# Development and validation of a nomogram for predicting bleeding risk in patients with pulmonary embolism

**Authors:** Tian Ye, Wanlin Lei, Maofeng Wang, Lili Xu

PMC · DOI: 10.3389/fmed.2025.1692156 · Frontiers in Medicine · 2025-10-09

## TL;DR

This study created a tool to predict bleeding risk in pulmonary embolism patients, aiming to improve anticoagulation treatment decisions.

## Contribution

A novel PE-specific bleeding risk prediction model was developed and validated for personalized anticoagulation management.

## Key findings

- The model identified six key predictors for bleeding risk, including prior bleeding history and renal insufficiency.
- The model showed strong discrimination with an AUC of 0.756 in development and 0.729 in validation.
- Using the model's optimal threshold reduced major bleeding by 42% compared to standard care.

## Abstract

Bleeding during anticoagulation therapy represents a critical challenge in pulmonary embolism (PE) management, this study aimed to develop and validate a PE-specific bleeding risk prediction model.

This retrospective cohort study utilized a clinical research big data platform, including 5,632 hospitalized PE patients (January 2013–December 2024). Significant bleeding within 6 months served as the primary outcome. After excluding variables with >20% missingness, 29 predictors were analyzed. The cohort was randomly split into development (n = 3,942) and validation sets (n = 1,690). LASSO regression identified key predictors, with multivariable logistic regression constructing the final model. Performance was assessed via AUC-ROC, calibration plots, and decision curve analysis (DCA).

The final model identified six predictors: prior bleeding history, renal insufficiency, red blood cell count, systolic pressure, cerebral infarction, and creatinine. The model demonstrated robust discrimination (development AUC: 0.756, 95%CI: 0.729–0.784; validation AUC: 0.729, 95%CI: 0.685–0.773) and calibration (validation slope: 0.810). DCA confirmed significant net benefit at 5–35% thresholds, with 30% as the optimal cut-off. At this threshold, the model reduced major bleeding by 42% versus standard care.

This novel PE-specific bleeding risk tool provides clinically actionable stratification, enabling personalized anticoagulation intensity adjustment. Implementation may reduce hemorrhage-related morbidity while optimizing resource utilization.

## Linked entities

- **Diseases:** pulmonary embolism (MONDO:0005279), renal insufficiency (MONDO:0001106), cerebral infarction (MONDO:0002679)

## Full-text entities

- **Diseases:** cerebral infarction (MESH:D002544), PE (MESH:D011655), Bleeding (MESH:D006470), renal insufficiency (MESH:D051437)
- **Chemicals:** creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12548197/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12548197/full.md

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Source: https://tomesphere.com/paper/PMC12548197