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Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations
BACKGROUND: For more than a decade, guidelines have recommended a limited 3 months of anticoagulation for the treatment of provoked venous thromboembolism (VTE). How closely real‐world practice follows guideline recommendations is not well described. METHODS AND RESULTS: In our multicenter, retrospe...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673630/ https://www.ncbi.nlm.nih.gov/pubmed/36285782 http://dx.doi.org/10.1161/JAHA.122.025471 |
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author | Joyce, Elizabeth Haymart, Brian Kong, Xiaowen Ali, Mona A. Carrigan, Mara Kaatz, Scott Shah, Vinay Kline‐Rogers, Eva Kozlowski, Jay Froehlich, James B. Barnes, Geoffrey D. |
author_facet | Joyce, Elizabeth Haymart, Brian Kong, Xiaowen Ali, Mona A. Carrigan, Mara Kaatz, Scott Shah, Vinay Kline‐Rogers, Eva Kozlowski, Jay Froehlich, James B. Barnes, Geoffrey D. |
author_sort | Joyce, Elizabeth |
collection | PubMed |
description | BACKGROUND: For more than a decade, guidelines have recommended a limited 3 months of anticoagulation for the treatment of provoked venous thromboembolism (VTE). How closely real‐world practice follows guideline recommendations is not well described. METHODS AND RESULTS: In our multicenter, retrospective cohort study, we evaluated trends in anticoagulation duration for patients enrolled in the MAQI(2) (Michigan Anticoagulation Quality Improvement Initiative) registry who were receiving anticoagulation for a provoked VTE. The MAQI(2) registry comprises 6 centers in Michigan that manage patients' long‐term anticoagulation. We identified 474 patients on warfarin and 302 patients on direct oral anticoagulants who were receiving anticoagulation for a primary indication of provoked VTE between 2008 and 2020. Using a predefined threshold of 120 days (3 months plus a buffer period), predictors of extended anticoagulant use were identified using multivariable logistic regression. Most patients received >120 days of anticoagulation, regardless of which medication was used. The median (25th–75th percentile) length of treatment for patients taking warfarin was 142 (91–234) days and for direct oral anticoagulants was 180 (101–360) days. Recurrent VTE (odds ratio [OR], 2.75 [95% CI, 1.67–4.53]), history of myocardial infarction (OR, 3.92 [95% CI, 1.32–11.7]), and direct oral anticoagulant rather than warfarin use (OR, 2.22 [95% CI, 1.59–3.08]) were independently associated with prolonged anticoagulation. CONCLUSIONS: In our cohort of patients with provoked VTE, most patients received anticoagulation for longer than the guideline‐recommended 3 months. This demonstrates a potential opportunity to improve care delivery and reduce anticoagulant‐associated bleeding risk. |
format | Online Article Text |
id | pubmed-9673630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96736302022-11-21 Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations Joyce, Elizabeth Haymart, Brian Kong, Xiaowen Ali, Mona A. Carrigan, Mara Kaatz, Scott Shah, Vinay Kline‐Rogers, Eva Kozlowski, Jay Froehlich, James B. Barnes, Geoffrey D. J Am Heart Assoc Original Research BACKGROUND: For more than a decade, guidelines have recommended a limited 3 months of anticoagulation for the treatment of provoked venous thromboembolism (VTE). How closely real‐world practice follows guideline recommendations is not well described. METHODS AND RESULTS: In our multicenter, retrospective cohort study, we evaluated trends in anticoagulation duration for patients enrolled in the MAQI(2) (Michigan Anticoagulation Quality Improvement Initiative) registry who were receiving anticoagulation for a provoked VTE. The MAQI(2) registry comprises 6 centers in Michigan that manage patients' long‐term anticoagulation. We identified 474 patients on warfarin and 302 patients on direct oral anticoagulants who were receiving anticoagulation for a primary indication of provoked VTE between 2008 and 2020. Using a predefined threshold of 120 days (3 months plus a buffer period), predictors of extended anticoagulant use were identified using multivariable logistic regression. Most patients received >120 days of anticoagulation, regardless of which medication was used. The median (25th–75th percentile) length of treatment for patients taking warfarin was 142 (91–234) days and for direct oral anticoagulants was 180 (101–360) days. Recurrent VTE (odds ratio [OR], 2.75 [95% CI, 1.67–4.53]), history of myocardial infarction (OR, 3.92 [95% CI, 1.32–11.7]), and direct oral anticoagulant rather than warfarin use (OR, 2.22 [95% CI, 1.59–3.08]) were independently associated with prolonged anticoagulation. CONCLUSIONS: In our cohort of patients with provoked VTE, most patients received anticoagulation for longer than the guideline‐recommended 3 months. This demonstrates a potential opportunity to improve care delivery and reduce anticoagulant‐associated bleeding risk. John Wiley and Sons Inc. 2022-10-26 /pmc/articles/PMC9673630/ /pubmed/36285782 http://dx.doi.org/10.1161/JAHA.122.025471 Text en © 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Joyce, Elizabeth Haymart, Brian Kong, Xiaowen Ali, Mona A. Carrigan, Mara Kaatz, Scott Shah, Vinay Kline‐Rogers, Eva Kozlowski, Jay Froehlich, James B. Barnes, Geoffrey D. Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations |
title | Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations |
title_full | Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations |
title_fullStr | Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations |
title_full_unstemmed | Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations |
title_short | Length of Anticoagulation in Provoked Venous Thromboembolism: A Multicenter Study of How Real‐World Practice Mirrors Guideline Recommendations |
title_sort | length of anticoagulation in provoked venous thromboembolism: a multicenter study of how real‐world practice mirrors guideline recommendations |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673630/ https://www.ncbi.nlm.nih.gov/pubmed/36285782 http://dx.doi.org/10.1161/JAHA.122.025471 |
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