Ofir Koren1,2
Vivek Patel1
Tarun Chakravarty1Hasan Jilaihawi1
Aakriti Gupta1Shirin Sadri3Raj R. Makkar1*
- 1Cedars–Sinai Medical Center, Smidt Heart Institute, Los Angeles, CA, United States
- 2Bruce Rappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel
- 3Department of Medicine, Stanford University, Stanford, CA, United States
Introduction: Transcatheter aortic valve intervention (TAVR) has emerged as a promising alternative to surgical aortic valve replacement for patients with severe aortic stenosis. However, leaflet thrombosis has raised concerns about the long-term durability and outcomes of TAVR. This study aims to provide an overview of the mechanisms, prevention strategies, and treatment options for leaflet thrombosis in TAVR.
Clinical evidence: Leaflet thrombosis refers to the formation of blood clots on bioprosthetic valve leaflets, leading to impaired leaflet mobility, early valve degeneration and dysfunction, and potential clinical implications. While the mechanisms underlying thrombus formation on valve leaflets are not fully understood, several factors, such as altered blood flow patterns within valve neosinuses, prothrombotic surfaces, and patient-related causes, have been implicated. Two distinct entities have been identified, namely, hypoattenuated leaflet thickening and restricted leaflet motion. Their occurrence appears dynamic over time and is related to the valve type. Imaging, including transesophageal echocardiography and multidetector computed tomography, plays a crucial role in the diagnosis and follow-up of leaflet thrombosis.
Prevention and treatment options: Preventing leaflet thrombosis requires a comprehensive and tailored approach involving identifying high-risk patients, close monitoring, and antithrombotic therapy. Antithrombotic therapy with dual antiplatelet agents or anticoagulation is commonly employed in TAVR patients, although the optimal regimen is yet to be defined. Novel antithrombotic agents, such as direct oral anticoagulants, are being investigated for their efficacy and safety in preventing leaflet thrombosis. When leaflet thrombosis is detected, treatment options include intensified antithrombotic therapy, valve-in-valve intervention, or balloon valvuloplasty. The long-term outcomes and impact of leaflet thrombosis on valve durability and patient prognosis are areas of ongoing research.
Summary: Leaflet thrombosis in TAVR is a considerable complication affecting valve function and patient outcomes. Understanding the mechanisms underlying thrombus formation and implementing appropriate prevention strategies are essential for mitigating this risk. Treatment options aim to restore leaflet mobility and optimize valve performance. Further research is needed to establish standardized protocols for antithrombotic therapy, identify high-risk patient populations, and determine the long-term consequences of leaflet thrombosis on TAVR outcomes.
Introduction
Leaflet thrombosis refers to the formation of both calcified and non-calcified thrombi on transcatheter heart valve (THV) leaflets, most commonly observed in transcatheter aortic valves (TAVs) made of bioprosthetic material (1). In 2015, Makkar et al. first recognized subclinical leaflet thrombosis (SLT) in transcatheter aortic valve intervention (TAVR). In their landmark study, they utilized multidetector computed tomography (CT) to assess leaflet abnormalities after balloon-expanding TAVR and demonstrated the occurrence of reduced leaflet motion associated with hypoattenuation opacities on CT in a subset of asymptomatic patients (2). This pioneering work prompted further investigation into its mechanisms, implications, and preventive and management strategies.
Mechanism
Pathophysiological mechanisms underlying leaflet thrombosis are still being elucidated. A modified Virchow's triad has been proposed, encompassing (i) hypercoagulability at the bioprosthetic surface, (ii) leaflet surface damage and/or endothelial injury during device deployment, and (iii) stasis and turbulent flow (3, 4). The formation of neosinuses between THV leaflets and the valve cage and between native leaflets and aortic wall creates semi-permeable barriers that lead to flow stasis and reduced washout forces (Figure 1) (5). Factors including larger-sized or overexpanded balloon-expandable valves, low-deployment depth of self-expanding valves (particularly CoreValve Evolut, Medtronic), intra-annular valve position, small annular perimeter, valve-in-valve (ViV) TAVR for stented surgical valves, non-commissural alignment, low coronary washout, small sinus size, and reduced flow can increase thrombosis risk (6–8). Valve maldeployment, which may occur due to factors such as extrinsic calcification or valve-in-valve deployment, can lead to incomplete cusp coaptation and excursion and increase thrombosis risk (9).
