Targeted prophylactic anticoagulation based on the TRiP(cast) score in patients with lower limb immobilisation: a multicentre, stepped wedge, randomised implementation trial.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
16 Mar 2024
Historique:
received: 23 08 2023
revised: 14 10 2023
accepted: 20 10 2023
medline: 18 3 2024
pubmed: 19 2 2024
entrez: 18 2 2024
Statut: ppublish

Résumé

Prophylactic anticoagulation in emergency department patients with lower limb trauma requiring immobilisation is controversial. The Thrombosis Risk Prediction for Patients with Cast Immobilisation-TRiP(cast)-score could identify a large subgroup of patients at low risk of venous thromboembolism for whom prophylactic anticoagulation can be safely withheld. We aimed to prospectively assess the safety of withholding anticoagulation for patients with lower limb trauma at low risk of venous thromboembolism, defined by a TRiP(cast) score of less than 7. CASTING was a stepped-wedge, multicentre, cluster-randomised trial with blinded outcome assessment. 15 emergency departments in France and Belgium were selected and randomly assigned staggered start dates for switching from the control phase (ie, anticoagulation prescription according to the physician's usual practice) to the intervention phase (ie, targeted anticoagulation according to TRiP(cast) score: no prescription if score <7 and anticoagulation if score was ≥7). Patients were included if they presented to a participating emergency department with lower limb trauma requiring immobilisation for at least 7 days and were aged 18 years or older. The primary outcome was the 3-month cumulative rate of symptomatic venous thromboembolism during the intervention phase in patients with a TRiP(cast) score of less than 7. The targeted strategy was considered safe if this rate was less than 1% with an upper 95% CI of less than 2%. The primary analysis was performed in the intention-to-treat population. This study is registered at ClinicalTrials.gov (NCT04064489). Between June 16, 2020, and Sept 15, 2021, 15 clusters and 2120 patients were included. Of the 1505 patients analysed in the intervention phase, 1159 (77·0%) had a TRiP(cast) score of less than 7 and did not receive anticoagulant treatment. The symptomatic venous thromboembolism rate was 0·7% (95% CI 0·3-1·4, n=8/1159). There was no difference between the control and the intervention phases in the cumulative rate of symptomatic venous thromboembolism or in bleeding rates. Patients with a TRiP(cast) score of less than 7 who are not receiving anticoagulation have a very low risk of venous thromboembolism. A large proportion of patients with lower limb trauma and immobilisation could safely avoid thromboprophylaxis. French Ministry of Health.

Sections du résumé

BACKGROUND BACKGROUND
Prophylactic anticoagulation in emergency department patients with lower limb trauma requiring immobilisation is controversial. The Thrombosis Risk Prediction for Patients with Cast Immobilisation-TRiP(cast)-score could identify a large subgroup of patients at low risk of venous thromboembolism for whom prophylactic anticoagulation can be safely withheld. We aimed to prospectively assess the safety of withholding anticoagulation for patients with lower limb trauma at low risk of venous thromboembolism, defined by a TRiP(cast) score of less than 7.
METHODS METHODS
CASTING was a stepped-wedge, multicentre, cluster-randomised trial with blinded outcome assessment. 15 emergency departments in France and Belgium were selected and randomly assigned staggered start dates for switching from the control phase (ie, anticoagulation prescription according to the physician's usual practice) to the intervention phase (ie, targeted anticoagulation according to TRiP(cast) score: no prescription if score <7 and anticoagulation if score was ≥7). Patients were included if they presented to a participating emergency department with lower limb trauma requiring immobilisation for at least 7 days and were aged 18 years or older. The primary outcome was the 3-month cumulative rate of symptomatic venous thromboembolism during the intervention phase in patients with a TRiP(cast) score of less than 7. The targeted strategy was considered safe if this rate was less than 1% with an upper 95% CI of less than 2%. The primary analysis was performed in the intention-to-treat population. This study is registered at ClinicalTrials.gov (NCT04064489).
FINDINGS RESULTS
Between June 16, 2020, and Sept 15, 2021, 15 clusters and 2120 patients were included. Of the 1505 patients analysed in the intervention phase, 1159 (77·0%) had a TRiP(cast) score of less than 7 and did not receive anticoagulant treatment. The symptomatic venous thromboembolism rate was 0·7% (95% CI 0·3-1·4, n=8/1159). There was no difference between the control and the intervention phases in the cumulative rate of symptomatic venous thromboembolism or in bleeding rates.
INTERPRETATION CONCLUSIONS
Patients with a TRiP(cast) score of less than 7 who are not receiving anticoagulation have a very low risk of venous thromboembolism. A large proportion of patients with lower limb trauma and immobilisation could safely avoid thromboprophylaxis.
FUNDING BACKGROUND
French Ministry of Health.

