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Aspirin and left ventricular assist devices: rationale and design for the international randomized, placebo‐controlled, non‐inferiority ARIES HM3 trial

dc.contributor.authorMehra, Mandeep R.
dc.contributor.authorCrandall, Daniel L.
dc.contributor.authorGustafsson, Finn
dc.contributor.authorJorde, Ulrich P.
dc.contributor.authorKatz, Jason N.
dc.contributor.authorNetuka, Ivan
dc.contributor.authorUriel, Nir
dc.contributor.authorConnors, Jean M.
dc.contributor.authorSood, Poornima
dc.contributor.authorHeatley, Gerald
dc.contributor.authorPagani, Francis D.
dc.date.accessioned2021-08-03T18:16:33Z
dc.date.available2022-08-03 14:16:32en
dc.date.available2021-08-03T18:16:33Z
dc.date.issued2021-07
dc.identifier.citationMehra, Mandeep R.; Crandall, Daniel L.; Gustafsson, Finn; Jorde, Ulrich P.; Katz, Jason N.; Netuka, Ivan; Uriel, Nir; Connors, Jean M.; Sood, Poornima; Heatley, Gerald; Pagani, Francis D. (2021). "Aspirin and left ventricular assist devices: rationale and design for the international randomized, placebo‐controlled, non‐inferiority ARIES HM3 trial." European Journal of Heart Failure 23(7): 1226-1237.
dc.identifier.issn1388-9842
dc.identifier.issn1879-0844
dc.identifier.urihttps://hdl.handle.net/2027.42/168502
dc.description.abstractAimsOver decades, left ventricular assist device (LVAD) technology has transitioned from less durable bulky pumps to smaller continuous‐flow pumps which have substantially improved long‐term outcomes and quality of life. Contemporary LVAD therapy is beleaguered by haemocompatibility‐related adverse events including thrombosis, stroke and bleeding. A fully magnetically levitated pump, the HeartMate 3 (HM3, Abbott, USA) LVAD, has been shown to be superior to the older HeartMate II (HMII, Abbott, USA) pump by improving haemocompatibility. Experience with the HM3 LVAD suggests near elimination of de‐novo pump thrombosis, a marked reduction in stroke rates, and only a modest decrease in bleeding complications. Since the advent of continuous‐flow LVAD therapy, patients have been prescribed a combination of aspirin and anticoagulation therapy on the presumption that platelet activation and perturbations to the haemostatic axis determine their necessity. Observational studies in patients implanted with the HM3 LVAD who suffer bleeding have suggested a signal of reduced subsequent bleeding events with withdrawal of aspirin. The notion of whether antiplatelet therapy can be avoided in an effort to reduce bleeding complications has now been advanced.MethodsTo evaluate this hypothesis and its clinical benefits, the Antiplatelet Removal and Hemocompatibility Events with the HeartMate 3 Pump (ARIES HM3) has been introduced as the first‐ever international prospective, randomized, double‐blind and placebo‐controlled, non‐inferiority trial in a patient population implanted with a LVAD.ConclusionThis paper reviews the biological and clinical role of aspirin (100 mg) with LVADs and discusses the rationale and design of the ARIES HM3 trial.This figure incorporates the rationale for ARIES HM3 (Antiplatelet Removal and Hemocompatibility Events with the HeartMate 3 Pump), the principal study hypothesis and a summary of its design. LVAD, left ventricular assist device.
dc.publisherJohn Wiley & Sons, Ltd.
dc.subject.otherAssist devices
dc.subject.otherLVAD
dc.subject.otherAspirin
dc.subject.otherOutcomes
dc.subject.otherHemocompatibility
dc.subject.otherBleeding
dc.subject.otherAdvanced heart failure
dc.subject.otherMechanical Circulatory Support
dc.titleAspirin and left ventricular assist devices: rationale and design for the international randomized, placebo‐controlled, non‐inferiority ARIES HM3 trial
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelCardiovascular Medicine
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/168502/1/ejhf2275.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/168502/2/ejhf2275_am.pdf
dc.identifier.doi10.1002/ejhf.2275
dc.identifier.sourceEuropean Journal of Heart Failure
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dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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