Cargando…

Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases

BACKGROUND: Acquired hemophilia A (AHA) is a rare autoimmune disease characterized by bleeding events. Recombinant activated factor VII (rFVIIa) is a first-line bypassing agent, which is effective against clinically significant bleeding. However, there is no standard way of tapering and discontinuin...

Descripción completa

Detalles Bibliográficos
Autores principales: Hosoi, Hiroki, Akagi, Yuina, Mushino, Toshiki, Takeyama, Masahiro, Minoura, Naoto, Hiroi, Takayuki, Furuya, Yoshiaki, Morimoto, Masaya, Murata, Shogo, Tamura, Shinobu, Sonoki, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109301/
https://www.ncbi.nlm.nih.gov/pubmed/35578257
http://dx.doi.org/10.1186/s12959-022-00387-x
_version_ 1784708872288600064
author Hosoi, Hiroki
Akagi, Yuina
Mushino, Toshiki
Takeyama, Masahiro
Minoura, Naoto
Hiroi, Takayuki
Furuya, Yoshiaki
Morimoto, Masaya
Murata, Shogo
Tamura, Shinobu
Sonoki, Takashi
author_facet Hosoi, Hiroki
Akagi, Yuina
Mushino, Toshiki
Takeyama, Masahiro
Minoura, Naoto
Hiroi, Takayuki
Furuya, Yoshiaki
Morimoto, Masaya
Murata, Shogo
Tamura, Shinobu
Sonoki, Takashi
author_sort Hosoi, Hiroki
collection PubMed
description BACKGROUND: Acquired hemophilia A (AHA) is a rare autoimmune disease characterized by bleeding events. Recombinant activated factor VII (rFVIIa) is a first-line bypassing agent, which is effective against clinically significant bleeding. However, there is no standard way of tapering and discontinuing rFVIIa, mainly because there is no established method for monitoring rFVIIa therapy for AHA. CASE PRESENTATION: Here, we report three AHA cases, in which we adjusted the rFVIIa dosing interval based on the results of thromboelastography (TEG) performed just before the administration of the next dose of rFVIIa. The dosing interval of rFVIIa was prolonged based on the reaction rate time (R) according to TEG, which is correlated with coagulation factor activity. The R-value reference range reported by the manufacturer of the TEG system was used as a threshold for making decisions. In these three cases, there was no rebleeding, and the patients’ ability to perform activities of daily living did not decline. CONCLUSION: Our cases suggest that conducting TEG-based monitoring just before the administration of the next dose of rFVIIa may be useful for guiding increases in the rFVIIa dosing interval without causing rebleeding events. Further investigations are warranted to examine how TEG could be used to determine the most appropriate rFVIIa dosing interval, e.g., through regular TEG-based monitoring, and the optimal TEG-derived threshold for indicating changes to the rFVIIa dosing interval.
format Online
Article
Text
id pubmed-9109301
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-91093012022-05-17 Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases Hosoi, Hiroki Akagi, Yuina Mushino, Toshiki Takeyama, Masahiro Minoura, Naoto Hiroi, Takayuki Furuya, Yoshiaki Morimoto, Masaya Murata, Shogo Tamura, Shinobu Sonoki, Takashi Thromb J Case Report BACKGROUND: Acquired hemophilia A (AHA) is a rare autoimmune disease characterized by bleeding events. Recombinant activated factor VII (rFVIIa) is a first-line bypassing agent, which is effective against clinically significant bleeding. However, there is no standard way of tapering and discontinuing rFVIIa, mainly because there is no established method for monitoring rFVIIa therapy for AHA. CASE PRESENTATION: Here, we report three AHA cases, in which we adjusted the rFVIIa dosing interval based on the results of thromboelastography (TEG) performed just before the administration of the next dose of rFVIIa. The dosing interval of rFVIIa was prolonged based on the reaction rate time (R) according to TEG, which is correlated with coagulation factor activity. The R-value reference range reported by the manufacturer of the TEG system was used as a threshold for making decisions. In these three cases, there was no rebleeding, and the patients’ ability to perform activities of daily living did not decline. CONCLUSION: Our cases suggest that conducting TEG-based monitoring just before the administration of the next dose of rFVIIa may be useful for guiding increases in the rFVIIa dosing interval without causing rebleeding events. Further investigations are warranted to examine how TEG could be used to determine the most appropriate rFVIIa dosing interval, e.g., through regular TEG-based monitoring, and the optimal TEG-derived threshold for indicating changes to the rFVIIa dosing interval. BioMed Central 2022-05-16 /pmc/articles/PMC9109301/ /pubmed/35578257 http://dx.doi.org/10.1186/s12959-022-00387-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Hosoi, Hiroki
Akagi, Yuina
Mushino, Toshiki
Takeyama, Masahiro
Minoura, Naoto
Hiroi, Takayuki
Furuya, Yoshiaki
Morimoto, Masaya
Murata, Shogo
Tamura, Shinobu
Sonoki, Takashi
Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases
title Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases
title_full Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases
title_fullStr Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases
title_full_unstemmed Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases
title_short Use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor VII in acquired hemophilia A: a report of three cases
title_sort use of thromboelastography before the administration of hemostatic agents to safely taper recombinant activated factor vii in acquired hemophilia a: a report of three cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109301/
https://www.ncbi.nlm.nih.gov/pubmed/35578257
http://dx.doi.org/10.1186/s12959-022-00387-x
work_keys_str_mv AT hosoihiroki useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT akagiyuina useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT mushinotoshiki useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT takeyamamasahiro useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT minouranaoto useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT hiroitakayuki useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT furuyayoshiaki useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT morimotomasaya useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT muratashogo useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT tamurashinobu useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases
AT sonokitakashi useofthromboelastographybeforetheadministrationofhemostaticagentstosafelytaperrecombinantactivatedfactorviiinacquiredhemophiliaaareportofthreecases