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Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis

The frequency of severe antithrombin deficiency (SAD) was examined in the hematopoietic disorder-, infectious-, and basic-types of the disseminated intravascular coagulation (DIC). A posthoc analysis of 3008 DIC patients (infectious-type, 1794; hematological disorder-type, 813; and basic-type, 401)...

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Autores principales: Wada, Hideo, Honda, Goichi, Kawano, Noriaki, Uchiyama, Toshimasa, Kawasugi, Kazuo, Madoiwa, Seiji, Takezako, Naoki, Suzuki, Kei, Seki, Yoshinobu, Ikezoe, Takayuki, Iba, Toshiaki, Okamoto, Kohji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448134/
https://www.ncbi.nlm.nih.gov/pubmed/32833540
http://dx.doi.org/10.1177/1076029620941112
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author Wada, Hideo
Honda, Goichi
Kawano, Noriaki
Uchiyama, Toshimasa
Kawasugi, Kazuo
Madoiwa, Seiji
Takezako, Naoki
Suzuki, Kei
Seki, Yoshinobu
Ikezoe, Takayuki
Iba, Toshiaki
Okamoto, Kohji
author_facet Wada, Hideo
Honda, Goichi
Kawano, Noriaki
Uchiyama, Toshimasa
Kawasugi, Kazuo
Madoiwa, Seiji
Takezako, Naoki
Suzuki, Kei
Seki, Yoshinobu
Ikezoe, Takayuki
Iba, Toshiaki
Okamoto, Kohji
author_sort Wada, Hideo
collection PubMed
description The frequency of severe antithrombin deficiency (SAD) was examined in the hematopoietic disorder-, infectious-, and basic-types of the disseminated intravascular coagulation (DIC). A posthoc analysis of 3008 DIC patients (infectious-type, 1794; hematological disorder-type, 813; and basic-type, 401) from post-marketing surveillance data of thrombomodulin alfa was performed. The clinical features of patients and outcomes were compared between patients with and without SAD, using an antithrombin cutoff value of 50%. Patients with SAD accounted for 40.4% of infectious-type DIC, 8.0% of hematopoietic disorder-type DIC, and 26.7% of basic-type DIC. There was no significant difference in thrombin–antithrombin complex levels between patients with and without SAD. The decreased fibrinogen level and differences in clinical features were significantly greater but the increases in fibrinolytic markers were significantly lower in patients with SAD than in those without. The 28-day survival rate was significantly lower in patients with SAD than in those without. Severe antithrombin deficiency was observed in all types of DIC, including hematopoietic disorders. Both hypofibrinolysis and hypercoagulability in patients with SAD may cause multiple organ failure and poor outcomes.
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spelling pubmed-74481342020-09-10 Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis Wada, Hideo Honda, Goichi Kawano, Noriaki Uchiyama, Toshimasa Kawasugi, Kazuo Madoiwa, Seiji Takezako, Naoki Suzuki, Kei Seki, Yoshinobu Ikezoe, Takayuki Iba, Toshiaki Okamoto, Kohji Clin Appl Thromb Hemost Original Article The frequency of severe antithrombin deficiency (SAD) was examined in the hematopoietic disorder-, infectious-, and basic-types of the disseminated intravascular coagulation (DIC). A posthoc analysis of 3008 DIC patients (infectious-type, 1794; hematological disorder-type, 813; and basic-type, 401) from post-marketing surveillance data of thrombomodulin alfa was performed. The clinical features of patients and outcomes were compared between patients with and without SAD, using an antithrombin cutoff value of 50%. Patients with SAD accounted for 40.4% of infectious-type DIC, 8.0% of hematopoietic disorder-type DIC, and 26.7% of basic-type DIC. There was no significant difference in thrombin–antithrombin complex levels between patients with and without SAD. The decreased fibrinogen level and differences in clinical features were significantly greater but the increases in fibrinolytic markers were significantly lower in patients with SAD than in those without. The 28-day survival rate was significantly lower in patients with SAD than in those without. Severe antithrombin deficiency was observed in all types of DIC, including hematopoietic disorders. Both hypofibrinolysis and hypercoagulability in patients with SAD may cause multiple organ failure and poor outcomes. SAGE Publications 2020-08-24 /pmc/articles/PMC7448134/ /pubmed/32833540 http://dx.doi.org/10.1177/1076029620941112 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Wada, Hideo
Honda, Goichi
Kawano, Noriaki
Uchiyama, Toshimasa
Kawasugi, Kazuo
Madoiwa, Seiji
Takezako, Naoki
Suzuki, Kei
Seki, Yoshinobu
Ikezoe, Takayuki
Iba, Toshiaki
Okamoto, Kohji
Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis
title Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis
title_full Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis
title_fullStr Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis
title_full_unstemmed Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis
title_short Severe Antithrombin Deficiency May be Associated With a High Risk of Pathological Progression of DIC With Suppressed Fibrinolysis
title_sort severe antithrombin deficiency may be associated with a high risk of pathological progression of dic with suppressed fibrinolysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448134/
https://www.ncbi.nlm.nih.gov/pubmed/32833540
http://dx.doi.org/10.1177/1076029620941112
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