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Métodos Terapêuticos e Terapias MTCI
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Thromb Haemost ; 117(3): 519-528, 2017 02 28.
Artigo em Inglês | MEDLINE | ID: mdl-28124061

RESUMO

Reliable detection of anticoagulation status in patients treated with non-vitamin K antagonist oral anticoagulants (NOACs) is challenging but of importance especially in the emergency setting. This study evaluated the potential of a whole-blood clotting time assay based on Surface Acoustic Waves (SAW-CT) in stroke-patients. The SAW-technology was used for quick and homogenous recalcification of whole blood inducing a surface-activated clotting reaction quantified and visualised by real-time fluorescence microscopy with automatic imaging processing. In 20 stroke or transient ischaemic attack (TIA)-patients taking NOACs kinetics of SAW-CT were assessed and correlated to other coagulation parameters (PT, aPTT) and NOAC-plasma concentration measured by tandem mass spectrometry (LC-MS/MS). In 225 emergency patients with suspicion of acute stroke or TIA, SAW-CT values were assessed. Mean (± SD) SAW-CT in non-anticoagulated stroke patients (n=180) was 124 s (± 21). In patients on dabigatran or rivaroxaban, SAW-CT values were significantly higher 2 and 8 hours (h) after intake rising up to 267 seconds (s) (dabigatran, 2 h after intake) and 250 s (rivaroxaban, 8 h after intake). In patients on apixaban, SAW-CT values were only moderately increased 2 h after intake (SAW-CT 153 s). In emergency patients, SAW-CT values were significantly higher in NOAC and vitamin K antagonist (VKA)-treated as compared to non-anticoagulated patients. In conclusion, the SAW-CT assay is capable to monitor anticoagulant level and effect in patients receiving dabigatran, rivaroxaban and the VKA phenprocoumon. It has a limited sensitivity for apixaban-detection. If specific SAW-CT results were used as cut-offs, SAW-CT yields high diagnostic accuracy to exclude relevant rivaroxaban and dabigatran concentrations in stroke-patients.


Assuntos
Anticoagulantes/administração & dosagem , Coagulação Sanguínea/efeitos dos fármacos , Dabigatrana/administração & dosagem , Monitoramento de Medicamentos/métodos , Ataque Isquêmico Transitório/tratamento farmacológico , Técnicas Analíticas Microfluídicas , Femprocumona/administração & dosagem , Pirazóis/administração & dosagem , Piridonas/administração & dosagem , Rivaroxabana/administração & dosagem , Acidente Vascular Cerebral/tratamento farmacológico , Tempo de Coagulação do Sangue Total , Administração Oral , Idoso , Idoso de 80 Anos ou mais , Anticoagulantes/efeitos adversos , Anticoagulantes/sangue , Automação Laboratorial , Cromatografia Líquida de Alta Pressão , Dabigatrana/efeitos adversos , Dabigatrana/sangue , Feminino , Humanos , Ataque Isquêmico Transitório/sangue , Ataque Isquêmico Transitório/diagnóstico , Masculino , Microscopia de Fluorescência , Pessoa de Meia-Idade , Femprocumona/efeitos adversos , Femprocumona/sangue , Valor Preditivo dos Testes , Pirazóis/efeitos adversos , Pirazóis/sangue , Piridonas/efeitos adversos , Piridonas/sangue , Reprodutibilidade dos Testes , Rivaroxabana/efeitos adversos , Rivaroxabana/sangue , Acidente Vascular Cerebral/sangue , Acidente Vascular Cerebral/diagnóstico , Espectrometria de Massas em Tandem , Fatores de Tempo , Resultado do Tratamento
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