Heart Failure Clinical Trial

Assessing Outcomes in ED Patients With RV Failure

Summary

Millions of Americans seek emergency care for acute shortness of breath, and many undergo computerized tomographic pulmonary angiography (CTPA) testing that is negative for acute disease. Management of patients with persistent shortness of breath despite normal testing continues to pose a challenge for clinicians. Right ventricular (RV) failure is a common cause of dyspnea that brings patients to the emergency department (ED), however, it is often not considered in the differential diagnosis, remains unrecognized, or patients are not properly followed up once diagnosed. Delays in diagnosis and management of RV failure are associated with poor outcomes. The investigators propose a novel clinical pathway, which entails identifying and enrolling patients with RV failure in the ED, then referring them to a specialized cardiovascular clinic where they will receive a standardized evaluation and management plan. Our hypothesis is that management of RV failure, through this pathway, will improve patient outcomes when compared to standard care. The primary outcome will assess 1-year unscheduled healthcare visits.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

adult patients > 18 years old,
with a non-significant CTPA scan (i.e. no acute disease), dyspnea PLUS an emergency physician performed echocardiogram with isolated RV failure OR CTPA scan with evidence of pulmonary hypertension OR comprehensive echocardiogram within 3 months of index hospital visit showing isolated RV dysfunction

Exclusion Criteria:

Currently being evaluated and/or treated for RV failure or PH,
those unable to have a comprehensive echocardiography performed,
those with indeterminate RV function OR LV dysfunction on comprehensive echocardiography, and
those patients with circumstances where they may be lost to follow-up (homeless, prisoner, severe psychiatric disorder, no reliable contact information).

Study is for people with:

Heart Failure

Estimated Enrollment:

2

Study ID:

NCT03073629

Recruitment Status:

Terminated

Sponsor:

Indiana University

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There is 1 Location for this study

See Locations Near You

Methodist Hospital
Indianapolis Indiana, 46203, United States

How clear is this clinincal trial information?

Study is for people with:

Heart Failure

Estimated Enrollment:

2

Study ID:

NCT03073629

Recruitment Status:

Terminated

Sponsor:


Indiana University

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider