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Direct oral anticoagulant concentrations and adherence in stroke patients.
Aakerøy, Rachel; Gynnild, Mari Nordbø; Løfblad, Lena; Dyrkorn, Roar; Ellekjaer, Hanne; Lydersen, Stian; Helland, Arne; Spigset, Olav.
Afiliação
  • Aakerøy R; Department of Clinical Pharmacology, St. Olav University Hospital, Trondheim, Norway.
  • Gynnild MN; Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
  • Løfblad L; Department of Stroke, Clinic of Medicine, St. Olav University Hospital, Trondheim, Norway.
  • Dyrkorn R; Clinic of Cardiology, St. Olav University Hospital, Trondheim, Norway.
  • Ellekjaer H; Department of Circulation and Medical Imaging, Norwegian University of Science and Technology, Trondheim, Norway.
  • Lydersen S; Department of Clinical Chemistry, St. Olav University Hospital, Trondheim, Norway.
  • Helland A; Department of Clinical Pharmacology, St. Olav University Hospital, Trondheim, Norway.
  • Spigset O; Department of Stroke, Clinic of Medicine, St. Olav University Hospital, Trondheim, Norway.
Basic Clin Pharmacol Toxicol ; 134(1): 175-185, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37845026
No therapeutic ranges linking drug concentrations of apixaban and rivaroxaban to clinical outcomes have been defined. We investigated whether direct oral anticoagulant (DOAC) concentrations among patients admitted to hospital with symptoms of stroke differed between those later verified to suffer an ischaemic cerebrovascular event (stroke or transient ischaemic attack) and those having other diagnoses (control group). Serum concentrations in 102 patients on DOAC for atrial fibrillation (84%) and thromboembolic disease (16%) were measured within 24 h of the acute event, employing ultra-high performance liquid chromatography with tandem mass spectrometry. We converted all concentrations to standardized trough levels. DOAC concentrations were lower in the 64 patients with verified ischaemic cerebrovascular event than in the 30 controls, 255 ± 155 versus 329 ± 144 nmol/L (p = 0.029), despite no statistically significant difference in self-reported adherence and daily dosages. Calculated concentrations were 5.4-596 nmol/L (median = 229 nmol/L) in the ischaemic stroke group and 41-602 nmol/L (median = 316 nmol/L) in controls. CHA2 DS2 -VASc score was significantly higher in the ischaemic stroke group than in controls (4.9 ± 1.6 versus 4.1 ± 1.7; p = 0.007). These results may suggest that patients with high cerebrovascular risk might benefit from higher DOAC levels than those with a lower risk.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Isquemia Encefálica / Acidente Vascular Cerebral / AVC Isquêmico Limite: Humans Idioma: En Revista: Basic Clin Pharmacol Toxicol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Isquemia Encefálica / Acidente Vascular Cerebral / AVC Isquêmico Limite: Humans Idioma: En Revista: Basic Clin Pharmacol Toxicol Ano de publicação: 2024 Tipo de documento: Article