American Society of Hirudotherapy

Direct oral anticoagulants vs. warfarin for left ventricular thrombus

Research article published in European heart journal open (2026)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportClinical TrialsKassab et al. · European heart journal open, 2026

Abstract

AIMS: Left ventricular (LV) thrombus carries a high risk of death and systemic embolism. While warfarin has been the standard treatment, evidence comparing direct oral anticoagulants (DOACs) with warfarin in this setting remains limited. This study aimed to compare real-world, risk-adjusted outcomes of DOAC vs. warfarin use in patients with LV thrombus. METHODS AND RESULTS: We conducted a retrospective cohort analysis using the TriNetX research network database. Adults (≥18 years) with echocardiographically confirmed LV thrombus from 2016 to 2022 were included. Patients with atrial fibrillation/flutter, venous thromboembolism, end-stage renal disease, mechanical/bioprosthetic valves, or therapy switch during follow-up were excluded. Propensity score matching (1:1) was used to balance covariates. The primary outcome was a composite of all-cause mortality and stroke/transient ischaemic attack at 30 days and 1 year. Secondary outcomes included major bleeding and LV thrombus resolution. Of 2488 eligible patients (DOAC: 950; warfarin: 1538), 945 matched pairs were analysed with all baseline covariates balanced. In the DOAC group, 74% received apixaban and 26% rivaroxaban. At 30 days and 1 year, the composite outcome did not differ significantly between DOAC and warfarin [13.3% vs. 15%; matched hazard ratio (HR): 0.90, P = 0.41, and 23.8% vs. 26.7%; matched HR: 0.93, P = 0.46, respectively]. Major bleeding rates were similar at 30 days and 1 year (1.18% vs. 1.54%; matched HR: 0.77, P = 0.54, and 4.8% vs. 4.7%; matched HR: 1.13, P = 0.58, respectively). Thrombus resolution at 6 months occurred in ∼81% of patients with follow-up imaging, with no difference by treatment group. CONCLUSION: In a large propensity-matched cohort, DOACs and warfarin demonstrated comparable effectiveness and safety for LV thrombus management, supporting DOACs as a reasonable alternative.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal Article

Summary

Peer-reviewed clinical and outcomes research relevant to medicinal leech therapy and its biology. Indexed in PubMed and verified against the NCBI record.

Why This Matters for Hirudotherapy

This retrospective propensity-matched cohort study, drawn from the TriNetX network, compared direct oral anticoagulants (DOACs) with warfarin in 945 matched pairs of patients with echocardiographically confirmed left ventricular thrombus and found no significant difference in the composite of mortality plus stroke/TIA at 30 days or 1 year, similar major-bleeding rates, and comparable (~81%) thrombus resolution at 6 months, concluding DOACs are a reasonable alternative to warfarin in this setting. For the hirudotherapy evidence picture it provides useful background on the modern systemic-anticoagulation landscape that frames how leech-derived anticoagulants (e.g., hirudin and its analogues) are positioned — namely as local or specialty agents rather than replacements for oral anticoagulation in conditions like LV thrombus. Honest caveat: this is observational, retrospective data subject to residual confounding despite matching, it concerns no leech product, and it informs systemic anticoagulant choice only, not the clinical use of medicinal leeches.

Citation

Direct oral anticoagulants vs. warfarin for left ventricular thrombus.

Kassab et al. · European heart journal open, 2026

Added to ASH library: May 28, 2026 · Site last updated: June 18, 2026

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