Evidence map›Paper›PMID 38420604›Full record

ArticleTrauma surgery & acute care open2024

Weight-based enoxaparin thromboprophylaxis in young trauma patients: analysis of the CLOTT-1 registry.

Sarah Lombardo, Marta McCrum, M Margaret Knudson, Ernest E Moore, Lucy Kornblith, Scott Brakenridge, Brandon Bruns, Mark D Cipolle, Todd W Costantini, Bruce Crookes and 16 more

Open access · goldAbstract read
In one paragraph

Article in Trauma surgery & acute care open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.2field-weighted citation impact, top 15% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Anti-xa guided enoxaparin thromboprophylaxis is associated with less thromboembolism than fixed dose dalteparin in trauma patients admitted to intensive care.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2025
    Observational
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

26 authors at 18 institutions in 1 country.

Sarah LombardoSurgery, University of Utah, Salt Lake City, Utah, USA.ORCID 0000-0002-1132-0881
Marta McCrumSurgery, University of Utah, Salt Lake City, Utah, USA.
M Margaret KnudsonSurgery, University of California San Francisco, San Francisco, California, USA.
Ernest E MooreDenver Health Medical Center, Denver, Colorado, USA.
Lucy KornblithSurgery, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0002-1861-9691
Scott BrakenridgeDepartment of Surgery, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-7327-3718
Brandon BrunsDepartment of Surgery, UT Southwestern Medical School, Dallas, Texas, USA.
Mark D CipolleLehigh Valley Health Network, Allentown, Pennsylvania, USA.
Todd W CostantiniSurgery, University of California San Francisco, San Francisco, California, USA.
Bruce CrookesSurgery, Medical University of South Carolina, Charleston, South Carolina, USA.
Elliott R HautSurgery, Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0001-7075-771X
Andrew J KerwinSurgery, University of Florida College of Medicine-Jacksonville, Jacksonville, Florida, USA.ORCID 0000-0003-4372-5813
Laszlo N KiralyOregon Health & Science University, Portland, Oregon, USA.
Lisa Marie KnowltonGeneral Surgery, Stanford University, Stanford, California, USA.ORCID 0000-0001-6046-5035
Matthew J MartinDivision of Trauma and Surgical Critical Care, LAC+USC Medical Center, Los Angeles, California, USA.
Michelle K McNuttSurgery, University of Texas Health Science Center at Houston, Houston, Texas, USA.
David J MiliaMedical College of Wisconsin, Milwaukee, Wisconsin, USA.
Alicia MohrSurgery, University of Florida College of Medicine-Jacksonville, Jacksonville, Florida, USA.
Frederick RogersLancaster General Health, Lancaster, Pennsylvania, USA.
Thomas ScaleaUniversity of Maryland School of Medicine, Baltimore, Maryland, USA.
Sherry SixtaSt Anthony Hospital & Medical Campus, Lakewood, Colorado, USA.
David SpainSurgery, Stanford University, Stanford, California, USA.ORCID 0000-0002-0477-7613
Charles E WadeSurgery, University of Texas Health Science Center at Houston, Houston, Texas, USA.
George C VelmahosMassachusetts General Hospital, Boston, Massachusetts, USA.
Ram NirulaUniversity of Utah School of Medicine, Salt Lake City, Utah, USA.
Jade NunezSurgery, University of Utah, Salt Lake City, Utah, USA.
University of Utah · USUniversity of California, San Francisco · USStanford University · USThe University of Texas Health Science Center at Houston · USUniversity of Florida · USDenver Health Medical Center · USJohns Hopkins University · USLAC+USC Medical Center · USLancaster General Hospital · USLehigh Valley Hospital-Pocono · USMassachusetts General Hospital · USMedical College of Wisconsin · USMedical University of South Carolina · USOregon Health & Science University · USSt. Anthony Hospital · USThe University of Texas Southwestern Medical Center · USUniversity of Maryland, Baltimore · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Optimal venous thromboembolism (VTE) enoxaparin prophylaxis dosing remains elusive. Weight-based (WB) dosing safely increases anti-factor Xa levels without the need for routine monitoring but it is unclear if it leads to lower VTE risk. We hypothesized that WB dosing would decrease VTE risk compared with standard fixed dosing (SFD). Methods: Patients from the prospective, observational CLOTT-1 registry receiving prophylactic enoxaparin (n=5539) were categorized as WB (0.45-0.55 mg/kg two times per day) or SFD (30 mg two times per day, 40 mg once a day). Multivariate logistic regression was used to generate a predicted probability of VTE for WB and SFD patients. Results: Of 4360 patients analyzed, 1065 (24.4%) were WB and 3295 (75.6%) were SFD. WB patients were younger, female, more severely injured, and underwent major operation or major venous repair at a higher rate than individuals in the SFD group. Obesity was more common among the SFD group. Unadjusted VTE rates were comparable (WB 3.1% vs. SFD 3.9%; p=0.221). Early prophylaxis was associated with lower VTE rate (1.4% vs. 5.0%; p=0.001) and deep vein thrombosis (0.9% vs. 4.4%; p<0.001), but not pulmonary embolism (0.7% vs. 1.4%; p=0.259). After adjustment, VTE incidence did not differ by dosing strategy (adjusted OR (aOR) 0.75, 95% CI 0.38 to 1.48); however, early administration was associated with a significant reduction in VTE (aOR 0.47, 95% CI 0.30 to 0.74). Conclusion: In young trauma patients, WB prophylaxis is not associated with reduced VTE rate when compared with SFD. The timing of the initiation of chemoprophylaxis may be more important than the dosing strategy. Further studies need to evaluate these findings across a wider age and comorbidity spectrum. Level of evidence: Level IV, therapeutic/care management.

Indexed as

Multiple Traumaobservational studyThromboembolismVenous thromboembolism

Identifiers

PMID38420604
PMCPMC10900334
OpenAlexW4392202449

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.