Retrospective Study of Airway Management in Dutch ED's

NCT ID: NCT06374030

Last Updated: 2024-07-03

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 1000 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-01-01
• Study Completion Date: 2024-12-31

Brief Summary

Describing characteristics of the practice of airway management in Dutch emergency departments, including information about patient demographics, indications, performer characteristics, equipment and medication used and complications due to intubation.

Detailed Description

Endotracheal intubation can be a lifesaving intervention for critically ill patients in the emergency department (ED). Endotracheal intubation is, however, a high-risk procedure with many potential complications, which seem to be even more prevalent when carried out in the ED compared to for example the operating theater. This is possibly due to multiple reasons such as a sicker population, non-elective setting, a higher variability among indications for intubation or competence of providers.

Internationally, large registries were established and multiple observational studies have been performed to gain more information about the methods, safety and complications of intubations in the ED. While in recent years these studies have added to our knowledge of ED airway management, there is still a lack of high-quality studies and there is a strong argument for increased research. To date, no studies have been published of airway management in Dutch EDs. The investigators therefore have no knowledge about any factors possibly influencing intubation outcomes and complications nor comparability with international data. Among these are factors that have been associated with preventable harm and death and insight into these factors could be used for improvement of the safety of airway management in Dutch EDs.

This study is therefore intended to provide a comprehensive review of the clinical practice and characteristics of endotracheal intubations within Dutch EDs. The results could potentially be used for comparative analysis against global datasets. Additionally, the insights gained from this study will shed light on existing gaps prevalent in the current registration processes of intubations in the Netherlands. Furthermore, these insights could act as a stepping stone for future investigations that can lead to a deeper understanding of the methodologies, safety protocols, and associated complications of endotracheal intubations within Dutch EDs

Conditions

Endotracheal Intubation

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: RETROSPECTIVE

Study Groups

patients who underwent the intervention of endotracheal intubation

Inclusion criteria:

All patients who underwent endotracheal intubation between 01-01-2019 and 31-12-2023 in the participating ED's.

Exclusion criteria:

Patients for which no information about the intubation can be found in the electronic patient chart will be excluded from the study.

Endotracheal intubation

Intervention Type: PROCEDURE

All endotracheal intubations carried out in the emergency department of one of the participating hospitals in the time period 01-01-2019 - 31-12-2023

Interventions

Endotracheal intubation

All endotracheal intubations carried out in the emergency department of one of the participating hospitals in the time period 01-01-2019 - 31-12-2023

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• All patients who underwent endotracheal intubation between 01-01-2019 and 31-12-2023 in the participating ED's

Exclusion Criteria

• Patients for which no information about the intubation can be found in the electronic patient chart will be excluded from the study.

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

VieCuri Medical Centre

OTHER

Sponsor Role: collaborator

Catharina Ziekenhuis Eindhoven

OTHER

Sponsor Role: collaborator

Rijnstate Hospital

OTHER

Sponsor Role: collaborator

Zuyderland Medical Centre

OTHER

Sponsor Role: collaborator

Frisius Medisch Centrum

OTHER

Sponsor Role: lead

Responsible Party

Peter Veldhuis

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Leeuwarden Medical Centre

Leeuwarden, , Netherlands

Site Status: RECRUITING

Countries

Netherlands

Central Contacts

Peter Veldhuis, MD

Role: CONTACT

peter.veldhuis@mcl.nl

+3158 286 6666

Facility Contacts

Peter Veldhuis, MD

Role: primary

peter.veldhuis@mcl.nl

+3158 286 6666

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

EDSAM2024

Identifier Type: -

Identifier Source: org_study_id