Syncope
Conditions
Keywords
syncope, point of care, ultrasound, echocardiography
Brief summary
The purpose of this study is to determine whether point-of-care (bedside) ultrasound assists physicians in the evaluation and management of patients with syncope.
Detailed description
Syncope is one of the more common presentations to the Emergency Department, representing between 1.2-1.5% of all evaluated patients and up to 6% of admissions. Due to an often broad and overlapping differential diagnosis, syncope represents a disease entity that often requires extensive workup. This typically involves laboratory tests, EKGs, x-rays, computed tomography, or other studies that are costly, time-consuming, and, in the case of diagnostic imaging, frequently involves ionizing radiation. Yet, despite extensive testing, an exact diagnosis is not made in up to 50% of cases. Cardiac causes of syncope include myocardial infarction, pericardial effusion, volume depletion, arrhythmia, among other entities, many of which are life threatening. Echocardiography (cardiac ultrasound) has been used for inpatient syncope evaluations for several decades. In the Emergency Department, echocardiography is currently being used at the point-of-care (POC) in a limited and focused approach to a variety of conditions. However, POC ultrasound has never been systematically evaluated as a diagnostic or prognostic tool specifically for syncope in the Emergency Department. We aim to determine if an ultrasound-based protocol is effective as an adjunct in the evaluation of syncope. Our research study will examine the utility of POC ultrasound in the diagnosis, imaging and laboratory utilization, and prognosis of syncope in the Emergency Department.
Interventions
OTHERPoint-of-Care Ultrasound
Performance of a focused cardiac ultrasound including a qualitative assessment of left ventricular function, pericardial effusion, right ventricular strain, proximal ascending aortic diameter, and inferior vena cava size and collapsibility
Sponsors
Yale University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 18 years and older presenting to the ED with acute syncope (defined as transient loss of consciousness) or near syncope (sensation of impending but not actual loss of consciousness) as a reason for ED visit.
Exclusion criteria
* persistent altered mental status * alcohol or illicit drug-related loss of consciousness * definite seizure, and transient loss of consciousness caused by head trauma.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to Final Emergency Department Disposition | Time at which an admit or discharge order is placed within the electronic medical record (estimated 2-3 hours) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time to therapeutic intervention | At onset of therapeutic interventions including but not limited to intravenous fluids and medications (estimated time frame 0 - 6 hours) | — |
| Time to clinical procedure | At onset of clinical procedures including but not limited to central line placement, pericardiocentesis, thoracentesis, etc. (estimated time frame 0-6 hours) | — |
| Number and Type of other imaging studies | End of Emergency Department Encounter (estimated time frame 1- 6 hours) | Other imaging studies to included radiographs, additional point-of-care ultrasound, computed tomography, etc. |
| Number and type of laboratory studies | estimated time frame 0-6 hours | — |
| Number of and time to consultant services | estimated time frame (0-6 hours) | Number of consults obtained and the time frame in which the consults were performed |
| Information Content provided by Point-of-Care Ultrasound | After performance of point-of-care ultrasound (estimated time frame 1- 6 hours) | calculating from pre and post test probability estimates and the number of diagnoses |
Other
| Measure | Time frame | Description |
|---|---|---|
| Short Term Adverse Outcome | 7 days from Emergency Department Visit | Adverse outcome defined as death, myocardial infarction, arrhythmia, pulmonary embolism, stroke, subarachnoid hemorrhage, significant hemorrhage, or any condition causing a return ED visit and hospitalization for a related event. |
Countries
United States
Outcome results
None listed