Cargando…

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)...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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
_version_ 1784570944767918080
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
work_keys_str_mv AT semmlergeorg safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT pomejkatharina safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT bauerdavidjm safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT balcarlorenz safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT simbrunnerbenedikt safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT binterteresa safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT hartllukas safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT beckerjeannette safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT pintermatthias safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT quehenbergerpeter safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT traunermichael safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT mandorfermattias safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT lismanton safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT reibergerthomas safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease
AT scheinerbernhard safetyofdirectoralanticoagulantsinpatientswithadvancedliverdisease