# Contemporary Challenges in Venous Thromboembolism: Evolving Populations and Implications for Management and Risk Stratification

**Authors:** Patrick Leung, Prahlad Ho, Hui Yin Lim

PMC · DOI: 10.3390/jcm15041509 · Journal of Clinical Medicine · 2026-02-14

## TL;DR

Venous thromboembolism is becoming more common due to changing demographics and new risk factors, requiring updated treatment and risk assessment strategies.

## Contribution

This review highlights emerging risk factors and treatment advances, emphasizing the need for revised risk models and novel biomarkers in VTE management.

## Key findings

- The incidence of VTE is rising due to demographic shifts and new risk factors like cancer treatments and hormonal therapies.
- Existing risk assessment models show limitations in contemporary patient populations, necessitating revisions and new biomarkers.
- DOACs have transformed VTE management, but complex cases require alternative strategies including interventional approaches.

## Abstract

Venous thromboembolism (VTE) remains a major cause of morbidity and mortality globally. The incidence of VTE continues to increase over time, contributed to by demographic shifts and emerging risk factors, such as novel cancer treatments and exposure to gender-affirming hormonal therapies. While the introduction of direct oral anticoagulants (DOACs) revolutionized VTE management, increasing complexity in select patient cohorts has driven the need for alternative treatment strategies, including pharmacological and interventional approaches. Concurrently, contemporary patient populations have exposed limitations in existing risk assessment models, highlighting the need for revision and consideration of novel biomarkers. In this review, we provide an overview of the changing VTE landscape, highlighting emerging risk factors, advances in treatment, and the utility of current risk stratification tools and novel biomarkers in guiding care.

## Linked entities

- **Diseases:** Venous thromboembolism (MONDO:0005399), cancer (MONDO:0004992)

## Full-text entities

- **Genes:** F11 (coagulation factor XI) [NCBI Gene 2160] {aka FXI, PTA}, F13A1 (coagulation factor XIII A chain) [NCBI Gene 2162] {aka F13A}, SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, F12 (coagulation factor XII) [NCBI Gene 2161] {aka HAE3, HAEX, HAF}, SELP (selectin P) [NCBI Gene 6403] {aka CD62, CD62P, GMP140, GRMP, LECAM3, PADGEM}, F8 (coagulation factor VIII) [NCBI Gene 2157] {aka AHF, DXS1253E, F8B, F8C, FVIII, HEMA}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}
- **Diseases:** pulmonary hypertension (MESH:D006976), chronic disease (MESH:D002908), PE (MESH:D011655), HIV (MESH:D015658), ventricular compromise (MESH:D014693), RAMs (MESH:D004195), coronary artery disease (MESH:D003324), Thrombophilia (MESH:D019851), stroke (MESH:D020521), right heart strain (MESH:D013180), Thromboembolic (MESH:D013923), B-cell lymphomas (MESH:D016393), bleeding (MESH:D006470), Obesity (MESH:D009765), breast cancer (MESH:D001943), advanced renal disease (MESH:D007674), AI (MESH:C538142), weight gain (MESH:D015430), CKD (MESH:D051436), DVT (MESH:D020246), acute lymphoblastic leukemia (MESH:D054198), thrombocytopenia (MESH:D013921), PTS (MESH:D000094025), end-stage renal failure (MESH:D007676), HD (MESH:D006816), FXI deficiency (MESH:D005173), CAT (MESH:D009369), right ventricular dysfunction (MESH:D018497), infections (MESH:D007239), multiple myeloma (MESH:D009101), cardiovascular disease (MESH:D002318), coagulation (MESH:D001778), intracranial haemorrhage (MESH:D013345), Atherosclerosis (MESH:D050197), venous obstruction (MESH:D006502), death (MESH:D003643), cervical cancer (MESH:D002583), VTE (MESH:D054556), gastrointestinal and genitourinary cancers (MESH:D014565), Thrombosis (MESH:D013927), lupus anticoagulant (MESH:C531622), injury to (MESH:D014947), complication (MESH:D008107), inflammation (MESH:D007249)
- **Chemicals:** enoxaparin (MESH:D017984), warfarin (MESH:D014859), abelacimab (MESH:C000718976), apixaban (MESH:C522181), rivaroxaban (MESH:D000069552), dabigatran (MESH:D000069604), dalteparin (MESH:D017985), CAR-T (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

161 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942584/full.md

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Source: https://tomesphere.com/paper/PMC12942584