In vitro evaluation of anticoagulant therapy management when urgent percutaneous coronary intervention is required in rivaroxaban-treated patients.


Journal

Naunyn-Schmiedeberg's archives of pharmacology
ISSN: 1432-1912
Titre abrégé: Naunyn Schmiedebergs Arch Pharmacol
Pays: Germany
ID NLM: 0326264

Informations de publication

Date de publication:
11 2023
Historique:
received: 28 11 2022
accepted: 15 05 2023
medline: 23 10 2023
pubmed: 20 5 2023
entrez: 20 5 2023
Statut: ppublish

Résumé

We investigated in vitro the management of intraprocedural anticoagulation in patients requiring immediate percutaneous coronary intervention (PCI) while using regular direct oral anticoagulants (DOACs). Twenty-five patients taking 20 mg of rivaroxaban once daily comprised the study group, while five healthy volunteers included the control group. In the study group, a beginning (24 h after the last rivaroxaban dose) examination was performed. Then, the effects of basal and four different anticoagulant doses (50 IU/kg unfractionated heparin (UFH), 100 IU/kg UFH, 0.5 mg/kg enoxaparin, and 1 mg/kg enoxaparin) on coagulation parameters were investigated at the 4th and 12th h following rivaroxaban intake. The effects of four different anticoagulant doses were evaluated in the control group. The anticoagulant activity was assessed mainly by anti-factor Xa (anti-Xa) levels. Beginning anti-Xa levels were significantly higher in the study group than in the control group (0.69 ± 0.77 IU/mL vs. 0.20 ± 0.14 IU/mL; p < 0.05). The study group's 4th and 12th-h anti-Xa levels were significantly higher than the beginning level (1.96 ± 1.35 IU/mL vs. 0.69 ± 0.77 IU/mL; p < 0.001 and 0.94 ± 1.21 IU/mL vs. 0.69 ± 0.77 IU/mL; p < 0.05, respectively). Anti-Xa levels increased significantly in the study group with the addition of UFH and enoxaparin doses at the 4th and 12th h than the beginning (p < 0.001 at all doses). The safest anti-Xa level (from 0.94 ± 1.21 to 2.00 ± 1.02 IU/mL) was achieved 12 h after rivaroxaban with 0.5 mg/kg enoxaparin. Anticoagulant activity was sufficient for urgent PCI at the 4th h after rivaroxaban treatment, and additional anticoagulant administration may not be required at this time. Twelve hours after taking rivaroxaban, administering 0.5 mg/kg of enoxaparin may provide adequate and safe anticoagulant activity for immediate PCI. This experimental study result should confirm with clinical trials (NCT05541757).

Identifiants

pubmed: 37209152
doi: 10.1007/s00210-023-02533-2
pii: 10.1007/s00210-023-02533-2
doi:

Substances chimiques

Enoxaparin 0
Heparin 9005-49-6
Rivaroxaban 9NDF7JZ4M3
Anticoagulants 0

Banques de données

ClinicalTrials.gov
['NCT05541757']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3221-3232

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Mehmet Melek (M)

Department of Cardiology, Bursa Postgraduate Hospital, Bursa, Turkey.

Hasan Ari (H)

Department of Cardiology, Bursa Postgraduate Hospital, Bursa, Turkey. hasanari03@yahoo.com.

Selma Ari (S)

Department of Cardiology, Bursa Postgraduate Hospital, Bursa, Turkey.

Mehmet Can Cilgin (MC)

Department of Cardiology, Bursa Postgraduate Hospital, Bursa, Turkey.

Mücahit Yarar (M)

Department of Cardiology, Bursa Postgraduate Hospital, Bursa, Turkey.

Kagan Huysal (K)

Department of Biochemistry, Bursa Postgraduate Hospital, Bursa, Turkey.

Fahriye Vatansever Ağca (FV)

Department of Cardiology, Bursa Postgraduate Hospital, Bursa, Turkey.

Tahsin Bozat (T)

Department of Cardiology, Bursa Postgraduate Hospital, Bursa, Turkey.

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