Evidence map›Paper›PMID 41216431›Full record

ArticleResearch and practice in thrombosis and haemostasis2025

Comparison of direct oral anticoagulants and vitamin K antagonists in the treatment of left ventricular thrombi: a retrospective cohort study.

Hossam Elbenawi, Kirsten Lipps, Samuel Heller, David A Liedl, Raymond C Shields, Ana I Casanegra, Stanislav Henkin, Thom W Rooke, Paul W Wennberg, Waldemar E Wysokinski and 2 more

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In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Hossam ElbenawiDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Kirsten LippsDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Samuel HellerSecond Faculty of Medicine, Charles University, Prague, Czech Republic.
David A LiedlGonda Vascular Center, Mayo Clinic, Rochester, Minnesota, USA.
Raymond C ShieldsDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Ana I CasanegraDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Stanislav HenkinDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Thom W RookeDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Paul W WennbergDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Waldemar E WysokinskiDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Robert D McBaneDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Damon E HoughtonDivision of Vascular Medicine, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Left ventricular thrombus (LVT) is a serious thromboembolic complication in patients with cardiomyopathies. Evidence supporting direct oral anticoagulant (DOAC) therapy in LVT is limited. Objectives: We evaluated the effectiveness and safety of DOACs compared with vitamin K antagonists (VKAs) in patients with LVT. Methods: A multisite retrospective cohort study was performed, including patients with LVT diagnosed by echocardiography from 2018-2023 who were treated with either DOACs or VKAs. Primary outcome was the incidence of stroke and systemic embolism (SSE). Secondary outcomes included LVT resolution, major bleeding, and all-cause mortality. Results: A total of 182 patients with LVT met inclusion criteria, of which 70 (38.5%) were treated with only DOACs and 112 (61.5%) with only VKAs. The mean age was 66 years, and 74% of the patients were male. The median follow-up duration was 363.5 days (IQR, 139-950). No significant difference between the groups was observed in the incidence of SSE (DOAC, 5.7% vs VKA, 5.4%; Conclusion: LVT treated solely with either DOACs or VKAs had similar incidences of SSE, LVT resolution, time to LVT resolution, and mortality. VKA therapy, however, was associated with a higher incidence of major bleeding events.

Indexed as

direct oral anti-coagulantleft ventricular thrombusstrokesystemic embolismvitamin K antagonists

Identifiers

PMID41216431
PMCPMC12596518

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.