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Safety of direct oral anticoagulants in patients with advanced liver disease
BACKGROUND & AIMS: While direct oral anticoagulants (DOACs) are increasingly used in patients with liver disease, safety data especially in advanced chronic liver disease (ACLD) are limited. METHODS: Liver disease patients receiving DOAC treatment (ACLD: n = 104; vascular liver disease: n = 29)...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456813/ https://www.ncbi.nlm.nih.gov/pubmed/34152697 http://dx.doi.org/10.1111/liv.14992 |
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author | Semmler, Georg Pomej, Katharina Bauer, David J. M. Balcar, Lorenz Simbrunner, Benedikt Binter, Teresa Hartl, Lukas Becker, Jeannette Pinter, Matthias Quehenberger, Peter Trauner, Michael Mandorfer, Mattias Lisman, Ton Reiberger, Thomas Scheiner, Bernhard |
author_facet | Semmler, Georg Pomej, Katharina Bauer, David J. M. Balcar, Lorenz Simbrunner, Benedikt Binter, Teresa Hartl, Lukas Becker, Jeannette Pinter, Matthias Quehenberger, Peter Trauner, Michael Mandorfer, Mattias Lisman, Ton Reiberger, Thomas Scheiner, Bernhard |
author_sort | Semmler, Georg |
collection | PubMed |
description | BACKGROUND & AIMS: While direct oral anticoagulants (DOACs) are increasingly used in patients with liver disease, safety data especially in advanced chronic liver disease (ACLD) are limited. METHODS: Liver disease patients receiving DOAC treatment (ACLD: n = 104; vascular liver disease: n = 29) or vitamin K antagonists (VKA)/low‐molecular‐weight heparin (LMWH; ACLD: n = 45; vascular: n = 13) between January 2010 and September 2020 were retrospectively included. Invasive procedures and bleeding events were recorded. Calibrated anti‐Xa peak levels and thrombomodulin‐modified thrombin generation assays (TM‐TGAs) were measured in a subgroup of 35/28 DOAC patients. RESULTS: Among patients receiving DOAC, 55 (41.3%) had advanced liver dysfunction (Child‐Pugh‐stage [CPS] B/C) and 66 (49.6%) had experienced decompensation. Overall, 205 procedures were performed in 60 patients and procedure‐related bleedings occurred in 7 (11.7%) patients. Additionally, 38 (28.6%) patients experienced spontaneous (15 minor, 23 major) bleedings during a median follow‐up of 10.5 (IQR: 4.0‐27.8) months. Spontaneous bleedings in ACLD patients were more common in CPS‐B/C (at 12 months: 36.9% vs CPS‐A: 15.9%, subdistribution hazard ratio [SHR]: 3.23 [95% CI: 1.59‐6.58], P < .001), as were major bleedings (at 12 months: 22.0% vs 5.0%, SHR: 5.82 [95% CI: 2.00‐16.90], P < .001). Importantly, CPS (adjusted SHR: 4.12 [91% CI: 1.82‐9.37], P < .001), but not the presence of hepatocellular carcinoma or varices, was independently associated with major bleeding during DOAC treatment. Additionally, ACLD patients experiencing bleeding had worse overall survival (at 12 months: 88.9% vs 95.0% without bleeding; P < .001). Edoxaban anti‐Xa peak levels were higher in patients with CPS‐B/C (345 [95% CI: 169‐395] vs CPS‐A: 137 [95% CI: 96‐248] ng/mL, P = .048) and were associated with lower TM‐TGA. Importantly, spontaneous bleeding rates were comparable to VKA/LMWH patients. CONCLUSIONS: Anticoagulants including DOACs should be used with caution in patients with advanced liver disease due to a significant rate of spontaneous bleeding events. |
format | Online Article Text |
