Evidence map›Paper›PMID 39305950›Full record

ArticleJournal of vascular surgery. Venous and lymphatic disorders2025

A composite risk assessment model for venous thromboembolism.

Mary Sixian Lin, Hilary Hayssen, Minerva Mayorga-Carlin, Shalini Sahoo, Tariq Siddiqui, Georges Jreij, Brian R Englum, Phuong Nguyen, Yelena Yesha, John David Sorkin and 1 more

Abstract read
In one paragraph

Article in Journal of vascular surgery. Venous and lymphatic disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Mary Sixian LinDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD.
Hilary HayssenDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD.
Minerva Mayorga-CarlinDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD.
Shalini SahooDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD.
Tariq SiddiquiDepartment of Surgery, Baltimore VA Medical Center, Baltimore, Baltimore, MD.
Georges JreijDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD.
Brian R EnglumDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD.
Phuong NguyenDepartment of Computer Science, University of Miami, Miami, FL.
Yelena YeshaDepartment of Computer Science, University of Miami, Miami, FL.
John David SorkinDepartment of Geriatric Research, Education, and Clinical Center, Baltimore VA Medical Center, Baltimore, MD; Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.
Brajesh K LalDepartment of Surgery, University of Maryland School of Medicine, Baltimore, MD; Department of Surgery, Baltimore VA Medical Center, Baltimore, Baltimore, MD. Electronic address: blal@som.umaryland.edu.

Funding

QAQC Johns Hopkins Institute for Clinical and Translational ResearchUL1TR003098 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2019 to 2023
$57.7M
CREST-2 Clinical Coordinating CenterU01NS080168 · NINDS · MAYO CLINIC JACKSONVILLE · PI Thomas G Brott, JAMES F MESCHIA · 2014 to 2026
$56.3M
University of Maryland Claude D. Pepper Older Americans Independence Center (UM-OAIC)P30AG028747 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI Stephen L. Seliger · 2006 to 2026
$28.9M
RESEARCH TRAINING IN THE EPIDEMIOLOGY OF AGINGT32AG000262 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI ANN L GRUBER-BALDINI, DENISE L ORWIG · 1998 to 2026
$8.2M
Healthy Aging Neighborhoods of Diversity Across LifespanZ01AG000513 · NIA · NATIONAL INSTITUTE ON AGING · PI EVANS, MICHELE K · 2001 to 2008
$6.8M
Carotid Revascularization and Medical Management for Asymptomatic CarotidStenosis Trial - Hemodynamics (CREST-H)R01NS097876 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI RONALD M LAZAR, DAVID SIGMUND LIEBESKIND · 2017 to 2026
$6.4M
CSRD VA I01 CX001621Intramural NIH HHS Z01 AG000513NCATS NIH HHS UL1 TR003098NIA NIH HHS P30 AG028747NIA NIH HHS T32 AG000262NINDS NIH HHS R01 NS097876NINDS NIH HHS U01 NS080168RRD VA I01 RX000995
6 · The paper itself

Abstract

objectiveVenous thromboembolism (VTE) is a preventable cause of hospitalization-related morbidity and mortality. VTE prevention requires accurate risk stratification. Federal agencies mandated VTE risk assessment for all hospital admissions. We have shown that the widely used Caprini (30 risk factors) and Padua (11 risk factors) VTE risk-assessment models (RAMs) have limited predictive ability for VTE when used for all general hospital admissions. Here, we test whether combining the risk factors from all 23 available VTE RAMs improves VTE risk prediction.

methodsWe analyzed data from the first hospitalizations of 1,282,014 surgical and non-surgical patients admitted to 1298 Veterans Affairs facilities nationwide between January 2016 and December 2021. We used logistic regression to predict VTE within 90 days of admission using risk factors from all 23 available VTE RAMs. Area under the receiver operating characteristic curves (AUC), sensitivity, specificity, and positive (PPV) and negative predictive values (NPV) were used to quantify the predictive power of our models. The metrics were computed at two diagnostic thresholds that maximized (1) the value of sensitivity + specificity-1; and (2) PPV and were compared using McNemar's test. The Delong-Delong test was used to compare AUCs.

resultsAfter excluding those with missing data, 1,185,633 patients (mean age, 66 years; 93% male; and 72% White) were analyzed, of whom 33,253 (2.8%) had a VTE (deep venous thrombosis [DVT], n = 19,218, 1.6%; pulmonary embolism [PE], n = 10,190, 0.9%; PE + DVT, n = 3845, 0.3%). Our composite RAM included 102 risk factors and improved prediction of VTE compared with the Caprini RAM risk factors (AUC composite model: 0.74; AUC Caprini risk-factor model: 0.63; P < .0001). When the sum of sensitivity and specificity-1 was maximized, the composite model demonstrated small improvements in sensitivity, specificity and PPV; NPV was high in both models. When PPV was maximized, the PPV of the composite model was improved but remained low. The nature of the relationship between NPV and PPV precluded any further gain in PPV by sacrificing NPV and sensitivity.

conclusionsUsing a composite of 102 risk factors from all available VTE RAMs, we improved VTE prediction in a large, national cohort of >1 million general hospital admissions. However, neither model has a sensitivity or PPV that permits it to be a reliable predictor of VTE. We demonstrate the limits of currently available VTE risk prediction tools; no available RAM is ready for widespread use in the general hospital population.

Indexed as

Decision Support TechniquesPredictive Value of TestsVenous ThromboembolismAgedAged, 80 and overDatabases, FactualFemaleHumansMaleMiddle AgedReproducibility of ResultsRetrospective StudiesRisk AssessmentRisk FactorsTime FactorsUnited StatesDeep venous thrombosisPreventionRisk assessmentRisk factorsVenous thromboembolism

Identifiers

PMID39305950
PMCPMC11764112

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.