State-of-the-Art Review
Thrombotic Risk and Antithrombotic Strategies After Transcatheter Mitral Valve Replacement

https://doi.org/10.1016/j.jcin.2019.07.055Get rights and content
Under an Elsevier user license
open archive

Highlights

  • The risk of THV thrombosis seems to be relevant after TMVR.

  • Routine anticoagulant therapy and serial clinical and imaging follow-up is suggested to mitigate this risk.

  • Future dedicated studies are needed to better investigate THV thrombosis and refine antithrombotic strategies after TMVR.

Abstract

Severe mitral regurgitation (MR) is fairly common in the general population and is associated with significant morbidity and mortality. Although surgical mitral valve (MV) repair and replacement are well established treatment options for MV disease, as much as one-half of patients with severe, symptomatic MR are not referred for surgery due to prohibitive procedural risk. Novel transcatheter alternatives are therefore being developed to provide an alternative treatment for these patients. A growing experience with transcatheter MV replacement (TMVR) strategies is accumulating and promising early results have been reported. However, the risk of transcatheter heart valve (THV) thrombosis seems to be relevant after TMVR, potentially higher than that observed after transcatheter aortic valve replacement, and routine anticoagulant therapy appears to be necessary to mitigate this risk. Hereafter, the authors: 1) review available evidence on thrombotic risk after TMVR (including new dedicated THVs for native MV, valve-in-valve, valve-in-ring, and valve-in-mitral annular calcification); and 2) discuss the antithrombotic treatment strategies after TMVR.

Key Words

antithrombotic therapy
anticoagulation
thrombosis
THV
TMVR

Abbreviations and Acronyms

CT
computed tomography
INR
international normalized ratio
MR
mitral regurgitation
MV
mitral valve
TAVR
transcatheter aortic valve replacement
THV
transcatheter heart valve
TMVR
transcatheter mitral valve replacement
ViMAC
valve-in-mitral annular calcification
ViR
valve-in-ring
ViV
valve-in-valve
VKA
vitamin K antagonist

Cited by (0)

Dr. Latib has served on the advisory board for Medtronic, Abbott Vascular, and Cardiovalve. Dr. Weisz has served on the medical advisory board for Corindus, Eco Fusion, Filterlex, Medivizor, and Trisol; and has received institutional research grants from Abbott Vascular, Corindus, Cardiovascular Systems, Inc., CSL Behring, RenalGuard, and Svelte. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.