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

DOAC VKA left ventricular thrombus meta-analysis oral anticoagulation

Journal

European heart journal. Cardiovascular pharmacotherapy
ISSN: 2055-6845
Titre abrégé: Eur Heart J Cardiovasc Pharmacother
Pays: England
ID NLM: 101669491

Informations de publication

Date de publication:
06 Jun 2024
Historique:
medline: 7 6 2024
pubmed: 7 6 2024
entrez: 7 6 2024
Statut: aheadofprint

Résumé

Direct oral anticoagulants (DOACs) are increasingly used off-label to treat patients with left ventricular thrombus (LVT). We analyzed available meta-data comparing DOACs and vitamin K antagonists (VKAs) for efficacy and safety. We conducted a systematic search and meta-analysis of observational and randomized data comparing DOACs versus 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-effect model meta-analysis, and their robustness was investigated using sensitivity and influential analyses. We identified 22 articles (18 observational studies, 4 small randomized clinical trials) reporting on a total of 3,587 patients (2,489 VKA vs. 1,098 DOAC therapy). The pooled estimates for stroke or systemic embolism (OR 0.81; 95% 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. DOAC use 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. 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 to 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.

Identifiants

pubmed: 38845369
pii: 7689204
doi: 10.1093/ehjcvp/pvae042
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Paul M Haller (PM)

Department of Cardiology, University Heart and Vascular Center Hamburg, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany.

Niema Kazem (N)

Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Stefan Agewall (S)

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

Claudio Borghi (C)

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

Claudio Ceconi (C)

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

Dobromir Dobrev (D)

Institute of Pharmacology, West German Heart and Vascular Center, University Duisburg-Essen, Essen, Germany.
Montréal Heart Institute, Université de Montréal, Montréal, Québec, Canada.
Department of Integrative Physiology, Baylor College of Medicine, Houston, TX, USA.

Elisabetta Cerbai (E)

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

Erik Lerkevang Grove (EL)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.

Juan Carlos Kaski (JC)

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

Basil S Lewis (BS)

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

Alexander Niessner (A)

Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Bianca Rocca (B)

Department of Preclinical and Clinical Pharmacology, University of Florence, Florence, Italy.
Department of Safety and Bioethics, Section of Pharmacology, Catholic University School of Medicine, Rome, Italy.

Giuseppe Rosano (G)

St George's Hospital Medical School, London, United Kingdom AND IRCCS San Raffaele Roma, Rome, Italy.

Gianluigi Savarese (G)

Division of Cardiology, Department of Medicine, Karolinska Institutet; and Heart and Vascular and Neurology Theme, Karolinska University Hospital, Stockholm, Sweden.

Renate Schnabel (R)

Department of Cardiology, University Heart and Vascular Center Hamburg, Hamburg, Germany.
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany.

Anne Grete Semb (AG)

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

Samuel Sossalla (S)

Department of Medicine I, Cardiology, Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen, Gießen, Germany AND Abteilung für Kardiologie, Kerckhoff-Klinik gGmbH, Bad Nauheim, Germany.

Sven Wassmann (S)

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

Patrick Sulzgruber (P)

Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Classifications MeSH