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Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa

BACKGROUND: In patients with infectious diseases, disseminated intravascular coagulation (DIC) is often diagnosed without the fibrinogen value. The relationship between hypofibrinogenemia and outcomes of DIC in infectious diseases has thus remained unclear. METHODS: We analyzed 3204 patients who rec...

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Autores principales: Kawasugi, Kazuo, Wada, Hideo, Honda, Goichi, Kawano, Noriaki, Uchiyama, Toshimasa, Madoiwa, Seiji, Takezako, Naoki, Suzuki, Kei, Seki, Yoshinobu, Ikezoe, Takayuki, Iba, Toshiaki, Okamoto, Kohji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908729/
https://www.ncbi.nlm.nih.gov/pubmed/33632246
http://dx.doi.org/10.1186/s12959-021-00264-z
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author Kawasugi, Kazuo
Wada, Hideo
Honda, Goichi
Kawano, Noriaki
Uchiyama, Toshimasa
Madoiwa, Seiji
Takezako, Naoki
Suzuki, Kei
Seki, Yoshinobu
Ikezoe, Takayuki
Iba, Toshiaki
Okamoto, Kohji
author_facet Kawasugi, