# Clinical significance of coagulation biomarkers in venous pressure therapy for preventing lower-extremity deep venous thromboembolism: A meta-analysis

**Authors:** Jingrong Niu, Shuang Zhou, Lijin Zhang, Chunmin Li, Hualiang Ren

PMC · DOI: 10.5937/jomb0-61632 · 2026-01-28

## TL;DR

Venous pressure therapy helps prevent blood clots by improving coagulation markers and blood flow, as shown in a meta-analysis of clinical studies.

## Contribution

This study demonstrates that venous pressure therapy modulates key coagulation biomarkers, offering a novel clinical approach for thrombosis prevention.

## Key findings

- Venous pressure therapy significantly reduced fibrinogen and D-dimer levels.
- The therapy prolonged APTT, PT, and TT, indicating improved anticoagulant activity.
- Improved venous blood flow velocity correlates with reduced thrombosis risk.

## Abstract

To evaluate the biochemical and clinical significance of venous pressure therapy in preventing venous thromboembolism (VTE) through analysis of coagulation and fibrinolysis biomarkers, including fibrinogen (FIB), D-dimer (D-D), and activated partial thromboplastin time (APTT).

Randomized controlled trials published between 2013 and 2025 were systematically retrieved from PubMed, CNKI, VIP, and Wanfang databases. Eligible studies investigated venous pressure therapy and reported coagulation-related indices. Pooled effect sizes were calculated for key biochemical markers (FIB, D-D, APTT, PT, TT) and venous hemodynamic outcomes.

Nineteen clinical studies met inclusion criteria. Meta-analysis revealed that venous pressure therapy significantly reduced plasma FIB and D-D levels, prolonged APTT, prothrombin time (PT), and thrombin time (TT), and improved venous blood flow velocity. These changes reflect improved anticoagulant activity, enhanced fibrinolysis, and reduced risk of thrombosis. Importantly, the observed modulation of biochemical markers correlated with a lower incidence of lower-extremity deep venous thrombosis.

Venous pressure therapy favorably alters coagulation and fibrinolytic biomarkers, underscoring their diagnostic value in monitoring therapeutic efficacy and thrombotic risk. These findings highlight the critical role of laboratory indices in guiding the prevention and management of VTE, supporting their integration into standardized clinical practice.

## Linked entities

- **Diseases:** venous thromboembolism (MONDO:0005399)

## Full-text entities

- **Genes:** F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}
- **Diseases:** coagulation (MESH:D001778), lower-extremity deep venous thrombosis (MESH:D020246), thrombosis (MESH:D013927), VTE (MESH:D054556)

## Figures

19 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12978355/full.md

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Source: https://tomesphere.com/paper/PMC12978355