[Theophylline adenosine dipyridamole (CTAD) and citrate evaluation to survey unfractionated heparin treatment: a delayed centrifugation validation for anti-Xa measurement?].

Évaluation du citrate théophylline adénosine dipyridamole (CTAD) et du citrate comme anticoagulant dans la surveillance du traitement par héparine non fractionnée : validation d’une centrifugation différée pour le dosage de l’anti-Xa.

Journal

Annales de biologie clinique
ISSN: 1950-6112
Titre abrégé: Ann Biol Clin (Paris)
Pays: France
ID NLM: 2984690R

Informations de publication

Date de publication:
01 02 2020
Historique:
entrez: 29 2 2020
pubmed: 29 2 2020
medline: 9 9 2020
Statut: ppublish

Résumé

Unfractionated heparin (UFH) is the main anticoagulante used in intensive care unit. The anticoagulant effect is monitored by activated partial thrombin time (aPTT) and anti-Xa activity (anti-Xa) measurement. However, delayed centrifugation induces platelet factor 4 (PF4) release and anti-Xa decrease. Several studies have concluded that aPTT and anti-Xa measurement should be performed within 2 hours in citrated anticoagulant but may be delayed longer in citrate theophylline adenosine and dypiridamol (CTAD) anticoagulant. The objective of this study was to compare the stability of both aPTT and anti-Xa in citrate and CTAD samples, and to determine the effect of delayed centrifugation on both aPTT, anti-Xa results, and PF4 release in citrate samples only. aPTT and anti-Xa were measured in citrate and CTAD anticoagulant samples from 93 patients. Delayed centrifugation was performed in citrate samples from 31 additional patients, with hourly aPTT and anti-Xa measurement from 1 to 6 hours. In 14 of these last patients, PF4 release was also evaluated with Human CXCL4/PF4 Quantikine ELISA Kit. We observed a significant correlation between citrate and CTAD anticoagulant for aPTT (r We have demonstrated that anti-Xa measurement for unfractionated heparin should be done 4 hours in citrated plasma and that CTAD was not better than citrate. However, these initial findings require confirmation using other aPTT and calibrated anti-Xa assays.

Identifiants

pubmed: 32108577
pii: abc.2020.1525
doi: 10.1684/abc.2020.1525
doi:

Substances chimiques

Anticoagulants 0
Factor Xa Inhibitors 0
Citric Acid 2968PHW8QP
Dipyridamole 64ALC7F90C
Heparin 9005-49-6
Theophylline C137DTR5RG
Factor Xa EC 3.4.21.6
Adenosine K72T3FS567

Types de publication

Evaluation Study Journal Article

Langues

fre

Sous-ensembles de citation

IM

Pagination

27-34

Auteurs

Paul Billoir (P)

Service d'hématologie biologique, CHU Charles Nicolle, Rouen, France, Inserm U1096, CHU Charles Nicolle, Rouen, France.

Thomas Clavier (T)

Département d'anesthésie-réanimation, Inserm U1096, CHU Charles Nicolle, Rouen, France, Inserm U1096, CHU Charles Nicolle, Rouen, France.

Arnaud Guilbert (A)

Département d'anesthésie-réanimation, Inserm U1096, CHU Charles Nicolle, Rouen, France.

Virginie Barbay (V)

Unité d'hémostase vasculaire, CHU Charles Nicolle, Rouen, France.

Marie Hélène Chrétien (MH)

Unité d'hémostase vasculaire, CHU Charles Nicolle, Rouen, France.

Marielle Fresel (M)

Unité d'hémostase vasculaire, CHU Charles Nicolle, Rouen, France.

Caroline Abriou (C)

Département d'anesthésie-réanimation, Inserm U1096, CHU Charles Nicolle, Rouen, France.

Christophe Girault (C)

Département de réanimation médicale, CHU Charles Nicolle, Rouen, France.

Véronique Le Cam Duchez (V)

Service d'hématologie biologique, CHU Charles Nicolle, Rouen, France, Inserm U1096, CHU Charles Nicolle, Rouen, France.

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Classifications MeSH