Figure 1. Leaflet thrombosis in TAVR—risk factors and mechanisms. Mechanisms of thrombus formation involve hemodynamic factors related to sinus anatomy and blood flow, as well as surface factors related to endothelial injury from valve deployment and valve surface. Risk factors are numerous and related to valve and annulus size and position as well as patient anatomy.
Two distinct entities have been identified, namely, hypoattenuated leaflet thickening (HALT) and restricted leaflet motion (RELM). HALT refers to the abnormal thrombotic thickening of valve leaflets. RELM occurs secondary to HALT and impairs valve functionality. The co-occurrence of HALT and RELM defines hypoattenuation affecting motion (HAM) (Figure 2) (10, 11).
Figure 2. Hypoattenuated leaflet thickening, restricted leaflet motion, and management strategies. (A) An example of a 30-day follow-up CT following TAVR indicating HALT and RELM on all three leaflets and HAM of the non-coronary cusps. If left untreated, SLT may progress to clinical thrombosis, although the absolute risk of this is not yet fully understood. (B) Treatment of SLT involves 3–6 months of oral anticoagulation followed by repeat imaging to determine resolution and subsequent treatment strategy. A follow-up CT of the same patient following 4 months of direct oral anticoagulation (rivaroxaban 10 mg daily) treatment indicated a significant resolution of leaflet thrombosis with HALT observed only on the left coronary cusp and no RELM or HAM. (C) Prevention of SLT involves dual antiplatelet therapy for 3–6 months followed by lifelong single antiplatelet therapy.
Prevalence
Clinical leaflet thrombosis after TAVR is rare, affecting approximately 0.5% of TAVR patients, and can manifest as increased valve gradient and double the risk of cerebrovascular events and embolization to other arterial beds (12–14).
SLT occurs more commonly in up to 15% of TAVR patients and can vary dynamically over time based on the valve type and position. Inherent differences in THV compared with surgical valves, including mounting the valve within a rigid vs. more flexible stent, valve crimping with delivery, and native calcification, may alter thrombotic risk (15). In the PARTNER-3 sub-study involving 435 low-risk patients, HALT was more than twice as common after TAVR as compared with surgical aortic valve replacement (SAVR) at 30 days (13% vs. 5%, respectively), but the difference was no longer seen after 1 year. In the Evolut Low-Risk Leaflet Thickening or Immobility (LTI) sub-study evaluating the frequency of HALT in 503 patients undergoing TAVR using the self-expanding Evolut THV or SAVR, there was no difference in HALT between TAVR and SAVR at 30 days and 1 year (16,17). Notably, a recent study examining ViV TAVR demonstrated no difference in HALT or RELM between ViV and native-valve TAVR, despite historical concerns about the impact of ViV on sinus thrombosis (18).
Diagnosis and clinical implications
Four-dimensional CT (4DCT) has emerged as a standard to identify HALT and RELM and is comparable to transesophageal echocardiology. Seen as hypoattenuating leaflet lesions on CT, HALT is assessed in diastole and requires visualization of leaflet coaptation. RELM is assessed in systole with maximal leaflet opening. Each leaflet is classified as mildly (<50%), moderately (50%–69%), or severely (70%–99%) restricted or immobile. HALT and >50% restriction signifies HAM (8).
The clinical significance of SLT is not well understood. Although the evidence is limited and conflicting, HALT may be associated with increased transient ischemic attack or stroke risk (RR: 2.6), with several studies showing no increase in cerebral ischemic events (19–21). If persistent or progressive, HALT minimally increases the valve gradient at 1 year compared with patients with no HALT or with spontaneously resolved HALT (17.8 vs. 12.7 mmHg, p = 0.04). An increase in the valve gradient appears concordant with the degree of HALT (17). Most studies have failed to demonstrate an association between HALT or RELM and heart failure symptomatology (22).
Prevention and management
Early prevention strategies centered on antiplatelets, based on expert consensus and extrapolation from coronary stenting and historical bioprosthesis studies. Single antiplatelet therapy (SAPT) is preferred over dual antiplatelet therapy (DAPT) for long-term prevention (23, 24).
