Drug–drug interaction of rivaroxaban and calcium channel blockers in patients aged 80 years and older with nonvalvular atrial fibrillation

Author:

Sychev Dmitry1ORCID,Mirzaev Karin2ORCID,Cherniaeva Marina34ORCID,Kulikova Maria1ORCID,Bochkov Pavel2ORCID,Shevchenko Roman2ORCID,Gorbatenkova Svetlana4,Golovina Olga1ORCID,Ostroumova Olga5ORCID,Bahteeva Damirya1ORCID,Rytkin Eric1ORCID

Affiliation:

1. Department of Clinical Pharmacology and Therapy of Federal State Budgetary Educational Institution of Further Professional Education “Russian Medical Academy of Continuous Professional Education” of the Ministry of Healthcare of the Russian Federation , Moscow , Russia

2. Department of Personalized Medicine , Research Institute of Molecular and Personalized Medicine of Federal State Budgetary Educational Institution of Further Professional Education “Russian Medical Academy of Continuous Professional Education” of the Ministry of Healthcare of the Russian Federation , Moscow , Russia

3. Department of Internal and Preventive Medicine of Federal State Budgetary Institution of Higher Professional Education “Central State Medical Academy of the Presidential Administration of the Russian Federation” , Marshal Timoshenko street,19, building 1A, 121359 , Moscow , Russia

4. State Budgetary Institution of Health “Hospital for War Veterans No. 2” of the Department of Health of Moscow , Volgogradsky prospect , Moscow , Russia

5. Department of Therapy and Polymorbid Pathology of Federal State Budgetary Educational Institution of Further Professional Education “Russian Medical Academy of Continuous Professional Education” of the Ministry of Healthcare of the Russian Federation , Moscow , Russia

Abstract

Abstract Objectives For revealing the peculiarities of the drug–drug interaction of rivaroxaban (substrate CYP3A4 and P-gp) and calcium channel blockers (CCBs) (verapamil – inhibitor CYP3A4 and P-gp and amlodipine – substrate CYP3A4) in patients 80 years and older with nonvalvular atrial fibrillation (NAF) we studied 128 patients. Methods All patients were divided into groups depending on the therapy taken: the 1st – rivaroxaban + amlodipine (n=51), the 2nd – rivaroxaban + verapamil (n=30), the control group – rivaroxaban without CCBs (n=47). A trough steady-state plasma concentration (C min,ss) of rivaroxaban, prothrombin time (PT) in the blood plasma and the event of clinically relevant non-major (CRNM) bleeding were assessed for each patient. Results Patient in group 2 had higher C min,ss of rivaroxaban, PT and CRNM than subjects in the control group (Me 73.8 [50.6–108.8] ng/mL vs. 40.5 [25.6–74.3] ng/mL; Me 14.8 [13.4–17.3] s vs. 13.8 [12.6–14.4] s; 34% vs. 13%, respectively, p<0.05 for all). When compared, the PT and complication rate in group 1 with the control group C min,ss of rivaroxaban were practically the same (p>0.05 for all). Conclusions In patients ≥80 years with NAF, the use of rivaroxaban in combination with verapamil may not be safe and can lead to CRNM bleeding.

Publisher

Walter de Gruyter GmbH

Subject

Pharmacology (medical)

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