SHORTness of Breath In the Emergency Department (SHORTIE)



Status:Completed
Conditions:Cardiology, Cardiology, Pulmonary
Therapuetic Areas:Cardiology / Vascular Diseases, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:April 2005
End Date:August 2007

Use our guide to learn which trials are right for you!

SHORTIE is a two-phase study to determine the impact of the Triage Profiler S.O.B.
(Shortness Of Breath) Panel on patient management, outcome, and cost.

Patients presenting to the ED with a primary complaint of shortness of breath will a have
blood sample collected at enrollment and tested using the Triage® Profiler S.O.B. Panel
(measuring creatine kinase MB [CK-MB], myoglobin, troponin I, B-type natriuretic peptide
[BNP], D-dimer). The test is used as an aid in the diagnosis of myocardial infarction (MI),
an aid in the diagnosis and assessment of severity of heart failure (HF), and an aid in the
assessment and evaluation of disseminated intravascular coagulation including pulmonary
embolism (PE). Phase I is an observational study and results of the Triage Profiler S.O.B.
panel will be blinded to all attending physicians and health care workers. In Phase II,
patients will be assigned to either the experimental arm or the control arm of the study. In
the experimental arm, the Triage Profiler S.O.B. Panel results will be available to the
treating physician and can be incorporated into the decision making process. In the control
arm, treating physicians and staff will be blinded to the Triage Profiler S.O.B. Panel
results. Time to appropriate treatment, length of ED stay, patient outcome and hospital
costs will be assessed in all patients and used to determine the impact of Triage Profiler
S.O.B Panel on these parameters. Furthermore, the diagnostic accuracy of the Triage Profiler
S.O.B Panel will be calculated.

Inclusion Criteria:

- Age 18 and older.

- Visit to the ED is due to a primary complaint of shortness of breath alone or
shortness of breath with associated chest pain, cough or edema.

Exclusion Criteria:

- Blood sample cannot be collected before treatment is initiated, specifically CPR or
treatment with i.v. diuretics, injectable anticoagulants, thrombolytics

- Patient is unwilling or unable to give consent to participate in the study

- Patient has renal disease requiring dialysis

- Patients with a clear exacerbation of isolated asthma

- Patients with trauma that interferes with normal breathing function
We found this trial at
5
sites
3400 Spruce St
Philadelphia, Pennsylvania 19104
 (215) 662-4000
Hospital of the University of Pennsylvania The Hospital of the University of Pennsylvania (HUP) is...
?
mi
from
Philadelphia, PA
Click here to add this to my saved trials
506 6th St
Brooklyn, New York 11215
(718) 780-3000
New York Methodist Hospital A voluntary, acute-care teaching hospital, New York Methodist Hospital's mission is...
?
mi
from
Brooklyn, NY
Click here to add this to my saved trials
Durham, North Carolina 27710
?
mi
from
Durham, NC
Click here to add this to my saved trials
Stony Brook, New York 11794
?
mi
from
Stony Brook, NY
Click here to add this to my saved trials
Worcester, Massachusetts 01655
?
mi
from
Worcester, MA
Click here to add this to my saved trials