id | pubmed-8456813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84568132021-09-27 Safety of direct oral anticoagulants in patients with advanced liver disease Semmler, Georg Pomej, Katharina Bauer, David J. M. Balcar, Lorenz Simbrunner, Benedikt Binter, Teresa Hartl, Lukas Becker, Jeannette Pinter, Matthias Quehenberger, Peter Trauner, Michael Mandorfer, Mattias Lisman, Ton Reiberger, Thomas Scheiner, Bernhard Liver Int Cirrhosis, Liver Failure and Transplantation BACKGROUND & AIMS: While direct oral anticoagulants (DOACs) are increasingly used in patients with liver disease, safety data especially in advanced chronic liver disease (ACLD) are limited. METHODS: Liver disease patients receiving DOAC treatment (ACLD: n = 104; vascular liver disease: n = 29) or vitamin K antagonists (VKA)/low‐molecular‐weight heparin (LMWH; ACLD: n = 45; vascular: n = 13) between January 2010 and September 2020 were retrospectively included. Invasive procedures and bleeding events were recorded. Calibrated anti‐Xa peak levels and thrombomodulin‐modified thrombin generation assays (TM‐TGAs) were measured in a subgroup of 35/28 DOAC patients. RESULTS: Among patients receiving DOAC, 55 (41.3%) had advanced liver dysfunction (Child‐Pugh‐stage [CPS] B/C) and 66 (49.6%) had experienced decompensation. Overall, 205 procedures were performed in 60 patients and procedure‐related bleedings occurred in 7 (11.7%) patients. Additionally, 38 (28.6%) patients experienced spontaneous (15 minor, 23 major) bleedings during a median follow‐up of 10.5 (IQR: 4.0‐27.8) months. Spontaneous bleedings in ACLD patients were more common in CPS‐B/C (at 12 months: 36.9% vs CPS‐A: 15.9%, subdistribution hazard ratio [SHR]: 3.23 [95% CI: 1.59‐6.58], P < .001), as were major bleedings (at 12 months: 22.0% vs 5.0%, SHR: 5.82 [95% CI: 2.00‐16.90], P < .001). Importantly, CPS (adjusted SHR: 4.12 [91% CI: 1.82‐9.37], P < .001), but not the presence of hepatocellular carcinoma or varices, was independently associated with major bleeding during DOAC treatment. Additionally, ACLD patients experiencing bleeding had worse overall survival (at 12 months: 88.9% vs 95.0% without bleeding; P < .001). Edoxaban anti‐Xa peak levels were higher in patients with CPS‐B/C (345 [95% CI: 169‐395] vs CPS‐A: 137 [95% CI: 96‐248] ng/mL, P = .048) and were associated with lower TM‐TGA. Importantly, spontaneous bleeding rates were comparable to VKA/LMWH patients. CONCLUSIONS: Anticoagulants including DOACs should be used with caution in patients with advanced liver disease due to a significant rate of spontaneous bleeding events. John Wiley and Sons Inc. 2021-07-10 2021-09 /pmc/articles/PMC8456813/ /pubmed/34152697 http://dx.doi.org/10.1111/liv.14992 Text en © 2021 The Authors. Liver International published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://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 | Cirrhosis, Liver Failure and Transplantation Semmler, Georg Pomej, Katharina Bauer, David J. M. Balcar, Lorenz Simbrunner, Benedikt Binter, Teresa Hartl, Lukas Becker, Jeannette Pinter, Matthias Quehenberger, Peter Trauner, Michael Mandorfer, Mattias Lisman, Ton Reiberger, Thomas Scheiner, Bernhard Safety of direct oral anticoagulants in patients with advanced liver disease |
title | Safety of direct oral anticoagulants in patients with advanced liver disease |
title_full | Safety of direct oral anticoagulants in patients with advanced liver disease |
title_fullStr | Safety of direct oral anticoagulants in patients with advanced liver disease |
title_full_unstemmed | Safety of direct oral anticoagulants in patients with advanced liver disease |
title_short | Safety of direct oral anticoagulants in patients with advanced liver disease |
title_sort | safety of direct oral anticoagulants in patients with advanced liver disease |
topic | Cirrhosis, Liver Failure and Transplantation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8456813/ https://www.ncbi.nlm.nih.gov/pubmed/34152697 http://dx.doi.org/10.1111/liv.14992 |
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