Oral anticoagulation (OAC)–based prevention strategies have produced mixed results. The GALILEO trial, which randomized 1,644 TAVR patients to either rivaroxaban (plus aspirin for 3 months) or antiplatelet (aspirin plus clopidogrel for 3 months) treatment, demonstrated a substantial reduction in HALT and RELM with the use of rivaroxaban. However, the trial was terminated early due to higher deaths and bleeding in the rivaroxaban treatment arm (25). The ATLANTIS study, which randomly assigned 1,500 TAVR patients to apixaban or standard care [vitamin K antagonist (VKA) or antiplatelet], demonstrated that apixaban vs. antiplatelet resulted in lower obstructive valve thrombosis but higher non-cardiovascular mortality with apixaban, while apixaban vs. VKA produced no difference in the primary outcome or safety (26). A small study randomizing TAVR patients to VKA plus aspirin or aspirin alone showed a reduction in the primary endpoint (7.0% vs. 26.5%), with VKA having no excess bleeding (27). Using routine OACs post-TAVR remains under debate, and future studies including comparisons of type and strength should be pursued.
The treatment selection for subclinical or clinical thrombosis requires careful assessment of thrombus burden and individual patient factors (Figure 2). Once confirmed on imaging, the preferred treatment involves OAC (apixaban, rivaroxaban, or warfarin) for 3–6 months until resolution. A reasonable approach is to monitor SLT in patients with a high bleeding risk because of its dynamic nature (17). Severe cases may require balloon valvuloplasty or transcatheter valve-in-valve implantation (17, 28).
Summary
Leaflet thrombosis is a dynamic phenomenon that relies on local and systemic factors to develop. The best prevention strategies are still under debate, arising from concerns about OAC bleeding risk with or without antiplatelet therapy. Further investigation is needed to improve the prevention strategies and better understand the clinical implications and progression to valve degeneration.
Author contributions
OK, VP, SS, RM reviewed the literature and conceptualization and composed the manuscript. TC, HJ, AG and RM provided critical feedback and helped shape the manuscript. All authors contributed to the article and approved the submitted version.
Acknowledgments
The study was supported in part by the California Chapter of the American College of Cardiology through the Save a Heart foundation.
Conflict of interest
RM received grant support from Edwards Lifesciences Corporation; he is a consultant for Abbott Vascular, Cordis, and Medtronic and holds equity in Entourage Medical. TC is a consultant, proctor, and speaker for Edwards Lifesciences and Medtronic; he is a consultant for Abbott Lifesciences and a consultant and speaker for Boston Scientific.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Imaeda S, Inohara T, Yoshijima N, Kobari Y, Myojin S, Ryuzaki T, et al. Natural history of leaflet thrombosis after transcatheter aortic valve replacement: a 5-year follow-up study. J Am Heart Assoc. (2022) 11(23): e026334. doi: 10.1161/JAHA.122.026334
2. Makkar RR, Fontana G, Jilaihawi H, Chakravarty T, Kofoed KF, De Backer O, et al. Possible subclinical leaflet thrombosis in bioprosthetic aortic valves. N Engl J Med. (2015) 373(21): 2015–24. doi: 10.1056/NEJMoa1509233
3. Sachdev S, Bardia N, Nguyen L, Omar B. Bioprosthetic valve thrombosis. Cardiol Res. (2018) 9(6): 335–42. doi: 10.14740/cr789
4. Jaffer IH, Fredenburgh JC, Hirsh J, Weitz JI. Medical device-induced thrombosis: what causes it and how can we prevent it? J Thromb Haemost. (2015) Suppl 1:S72–81. doi: 10.1111/jth.12961
