Propensity weighted analysis of chemical venous thromboembolism prophylaxis agents in isolated severe traumatic brain injury: An EAST sponsored multicenter study.

Severe TBI VTE VTE agent VTE prophylaxis

Journal

Injury
ISSN: 1879-0267
Titre abrégé: Injury
Pays: Netherlands
ID NLM: 0226040

Informations de publication

Date de publication:
09 Apr 2024
Historique:
received: 27 10 2023
revised: 09 03 2024
accepted: 01 04 2024
medline: 14 4 2024
pubmed: 14 4 2024
entrez: 13 4 2024
Statut: aheadofprint

Résumé

In patients with severe traumatic brain injury (TBI), clinicians must balance preventing venous thromboembolism (VTE) with the risk of intracranial hemorrhagic expansion (ICHE). We hypothesized that low molecular weight heparin (LMWH) would not increase risk of ICHE or VTE as compared to unfractionated heparin (UH) in patients with severe TBI. Patients ≥ 18 years of age with isolated severe TBI (AIS ≥ 3), admitted to 24 level I and II trauma centers between January 1, 2014 to December 31, 2020 and who received subcutaneous UH and LMWH injections for chemical venous thromboembolism prophylaxis (VTEP) were included. Primary outcomes were VTE and ICHE after VTEP initiation. Secondary outcomes were mortality and neurosurgical interventions. Entropy balancing (EBAL) weighted competing risk or logistic regression models were estimated for all outcomes with chemical VTEP agent as the predictor of interest. 984 patients received chemical VTEP, 482 UH and 502 LMWH. Patients on LMWH more often had pre-existing conditions such as liver disease (UH vs LMWH 1.7 % vs. 4.4 %, p = 0.01), and coagulopathy (UH vs LMWH 0.4 % vs. 4.2 %, p < 0.001). There were no differences in VTE or ICHE after VTEP initiation. There were no differences in neurosurgical interventions performed. There were a total of 29 VTE events (3 %) in the cohort who received VTEP. A Cox proportional hazards model with a random effect for facility demonstrated no statistically significant differences in time to VTE across the two agents (p = 0.44). The LMWH group had a 43 % lower risk of overall ICHE compared to the UH group (HR = 0.57: 95 % CI = 0.32-1.03, p = 0.062), however was not statistically significant. In this multi-center analysis, patients who received LMWH had a decreased risk of ICHE, with no differences in VTE, ICHE after VTEP initiation and neurosurgical interventions compared to those who received UH. There were no safety concerns when using LMWH compared to UH. Level III, Therapeutic Care Management.

Sections du résumé

BACKGROUND BACKGROUND
In patients with severe traumatic brain injury (TBI), clinicians must balance preventing venous thromboembolism (VTE) with the risk of intracranial hemorrhagic expansion (ICHE). We hypothesized that low molecular weight heparin (LMWH) would not increase risk of ICHE or VTE as compared to unfractionated heparin (UH) in patients with severe TBI.
METHODS METHODS
Patients ≥ 18 years of age with isolated severe TBI (AIS ≥ 3), admitted to 24 level I and II trauma centers between January 1, 2014 to December 31, 2020 and who received subcutaneous UH and LMWH injections for chemical venous thromboembolism prophylaxis (VTEP) were included. Primary outcomes were VTE and ICHE after VTEP initiation. Secondary outcomes were mortality and neurosurgical interventions. Entropy balancing (EBAL) weighted competing risk or logistic regression models were estimated for all outcomes with chemical VTEP agent as the predictor of interest.
RESULTS RESULTS
984 patients received chemical VTEP, 482 UH and 502 LMWH. Patients on LMWH more often had pre-existing conditions such as liver disease (UH vs LMWH 1.7 % vs. 4.4 %, p = 0.01), and coagulopathy (UH vs LMWH 0.4 % vs. 4.2 %, p < 0.001). There were no differences in VTE or ICHE after VTEP initiation. There were no differences in neurosurgical interventions performed. There were a total of 29 VTE events (3 %) in the cohort who received VTEP. A Cox proportional hazards model with a random effect for facility demonstrated no statistically significant differences in time to VTE across the two agents (p = 0.44). The LMWH group had a 43 % lower risk of overall ICHE compared to the UH group (HR = 0.57: 95 % CI = 0.32-1.03, p = 0.062), however was not statistically significant.
CONCLUSION CONCLUSIONS
In this multi-center analysis, patients who received LMWH had a decreased risk of ICHE, with no differences in VTE, ICHE after VTEP initiation and neurosurgical interventions compared to those who received UH. There were no safety concerns when using LMWH compared to UH.
LEVEL OF EVIDENCE METHODS
Level III, Therapeutic Care Management.

Identifiants

pubmed: 38614835
pii: S0020-1383(24)00210-9
doi: 10.1016/j.injury.2024.111523
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111523

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors have no conflict of interest to disclose.

Auteurs

Asanthi M Ratnasekera (AM)

Department of Surgery, Division of Trauma and Surgical Critical Care, Associate Professor of Surgery, Drexel College of Medicine, Philadelphia, PA, United States; Crozer Health Upland PA, Currently at Christianacare Health, Newark, DE, United States. Electronic address: ashanthi27@hotmail.com.

Sirivan S Seng (SS)

Department of Surgery, Crozer Health, Upland, PA, United States.

Daniel Kim (D)

Department of Surgery, Crozer Health, Upland, PA, United States.

Wenyan Ji (W)

Center for Biostatistics and Health Data Science, Department of Statistics, Virginia Polytechnic Institute and State University, Roanoke, VA, United States.

Christina L Jacovides (CL)

Department of Surgery, University of Pennsylvania, Philadelphia, PA, United States; Currently at Temple University, Philadelphia, PA, United States.

