Heart Failure
Conditions
Keywords
Ventricular Assist Device, Cardiac Resynchronization Therapy
Brief summary
Left Ventricular Assist Devices (LVAD) are mechanical heart pumps that are increasingly being implanted in patients with severe heart failure which have failed medical therapy. In patients with LVADs, right ventricular failure, which is not supported by the LVAD pump, is a major problem that affects quality-of-life and survival. Cardiac Resynchronization Therapy (CRT) aims to restore the synchronized contraction of the heart and has proven to be beneficial for improving ejection fraction of both right and left ventricle as well as quality of life in selected heart failure patients. The role of CRT in patients with LVADs is unknown. We hypothesize that CRT can exert a beneficial impact on right ventricular function in LVAD patients and improve their quality-of-life. The specific questions that this study aims to answer are: 1. What are the effects of CRT on the function of the non-supported right ventricle in patients with an implanted LVAD? 2. Can the effects of CRT on cardiac function positively impact quality-of-life and exercise capacity in LVAD recipients? In this study patients with a previously implanted CRT device, who later receives an LVAD, will be randomly assigned to have the CRT turned off (CRT-off) or on (CRT-on). The patients will be followed for an 8-week period, and then switched over to the opposite CRT status. The total participation in this study will last for 16 ± 1 weeks, and will involve 3 clinic visits of approximately 3 hour duration (initial visit, 8 week visit, and 16 week final visit), plus 2 quick checks of the pacemaker/defibrillator in-between the visits. Heart function will be assessed with comprehensive echocardiographic studies during the CRT on and CRT off periods. Quality-of-life and exercise capacity will be assessed with a standardized questionnaire and a 6-Minute Walk Test.
Interventions
DEVICECardiac Resynchronization Therapy
The cardiac resynchronization therapy of the ICD/Pacemaker device of the patients enrolled in the study will be programed under a standardized protocol and enabled or disabled in a crossover fashion during the study.
Sponsors
University of Louisville
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Heart failure patients with previously implanted Bi-Ventricular pacemaker / defibrillator, and continuous flow LVAD (Heart Mate II® or HeartWare®) * The LVAD must be implanted between 8 weeks and 18 months prior to enrollment * Patients should be at least 3 weeks post discharge from the LVAD implant hospitalization
Exclusion criteria
* Severe decompensated right ventricular failure defined as requiring any of the following: * Hospitalization for heart failure within last 30 days * Need for inotropic infusion for \> 48h within the last 14 days * Increase of \> 100% diuretic dose within last 14 days * Severe aortic regurgitation documented by echocardiography or cardiac catheterization * Stage IV or greater kidney disease (GFR \< 30 mL/min/1.73 m2) * Active infection (not including controlled chronic driveline infection on suppressive antibiotic therapy) * Biventricular pacing \< 90 % of time due to uncontrolled arrhythmias * LVAD malfunction * Inability to follow study protocol * Non-functional LV lead (i.e. high capture threshold that cannot be corrected with programming changes)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Right ventricular function | 8 weeks | The primary cardiac performance endpoint is global longitudinal right ventricular (RV) function assessed by myocardial strain analysis using Speckle Tracking Echocardiography (STE). Other traditional echocardiographic RV function indexes will also be evaluated. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Functional capacity | 8 weeks | Will be assessed by 6-Minute Walk Test |
Other
| Measure | Time frame | Description |
|---|---|---|
| Quality-of-Life | 8 weeks | Assessed by standardized self administered Minnesota Living with Heart Failure Questionnaire (MLHFQ) |
Countries
United States
Outcome results
None listed