Identifiants

pubmed: 38368901
pii: S0140-6736(23)02369-3
doi: 10.1016/S0140-6736(23)02369-3
pii:
doi:

Substances chimiques

Anticoagulants 0

Banques de données

ClinicalTrials.gov
['NCT04064489']

Types de publication

Randomized Controlled Trial Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1051-1060

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests AP reports receiving personal fees from Daiichi, Bayer, Bristol Myers Squibb, Pfizer, Stago, Alnylam, Sanofi, Viatris, Boehringer, and Leo Pharma. SL reports receiving personal fees from Brahms. TD reports receiving personal fees from Sanofi Aventis. TM reports receiving personal fees from Bristol Myers Squibb. P-MR reports receiving personal fees from Aspen, Bayer, Boehringer Ingelheim, Sanofi Aventis, Pfizer, Bristol Myers Squibb, and Viatis. All other authors declare no competing interests.

Auteurs

Delphine Douillet (D)

Emergency Department, Health Faculty, Angers University Hospital, Angers, France; UMR MitoVasc CNRS 6015 - INSERM 1083, Equipe CARME, UNIV Angers, Angers, France; F-CRIN INNOVTE Network, Saint-Etienne, France. Electronic address: delphine.douillet@chu-angers.fr.

Andrea Penaloza (A)

F-CRIN INNOVTE Network, Saint-Etienne, France; Emergency Department, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

Damien Viglino (D)

Emergency Department, University Hospital of Grenoble Alpes, University Grenoble-Alpes, Grenoble, France; HP2 Laboratory, Grenoble Alpes University, INSERM U1300, Grenoble, France.

Jean-Jacques Banihachemi (JJ)

Department of Trauma and Musculo-Skeletal Emergency, University Hospital and Medical Centre of Grenoble-Alpes Hospital South, Grenoble, France.

Anmar Abboodi (A)

Emergency Department, Cholet Hospital, Cholet, France.

Mathilde Helderlé (M)

Emergency Department, Le Mans Hospital, Le Mans, France.

Emmanuel Montassier (E)

Emergency Department, Nantes University Hospital, Nantes, France; MiHAR Laboratary, EE1701, University of Nantes, Nantes, France.

Fréderic Balen (F)

Department of Emergency Medicine, Toulouse University Hospital, Toulouse, France.

Christian Brice (C)

Emergency Department, Centre Hospitalier de Saint-Brieuc, Saint-Brieuc, France.

Saïd Laribi (S)

Emergency Department, Tours University Hospital, Tours, France.

Thibault Duchenoy (T)

Emergency Department, AP-HP Cochin, Paris, France.

Philippe Vives (P)

Emergency Department, Agen Hospital, Agen, France.

Louis Soulat (L)

Emergency Department, Rennes University Hospital, Rennes, France.

Nicolas Marjanovic (N)

Emergency Department, Poitiers University Hospital, Poitiers, France.

Thomas Moumneh (T)

Emergency Department, Health Faculty, Angers University Hospital, Angers, France; F-CRIN INNOVTE Network, Saint-Etienne, France.

Dominique Savary (D)

Emergency Department, Health Faculty, Angers University Hospital, Angers, France.

Jérémie Riou (J)

Methodology and Biostatistics Department, Delegation to Clinical Research and Innovation, Angers University Hospital, Angers, France.

Pierre-Marie Roy (PM)

Emergency Department, Health Faculty, Angers University Hospital, Angers, France; UMR MitoVasc CNRS 6015 - INSERM 1083, Equipe CARME, UNIV Angers, Angers, France; F-CRIN INNOVTE Network, Saint-Etienne, France.

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Classifications MeSH