Oral anticoagulation in patients with left ventricular thrombus: a systematic review and meta-analysis

Author:

Haller Paul M12ORCID,Kazem Niema3ORCID,Agewall Stefan4,Borghi Claudio5ORCID,Ceconi Claudio6,Dobrev Dobromir789ORCID,Cerbai Elisabetta10ORCID,Grove Erik Lerkevang1112,Kaski Juan Carlos13,Lewis Basil S14,Niessner Alexander3ORCID,Rocca Bianca1015ORCID,Rosano Giuseppe1617ORCID,Savarese Gianluigi1819,Schnabel Renate B12ORCID,Semb Anne Grete20,Sossalla Samuel21222324,Wassmann Sven25,Sulzgruber Patrick3ORCID

Affiliation:

1. Department of Cardiology, University Heart and Vascular Center Hamburg , Building O50, Empore, Martinistrasse 52, 20246 Hamburg , Germany

2. German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck , Hamburg 20246 , Germany

3. Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna , Währinger Gürtel 18-20, 1090 Vienna , Austria

4. Division of Clinical Science, Danderyd hospital, Karolinska Institute, Stockholm 171 77 , Sweden

5. Department of Medical and Surgical Sciences, University of Bologna, IRCCS Azienda Ospedaliero-Universitaria di Bologna,   Bologna 40126 , Italy

6. Cardiovascular Institute, Azienda Ospedaliera Universitaria S. Anna , Ferrara 44124 , Italy

7. Institute of Pharmacology, West German Heart and Vascular Center, University Duisburg-Essen , Essen 45122 , Germany

8. Montréal Heart Institute, Université de Montréal , Montréal, Québec H1T 1C8 , Canada

9. Department of Integrative Physiology, Baylor College of Medicine , Houston, TX 77030 , USA

10. Department of Preclinical and Clinical Pharmacology, University of Florence , Florence 50121 , Italy

11. Department of Cardiology, Aarhus University Hospital , Aarhus 8200, Denmark

12. Department of Clinical Medicine, Faculty of Health, Aarhus University , Aarhus 8200 , Denmark

13. Molecular and Clinical Sciences Research Institute, St George's, University of London , London SW17 ORE , UK

14. Lady Davis Carmel Medical Center and Technion-Israel Institute of Technology , Haifa 3436212 , Israel

15. Department of Safety and Bioethics, Section of Pharmacology, Catholic University School of Medicine , Rome 00168 , Italy

16. St George's Hospital Medical School , London SW17 0RE , UK

17. IRCCS San Raffaele Roma , Rome 00163 , Italy

18. Division of Cardiology, Department of Medicine, Karolinska Institutet , Stockholm 171 77 , Sweden

19. Heart and Vascular and Neurology Theme, Karolinska University Hospital , Stockholm 171 77 , Sweden

20. Division of Research and Innovation, REMEDY, Centre for Treatment of Rheumatic and Musculoskeletal Diseases, Diakonhjemmet Hospital , Oslo 0319 , Norway

21. Department   Gießen 35392   Germany

22. of Medicine I, Cardiology, Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen,   Gießen 35392   Germany

23. ,   Gießen 35392   Germany

24. Abteilung für Kardiologie, Kerckhoff-Klinik GmbH , Bad Nauheim 61231, Germany

25. Cardiology Pasing, Munich, and Faculty of Medicine, University of the Saarland , Homburg/Saar 66123 , Germany

Abstract

Abstract Aims Direct oral anticoagulants (DOACs) are increasingly used off-label to treat patients with left ventricular thrombus (LVT). We analysed available meta-data comparing DOACs and vitamin K antagonists (VKAs) for efficacy and safety. Methods We conducted a systematic search and meta-analysis of observational and randomized data comparing DOACs vs. VKAs in patients with LVT. Endpoints of interest were stroke or systemic embolism, thrombus resolution, all-cause death, and a composite bleeding endpoint. Estimates were pooled using a random-effects model meta-analysis, and their robustness was investigated using sensitivity and influential analyses. Results We identified 22 articles (18 observational studies, 4 small randomized clinical trials) reporting on a total of 3587 patients (2489 VKA vs. 1098 DOAC therapy). The pooled estimates for stroke or systemic embolism [odds ratio (OR): 0.81; 95% confidence interval (CI): 0.57, 1.15] and thrombus resolution (OR: 1.12; 95% CI: 0.86, 1.46) were comparable, and there was low heterogeneity overall across the included studies. The use of DOACs was associated with lower odds of all-cause death (OR: 0.65; 95% CI: 0.46, 0.92) and a composite bleeding endpoint (OR: 0.67; 95% CI: 0.47, 0.97). A risk of bias was evident particularly for observational reports, with some publication bias suggested in funnel plots. Conclusion In this comprehensive analysis of mainly observational data, the use of DOACs was not associated with a significant difference in stroke or systemic embolism, or thrombus resolution, compared with VKA therapy. The use of DOACs was associated with a lower rate of all-cause death and fewer bleeding events. Adequately sized randomized clinical trials are needed to confirm these findings, which could allow a wider adoption of DOACs in patients with LVT.

Publisher

Oxford University Press (OUP)

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