PREDIHCA: Prediction of Intrahospital Cardiac Arrest Outcomes

Sponsor
Kepler University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05466188
Collaborator
(none)
668
1
2
338.9

Study Details

Study Description

Brief Summary

Intrahospital cardiovascular arrest is one of the most common causes of death in hospitalized patients. In contrast to extramural cases of cardiovascular arrest, hospitalized patients often have severe medical conditions that can affect the outcome of resuscitation. Nevertheless, survival rates from resuscitation are better in hospitals than outside, because there is often a rapid start of resuscitation measures and predefined resuscitation standards. Regular CPR training and the availability of defibrillators in all bedside units can also positively influence outcome. Despite these many efforts, survival rates, especially of patients with good neurological outcome, remained stable at low levels even within hospitals in recent years and did not improve.

Most outcome parameters are nowadays well known. (e.g., initial rhythm, age, early defibrillation, etc.) Nevertheless, we still do not know today how relevant the corresponding factors actually are, especially in relation to each other. One approach to this might be machine learning methods such as "random forest", which might be able to create a predictive model. However, this has not been attempted to date.

The hypothesis of this work is to find out if it is possible to accurately predict the probability of surviving an in-hospital resuscitation using the machine learning method "random forest" and if particularly relevant outcome parameters can be identified.

Design: retrospective data analysis of all data sets recorded in the resuscitation register of Kepler University Hospital.

Measures and Procedure: Review of the registry for missing data as well as false alarms of the CPR team and, if necessary, exclusion of these data sets; evaluation of the data sets using the machine learning method random forest.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: CPC

Study Design

Study Type:
Observational
Actual Enrollment :
668 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Prediction of Intrahospital Cardiac Arrest Outcomes
Actual Study Start Date :
Jun 1, 2022
Actual Primary Completion Date :
Jul 31, 2022
Actual Study Completion Date :
Jul 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Outcome CPC Positive

Outcome CPC Positive

Diagnostic Test: CPC
CPC

Outcome CPC Negative

Outcome CPC Negative

Diagnostic Test: CPC
CPC

Outcome Measures

Primary Outcome Measures

  1. AUROC for Classification of Outcome CPC [2006-01-01 to 2018-12-31]

    AUROC for Classification of Outcome CPC

Secondary Outcome Measures

  1. Confusion Matrix [2006-01-01 to 2018-12-31]

    Confusion Matrix Results: true positives, true negatives, false positive, false negatives and values calculated from these results.

  2. Descriptive Statistics [2006-01-01 to 2018-12-31]

    Descriptive Statistics (age in years, delay in seconds, gender as male/female, agonal breathing/initial rhythm/airway management/iv-access/witnessed cardiac arrest/use of AED/chest compressions as binary features) This outcome measure will compare the individual feature (e. g. height in cm) in one group vs. the other. Significant difference will be described by p-value.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • All adults patients suffering cardiac arrest and having been resuscitated by the medical emergency team of the Kepler University Hospital, Linz, Austria in the period of 2006-01-01 to 2018-10-31.
Exclusion Criteria:
  • None.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Kepler University Hospital Linz Upper Austria Austria 4021

Sponsors and Collaborators

  • Kepler University Hospital

Investigators

  • Principal Investigator: Thomas Tschoellitsch, MD, Kepler University Hospital and Johannes Kepler University, Linz, Austria

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kepler University Hospital
ClinicalTrials.gov Identifier:
NCT05466188
Other Study ID Numbers:
  • PREDIHCA
First Posted:
Jul 20, 2022
Last Update Posted:
Aug 17, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 17, 2022