# Do Patients with Antiphospholipid Syndrome Present with More Significant Venous Thromboembolic Clot Burden? A Retrospective Single-Center Study

**Authors:** Joseph Liput, Rahim Jiwani, Rachel DiLeo, Ryan Moll, Abigail Arrigo, Yazan Samhouri, Deep Shah

PMC · DOI: 10.3390/hematolrep18020021 · 2026-03-10

## TL;DR

This study found no evidence that patients with antiphospholipid syndrome have more severe venous blood clots compared to those without the condition.

## Contribution

The study provides new clinical evidence that APS status does not correlate with increased clot burden in venous thromboembolic events.

## Key findings

- APS patients had similar rates of significant clot burden as non-APS patients (38.7% vs 40.0%).
- No clinical or laboratory predictors of significant clot burden were identified in multivariable analysis.
- Triple-positive APS and primary APS were not associated with increased clot burden.

## Abstract

Background/Objectives: Venous thromboembolic disease (VTE) is the most common initial manifestation of antiphospholipid syndrome (APS). Determining which patients with VTE to test for APS can be a challenging clinical decision. We aimed to determine if patients with APS present with more significant venous thromboembolic clot burden, as compared to patients with VTE without a diagnosis of APS. Methods: A multi-hospital single-institution retrospective cohort study was designed. Patients with a diagnosis of VTE who had been tested for APS from 1 December 2019 to 31 January 2022 were included. Patients were stratified based on the presence of APS (APS versus non-APS). Significant venous thromboembolic clot burden was defined as PE involving the main and/or lobar pulmonary arteries or DVT involving the iliofemoral veins. Assessment of clot burden was performed by review of radiology reports of the index clotting event. Results: We included 748 patients with a history of VTE who had been tested for APS; 75 patients (10%) were positive for APS. Significant clot burden was present in 29 (38.7%) APS patients and 269 (40.0%) non-APS patients (OR 0.95, 95% CI 0.58–1.56; p = 0.85). No predictors for significant clot burden were found on multivariable analysis. Triple-positive APS (OR 0.83, 95% CI 0.16–4.21; p = 0.82) and primary APS (OR 0.72, 95% CI 0.15–3.45; p = 0.68) were not associated with more significant clot burden. Conclusions: This retrospective single-institution analysis suggests that patients with APS may not present with more significant venous thromboembolic clot burden than patients with VTE without APS.

## Linked entities

- **Diseases:** antiphospholipid syndrome (MONDO:0017278), pulmonary embolism (MONDO:0005279)

## Full-text entities

- **Genes:** F5 (coagulation factor V) [NCBI Gene 2153] {aka FVL, PCCF, RPRGL1, THPH2, fV}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}
- **Diseases:** arterial thrombosis (MESH:D002341), DVT (OMIM:612862), Cancer (MESH:D009369), PE (MESH:D011655), APS (MESH:D016736), systemic lupus erythematosus (MESH:D008180), injury to (MESH:D014947), emboli (MESH:D020766), inherited and acquired thrombophilia (MESH:C540694), clot (MESH:D013927), protein S deficiency (MESH:D018455), antithrombin III deficiency (MESH:D020152), COVID infection (MESH:D000086382), VTE (MESH:D054556), DVT (MESH:D020246), LAC (MESH:C531622), protein C deficiency (MESH:D020151), thrombophilia (MESH:D019851)
- **Chemicals:** phospholipid (MESH:D010743), DOAC (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC13010601/full.md

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Source: https://tomesphere.com/paper/PMC13010601