Evidence map›Paper›PMID 41140656›Full record

ArticleFrontiers in medicine2025

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

Tian Ye, Wanlin Lei, Maofeng Wang, Lili Xu

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Tian Ye *Department of Emergency, Affiliated Dongyang Hospital, Wenzhou Medical University, Dongyang, Zhejiang, China.
Wanlin Lei *Department of Biomedical Sciences Laboratory, Affiliated Dongyang Hospital, Wenzhou Medical University, Dongyang, Zhejiang, China.
Maofeng WangDepartment of Biomedical Sciences Laboratory, Affiliated Dongyang Hospital, Wenzhou Medical University, Dongyang, Zhejiang, China.
Lili XuDepartment of Obstetrics, Affiliated Dongyang Hospital, Wenzhou Medical University, Dongyang, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: 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. Methods: 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 ( Results: 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. Conclusion: 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.

Indexed as

adverse effectsanticoagulantsbleedingnomogrampulmonary embolismrisk prediction model

Identifiers

PMID41140656
PMCPMC12548197

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.