5. Trusty PM, Sadri V, Madukauwa-David ID, Funnell E, Kamioka N, Sharma R, et al. Neosinus flow stasis correlates with thrombus volume post-tavr: a patient-specific in vitro study. JACC Cardiovasc Interv. (2019) 12(13): 1288–90. doi: 10.1016/j.jcin.2019.03.022
6. Madukauwa-David ID, Sadri V, Kamioka N, Midha PA, Raghav V, Oshinski JN, et al. Transcatheter aortic valve deployment influences neo-sinus thrombosis risk: An in vitro flow study. Catheter Cardiovasc Interv. (2020) 95(5): 1009–16. doi: 10.1002/ccd.28388
7. D'Ascenzo F, Salizzoni S, Saglietto A, Cortese M, Latib A, Franzone A, Barbanti M, et al. Incidence, predictors and cerebrovascular consequences of leaflet thrombosis after transcatheter aortic valve implantation: a systematic review and meta-analysis. Eur J Cardiothorac Surg. (2019) 56(3): 488–94. doi: 10.1093/ejcts/ezz099
8. Hansson NC, Grove EL, Andersen HR, Leipsic J, Mathiassen ON, Jensen JM, et al. Transcatheter aortic valve thrombosis: incidence, predisposing factors, and clinical implications. J Am Coll Cardiol. (2016) 68(19):2059–69. doi: 10.1016/j.jacc.2016.08.010
9. Mangione FM, Jatene T, Gonçalves A, Fishbein GA, Mitchell RN, Pelletier MP, et al. Leaflet thrombosis in surgically explanted or post-mortem tavr valves. JACC Cardiovasc Imaging. (2017) 10(1):82–5. doi: 10.1016/j.jcmg.2016.11.009
10. Jilaihawi H, Asch FM, Manasse E, Ruiz CE, Jelnin V, Kashif M, et al. Systematic CT methodology for the evaluation of subclinical leaflet thrombosis. JACC Cardiovasc Imaging. (2017) 10(4):461–70. doi: 10.1016/j.jcmg.2017.02.005. Erratum in: JACC Cardiovasc Imaging. (2017 10(6):718. PMID: 28385256.28385256
11. Sannino A, Hahn RT, Leipsic J, Mack MJ, Grayburn PA. Meta-analysis of Incidence, predictors and consequences of clinical and subclinical bioprosthetic leaflet thrombosis after transcatheter aortic valve implantation. Am J Cardiol. (2020) 132: 106–13. doi: 10.1016/j.amjcard.2020.07.018
12. Rosseel L, De Backer O, Søndergaard L. Clinical valve thrombosis and subclinical leaflet thrombosis following transcatheter aortic valve replacement: is there a need for a patient-tailored antithrombotic therapy? Front Cardiovasc Med. (2019) 6:44. doi: 10.3389/fcvm.2019.00044
13. Bogyi M, Schernthaner RE, Loewe C, Gager GM, Dizdarevic AM, Kronberger C, et al. Subclinical leaflet thrombosis after transcatheter aortic valve replacement: a meta-analysis. JACC Cardiovasc Interv. (2021) 14(24): 2643–56. doi: 10.1016/j.jcin.2021.09.019
14. Chakravarty T, Søndergaard L, Friedman J, De Backer O, Berman D, Kofoed KF, et al. Subclinical leaflet thrombosis in surgical and transcatheter bioprosthetic aortic valves: an observational study. Lancet. (2017) 389(10087): 2383–92. doi: 10.1016/S0140-6736(17)30757-2
15. Puri R, Auffret V, Rodés-Cabau J. Bioprosthetic valve thrombosis. J Am Coll Cardiol. (2017) 69(17):2193–211. doi: 10.1016/j.jacc.2017.02.051. Erratum in: J Am Coll Cardiol. (2017) 70(1):121. PMID: 28449781.28449781
16. Blanke P, Leipsic JA, Popma JJ, Yakubov SJ, Deeb GM, Gada H, et al. Bioprosthetic aortic valve leaflet thickening in the evolut low risk sub-study. J Am Coll Cardiol. (2020) 75(19):2430–42. doi: 10.1016/j.jacc.2020.03.022
17. Makkar RR, Blanke P, Leipsic J, Thourani V, Chakravarty T, Brown D, et al. Subclinical leaflet thrombosis in transcatheter and surgical bioprosthetic valves: partner 3 cardiac computed tomography substudy. J Am Coll Cardiol. (2020) 75(24): 3003–15. doi: 10.1016/j.jacc.2020.04.043.
