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Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions

AIM: The aim of the present study was to analyse concomitant drug use and its association with outcome in patients (N = 17 701) receiving rivaroxaban or standard of care (SOC) for the prevention of venous thromboembolism after major orthopaedic surgery in the non‐interventional, phase IV XAMOS (Xare...

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Autores principales: Kreutz, Reinhold, Haas, Sylvia, Holberg, Gerlind, Lassen, Michael R., Mantovani, Lorenzo G., Schmidt, André, Turpie, Alexander G. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799939/
https://www.ncbi.nlm.nih.gov/pubmed/26580706
http://dx.doi.org/10.1111/bcp.12836
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author Kreutz, Reinhold
Haas, Sylvia
Holberg, Gerlind
Lassen, Michael R.
Mantovani, Lorenzo G.
Schmidt, André
Turpie, Alexander G. G.
author_facet Kreutz, Reinhold
Haas, Sylvia
Holberg, Gerlind
Lassen, Michael R.
Mantovani, Lorenzo G.
Schmidt, André
Turpie, Alexander G. G.
author_sort Kreutz, Reinhold
collection PubMed
description AIM: The aim of the present study was to analyse concomitant drug use and its association with outcome in patients (N = 17 701) receiving rivaroxaban or standard of care (SOC) for the prevention of venous thromboembolism after major orthopaedic surgery in the non‐interventional, phase IV XAMOS (Xarelto® in the prophylaxis of post‐surgical venous thromboembolism after elective major orthopaedic surgery of hip or knee) study. METHODS: Concomitant drug use was at the discretion of the treating physician. Prespecified co‐medications of interest were cytochrome P450 (CYP) 3A4/P‐glycoprotein inhibitors/inducers, platelet aggregation inhibitors (PAIs) and nonsteroidal anti‐inflammatory drugs (NSAIDs). Crude event incidences were compared between rivaroxaban and SOC groups. RESULTS: CYP3A4/P‐glycoprotein inhibitor/inducer use was infrequent, in contrast to PAI (~7%) and NSAID (~52%) use. Rivaroxaban was associated with a lower incidence of overall symptomatic thromboembolic events compared with SOC, regardless of co‐medication use. In both treatment groups, PAI users, with higher age and prevalence of cardiovascular co‐morbidities, had similar higher (>7‐fold) incidences of symptomatic arterial but not venous thromboembolic events compared with non‐users. NSAID use had no influence on thromboembolic events. However, odds ratios (ORs) for major bleeding events (European Medicines Agency definition) were higher in NSAID users compared with non‐users in rivaroxaban [OR = 1.50; 95% confidence interval (CI) 1.06, 2.13] and SOC (OR = 1.70; CI 1.16, 2.49) groups. In PAI users, ORs for major bleeding events were no different from those of non‐users in both the rivaroxaban (OR = 1.49; CI 0.84, 2.65) and SOC (OR = 1.46; CI 0.82, 2.62) groups. CONCLUSIONS: Use of NSAIDs in XAMOS was frequent and associated with a higher frequency of bleeding events in patients receiving rivaroxaban or SOC, although the benefit–risk profile of rivaroxaban compared with SOC was maintained.
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spelling pubmed-47999392016-11-01 Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions Kreutz, Reinhold Haas, Sylvia Holberg, Gerlind Lassen, Michael R. Mantovani, Lorenzo G. Schmidt, André Turpie, Alexander G. G. Br J Clin Pharmacol Drug Interactions AIM: The aim of the present study was to analyse concomitant drug use and its association with outcome in patients (N = 17 701) receiving rivaroxaban or standard of care (SOC) for the prevention of venous thromboembolism after major orthopaedic surgery in the non‐interventional, phase IV XAMOS (Xarelto® in the prophylaxis of post‐surgical venous thromboembolism after elective major orthopaedic surgery of hip or knee) study. METHODS: Concomitant drug use was at the discretion of the treating physician. Prespecified co‐medications of interest were cytochrome P450 (CYP) 3A4/P‐glycoprotein inhibitors/inducers, platelet aggregation inhibitors (PAIs) and nonsteroidal anti‐inflammatory drugs (NSAIDs). Crude event incidences were compared between rivaroxaban and SOC groups. RESULTS: CYP3A4/P‐glycoprotein inhibitor/inducer use was infrequent, in contrast to PAI (~7%) and NSAID (~52%) use. Rivaroxaban was associated with a lower incidence of overall symptomatic thromboembolic events compared with SOC, regardless of co‐medication use. In both treatment groups, PAI users, with higher age and prevalence of cardiovascular co‐morbidities, had similar higher (>7‐fold) incidences of symptomatic arterial but not venous thromboembolic events compared with non‐users. NSAID use had no influence on thromboembolic events. However, odds ratios (ORs) for major bleeding events (European Medicines Agency definition) were higher in NSAID users compared with non‐users in rivaroxaban [OR = 1.50; 95% confidence interval (CI) 1.06, 2.13] and SOC (OR = 1.70; CI 1.16, 2.49) groups. In PAI users, ORs for major bleeding events were no different from those of non‐users in both the rivaroxaban (OR = 1.49; CI 0.84, 2.65) and SOC (OR = 1.46; CI 0.82, 2.62) groups. CONCLUSIONS: Use of NSAIDs in XAMOS was frequent and associated with a higher frequency of bleeding events in patients receiving rivaroxaban or SOC, although the benefit–risk profile of rivaroxaban compared with SOC was maintained. John Wiley and Sons Inc. 2016-02-12 2016-04 /pmc/articles/PMC4799939/ /pubmed/26580706 http://dx.doi.org/10.1111/bcp.12836 Text en © 2015 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of The British Pharmacological Society. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Drug Interactions
Kreutz, Reinhold
Haas, Sylvia
Holberg, Gerlind
Lassen, Michael R.
Mantovani, Lorenzo G.
Schmidt, André
Turpie, Alexander G. G.
Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions
title Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions
title_full Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions
title_fullStr Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions
title_full_unstemmed Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions
title_short Rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions
title_sort rivaroxaban compared with standard thromboprophylaxis after major orthopaedic surgery: co‐medication interactions
topic Drug Interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4799939/
https://www.ncbi.nlm.nih.gov/pubmed/26580706
http://dx.doi.org/10.1111/bcp.12836
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