Evidence map›Paper›PMID 42421880›Full record

ArticleFrontiers in surgery2026

Weight-based, anti-Xa guided enoxaparin after spine trauma surgery: target attainment and safety in a retrospective cohort.

Dallas L Sheinberg, David Travis Johnston, Brendan T O'Reilly, Gabriel Galan Castro, Jawad R Khazaal, Joseph S Withrow, Duncan J Trimble, Ankush Chandra, Anthony J Lim, Derek S Sheinberg and 3 more

Abstract read
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Article in Frontiers in surgery, 2026. 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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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

13 authors.

Dallas L SheinbergDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
David Travis JohnstonDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Brendan T O'ReillyDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Gabriel Galan CastroDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Jawad R KhazaalDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Joseph S WithrowCarolina Neurosurgery & Spine Associates, Charlotte, NC, United States.
Duncan J TrimbleDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Ankush ChandraDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Anthony J LimDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Derek S SheinbergUniversity of Miami Miller School of Medicine, Miami, FL, United States.
Jennifer ZaragozaDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
Wen LiDepartment of Internal Medicine, McGovern Medical School at UTHealth Houston, Houston, TX, United States.
John R WilliamsDepartment of Neurosurgery, McGovern Medical School at UTHealth Houston, Houston, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and purpose: Patients undergoing surgery for traumatic spine injuries have a high risk of venous thromboembolism (VTE). Standard fixed or weight-based enoxaparin regimens may leave some patients below prophylactic anti-factor Xa (anti-Xa) target ranges. Whether anti-Xa-guided enoxaparin dose adjustment can be implemented while maintaining acceptable observed bleeding outcomes has not been studied specifically in postoperative spine trauma patients. This study evaluates anti-Xa target attainment, symptomatic VTE, and safety outcomes after anti-Xa-guided enoxaparin titration. Methods: We performed a retrospective cohort study of adults (≥18 years old) who underwent operative treatment for traumatic spine injuries at a Level I trauma center. All patients received weight-based enoxaparin starting 24 h postoperatively (30 mg every 12 h if <90 kg, 40 mg every 12 h if ≥90 kg) plus mechanical VTE prophylaxis and early mobilization. In the anti-Xa cohort, levels were obtained 4 h after the third dose (target 0.2-0.4 IU/mL) and doses were adjusted by 10 mg if outside this range. A comparison cohort received the same initial dosing without anti-Xa monitoring. The primary outcome was symptomatic postoperative VTE. Secondary outcomes included bleeding requiring transfusion, spinal epidural hematoma, hospital length of stay, and ambulation at discharge. Results: A total of 354 patients were included (170 anti-Xa; 184 fixed dose). Symptomatic VTE was rare and similar between groups (1.1% vs. 1.6%). No postoperative epidural hematomas occurred. In the anti-Xa cohort, 28% required dose escalation and 7% required more than one adjustment. In exploratory adjusted analyses, bleeding requiring transfusion and length of stay did not differ between groups. Conclusions: Weight-based enoxaparin with anti-Xa-guided titration was feasible after spine trauma surgery and identified a substantial subset of patients below the prespecified prophylactic anti-Xa target range. Protocol-based dose escalation was not associated with an observed increase in bleeding requiring transfusion, and no postoperative epidural hematomas occurred. Larger prospective studies are needed to determine whether improved anti-Xa target attainment translates into lower VTE rates.

Indexed as

anti-factor Xa monitoringdeep vein thrombosisenoxaparinepidural hematomaspinal cord injuryspinal traumaspine surgeryvenous thromboembolism

Identifiers

PMID42421880
PMCPMC13341635

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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.