Heart Failure and Risk of Re-Admissions Determined by Abnormal REVEAL Parameters
| Status: | Recruiting |
|---|---|
| Conditions: | Cardiology |
| Therapuetic Areas: | Cardiology / Vascular Diseases |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 11/18/2012 |
| Start Date: | May 2011 |
| Contact: | David J Whellan, MD |
| Email: | david.whellan@jefferson.edu |
| Phone: | 215-955-2007 |
Phase 4 Registry Study Will Evaluate the Ability of Cardiac Rhythm (Cardiac Compass) Data to Predict Future Cardiac Events in Heart Failure (HF) Patients Recently Discharged After a Hospitalization for Heart Failure Who Have or Plan to Have a Implanted Loop Recorder (ILR), Specifically, the Reveal XT Device.
The purpose of the Heart Failure and Risk of re-Admissions Determined by Abnormal REVEAL
Parameters (HF RADAR) study is to evaluate the ability of cardiac rhythm (Cardiac Compass)
data to predict future cardiac events in heart failure (HF) patients recently discharged
after a hospitalization for heart failure who have or plan to have a implanted loop recorder
(ILR), specifically, the Reveal XT device. The study will enroll 40 HF patients (with LV
function ≥ 40%) admitted to an acute care facility (observation status or hospital stay) for
heart failure who either have a Reveal XT device in place or plan to have the ILR device
inserted for clinical indication within 14 days of discharge from the hospitalization. HF
patients will be followed for 6 months. Device date will be captured during normal clinic
visits and at 6 months.
Inclusion Criteria:
1. Men and non-pregnant/non lactating women ≥ 18 years.
2. Admission to hospital or observation unit for worsening heart failure.
3. Has a Reveal XT device or has plans for a device implant for a clinical indication
within 14 days of discharge.
4. Ejection fraction ≥40% by echocardiogram within 6 months of enrollment
5. Able to participate in the study for at least 6 months.
6. Not currently enrolled in another study.
7. Able to provide informed consent and complete scheduled study visits.
Exclusion Criteria:
1. Has a clinical indication for a therapeutic cardiac device (pacemaker or
defibrillator)
2. History of permanent atrial fibrillation or atrial flutter.
3. History of uncontrolled hypertension (high blood pressure)
4. Has a previously implanted cardiac device (pacemaker or defibrillator) in place.
5. Stage IV or V chronic renal dysfunction (estimated GFR <25 ml/min per 1.73 m2)
6. End-stage (Stage D) HF, including chronic ionotropic drugs infusions or left
ventricular assist device
7. Waiting on the transplant list as an UNOS status 1A or 1B patient
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