Heart failure is a common condition, and the number of people with advanced disease continues to increase. We need new treatments that improve patients' symptoms and extend life. Recently the new CircuLite Synergy pump has come into use. It is the smallest pump manufactured to date and does not cover the full work of the heart, instead providing "partial" support. One interesting thing about this is that taking some strain off the heart might allow the muscle to repair and rebuild its own strength. This process is called reverse remodelling, and is the topic of this research. Our hypothesis is that "partial" support improves patients' symptoms and causes improvement in heart muscle function. We also want to examine the best techniques for assessing this, including new scanning and molecular tests, and study some practical aspects of the pump to do with blood clotting.
The CircuLite Synergy pump is a new minimally-invasive partial support left ventricular assist device (LVAD) that pumps blood from the left atrium to the right subclavian artery. Ex vivo pilot data suggests that the Synergy pump induces structural reverse remodelling, which proposes the Synergy device as a new disease-modifying therapy. We will assess whether the Synergy pump facilitates functional, structural and molecular LV reverse remodelling in vivo; assess how this can be determined and predicted by analysis of circulating micro RNA profiles and specific echocardiographic parameters; and evaluate the haematological abnormalities associated with this new LVAD. We will address these questions with a prospective, observational study comparing patients implanted with the Synergy device with matched heart failure controls. The two study centres will be Royal Brompton \& Harefield NHS Foundation Trust (Harefield Hospital) and University Hospitals Leuven, Belgium. We will recruit a total of 64 patients. The primary outcome will be change in peak VO2 at 6 months. Secondary outcomes will include functional parameters, profiling of circulating microRNA, multimodal echocardiographic assessment and comprehensive assessment of platelet activation and coagulopathy. We will quantify the LV reverse remodelling associated with partial support; define new echo and microRNA markers of reverse remodelling for clinical use, with insights into underlying pathophysiology; and describe the haematological profile of these patients to guide future antiplatelet and anticoagulant therapy.
Study Type
OBSERVATIONAL
Enrollment
2
Universitaire Ziekenhuizen Leuven
Leuven, Belgium
Royal Brompton & Harefield NHS Foundation Trust
London, United Kingdom
Change in maximal aerobic exercise capacity (peak VO2)
Time frame: 6 months
Change in 6-minute walk distance
Time frame: 6 months
Change in New York Heart Association (NYHA) functional class
Time frame: 6 months
Change in B-type natriuretic peptide
Time frame: 6 months
Change in ventricular dimensions as measured by echocardiography
Time frame: 6 months
Change in ventricular strain as measured by echocardiography
Time frame: 6 months
Change in circulating microRNA expression profile
Time frame: 6 months
Change in ventilatory equivalent for carbon dioxide (VE/VCO2) slope
Time frame: 6 months
Change in haemodynamic parameters at right heart catheterisation
Time frame: 6 months
Change in quality of life score
Time frame: 6 months
Accumulated days of hospital inpatient stay due to cardiovascular reasons
Time frame: 6 months
Incidence of significant haematological derangements
Time frame: 6 months
Number of participants suffering adverse events
'Adverse events' are defined as major bleeding, thromboembolism, stroke, infection, perioperative complications, right ventricular failure, device-related morbidity and device failure.
Time frame: 6 months
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