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Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis

Introduction. Low molecular weight heparin (LMWH) is preferred for malignancy-associated venous thromboembolism (VTE). Many providers monitor LMWH with anti-Xa levels, despite little validation on correspondence with patient outcome. Methods. This is a retrospective, single institution study of anti...

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Autores principales: Yentz, Sarah, Onwuemene, Oluwatoyosi A., Stein, Brady L., Cull, Elizabeth H., McMahon, Brandon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620379/
https://www.ncbi.nlm.nih.gov/pubmed/26543644
http://dx.doi.org/10.1155/2015/126975
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author Yentz, Sarah
Onwuemene, Oluwatoyosi A.
Stein, Brady L.
Cull, Elizabeth H.
McMahon, Brandon
author_facet Yentz, Sarah
Onwuemene, Oluwatoyosi A.
Stein, Brady L.
Cull, Elizabeth H.
McMahon, Brandon
author_sort Yentz, Sarah
collection PubMed
description Introduction. Low molecular weight heparin (LMWH) is preferred for malignancy-associated venous thromboembolism (VTE). Many providers monitor LMWH with anti-Xa levels, despite little validation on correspondence with patient outcome. Methods. This is a retrospective, single institution study of anti-Xa measurement in malignancy-associated thrombosis. Cases were identified using the Electronic Data Warehouse, and inclusion was confirmed by two independent reviewers. Malignancy type, thrombotic history, measurement rationale and accuracy, clinical context, and management changes were evaluated. Results. 167 cases met inclusion criteria. There was no clear rationale for anti-Xa testing in 56%. Impaired renal function (10%), documented or suspected recurrent thrombosis despite anticoagulation (9%), and bleeding (6%) were the most common reasons for testing. Incorrect measurement occurred in 44%. Renal impairment was not a significant impetus for testing, as 70% had a GFR > 60. BMI > 30 was present in 40%, and 28% had a BMI < 25. Clinical impact was low, as only 11% of patients had management changes. Conclusions. Provider education in accuracy and rationale for anti-Xa testing is needed. Our study illustrates uncertainty of interpretation and clinical impact of routine anti-Xa testing, as management was affected in few patients. It is not yet clear in which clinical context providers should send anti-Xa levels.
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spelling pubmed-46203792015-11-05 Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis Yentz, Sarah Onwuemene, Oluwatoyosi A. Stein, Brady L. Cull, Elizabeth H. McMahon, Brandon Thrombosis Research Article Introduction. Low molecular weight heparin (LMWH) is preferred for malignancy-associated venous thromboembolism (VTE). Many providers monitor LMWH with anti-Xa levels, despite little validation on correspondence with patient outcome. Methods. This is a retrospective, single institution study of anti-Xa measurement in malignancy-associated thrombosis. Cases were identified using the Electronic Data Warehouse, and inclusion was confirmed by two independent reviewers. Malignancy type, thrombotic history, measurement rationale and accuracy, clinical context, and management changes were evaluated. Results. 167 cases met inclusion criteria. There was no clear rationale for anti-Xa testing in 56%. Impaired renal function (10%), documented or suspected recurrent thrombosis despite anticoagulation (9%), and bleeding (6%) were the most common reasons for testing. Incorrect measurement occurred in 44%. Renal impairment was not a significant impetus for testing, as 70% had a GFR > 60. BMI > 30 was present in 40%, and 28% had a BMI < 25. Clinical impact was low, as only 11% of patients had management changes. Conclusions. Provider education in accuracy and rationale for anti-Xa testing is needed. Our study illustrates uncertainty of interpretation and clinical impact of routine anti-Xa testing, as management was affected in few patients. It is not yet clear in which clinical context providers should send anti-Xa levels. Hindawi Publishing Corporation 2015 2015-10-12 /pmc/articles/PMC4620379/ /pubmed/26543644 http://dx.doi.org/10.1155/2015/126975 Text en Copyright © 2015 Sarah Yentz et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yentz, Sarah
Onwuemene, Oluwatoyosi A.
Stein, Brady L.
Cull, Elizabeth H.
McMahon, Brandon
Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis
title Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis
title_full Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis
title_fullStr Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis
title_full_unstemmed Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis
title_short Clinical Use of Anti-Xa Monitoring in Malignancy-Associated Thrombosis
title_sort clinical use of anti-xa monitoring in malignancy-associated thrombosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620379/
https://www.ncbi.nlm.nih.gov/pubmed/26543644
http://dx.doi.org/10.1155/2015/126975
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