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Oral anticoagulation in patients with left ventricular thrombus: a systematic review and meta-analysis.
Haller, Paul M; Kazem, Niema; Agewall, Stefan; Borghi, Claudio; Ceconi, Claudio; Dobrev, Dobromir; Cerbai, Elisabetta; Grove, Erik Lerkevang; Kaski, Juan Carlos; Lewis, Basil S; Niessner, Alexander; Rocca, Bianca; Rosano, Giuseppe; Savarese, Gianluigi; Schnabel, Renate B; Semb, Anne Grete; Sossalla, Samuel; Wassmann, Sven; Sulzgruber, Patrick.
Affiliation
  • Haller PM; Department of Cardiology, University Heart and Vascular Center Hamburg, Building O50, Empore, Martinistrasse 52, 20246 Hamburg, Germany.
  • Kazem N; German Center for Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Hamburg 20246, Germany.
  • Agewall S; Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
  • Borghi C; Division of Clinical Science, Danderyd hospital, Karolinska Institute, Stockholm 171 77, Sweden.
  • Ceconi C; Department of Medical and Surgical Sciences, University of Bologna, IRCCS Azienda Ospedaliero-Universitaria di Bologna,  Bologna 40126, Italy.
  • Dobrev D; Cardiovascular Institute, Azienda Ospedaliera Universitaria S. Anna, Ferrara 44124, Italy.
  • Cerbai E; Institute of Pharmacology, West German Heart and Vascular Center, University Duisburg-Essen, Essen 45122, Germany.
  • Grove EL; Montréal Heart Institute, Université de Montréal, Montréal, Québec H1T 1C8, Canada.
  • Kaski JC; Department of Integrative Physiology, Baylor College of Medicine, Houston, TX 77030, USA.
  • Lewis BS; Department of Preclinical and Clinical Pharmacology, University of Florence, Florence 50121, Italy.
  • Niessner A; Department of Cardiology, Aarhus University Hospital, Aarhus 8200, Denmark.
  • Rocca B; Department of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus 8200, Denmark.
  • Rosano G; Molecular and Clinical Sciences Research Institute, St George's, University of London, London SW17 ORE, UK.
  • Savarese G; Lady Davis Carmel Medical Center and Technion-Israel Institute of Technology, Haifa 3436212, Israel.
  • Schnabel RB; Division of Cardiology, Department of Internal Medicine II, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
  • Semb AG; Department of Preclinical and Clinical Pharmacology, University of Florence, Florence 50121, Italy.
  • Sossalla S; Department of Safety and Bioethics, Section of Pharmacology, Catholic University School of Medicine, Rome 00168, Italy.
  • Wassmann S; St George's Hospital Medical School, London SW17 0RE, UK.
  • Sulzgruber P; IRCCS San Raffaele Roma, Rome 00163, Italy.
Eur Heart J Cardiovasc Pharmacother ; 10(5): 444-453, 2024 Aug 14.
Article in En | MEDLINE | ID: mdl-38845369
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Heart Diseases / Hemorrhage Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Eur Heart J Cardiovasc Pharmacother Year: 2024 Document type: Article Affiliation country: Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombosis / Heart Diseases / Hemorrhage Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Eur Heart J Cardiovasc Pharmacother Year: 2024 Document type: Article Affiliation country: Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM