Drug-drug interaction of rivaroxaban and calcium channel blockers in patients aged 80 years and older with nonvalvular atrial fibrillation.
Dmitry Alekseevich SychevKarin Badavievich MirzaevMarina S CherniaevaMaria KulikovaPavel O BochkovRoman ShevchenkoSvetlana GorbatenkovaOlga GolovinaOlga Dmitrievna OstroumovaDamirya BahteevaEric RytkinPublished in: Drug metabolism and personalized therapy (2020)
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.
Keyphrases
- atrial fibrillation
- end stage renal disease
- venous thromboembolism
- ejection fraction
- newly diagnosed
- chronic kidney disease
- pulmonary embolism
- heart failure
- oral anticoagulants
- stem cells
- direct oral anticoagulants
- blood pressure
- coronary artery disease
- emergency department
- bone marrow
- patient reported outcomes
- acute coronary syndrome
- left ventricular
- angiotensin converting enzyme
- adverse drug
- hypertensive patients