Post-Resuscitation Pneumothorax - Analysis of Incidence, Risk Factors and Outcome Relevance

NCT ID: NCT06182007

Last Updated: 2023-12-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

237 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-02-02

Study Completion Date

2022-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

In this retrospective study, the investigators seek to investigate the incidence of pneumothorax following possible risk factors, and elucidate its association with outcomes.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This is a retrospective analysis of routine data, collected by a single Emergency Medical System (EMS). Adult patients (≥18 years) hospitalised after Out-of-Hospital Cardiac Arrest (OHCA) who received chest compressions and underwent chest imaging within 12 hours after hospital admission were included.

Variables and outcomes ascertained are built up of the core elements of the latest version of the Utstein Resuscitation Registry Template for OHCA. This includes sex, age, aetiology of arrest, response times of the first emergency medical service team and emergency physician, witnessed cardiac arrest, bystander CPR/AED, arrest location, first monitored rhythm, defibrillation time, drugs given, reperfusion attempted and target temperature management. Additional variables studied were pre-existing health status represented by the Pre Emergency Status Assessment (PESA), history of lung disease, no-flow-time (time from collapse until initiation of CPR), use of a mechanical chest compression device and prehospital CPR duration.

The primary outcome is incidence of pneumothorax, secondary outcomes are survival to hospital discharge and favourable neurological condition at hospital discharge defined by a cerebral performance category (CPC) of 1 or 2.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cardiac Arrest Pneumothorax Resuscitation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

No Pneumothorax

Patients with no pneumothorax reported from the first chest imaging after hospital admission.

Cardiopulmonary Resuscitation

Intervention Type PROCEDURE

Cardiopulmonary Resuscitation (Advanced Life Support) according to current guidelines

Pneumothorax

Patients with a pneumothorax reported from the first chest imaging after hospital admission.

Cardiopulmonary Resuscitation

Intervention Type PROCEDURE

Cardiopulmonary Resuscitation (Advanced Life Support) according to current guidelines

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Cardiopulmonary Resuscitation

Cardiopulmonary Resuscitation (Advanced Life Support) according to current guidelines

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Hospitalized after out of hospital cardiac arrest
* Chest compressions received
* Chest imaging within the first 12 hours of admission

Exclusion Criteria

* Traumatic cardiac arrest
* Chest trauma/surgery/pneumothorax one month prior to cardiac arrest
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Auinger, Daniel MD

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Auinger, Daniel MD

MD

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Gerhard Prause, Prof.

Role: STUDY_DIRECTOR

Medical University of Graz

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Medical University of Graz

Graz, Styria, Austria

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Austria

References

Explore related publications, articles, or registry entries linked to this study.

Auinger D, Hotzer D, Zajic P, Orlob S, Heschl S, Fida S, Zoidl P, Honnef G, Friedl H, Smolle-Juttner FM, Prause G. Post-resuscitation pneumothorax: retrospective analysis of incidence, risk factors and outcome-relevance. Scand J Trauma Resusc Emerg Med. 2024 Sep 5;32(1):82. doi: 10.1186/s13049-024-01260-8.

Reference Type DERIVED
PMID: 39238051 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

PostCPRptx

Identifier Type: -

Identifier Source: org_study_id