Timing of pharmacologic venous thromboembolism prophylaxis initiation for trauma patients with nonoperatively managed blunt abdominal solid organ injury: a systematic review and meta-analysis.


Journal

World journal of emergency surgery : WJES
ISSN: 1749-7922
Titre abrégé: World J Emerg Surg
Pays: England
ID NLM: 101266603

Informations de publication

Date de publication:
25 04 2022
Historique:
received: 22 01 2022
accepted: 15 04 2022
entrez: 26 4 2022
pubmed: 27 4 2022
medline: 28 4 2022
Statut: epublish

Résumé

Blunt abdominal solid organ injury is common and is often managed nonoperatively. Clinicians must balance risk of both hemorrhage and thrombosis. The optimal timing of pharmacologic venous thromboembolism prophylaxis (VTEp) initiation in this population is unclear. The objective was to evaluate early (< 48 h) compared to late initiation of VTEp in adult trauma patients with blunt abdominal solid organ injury managed nonoperatively. Embase, MEDLINE, and the Cochrane Central Register of Controlled Trials were searched from inception to March 2021. Studies comparing timeframes of VTEp initiation were considered. The primary outcome was failure of nonoperative management (NOM) after VTEp initiation. Secondary outcomes included risk of transfusion, other bleeding complications, risk of deep vein thrombosis (DVT) and pulmonary embolism, and mortality. Ten cohort studies met inclusion criteria, with a total of 4642 patients. Meta-analysis revealed a statistically significant increase in the risk of failure of NOM among patients receiving early VTEp (OR 1.76, 95% CI 1.01-3.05, p = 0.05). There was no significant difference in risk of transfusion. Odds of DVT were significantly lower in the early group (OR 0.36, 95% CI 0.22-0.59, p < 0.0001). There was no difference in mortality (OR 1.50, 95% CI 0.82-2.75, p = 0.19). All studies were at serious risk of bias due to confounding. Initiation of VTEp earlier than 48 h following hospitalization is associated with an increased risk of failure of NOM but a decreased risk of DVT. Absolute failure rates of NOM are low. Initiation of VTEp at 48 h may balance the risks of bleeding and VTE.

Sections du résumé

BACKGROUND
Blunt abdominal solid organ injury is common and is often managed nonoperatively. Clinicians must balance risk of both hemorrhage and thrombosis. The optimal timing of pharmacologic venous thromboembolism prophylaxis (VTEp) initiation in this population is unclear. The objective was to evaluate early (< 48 h) compared to late initiation of VTEp in adult trauma patients with blunt abdominal solid organ injury managed nonoperatively.
METHODS
Embase, MEDLINE, and the Cochrane Central Register of Controlled Trials were searched from inception to March 2021. Studies comparing timeframes of VTEp initiation were considered. The primary outcome was failure of nonoperative management (NOM) after VTEp initiation. Secondary outcomes included risk of transfusion, other bleeding complications, risk of deep vein thrombosis (DVT) and pulmonary embolism, and mortality.
RESULTS
Ten cohort studies met inclusion criteria, with a total of 4642 patients. Meta-analysis revealed a statistically significant increase in the risk of failure of NOM among patients receiving early VTEp (OR 1.76, 95% CI 1.01-3.05, p = 0.05). There was no significant difference in risk of transfusion. Odds of DVT were significantly lower in the early group (OR 0.36, 95% CI 0.22-0.59, p < 0.0001). There was no difference in mortality (OR 1.50, 95% CI 0.82-2.75, p = 0.19). All studies were at serious risk of bias due to confounding.
CONCLUSIONS
Initiation of VTEp earlier than 48 h following hospitalization is associated with an increased risk of failure of NOM but a decreased risk of DVT. Absolute failure rates of NOM are low. Initiation of VTEp at 48 h may balance the risks of bleeding and VTE.

Identifiants

pubmed: 35468835
doi: 10.1186/s13017-022-00423-1
pii: 10.1186/s13017-022-00423-1
pmc: PMC9036793
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Meta-Analysis Systematic Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

19

Informations de copyright

© 2022. The Author(s).

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Auteurs

Tyler Lamb (T)

Division of General Surgery, Department of Surgery, The Ottawa Hospital, 725 Parkdale Avenue, Ottawa, ON, K1Y 1J8, Canada. tlamb@toh.ca.
School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada. tlamb@toh.ca.

Tori Lenet (T)

Division of General Surgery, Department of Surgery, The Ottawa Hospital, 725 Parkdale Avenue, Ottawa, ON, K1Y 1J8, Canada.
School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.

Amin Zahrai (A)

School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.

Joseph R Shaw (JR)

School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
The Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Ryan McLarty (R)

School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Division of Urology, Department of Surgery, The Ottawa Hospital, Ottawa, ON, Canada.

Risa Shorr (R)

Library and Information Sciences, The Ottawa Hospital, Ottawa, ON, Canada.

Grégoire Le Gal (G)

Division of Hematology, Department of Medicine, The Ottawa Hospital, Ottawa, ON, Canada.
The Ottawa Hospital Research Institute, Ottawa, ON, Canada.

Peter Glen (P)

Division of General Surgery, Department of Surgery, The Ottawa Hospital, 725 Parkdale Avenue, Ottawa, ON, K1Y 1J8, Canada.
The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Ottawa Regional Trauma Program, The Ottawa Hospital, Ottawa, ON, Canada.

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