18. Koren O, Patel V, Naami R, Naami E, Nagasaka T, Shechter A, et al. New adverse coronary events in valve-in-valve TAVR and native TAVR-A 2-year matched cohort. Front Cardiovasc Med. (2022) 9:1004103. doi: 10.3389/fcvm.2022.1004103
19. Rashid HN, Gooley RP, Nerlekar N, Ihdayhid AR, McCormick LM, Nasis A, et al. Bioprosthetic aortic valve leaflet thrombosis detected by multidetector computed tomography is associated with adverse cerebrovascular events: a meta-analysis of observational studies. EuroIntervention. 2018 Feb 2;13(15):e1748–e1755. doi: 10.4244/EIJ-D-17-01062. PMID: 29235436.29235436
20. Pache G, Schoechlin S, Blanke P, Dorfs S, Jander N, Arepalli CD, et al. Early hypo-attenuated leaflet thickening in balloon-expandable transcatheter aortic heart valves. Eur Heart J. (2016) 37(28):2263–71. doi: 10.1093/eurheartj/ehv526
21. Yanagisawa R, Hayashida K, Yamada Y, Tanaka M, Yashima F, Inohara T, et al. Incidence, predictors, and mid-term outcomes of possible leaflet thrombosis after tavr. J Am Coll Cardiol Img. (2017) 10(1): 1–11. doi: 10.1016/j.jcmg.2016.11.005
22. Ng ACT, Holmes DR, Mack MJ, Delgado V, Makkar R, Blanke P, et al. Leaflet immobility and thrombosis in transcatheter aortic valve replacement. Eur Heart J. (2020); 41(33): 3184–97. doi: 10.1093/eurheartj/ehaa542
23. Maes F, Stabile E, Ussia GP, Tamburino C, Pucciarelli A, Masson JB, et al. Meta-analysis comparing single versus dual antiplatelet therapy following transcatheter aortic valve implantation. Am J Cardiol. (2018) 122(2):310–5. doi: 10.1016/j.amjcard.2018.04.006
24. Brouwer J, Nijenhuis VJ, Delewi R, Hermanides RS, Holvoet W, Dubois CLF, et al. Aspirin with or without clopidogrel after transcatheter aortic-valve implantation. N Engl J Med. (2020) 383(15):1447–57. doi: 10.1056/NEJMoa2017815
25. Dangas GD, Tijssen JGP, Wöhrle J, Søndergaard L, Gilard M, Möllmann H, et al. A controlled trial of rivaroxaban after transcatheter aortic-valve replacement. N Engl J Med. (2020) 382(2): 120–9. doi: 10.1056/NEJMoa1911425
26. Collet JP, Berti S, Cequier A, Van Belle E, Lefevre T, Leprince P, et al. Oral anti-Xa anticoagulation after trans-aortic valve implantation for aortic stenosis: The randomized ATLANTIS trial. Am Heart J. (2018) 200: 44–50. doi: 10.1016/j.ahj.2018.03.008
27. Rogers T, Shults C, Torguson R, Shea C, Parikh P, Bilfinger T, et al. Randomized trial of aspirin versus warfarin after transcatheter aortic valve replacement in low-risk patients. Circ Cardiovasc Interv. (2021) 14(1):e009983. doi: 10.1161/CIRCINTERVENTIONS.120.009983
Keywords: TAVR, leaflet thrombosis, mechanism, prevention, prevalence, review
Citation: Koren O, Patel V, Chakravarty T, Jilaihawi H, Gupta A, Sadri S and Makkar RR (2023) Leaflet thrombosis in transcatheter aortic valve intervention: mechanisms, prevention, and treatment options. Front. Cardiovasc. Med. 10:1249604. doi: 10.3389/fcvm.2023.1249604
Received: 28 June 2023; Accepted: 19 September 2023;
Published: 6 October 2023.
Edited by:
Elisabetta Ricottini, Campus Bio-Medico University, ItalyReviewed by:
Richard Mitchell, Brigham and Women's Hospital, United StatesMichele Gallo, University of Louisville, United States
Yung-Tsai Lee, Cheng Hsin General Hospital, Taiwan
© 2023 Koren, Patel, Chakravarty, Jilaihawi, Gupta, Sadri and Makkar. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Raj R. Makkar cmFqLm1ha2thckBjc2hzLm9yZw==