Elinore J Kaufman (EJ)

Department of Surgery, University of Pennsylvania, Philadelphia, PA, United States.

Hannah M Sadek (HM)

Department of Surgery, Virginia Commonwealth University, Richmond, VA, United States.

Lindsey L Perea (LL)

Department of Surgery, Penn Medicine Lancaster General Health, Lancaster, PA, United States.

Christina Monaco Poloni (CM)

Department of Surgery, Philadelphia College of Osteopathic Medicine, Philadelphia, PA, United States.

Ilya Shnaydman (I)

Department of Surgery, Medical Director, Surgical Intensive Care Unit, New York Medical College, West Chester Medical Center, Valhalla, NY, United States.

Alexandra Jeongyoon Lee (AJ)

Department of Surgery, West Chester Medical Center, Valhalla, NY, United States.

Victoria Sharp (V)

Department of Surgery, Trinity Health Ann Arbor, Ypsilanti, MI, United States.

Angela Miciura (A)

Department of Surgery, Trinity Health Ann Arbor, Ypsilanti, MI, United States.

Eric Trevizo (E)

Department of Surgery, Loma Linda University Medical Center, Loma Linda, CA, United States.

Martin G Rosenthal (MG)

Department of Surgery, Loma Linda University Medical Center, Loma Linda, CA, United States.

Lawrence Lottenberg (L)

Department of Surgery, St. Mary's Medical Center, West Palm Beach, FL, United States; Florida Atlantic University, Boca Raton, FL, United States.

William Zhao (W)

Department of Surgery, St. Mary's Medical Center, West Palm Beach, FL, United States; Florida Atlantic University, Boca Raton, FL, United States.

Alicia Keininger (A)

Department of Surgery, Trinity Health Oakland, Pontiac, MI, United States.

Michele Hunt (M)

Department of Surgery, Trinity Health Oakland, Pontiac, MI, United States.

John Cull (J)

Department of Surgery, Prisma Health Upstate, Greenville, SC, United States.

Chassidy Balentine (C)

Department of Surgery, Prisma Health Upstate, Greenville, SC, United States.

Tanya Egodage (T)

Department of Surgery, Cooper University Hospital, Camden, NJ, United States.

Aleem T Mohamed (AT)

Department of Surgery, Cooper University Hospital, Camden, NJ, United States.

Michelle Kincaid (M)

Department of Surgery, Ohio Health Grant Medical Center, Columbus, OH, United States.

Stephanie Doris (S)

Department of Surgery, Ohio Health Grant Medical Center, Columbus, OH, United States.

Robert Cotterman (R)

Department of Surgery, Promedica Toledo Hospital, Toledo, OH, United States.

Sara Seegert (S)

Department of Research, Promedica Toledo Hospital, Toledo, OH, United States.

Lewis E Jacobson (LE)

Department of Surgery, Ascension St. Vincent Hospital, Indianapolis, IN, United States.

Jamie Williams (J)

Department of Surgery, Ascension St. Vincent Hospital, Indianapolis, IN, United States.

Melissa Moncrief (M)

Department of Trauma & Acute Care Surgery, Kettering Health Main Campus, Kettering, OH, United States.

Brandi Palmer (B)

Department of Trauma & Acute Care Surgery, Kettering Health Main Campus, Kettering, OH, United States.

Caleb Mentzer (C)

Department of Surgery, Spartanburg Medical Center, Spartanburg, SC, United States.

Nichole Tackett (N)

Department of Surgery, Spartanburg Medical Center, Spartanburg, SC, United States.

Tjasa Hranjec (T)

Department of Surgery, Memorial Healthcare System, Hollywood, FL, United States.

Thomas Dougherty (T)

Department of Surgery, Memorial Healthcare System, Hollywood, FL, United States.

Shawna Morrissey (S)

Department of Surgery, Conemaugh Memorial Medical Center, Johnstown, PA, United States.

Lauren Donatelli-Seyler (L)

Department of Surgery, University Hospitals Cleveland Medical Center, Cleveland, OH, United States.

Amy Rushing (A)

Department of Surgery, University Hospitals Cleveland Medical Center, Cleveland, OH, United States.

Leah C Tatebe (LC)

Department of Surgery, Cook County Hospital, Chicago, IL, United States; Currently at Northwestern Memorial Hospital, Chicago, IL, United States.

Tiffany J Nevill (TJ)

Department of Surgery, Cook County Hospital, Chicago, IL, United States.

Michel B Aboutanos (MB)

Department of Surgery, Virginia Commonwealth University, Richmond, VA, United States.

David Hamilton (D)

Department of Surgery, Penrose Hospital, Colorado Springs, CO, United States.

Diane Redmond (D)

Department of Surgery, Penrose Hospital, Colorado Springs, CO, United States.

Daniel C Cullinane (DC)

Department of Surgery, Maine Medical Center, Portland, ME, United States.

Carolyne Falank (C)

Department of Surgery, Maine Medical Center, Portland, ME, United States.

Mark McMellen (M)

Department of Surgery, St. Anthony Hospital, Lakewood, CO, United States.

Chris Duran (C)

Department of Surgery, St. Anthony Hospital, Lakewood, CO, United States.

Jennifer Daniels (J)

Department of Surgery, University of California San Francisco, Fresno, CA, United States.

Shana Ballow (S)

Department of Surgery, University of California San Francisco, Fresno, CA, United States.

Kevin M Schuster (KM)

Department of Surgery, Yale School of Medicine, New Haven, CT, United States.

Paula Ferrada (P)

Department of Surgery, INOVA Fairfax Health System, Fairfax, VA, United States.

Classifications MeSH