Impact of Hemodynamic Ramp Test-Guided HVAD RPM and Medication Adjustments on Exercise Tolerance and Quality of Life
- Conditions
- Continous Flow Left Ventricular Device
- Interventions
- Procedure: Hemodynamic-Echo Ramp Testing -Procedure: Echo Guided Testing
- Registration Number
- NCT03021239
- Lead Sponsor
- University of Chicago
- Brief Summary
The main purpose of this study is to compare Echo-guided testing to the Hemodynamic-Echo Ramp Tests to determine which method of testing provides better information for adjusting pump speed and medical treatment for Left Ventricular Assist Device (LVAD) patients. Better adjustments may provide better quality of life, exercise tolerance and reduced unwanted cardiac events over a 6-month period.
- Detailed Description
All Left Ventricular Assist Device (LVAD)patients undergo testing to determine the best pumping speed for their Left Ventricular Assist Device (LVAD) and to gather measurements that help guide medical treatment. The testing uses echocardiography ("echo", ultrasound images of the heart) to create heart images and make measurements while gradually increasing the Left Ventricular Assist Device (LVAD) heart pump speed. Each time the pump speed is increased, images and measurements are taken. This is called a ramp test.
The ramp testing may also be performed during a right heart catheterization procedure. In a catheterization procedure, a doctor inserts a thin, flexible tube (catheter) into a vein or artery in the upper leg (groin), arm or neck and guides it to the heart using X-ray imaging. Doctors normally perform this procedure to measure the pressure and blood flow in the heart (otherwise called hemodynamic measurements). If the ramp testing is performed during this procedure, then the doctors have additional measurements to consider before choosing a final speed for the Left Ventricular Assist Device (LVAD) pump and appropriate medical treatment.
All of the procedures in this study are considered standard of care. The research part is randomly assigning the subject to one of the two methods of testing in this study. Subjects have a 50/50 chance of being in either testing group.
Baseline Visit (1 - 3 months after Left Ventricular Assist Device (LVAD) implant)
The following will be performed:
* Subjects will be asked to sign this consent form.
* Physical exam with an assessment of heart failure symptoms, and medical history will be recorded
* Routine blood tests (about 1 tablespoon will be drawn)
* Subjects will be randomly assigned to one of the two testing groups. If there is time, the ramp test can be performed at this visit, but usually it will be scheduled to occur a different day in about 1 to 4 weeks.
* 6 Minute Walk Test. This test measures how far the subject can walk in 6 minutes. If needed, this can be completed the day of the ramp test.
* Subjects will be asked to complete a questionnaire about their current quality of life. This will take about 10 minutes. If needed, this can be completed the day of the ramp test.
Ramp Testing Groups:
1. Echo Guided Testing - This testing uses echocardiography to create images of the heart and make measurements while gradually increasing the heart pump speed. The final pump speed and medical treatment are determined using the echo measurements. This will take about 45 minutes.
OR
2. Hemodynamic-Echo Ramp Testing - This testing is performed during a right heart catheterization procedure which provides hemodynamic measurements (pressure and blood flow) in addition to the echocardiography measurements. With this method, more echo images and measurements are taken. The final pump speed and medical treatment adjustments are made using the hemodynamic measurements as well as the information from the echo. This test will take about 1 hour and 45 minutes.
6 Months after Baseline Visit
The following will be performed:
* Physical exam with an assessment of heart failure symptoms, and medical history will be recorded
* Routine blood tests (about 1 tablespoon will be drawn)
* 6 Minute Walk Test. This test measures how far the subject can walk in 6 minutes.
* Subjects will be asked to complete a questionnaire about their current quality of life. This will take about 10 minutes.
* All subjects will undergo a Hemodynamic-Echo Ramp Test at 6 months after the baseline visit.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- Patient older than 18 years
- Newly implanted HVAD
- HVAD support anticipated for at least 6 months
- Patient is ambulatory and discharged from hospital without inotropes
- Patient is between 1 and 3 months post implant
- Patient has not had a right heart catheterization since discharged from HVAD implantation hospitalization
- The current HVAD is a replacement device
- Patients currently has Right Ventricle (RV) failure requiring home inotropes
- Inability to preformed right heart cath
- Inadequate echocardiographic windows
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description 1) Echo Guided Testing - Hemodynamic-Echo Ramp Testing - This testing uses echocardiography to create images of the heart and make measurements while gradually increasing the heart pump speed. The final pump speed and medical treatment are determined using the echo measurements. This will take about 45 minutes. 2) Hemodynamic-Echo Ramp Testing - Echo Guided Testing This testing is performed during a right heart catheterization procedure which provides hemodynamic measurements (pressure and blood flow) in addition to the echocardiography measurements. With this method, more echo images and measurements are taken. The final pump speed and medical treatment adjustments are made using the hemodynamic measurements as well as the information from the echo. This test will take about 1 hour and 45 minutes.
- Primary Outcome Measures
Name Time Method Clinical parameters most likely to be impacted by hemodynamic-echo ramp tests 6 Months 6 Walk Test
New York Heart Association (NYHA) Class 6 Months Heart Failure Readmission 6 Months Composite end-point of heart failure readmission.
Quality of Life: Kansas City Cardiomyopathy Questionnaire (KCCQ) 6 Months Kansas City Cardiomyopathy Questionnaire (KCCQ) a summary score can be derived from the physical function, symptom (frequency and severity), social function and quality of life domains in which scores are transformed to a range of 0-100.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (8)
Stanford Medical Center
🇺🇸Stanford, California, United States
Northwestern University
🇺🇸Chicago, Illinois, United States
UC San Diego Medical Center
🇺🇸San Diego, California, United States
The University of Chicago
🇺🇸Chicago, Illinois, United States
Hospital of the University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States
University of Pittsburgh Medical Center
🇺🇸Pittsburgh, Pennsylvania, United States
University of Washington School of Medicine
🇺🇸Seattle, Washington, United States
Montefiore Medical Center
🇺🇸Bronx, New York, United States