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Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis

BACKGROUND: Multiple myeloma (MM) is associated with high risk of venous thromboembolism (VTE). Thromboprophylaxis is thoroughly studied in MM. Contrarily, studies assessing the risk of bleeding in people with MM on anticoagulation are lacking. OBJECTIVES: To determine the rate of serious bleeding i...

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Autores principales: Adrianzen-Herrera, Diego, Lutsey, Pamela L., Giorgio, Katherine, Walker, Robert F., Zakai, Neil A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982328/
https://www.ncbi.nlm.nih.gov/pubmed/36873562
http://dx.doi.org/10.1016/j.rpth.2022.100024
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author Adrianzen-Herrera, Diego
Lutsey, Pamela L.
Giorgio, Katherine
Walker, Robert F.
Zakai, Neil A.
author_facet Adrianzen-Herrera, Diego
Lutsey, Pamela L.
Giorgio, Katherine
Walker, Robert F.
Zakai, Neil A.
author_sort Adrianzen-Herrera, Diego
collection PubMed
description BACKGROUND: Multiple myeloma (MM) is associated with high risk of venous thromboembolism (VTE). Thromboprophylaxis is thoroughly studied in MM. Contrarily, studies assessing the risk of bleeding in people with MM on anticoagulation are lacking. OBJECTIVES: To determine the rate of serious bleeding in patients with MM receiving anticoagulation for VTE and the clinical factors associated with bleeding risk. METHODS: Using the MarketScan commercial database, we identified 1298 people with MM treated with anticoagulation for incident VTE events between 2011 and 2019. Hospitalized bleeding was identified using the Cunningham algorithm. Rates of bleeding were calculated and Cox regression identified risk factors for bleeding. RESULTS: Bleeding occurred in 51 (3.9%) cases during median follow-up of 1.13 years. Rate of bleeding among patients with MM on anticoagulation was 24.0 per 1000 person-years. In adjusted regression, factors associated with increased bleeding included age (HR, 1.31 per 10-year increase; 95% CI, 1.03-1.65), Charlson comorbidity index (HR, 1.29 per SD increase; 95% CI, 1.02-1.58), use of antiplatelet agents (HR, 2.4; 95% CI, 1.03-5.68), diabetes (HR, 1.85; 95% CI, 1.06-3.26), and renal disease (HR, 1.80; 95% CI, 1.05-3.16). Cumulative incidence of bleeding was 4.7%, 3.2%, and 3.4% for warfarin, low molecular weight heparin, and direct oral anticoagulants, respectively. CONCLUSION: In this real-world analysis, the rate of bleeding in people with MM on anticoagulation was comparable to those in other subsets of cancer-related VTE. Bleeding rate was lower with low molecular weight heparin and direct oral anticoagulants than warfarin. Higher comorbidity index, diabetes, antiplatelet agent use, and renal disease were risk factors for serious bleeding.
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spelling pubmed-99823282023-03-04 Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis Adrianzen-Herrera, Diego Lutsey, Pamela L. Giorgio, Katherine Walker, Robert F. Zakai, Neil A. Res Pract Thromb Haemost Brief Report BACKGROUND: Multiple myeloma (MM) is associated with high risk of venous thromboembolism (VTE). Thromboprophylaxis is thoroughly studied in MM. Contrarily, studies assessing the risk of bleeding in people with MM on anticoagulation are lacking. OBJECTIVES: To determine the rate of serious bleeding in patients with MM receiving anticoagulation for VTE and the clinical factors associated with bleeding risk. METHODS: Using the MarketScan commercial database, we identified 1298 people with MM treated with anticoagulation for incident VTE events between 2011 and 2019. Hospitalized bleeding was identified using the Cunningham algorithm. Rates of bleeding were calculated and Cox regression identified risk factors for bleeding. RESULTS: Bleeding occurred in 51 (3.9%) cases during median follow-up of 1.13 years. Rate of bleeding among patients with MM on anticoagulation was 24.0 per 1000 person-years. In adjusted regression, factors associated with increased bleeding included age (HR, 1.31 per 10-year increase; 95% CI, 1.03-1.65), Charlson comorbidity index (HR, 1.29 per SD increase; 95% CI, 1.02-1.58), use of antiplatelet agents (HR, 2.4; 95% CI, 1.03-5.68), diabetes (HR, 1.85; 95% CI, 1.06-3.26), and renal disease (HR, 1.80; 95% CI, 1.05-3.16). Cumulative incidence of bleeding was 4.7%, 3.2%, and 3.4% for warfarin, low molecular weight heparin, and direct oral anticoagulants, respectively. CONCLUSION: In this real-world analysis, the rate of bleeding in people with MM on anticoagulation was comparable to those in other subsets of cancer-related VTE. Bleeding rate was lower with low molecular weight heparin and direct oral anticoagulants than warfarin. Higher comorbidity index, diabetes, antiplatelet agent use, and renal disease were risk factors for serious bleeding. Elsevier 2022-12-23 /pmc/articles/PMC9982328/ /pubmed/36873562 http://dx.doi.org/10.1016/j.rpth.2022.100024 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Adrianzen-Herrera, Diego
Lutsey, Pamela L.
Giorgio, Katherine
Walker, Robert F.
Zakai, Neil A.
Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis
title Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis
title_full Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis
title_fullStr Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis
title_full_unstemmed Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis
title_short Bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a MarketScan analysis
title_sort bleeding risk in patients with multiple myeloma treated for venous thromboembolism: a marketscan analysis
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982328/
https://www.ncbi.nlm.nih.gov/pubmed/36873562
http://dx.doi.org/10.1016/j.rpth.2022.100024
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