Anti-Factor-Xa and Activated Partial Thromboplastin Time Concordance and Outcomes in Adults Undergoing Extracorporeal Membrane Oxygenation: A Secondary Analysis of the Pilot Low-Dose Heparin in Critically Ill Patients Undergoing Extracorporeal Membrane Oxygenation Randomized Trial.

activated partial thromboplastin time anti-factor-Xa anticoagulation extracorporeal membrane oxygenation heparin resistance

Journal

Critical care explorations
ISSN: 2639-8028
Titre abrégé: Crit Care Explor
Pays: United States
ID NLM: 101746347

Informations de publication

Date de publication:
Nov 2023
Historique:
medline: 13 11 2023
pubmed: 13 11 2023
entrez: 13 11 2023
Statut: epublish

Résumé

To determine the concordance between activated partial thromboplastin time (aPTT) and anti-factor-Xa (anti-Xa) in adults undergoing extracorporeal membrane oxygenation (ECMO) and to identify the factors associated with discordant paired aPTT/anti-Xa. Pre-planned secondary analysis of the Low-Dose Heparin in Critically Ill Patients Undergoing Extracorporeal Membrane Oxygenation pilot randomized unblinded, parallel-group controlled trial. Two ICUs in two university hospitals. Thirty-two critically ill patients who underwent ECMO and who had at least one paired aPTT and anti-Xa assay performed at the same time. We analyzed the concordance between aPTT and anti-Xa and identified factors associated with discordant paired aPTT/anti-Xa based on their respective therapeutic ranges. We also compared biological parameters between heparin resistance episode and no heparin resistance. Of the 32 patients who were included in this study, 24 (75%) had at least one discordant paired aPTT/anti-Xa. Of the 581 paired aPTT/anti-Xa that were analyzed, 202 were discordant. The aPTT was relatively lower than anti-Xa in 66 cases (32.7%) or relatively higher than anti-Xa in 136 cases (67.3%). Thirty-three heparin resistance episodes were identified in six patients (19%). In these critically ill patients undergoing ECMO, one third of paired aPTT/anti-Xa measures was discordant. Coagulopathy and heparin resistance might be the reasons for discordance. Our results support the potential importance of routinely monitoring both tests in this setting.

Identifiants

pubmed: 37954899
doi: 10.1097/CCE.0000000000000999
pmc: PMC10635598
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e0999

Informations de copyright

Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine.

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Auteurs

Cécile Aubron (C)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.
Département de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Brest, site La Cavale Blanche, Université de Bretagne Occidentale, Brest, France.

Xavier Chapalain (X)

Département d'anesthésie réanimation, Centre Hospitalier Universitaire de Brest, site La Cavale Blanche, Université de Bretagne Occidentale, Brest, France.

Michael Bailey (M)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.

Jasmin Board (J)

Intensive Care Unit, Alfred Hospital, Melbourne, VIC, Australia.

Heidi Buhr (H)

Intensive Care Service, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

Bruce Cartwright (B)

Department of Anaesthesia, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

Mark Dennis (M)

Cardiology Department, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

Carol Hodgson (C)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.

Paul Forrest (P)

Department of Anaesthesia, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

David McIlroy (D)

Department of Anaesthesia & Perioperative Medicine, Alfred Hospital, Melbourne, VIC, Australia.

Deirdre Murphy (D)

Intensive Care Unit, Alfred Hospital, Melbourne, VIC, Australia.

Lynne Murray (L)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.

Vincent Pellegrino (V)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.
Intensive Care Unit, Alfred Hospital, Melbourne, VIC, Australia.

David Pilcher (D)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.
Intensive Care Unit, Alfred Hospital, Melbourne, VIC, Australia.

Jayne Sheldrake (J)

Intensive Care Unit, Alfred Hospital, Melbourne, VIC, Australia.

Huyen Tran (H)

Clinical Haematology Department, Alfred Hospital, Melbourne, VIC, Australia.

Shirley Vallance (S)

Intensive Care Unit, Alfred Hospital, Melbourne, VIC, Australia.

D James Cooper (DJ)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.
Intensive Care Unit, Alfred Hospital, Melbourne, VIC, Australia.

Zoe McQuilten (Z)

Department of Epidemiology and Preventive Medicine, Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), Monash University, Melbourne, VIC, Australia.

Classifications MeSH