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Review
. 2015 Dec;7(12):2129-38.
doi: 10.3978/j.issn.2072-1439.2015.10.65.

Anticoagulation management in mechanical circulatory support

Affiliations
Review

Anticoagulation management in mechanical circulatory support

Sirtaz Adatya et al. J Thorac Dis. 2015 Dec.

Abstract

Heart failure continues to be a worldwide epidemic, effecting over 23 million persons. Despite advances in medical therapy, the disease is progressive and a significant proportion of patients will need advanced heart replacement therapy. Continuous flow assist devices have become a standard approach for many patients both as a bridge to cardiac transplantation and as destination therapy (DT). However, device related complications such as bleeding and thrombosis continue to hinder further advancements of this technology. The field is rapidly advancing and efforts to reduce pump complications are directed towards improving hemocompatibility and maximizing blood flow without clinically significant hemolysis, areas of stasis or turbulent flow.

Keywords: Anticoagulation; acquired von Willebrand syndrome; anti-factor Xa (anti-FXa); continuous-flow left ventricular assist device (CF-LVAD); device thrombosis; mean arterial pressure; mechanical circulatory support.

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Conflict of interest statement

Conflicts of Interest: The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Trends in patient profiles, left ventricular assist device volumes, and management strategies, 2008-2013 [(Reprinted with permission) (24)]. AV, aortic valve; BTT, bridge to transplant; DT, destination therapy; FDA, Food and Drug Administration; GI, gastrointestinal; HMII, HeartMate II; HVAD, HeartWare Ventricular Assist Device; INTERMACS, Interagency Registry for Mechanically Assisted Circulatory Support; LVAD, left ventricular assist device; vWF, von Willebrand factor.
Figure 2
Figure 2
Multivariable risk factors for bleeding, hemorrhagic stroke, ischemic stroke, and pump thrombosis. Hazard rations for severe thrombotic and hemorrhagic events [(Reprinted with permission) (25)]. BMI, body mass index; HCT, hematocrit.
Figure 3
Figure 3
Anti-factor Xa (anti-FXa) determines anticoagulant activity by measuring the ability of the heparin-antithrombin complex to inhibit activated coagulation factor X. Measuring the inhibition of a single enzyme is a more direct measure of unfractionated heparin (UFH) activity than activated partial thromboplastin time (aPTT), which assesses the intrinsic coagulation and final common pathway [(Reprinted with permission) (32)].

References

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