Evidence map›Paper›PMID 41056444›Full record

ArticleJournal of orthopaedic trauma2025

Effect of Aspirin Versus Low-Molecular-Weight Heparin for Thromboprophylaxis in High-Risk and Fracture Location Subpopulations: A Secondary Analysis of the PREVENT CLOT Trial.

Sandip P Tarpada, Nathan N O'Hara, Deborah M Stein, Anthony J DeSantis, Renan C Castillo, Katherine P Frey, Gerard P Slobogean, I Leah Gitajn, Greg E Gaski, Laurence B Kempton and 8 more

Abstract read
In one paragraph

Article in Journal of orthopaedic trauma, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

18 authors.

Sandip P TarpadaDepartment of Orthopaedics, R Adams Cowley Shock Trauma Center, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0003-0532-5552
Nathan N O'HaraDepartment of Orthopaedics, R Adams Cowley Shock Trauma Center, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0003-0537-3474
Deborah M SteinProgram in Trauma/Department of Surgery, R Adams Cowley Shock Trauma Center, University of Maryland School of Medicine, MD, Baltimore, MD.
Anthony J DeSantisProgram in Trauma/Department of Surgery, R Adams Cowley Shock Trauma Center, University of Maryland School of Medicine, MD, Baltimore, MD.ORCID 0000-0002-0746-8605
Renan C CastilloDepartment of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Katherine P FreyDepartment of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.ORCID 0000-0001-5305-1774
Gerard P SlobogeanDepartment of Orthopaedics, R Adams Cowley Shock Trauma Center, University of Maryland School of Medicine, Baltimore, MD.ORCID 0000-0002-9111-9239
I Leah GitajnDepartment of Orthopaedics, Dartmouth Hitchcock Medical Center, Lebanon, NH.
Greg E GaskiDepartment of Orthopaedic Surgery, Inova Fairfax Medical Campus, Fairfax, VA.ORCID 0000-0002-2795-4029
Laurence B KemptonDepartment of Orthopaedic Surgery, Carolinas Medical Center, Atrium Health Musculoskeletal Institute, Charlotte, NC.ORCID 0000-0003-2185-9730
Conor P KlewenoDepartment of Orthopaedic Surgery, Harborview Medical Center at the University of Washington, Seattle, WA.ORCID 0000-0002-2113-9146
Reza FiroozabadiDepartment of Orthopaedic Surgery, Harborview Medical Center at the University of Washington, Seattle, WA.ORCID 0000-0001-6171-489
Joseph CuschieriDepartment of Surgery, University of California, San Francisco, San Francisco, CA.ORCID 0000-0003-1456-6841
A Britton ChristmasDepartment of Surgery, Atrium Health-Carolinas Medical Center, Charlotte, NC.
Jeffery A ClaridgeDepartment of General Surgery, The Cleveland Clinic Health Care System, Cleveland, OH.
Debra MarvelPREVENT CLOT Patient Stakeholder.ORCID 0000-0002-0983-8630
Robert V O'TooleDepartment of Orthopaedics, R Adams Cowley Shock Trauma Center, University of Maryland School of Medicine, Baltimore, MD.
METRC

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo compare the effectiveness and safety of aspirin versus low-molecular-weight heparin (LMWH) for thromboprophylaxis in 11 high-risk or fracture location subpopulations.

methodsDesign: A post-hoc secondary analysis of the published PREVENT CLOT trial.

setting21 trauma centers. PATIENT SELECTION CRITERIA: Adult patients with an operatively treated extremity fracture or any pelvic or acetabular fracture were enrolled from April 2017 through August 2021. Patients with only hand or foot fractures, presenting >48 hours after injury, or with a history of VTE within 6 months of injury were excluded. The 11 subpopulations included i) a head injury, ii) an abdominal injury, iii) a spinal injury, iv) a thoracic injury, v) multiply injured patients, vi) obesity, vii) previous VTE ≥ 6 months, viii) isolated upper extremity fracture, ix) isolated lower extremity fracture, x) isolated pelvic or acetabular fracture, and xi) geriatric femur fracture. OUTCOME MEASURES AND COMPARISONS: The primary outcome was 90-day all-cause mortality. Secondary outcomes included non-fatal pulmonary embolism, proximal deep vein thrombosis (DVT), distal DVT, and bleeding events. Outcomes were assessed using Kaplan-Meier estimators and Cox proportional hazards models comparing 81 mg of aspirin versus 30 mg of LMWH twice daily. The threshold for statistical significance was a Bonferroni-corrected alpha of 0.001 to account for multiple comparisons.

resultsThe largest subpopulations were isolated lower extremity fractures (n=6,289), obesity (n=4,234), and polytrauma with Injury Severity Score (ISS) >16 (n=1,596). No comparison of aspirin vs LMWH within the 11 subpopulations for the 5 outcomes reached the corrected threshold for statistical significance of P < 0.001. However, 5 comparisons of aspirin vs LMWH were less than the conventional P-value of 0.05. Specifically, the aspirin group demonstrated lower mortality in patients with a head injury (difference, -3.2%; 95% CI -6.1% to -0.3%; P = 0.03) or a spine injury (difference, -6.0%; 95% CI -11.7% to -0.3%; P = 0.04) than the LMWH group. The LMWH group demonstrated a lower rate of distal DVTs for patients with a head injury (difference, 4.4%; 95% CI, 0.8% to 8.1%; P = 0.03), thoracic injury (difference, 1.5%; 95% CI, 0.0% to 2.9%; P=0.034) or with ISS >16 (difference, 1.7%; 95% CI, 0.2% to 3.3; P = 0.03) than the aspirin group.

conclusionsWithin 11 high-risk or fracture location-specific subpopulations, there were no statistically significant differences between aspirin or LMWH in the 90-day rates of all-cause mortality, non-fatal PE, proximal DVT, distal DVT, or bleeding complications at a threshold corrected for multiple comparisons (P < 0.001). LEVEL OF EVIDENCE: Therapeutic Level I.

Indexed as

aspirinclinical trialhigh-risklow-molecular-weight heparinorthopaedic traumathromboprophylaxistraumavenous thromboembolism

Identifiers

PMID41056444
PMCPMC12704675

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.