Heart Failure Clinical Trial
Official title:
Multi-Modality Imaging Assessment for Pacing Interventions in Heart Failure: Targeting Optimal Sites and Outcomes
Patients with heart failure and cardiomyopathy that have been referred for Cardiac Resynchronization Therapy (CRT) will have their CRT devices implanted using an image guided treatment plan for optimal lead delivery. The validation of image-guided CRT lead delivery will significantly advance the field of heart failure therapy.
Objective 1: Using established study data from our previous study (Multimodality imaging
Assessment of Pacing InTervention in Heart Failure Heart Failure or MAPIT HF) define
characteristics of the "optimal myocardial target" that maximally yields clinical response to
CRT.
Objective 2: Using established MAPIT-HF study data identify whether alternate coronary venous
pathways to "optimal myocardial targets" exists in clinical non-responders.
Objective 3: Evaluate the feasibility of guiding the delivery of CRT leads to "optimal
myocardial targets" through the use of an interactive, 3D "integrated cardiac model" of
coronary vein anatomy, myocardial scar and mechanical dyssynchrony.
Currently there is no standard definition for response to CRT. Of importance is that measures
of clinical response appear to be incongruent with echocardiographic parameters of reverse
remodeling following CRT. The primary endpoint of clinical response will be an improvement in
Left ventricular end systolic volume (LVESV) by ≥ 15% at 3 months following CRT, as validated
in prior studies. Secondary clinical endpoints will also be evaluated; 1) Improvement in
ejection fraction ≥ 5 percentage points, 2) Improvement in 6-minute hall walk ≥ 30 meters or
≥ 10%, 3) Improvement in NYHA (New York Heart Association) functional class by 1, or Specific
Activity Score by 1, and 4) Improvement in Quality of Life (Minnesota Living with Heart
Failure) by 10 points.
Our hypothesis is that a single 3D dataset can be developed from multiple MRI datasets for
the simultaneous display of coronary venous anatomy, myocardial scar, and mechanical
dyssynchrony, the latter being derived from tagged MRI data. The investigators hypothesize
that the availability of this 3D model during fluoroscopic CRT lead placement will result in
improved rates of lead tip delivery to "optimal myocardial targets" and improved clinical
response. Our specific hypotheses of Project 2 are as follows;
1. The generation of an integrated cardiac model of venous anatomy, myocardial scar and
dyssynchrony is feasible using multiple MRI-derived datasets.
2. The availability of this interactive 3D cardiac model during fluoroscopic CRT lead
delivery will increase the occurrence of CRT lead tips being delivered to "optimal
myocardial segments" when compared to historic control data within the MAPIT-HF study
cohort.
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