In the Netherlands, TEE is currently not used in emergency departments during cardiac arrest. The purpose of this study is to investigate if point-of-care TEE can be used effectively and safely in patients with cardiac arrest.
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
Alle aandoeningen leidend tot een reanimatiesetting.
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The percentage of patients with cardiac arrest in which providers are able to
determine the AMC with the use of TEE.
Secondary outcome
- The AMC location during cardiac arrest
- The accuracy of reported AMC
- Safety of using TEE in patients with cardiac arrest in the ED
- Need for intubation and prolonged intubation attempts
- Time from start ED treatment to first images
Background summary
Point-of-care ultrasound is a valuable diagnostic tool during cardiopulmonary
resuscitation (CPR) in cardiac arrest and its use is recommended by
international guidelines. Transthoracic echocardiography (TTE) is most commonly
used, but has certain limitations. Image acquisition can be challenging due to
patient specific factors such as body habitus. Also image quality may be
impacted by the limited acquisition time during CPR pulse checks. Furthermore,
observational data suggests that pulse checks are prolonged due to TTE, while
minimizing interruption of chest compressions is emphasized for better CPR
outcomes in the guidelines. Transesophageal ultrasound (TEE) is a possible
alternative for TTE. It has the theoretical advantage of superior image quality
and thereby possible reductions of chest compression delays. Furthermore, TEE
gives the opportunity determine which part of the heart is compressed most
effectively, which is referred to as the area of maximal compression (AMC).
Animal studies showed that an AMC located over the left ventricle positively
influenced hemodynamics and return of spontaneous circulation (ROSC) compared
to an AMC over the aortic root. In human studies, data also suggests that AMC
located on the left ventricle, as measured by TEE, may positively influence
prognosis.
In the Netherlands, TEE is currently not used in emergency departments during
cardiac arrest. The purpose of this study is to investigate if point-of-care
TEE can be used effectively and safely by providers and teams that have not
previously used this modality. Given the paramount importance of quality of
chest compressions, the ability of the providers to assess the location of the
AMC will be the main focus of this feasibility study.
Study objective
In the Netherlands, TEE is currently not used in emergency departments during
cardiac arrest. The purpose of this study is to investigate if point-of-care
TEE can be used effectively and safely in patients with cardiac arrest.
Study design
Prospective observational feasibility study.
Intervention
Point-of-care transoesophageal echocardiography will be used as diagnostic
modality during cardiac arrest.
Study burden and risks
TEE will be used during the study period during cardiac arrest. TEE is widely
used in the hospital in multiple departments. In previous studies concerning
the use of TEE during cardiac arrest no complications of TEE have been
reported. While rare, complications of the use of TEE in general have been
reported. The potential risks are described in more detail in section 4 and 6
of the protocol. The possible benefits include superior diagnostic
characteristics, shorter compression pauses, continuous assessment and
enhancement of chest compressions (see section 1 of the protocol).
Henri Dunantweg 2
Leeuwarden 8934 AD
NL
Henri Dunantweg 2
Leeuwarden 8934 AD
NL
Listed location countries
Age
Inclusion criteria
Cardiac arrest patients in the emergency department.
Exclusion criteria
Patients <18 years old
Pregnant patients
Traumatic cardiac arrest
Increased risk of esophageal trauma (malignancy or stricture of the upper
gastro-intestinal tract. previous radiation or surgery of the esophagus,
esophageal varices)
Do not resuscitate order
Design
Recruitment
Medical products/devices used
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL84790.099.24 |