Urine-based point-of-care testing for factor-Xa-inhibitors in acute ischemic stroke patients: a feasibility study
dc.contributor.author | Doeppner, Thorsten R. | |
dc.contributor.author | Olbricht, Linus | |
dc.contributor.author | Maxhuni, Toska | |
dc.contributor.author | Alhaj Omar, Omar | |
dc.contributor.author | Sachs, Ulrich J. | |
dc.contributor.author | Juenemann, Martin B. | |
dc.contributor.author | Huttner, Hagen B. | |
dc.contributor.author | Gerner, Stefan T. | |
dc.date.accessioned | 2024-10-02T07:33:40Z | |
dc.date.available | 2024-10-02T07:33:40Z | |
dc.date.issued | 2023 | |
dc.description.abstract | Introduction: Direct oral anticoagulants (DOACs) have become widely used in clinical practice for preventing thromboembolic events. Point-of-care testing methods, particularly those based on urine samples, offer a promising approach for rapid and accurate assessment of DOAC presence. This pilot study aims to evaluate the utility of a urine-based DOAC dipstick test as a point-of-care tool for identifying DOAB presence in acute ischemic stroke (AIS) or transient ischemic attack (TIA) patients. Patients and methods: This prospective pilot study included patients with AIS/TIA eligible for DOAC-measurement. After exclusion of 3 patients, 23 patients with DOAC-intake (DOAC group; factor-Xa-inhibitors; n = 23) and 21 patients without DOAC-intake (control-group) remained for analyses. The urine-based DOAC dipstick test and parallel blood-based specific DOAC-level assessment were performed in all patients. Time-intervals of sampling urine/blood sampling and result of DOAC-test were recorded to analyze a potential time benefit based on dipstick evaluation. Results: The urine-based DOAC dipstick test demonstrated high sensitivity (100%) and specificity (100%), correctly identifying all patients with anticoagulatory activity due to DOAC intake (i.e., anti-Xalevel ≥30 ng/mL). Moreover, the visual readout of the test provided semiquantitative information on drug-specific anti-Xa levels, showing a sensitivity of 83% and specificity of 93% to detect anti-Xa levels ≥120 ng/mL. The dipstick test exhibited a median time-benefit of 2:25 h compared to standard blood-based DOAC-level testing. Discussion: The results of this pilot study underline the efficacy of urine-based point-of-care testing as a rapid and reliable method for assessing DOAC presence in patients with acute ischemic stroke. Conclusion: The value of this tool for clinical decision-making in stroke management needs to be established in future trials. | en |
dc.identifier.uri | https://jlupub.ub.uni-giessen.de/handle/jlupub/19560 | |
dc.identifier.uri | https://doi.org/10.22029/jlupub-18918 | |
dc.language.iso | en | |
dc.rights | Namensnennung 4.0 International | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject.ddc | ddc:610 | |
dc.title | Urine-based point-of-care testing for factor-Xa-inhibitors in acute ischemic stroke patients: a feasibility study | |
dc.type | article | |
local.affiliation | FB 11 - Medizin | |
local.source.articlenumber | 1330421 | |
local.source.epage | 7 | |
local.source.journaltitle | Frontiers in neurology | |
local.source.spage | 1 | |
local.source.uri | https://doi.org/10.3389/fneur.2023.1330421 | |
local.source.volume | 14 |
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