Left-ventricular assist devices (LVADs) improve outcomes in end-stage heart failure patients. Two centrifugal-flow LVAD systems are currently approved, HeartMate 3 (HM3) and Medtronic/Heartware HVAD (HVAD). Clinical findings suggest differences in thrombogenicity between both systems. We compared markers of platelet activation and aggregation between HM3 and HVAD. We prospectively included 59 LVAD patients (40 HM3, 19 HVAD). Platelet -selectin expression, activated glycoprotein (GP) IIb/IIIa and monocyte-platelet aggregates (MPA) were assessed by flow-cytometry. Platelet aggregation was measured by light-transmission aggregometry (LTA) and multiple-electrode aggregometry (MEA). Von-Willebrand factor (VWF) antigen (VWF:Ag), VWF activity (VWF:Ac), and VWF multimer pattern analysis were determined. Soluble -selectin (sP-selectin) was measured with an enzyme-linked immunoassay. -selectin, GPIIb/IIIa and MPA levels and in response to arachidonic acid, adenosine diphosphate, and thrombin receptor activating peptide were similar between HM3 and HVAD (all > .05). Likewise, agonist-inducible platelet aggregation by LTA and MEA did not differ between HM3 and HVAD (all > .05). VWF:Ag levels and FVIII:C were similar between both systems (both > .05), but patients with HVAD had significantly lower VWF:Ac ( = .011) and reduced large VWF multimers ( = .013). Finally, sP-selectin levels were similar in patients with HVAD and HM3 ( = .845). In conclusion, on-treatment platelet activation and aggregation are similar in HM3 and HVAD patients. Potential clinical implications of observed differences in VWF profiles between both LVAD systems need to be addressed in future clinical trials.
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http://dx.doi.org/10.1080/09537104.2021.1881950 | DOI Listing |
Circ Heart Fail
November 2024
Division of Cardiology, Department of Medicine (A.T., S.C., J.E.W.), Northwestern University, Chicago, IL.
Background: In October 2018, the US heart transplant (HT) allocation system was revised giving patients with left ventricular assist device (LVAD) intermediate priority status. Few studies have examined the impact of this policy change on outcomes among patients with LVAD. We sought to determine how the allocation change impacted waitlist and posttransplant mortality in patients with LVAD.
View Article and Find Full Text PDFSAGE Open Med
August 2024
Division of Cardiothoracic and Vascular Surgery, Department of Surgery, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia.
Objective: Ventricular assist device is one of the treatment options for heart failure patients. Therefore, the purpose of this review is to aid in clinical decision-making of exchanging previous older ventricular assist device models to the newest one, HM3.
Methods: The search was conducted across several databases until February 25, 2023, and was registered with the ID of CRD42023405367.
ASAIO J
December 2024
From the Utah Cardiac Recovery (UCAR) Program (Divisions of Cardiology and Cardiothoracic Surgery at University of Utah Health & School of Medicine, Intermountain Medical Center, and George E. Wahlen Department of Veterans Affairs Medical Center), Salt Lake City, Utah.
J Biomech Eng
October 2024
Clean Mobility & Thermofluids, Universitat Politècnica de València, Camino de Vera, s/n, València 46022, Spain.
Artif Organs
August 2024
Stony Brook University Hospital, Renaissance School of Medicine at Stony Brook University, Stony Brook, New York, USA.
Background: The efficacy of extracorporeal membrane oxygenation (ECMO) as a bridge to left ventricular assist device (LVAD) remains unclear, and recipients of the more contemporary HeartMate 3 (HM3) LVAD are not well represented in previous studies. We therefore undertook a multicenter, retrospective study of this population.
Methods And Results: INTERMACS 1 LVAD recipients from five U.
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