Management of urgent invasive procedures in patients treated with direct oral anticoagulants: An observational registry analysis.

Activated prothrombin complex concentrates Anticoagulant Apixaban Bleeding Dabigatran Delay Direct oral anticoagulant Prothrombin complex concentrates Rivaroxaban Urgent procedure

Journal

Thrombosis research
ISSN: 1879-2472
Titre abrégé: Thromb Res
Pays: United States
ID NLM: 0326377

Informations de publication

Date de publication:
08 2022
Historique:
received: 23 02 2022
revised: 07 06 2022
accepted: 14 06 2022
pubmed: 6 7 2022
medline: 20 7 2022
entrez: 5 7 2022
Statut: ppublish

Résumé

Patients treated with direct oral anticoagulants (DOACs) may require urgent procedures. Managing these patients is challenging due to different bleeding risks and may include laboratory testing, procedural delays, or haemostatic/reversal agent administration. We evaluated management strategies and outcomes of urgent, non-haemostatic invasive procedures in patients treated with DOACs. In a descriptive cohort study, we prospectively evaluated 478 patients in the GIHP-NACO registry, from June 2013 to November 2015. Hospitalised patients receiving dabigatran (n = 160), rivaroxaban (n = 274), or apixaban (n = 44) requiring urgent, procedural interventions were evaluated, of which 384/478 (80 %) were surgical procedures. Orthopaedic surgery included 216/384 patients (56 %), while gastrointestinal surgery included 75/384 (20 %) patients. On admission, the median age was 79 (70-85), and creatinine clearance was <60 mL·min In the GIHP-NACO registry, before specific antidotes were available, DOAC treated patients undergoing urgent invasive procedures were delayed in nearly half of the cases, and showed a low rate of excessive bleeding, suggesting that most urgent procedures can be performed safely without DOAC reversal. www. gov. Identifier: NCT02185027.

Sections du résumé

BACKGROUND
Patients treated with direct oral anticoagulants (DOACs) may require urgent procedures. Managing these patients is challenging due to different bleeding risks and may include laboratory testing, procedural delays, or haemostatic/reversal agent administration.
OBJECTIVE
We evaluated management strategies and outcomes of urgent, non-haemostatic invasive procedures in patients treated with DOACs.
METHODS AND RESULTS
In a descriptive cohort study, we prospectively evaluated 478 patients in the GIHP-NACO registry, from June 2013 to November 2015. Hospitalised patients receiving dabigatran (n = 160), rivaroxaban (n = 274), or apixaban (n = 44) requiring urgent, procedural interventions were evaluated, of which 384/478 (80 %) were surgical procedures. Orthopaedic surgery included 216/384 patients (56 %), while gastrointestinal surgery included 75/384 (20 %) patients. On admission, the median age was 79 (70-85), and creatinine clearance was <60 mL·min
CONCLUSIONS
In the GIHP-NACO registry, before specific antidotes were available, DOAC treated patients undergoing urgent invasive procedures were delayed in nearly half of the cases, and showed a low rate of excessive bleeding, suggesting that most urgent procedures can be performed safely without DOAC reversal.
CLINICAL TRIAL REGISTRATION
www.
CLINICALTRIALS
gov. Identifier: NCT02185027.

Identifiants

pubmed: 35785621
pii: S0049-3848(22)00298-5
doi: 10.1016/j.thromres.2022.06.005
pii:
doi:

Substances chimiques

Anticoagulants 0
Pyridones 0
Rivaroxaban 9NDF7JZ4M3
Dabigatran I0VM4M70GC

Banques de données

ClinicalTrials.gov
['NCT02185027']

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

106-112

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

Alexandre Godon (A)

Department of Anesthesiology and Critical Care, CHU Grenoble Alpes, Université Grenoble Alpes, Grenoble, France. Electronic address: agodon1@chu-grenoble.fr.

Manon Gabin (M)

Department of Anesthesiology and Critical Care, CHU Grenoble Alpes, Université Grenoble Alpes, Grenoble, France.

Jerrold H Levy (JH)

Department of Anesthesiology, Critical Care, and Surgery, Duke University School of Medicine, Durham, NC, United States.

Olivier Huet (O)

Department of Anesthesiology and Critical Care, CHRU de Brest, UFR de Médecine, 29200 Brest, France.

Xavier Chapalain (X)

Department of Anesthesiology and Critical Care, CHRU de Brest, UFR de Médecine, 29200 Brest, France.

Jean-Stéphane David (JS)

Department of Anesthesiology and Critical Care, Centre hospitalier Lyon Sud, Hospices Civils de Lyon, F-69495 Pierre Benite, France; School of Medicine, Université Claude Bernard Lyon 1, Lyon, France; Research on Healthcare Performance (RESHAPE), INSERM U1290, Université Claude Bernard Lyon 1, Lyon, France.

Charles Tacquard (C)

Department of Anesthesiology and Intensive Care, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Laurent Sattler (L)

Laboratory of Haematology, Haemostasis Unit, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

Vincent Minville (V)

Department of Anesthesiology and Intensive Care, University Hospital of Toulouse, RESTORE, UMR 1301Inserm - 5070 CNRS -University Paul Sabatier, Toulouse, France.

Vincent Mémier (V)

Laboratory of Hematology, University Hospital of Toulouse, Toulouse, France.

Antonia Blanié (A)

Department of Anesthesiology and Intensive Care, CHU Bicêtre, AP-HP, Paris Saclay University, Le Kremlin Bicêtre, France.

Thomas Godet (T)

Department of Anesthesiology, Critical Care and Perioperative Medicine, CHU de Clermont-Ferrand, Université Clermont-Auvergne, UFR de Médecine, 63000 Clermont-Ferrand, France.

Marc Leone (M)

Department of Anesthesiology and Intensive Care Unit, Aix Marseille University, Assistance Publique Hôpitaux de Marseille, North Hospital, Marseille, France.

Emmanuel De Maistre (E)

Haemostasis Unit, University Hospital of Dijon, Dijon, France.

Yves Gruel (Y)

Department of Haematology-Haemostasis, Trousseau Hospital, CHU Tours, 37044 Tours Cedex, France.

Stéphanie Roullet (S)

Department of Anesthesiology and Critical Care, CHU Bordeaux, Bordeaux, France.

Céline Vermorel (C)

Data-stat Department, Grenoble Alpes University Hospital, Grenoble, France.

Charles Marc Samama (CM)

Université de Paris, INSERM, Innovative Therapies in Haemostasis, F-75006 Paris, France; Department of Anaesthesia, Intensive Care and Perioperative Medicine, GHU AP-HP, Centre - Université de Paris - Cochin Hospital, Paris, France.

Jean-Luc Bosson (JL)

Data-stat Department, Grenoble Alpes University Hospital, Grenoble, France.

Pierre Albaladejo (P)

Department of Anesthesiology and Critical Care, CHU Grenoble Alpes, Université Grenoble Alpes, Grenoble, France.

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