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A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting

Determining whether a patient has taken a direct oral anticoagulant (DOAC) is critical during the periprocedural and preoperative period in the emergency department. However, the inaccessibility of complete medical records, along with the generally inconsistent sensitivity of conventional coagulatio...

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Autores principales: Frydman, Galit H., Ellett, Felix, Van Cott, Elizabeth M., Hayden, Douglas, Majmudar, Maulik, Vanderburg, Charles R., Dalzell, Haley, Padmanabhan, Divya L., Davis, Nick, Jorgensen, Julianne, Toner, Mehmet, Fox, James G., Tompkins, Ronald G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063952/
https://www.ncbi.nlm.nih.gov/pubmed/32166266
http://dx.doi.org/10.1097/CCE.0000000000000024
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author Frydman, Galit H.
Ellett, Felix
Van Cott, Elizabeth M.
Hayden, Douglas
Majmudar, Maulik
Vanderburg, Charles R.
Dalzell, Haley
Padmanabhan, Divya L.
Davis, Nick
Jorgensen, Julianne
Toner, Mehmet
Fox, James G.
Tompkins, Ronald G.
author_facet Frydman, Galit H.
Ellett, Felix
Van Cott, Elizabeth M.
Hayden, Douglas
Majmudar, Maulik
Vanderburg, Charles R.
Dalzell, Haley
Padmanabhan, Divya L.
Davis, Nick
Jorgensen, Julianne
Toner, Mehmet
Fox, James G.
Tompkins, Ronald G.
author_sort Frydman, Galit H.
collection PubMed
description Determining whether a patient has taken a direct oral anticoagulant (DOAC) is critical during the periprocedural and preoperative period in the emergency department. However, the inaccessibility of complete medical records, along with the generally inconsistent sensitivity of conventional coagulation tests to these drugs, complicates clinical decision making and puts patients at risk of uncontrollable bleeding. In this study, we evaluate the utility of inhibitor-II-X (i-II-X), a novel, microfluidics-based diagnostic assay for the detection and identification of Factor Xa inhibitors (FXa-Is) in an acute care setting. DESIGN: First-in-human, 91-patient, single-center retrospective pilot study. SETTING: Emergency room. PATIENTS: Adult patients admitted into the emergency department, which received any clinician-ordered coagulation test requiring a 3.2% buffered sodium citrate blood collection tube. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Plasma samples from patients admitted to the emergency department were screened for the use of FXa-Is, including apixaban and rivaroxaban, within the past 24 hours using our new i-II-X microfluidic test. i-II-X results were then compared with results from conventional coagulation tests, including prothrombin time (PT) and international normalized ratio (INR), which were ordered by treating clinicians, and an anti-Xa assay for rivaroxaban. The i-II-X test detected DOACs in samples collected from the emergency department with 95.20% sensitivity and 100.00% specificity. Unlike PT and INR, i-II-X reliably identified patients who had prolonged clotting times secondary to the presence of a FXa-I. CONCLUSIONS: The i-II-X test overcomes the limitations of currently available coagulation tests and could be a useful tool by which to routinely screen patients for DOACs in emergency and critical care settings. Our new diagnostic approach is particularly relevant in clinical situations where medical records may be unavailable, or where precautions need to be taken prior to invasive interventions, such as specific reversal agent administration.
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spelling pubmed-70639522020-03-12 A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting Frydman, Galit H. Ellett, Felix Van Cott, Elizabeth M. Hayden, Douglas Majmudar, Maulik Vanderburg, Charles R. Dalzell, Haley Padmanabhan, Divya L. Davis, Nick Jorgensen, Julianne Toner, Mehmet Fox, James G. Tompkins, Ronald G. Crit Care Explor Original Clinical Report Determining whether a patient has taken a direct oral anticoagulant (DOAC) is critical during the periprocedural and preoperative period in the emergency department. However, the inaccessibility of complete medical records, along with the generally inconsistent sensitivity of conventional coagulation tests to these drugs, complicates clinical decision making and puts patients at risk of uncontrollable bleeding. In this study, we evaluate the utility of inhibitor-II-X (i-II-X), a novel, microfluidics-based diagnostic assay for the detection and identification of Factor Xa inhibitors (FXa-Is) in an acute care setting. DESIGN: First-in-human, 91-patient, single-center retrospective pilot study. SETTING: Emergency room. PATIENTS: Adult patients admitted into the emergency department, which received any clinician-ordered coagulation test requiring a 3.2% buffered sodium citrate blood collection tube. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Plasma samples from patients admitted to the emergency department were screened for the use of FXa-Is, including apixaban and rivaroxaban, within the past 24 hours using our new i-II-X microfluidic test. i-II-X results were then compared with results from conventional coagulation tests, including prothrombin time (PT) and international normalized ratio (INR), which were ordered by treating clinicians, and an anti-Xa assay for rivaroxaban. The i-II-X test detected DOACs in samples collected from the emergency department with 95.20% sensitivity and 100.00% specificity. Unlike PT and INR, i-II-X reliably identified patients who had prolonged clotting times secondary to the presence of a FXa-I. CONCLUSIONS: The i-II-X test overcomes the limitations of currently available coagulation tests and could be a useful tool by which to routinely screen patients for DOACs in emergency and critical care settings. Our new diagnostic approach is particularly relevant in clinical situations where medical records may be unavailable, or where precautions need to be taken prior to invasive interventions, such as specific reversal agent administration. Wolters Kluwer Health 2019-08-20 /pmc/articles/PMC7063952/ /pubmed/32166266 http://dx.doi.org/10.1097/CCE.0000000000000024 Text en Copyright © 2019 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the Society of Critical Care Medicine. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Clinical Report
Frydman, Galit H.
Ellett, Felix
Van Cott, Elizabeth M.
Hayden, Douglas
Majmudar, Maulik
Vanderburg, Charles R.
Dalzell, Haley
Padmanabhan, Divya L.
Davis, Nick
Jorgensen, Julianne
Toner, Mehmet
Fox, James G.
Tompkins, Ronald G.
A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting
title A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting
title_full A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting
title_fullStr A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting
title_full_unstemmed A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting
title_short A New Test for the Detection of Direct Oral Anticoagulants (Rivaroxaban and Apixaban) in the Emergency Room Setting
title_sort new test for the detection of direct oral anticoagulants (rivaroxaban and apixaban) in the emergency room setting
topic Original Clinical Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063952/
https://www.ncbi.nlm.nih.gov/pubmed/32166266
http://dx.doi.org/10.1097/CCE.0000000000000024
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