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

Author:

Aubron Cécile12,Chapalain Xavier3,Bailey Michael1,Board Jasmin4,Buhr Heidi5,Cartwright Bruce6,Dennis Mark7,Hodgson Carol1,Forrest Paul6,McIlroy David8,Murphy Deirdre4,Murray Lynne1,Pellegrino Vincent14,Pilcher David14,Sheldrake Jayne4,Tran Huyen9,Vallance Shirley4,Cooper D. James14,McQuilten Zoe1

Affiliation:

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

2. Département de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Brest, site La Cavale Blanche, Université de Bretagne Occidentale, Brest, France.

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

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

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

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

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

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

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

Abstract

OBJECTIVES: 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. DESIGN: Pre-planned secondary analysis of the Low-Dose Heparin in Critically Ill Patients Undergoing Extracorporeal Membrane Oxygenation pilot randomized unblinded, parallel-group controlled trial. SETTING: Two ICUs in two university hospitals. PATIENTS: 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. INTERVENTIONS: 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. MEASUREMENTS AND MAIN RESULTS: 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%). CONCLUSIONS: 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.

Funder

Australian and New Zealand College of Anaesthetists

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Critical Care and Intensive Care Medicine

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