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The DOAC (direct oral anticoagulant) Dipstick reliably excludes residual FXa inhibitors levels in the preoperative setting

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Résumé

Highlights
- Preoperative point-of-care test to determine DOAC levels in plasma
- Comparison of the performance of a point-of-care test, UHPLC-MS/MS and a chromogenic assay
- A negative DOAC Dipstick excludes residual levels of FXa inhibitors in plasma.
- Reference standard test significantly impacts the performance of the index test.
- Chromogenic anti-FXa assays should be validated against UHPLC-MS/MS.
langue originaleAnglais
Numéro d'article109023
journalThrombosis Research
Volume239
Numéro de publicationJuly 2024
Les DOIs
Etat de la publicationPublié - juil. 2024

Financement

This work was partially supported by Doasense GmbH, Germany, by the NorthShore Vascular Medicine Research fund, and by the Cardiovascular Research Institute of Loyola University Chicago.

Bailleurs de fonds
DOASENSE GmbH
NorthShore Vascular
Cardiovascular Research Institute of Loyola University Chicago

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