# Efficacy and safety of direct oral anticoagulants versus warfarin in patients with a left ventricular thrombus: an updated systematic review and meta-analysis of randomised controlled trials

**Authors:** Thomaz Alexandre Costa, Gabriel Cavalcante Lima Chagas, Luma Maria Tavares de Sousa, Bruno Lins de Souza, Nicole Felix, Josephine Harrington, Bruno Bezerra Lima

PMC · DOI: 10.1136/openhrt-2025-003542 · Open Heart · 2025-11-19

## TL;DR

This study compares the effectiveness and safety of direct oral anticoagulants (DOACs) and warfarin for treating left ventricular thrombus, finding them equally effective and safe.

## Contribution

An updated meta-analysis including the RIVAWAR trial, showing DOACs are as effective and safe as warfarin for managing left ventricular thrombus.

## Key findings

- DOACs and warfarin showed similar thrombus resolution rates at 3 months.
- No significant differences were found in major adverse events or bleeding risks between DOACs and warfarin.
- Results were consistent across subgroup and sensitivity analyses.

## Abstract

Left ventricular (LV) thrombus is a complication of myocardial infarction and dilated cardiomyopathy and is associated with a high thromboembolic risk. Although warfarin has traditionally been used, direct oral anticoagulants (DOACs) offer a more convenient alternative. With the addition of the RIVAWAR trial, we conducted an updated systematic review and meta-analysis to assess the efficacy and safety of DOACs compared with warfarin in patients with LV thrombus.

A systematic search of electronic databases (PubMed, EMBASE, Cochrane and clinicaltrials.gov) from inception to April 2025 identified randomised clinical trials (RCTs) comparing DOACs with warfarin for the treatment of LV thrombus. The main outcome of interest was thrombus resolution at 3 months. Risk ratios (RRs) with 95% CIs were calculated using random-effects models.

Seven RCTs comprising 554 patients were included. Non-contrast transthoracic echocardiography was used for LV thrombus assessment in all RCTs. There was no difference between DOACs and warfarin in thrombus resolution at 3 months (RR 1.02; 95% CI 0.95 to 1.09), major adverse cardiovascular events (RR 0.50; 95% CI 0.16 to 1.54), all-cause mortality (RR 0.92; 95% CI 0.36 to 2.31), stroke/systemic embolism (RR 0.76; 95% CI 0.12 to 4.68), rehospitalisation (RR 1.36; 95% CI 0.47 to 3.94) or major bleeding (RR 0.54; 95% CI 0.20 to 1.48). Subgroup and sensitivity analyses confirmed the robustness of these results.

DOACs demonstrated similar efficacy and safety to warfarin for LV thrombus management in this meta-analysis, supporting their use for the treatment of LV thrombus. However, large-scale RCTs with longer follow-up periods and using diagnostic modalities with higher sensitivity and specificity for detecting LV thrombus resolution are warranted to confirm these findings and clarify long-term outcomes.

CRD420251023513.

## Linked entities

- **Diseases:** myocardial infarction (MONDO:0005068), dilated cardiomyopathy (MONDO:0005021)

## Full-text entities

- **Diseases:** dilated cardiomyopathy (MESH:D002311), thromboembolic (MESH:D013923), LV thrombus (MESH:D013927), systemic embolism (MESH:D004617), bleeding (MESH:D006470), myocardial infarction (MESH:D009203), stroke (MESH:D020521)
- **Chemicals:** warfarin (MESH:D014859), direct (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12636967/full.md

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Source: https://tomesphere.com/paper/PMC12636967