# Eosinophilia and Risk of Thrombosis and Mortality in Hospitalized Patients: A Retrospective Cohort Study

**Authors:** Ronen Shavit, Adi Kidron, Ramit Maoz Segal, Stanley Niznik, Soad Haj Yahia, Mona Iancovici-Kidon, Irena Offengenden, Diti Machnes Maayan, Yulia Lifshitz-Tunitsky, Liraz Olmer, Nancy Agmon-Levin

PMC · DOI: 10.3390/life16020241 · Life · 2026-02-02

## TL;DR

High eosinophil counts in hospitalized patients are linked to increased risk of blood clots and death.

## Contribution

This study identifies a novel association between eosinophilia and thromboembolic events and mortality in hospitalized patients.

## Key findings

- Eosinophilia was associated with a 33% increased risk of thromboembolic events.
- Patients with eosinophilia had a 17% higher mortality risk compared to controls.

## Abstract

Background: Eosinophilia, defined as peripheral blood eosinophil counts > 0.5 K/μL, is associated with various clinical conditions, including allergic, infectious, and malignant diseases. Emerging evidence suggests that eosinophils may contribute to thrombo-inflammatory processes, but their association with thromboembolic events and mortality remains insufficiently characterized. This study aimed to evaluate whether eosinophilia is independently associated with increased risk of thromboembolic events and mortality in hospitalized patients. Methods: We conducted a retrospective cohort study using electronic medical records from Sheba Medical Center (2011–2020). Eosinophilia was classified as mild (0.5–1.5 K/μL) or hypereosinophilia (HE, >1.5 K/μL). Patients with eosinophilia were matched 1:1 to controls with normal eosinophil counts based on age, sex, and follow-up duration. Results: Among 93,320 patients (46,660 with eosinophilia and 46,660 controls), thromboembolic events occurred in 20.9% of eosinophilic patients vs. 9.8% of controls. Eosinophilia was independently associated with thrombosis (OR = 1.33; 95% CI, 1.28–1.38; p < 0.0001), with increased risk from counts ≥ 0.7 K/μL. Mortality was also higher among eosinophilic patients (HR = 1.17; 95% CI, 1.13–1.20; p < 0.0001). Conclusions: Eosinophilia is associated with increased thromboembolic and mortality risk, highlighting the importance of eosinophil monitoring in clinical practice.

## Full-text entities

- **Genes:** EPX (eosinophil peroxidase) [NCBI Gene 8288] {aka EPO, EPP, EPX-PEN, EPXD}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}, SIGLEC8 (sialic acid binding Ig like lectin 8) [NCBI Gene 27181] {aka SAF2, SIGLEC-8, SIGLEC8L}
- **Diseases:** thrombophilia (MESH:D019851), acute and chronic kidney failure (MESH:D058186), inherited thrombophilic disorders (MESH:C540694), allergic and immune-mediated diseases (MESH:D006969), strokes (MESH:D020521), chronic obstructive lung disease (MESH:D029424), cardiomyopathies (MESH:D009202), Hodgkin lymphoma (MESH:D006689), autoimmune diseases (MESH:D001327), neurologic disease (MESH:D020271), obesity (MESH:D009765), interstitial nephritis (MESH:D009395), hematologic malignancies (MESH:D019337), PE (MESH:D011655), acute and chronic myeloid leukemias (MESH:D015470), metabolic diseases (MESH:D008659), dyslipidemia (MESH:D050171), asthmatic (MESH:D013224), injury to (MESH:D014947), vasculitis (MESH:D014657), inflammation (MESH:D007249), asthma (MESH:D001249), Eosinophilia (MESH:D004802), diabetes (MESH:D003920), valve diseases (MESH:D006349), lung diseases (MESH:D008171), malignancies (MESH:D009369), dementia (MESH:D003704), non-Hodgkin lymphoma (MESH:D008228), aggression (MESH:D010554), cardiac and neurologic diseases (MESH:D006331), allergic disorders (MESH:D004342), parasitic infections (MESH:D010272), thromboembolic (MESH:D013923), hepatic diseases (MESH:D056486), interstitial lung disease (MESH:D017563), heart failure (MESH:D006333), kidney disease (MESH:D007674), allergic, infectious, and malignant diseases (MESH:D003141), solid (MESH:D018250), chronic myelomonocytic leukemia (MESH:D015477), movement disorders (MESH:D009069), alcoholic cirrhosis (MESH:D008104), HES (MESH:D017681), hypertension (MESH:D006973), Mortality (MESH:D003643), VTE (MESH:D054556), Thrombosis (MESH:D013927), glomerulonephritis (MESH:D005921), vascular injury (MESH:D057772), antiphospholipid syndrome (MESH:D016736), DVT (MESH:D020246), acute and chronic lymphoid leukemias (MESH:D054198), heart attacks (MESH:D009203), helminthic infections (MESH:D007239), coagulation (MESH:D001778), cardiovascular and metabolic diseases (MESH:D002318)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942559/full.md

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Source: https://tomesphere.com/paper/PMC12942559