Clinical Trials Directory

Trials / Completed

CompletedNCT02663505

Development of an ICU Risk Score

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

Status
Completed
Phase
Study type
Observational
Enrollment
6,918 (actual)
Sponsor
University Hospital Schleswig-Holstein · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREPatients receiving the surgery planned for themFor each patient the following potential influence (risk) factors are documented: sex, urgency of the operation, BMI, age, ASA classification, preconditions, physical fitness, Hb value. In phase 2 only selected influence factors will be recorded. No intervention will be performed apart from the surgery planned for each patient.

Timeline

Start date
2016-02-01
Primary completion
2017-07-01
Completion
2017-07-01
First posted
2016-01-26
Last updated
2018-01-25

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02663505. Inclusion in this directory is not an endorsement.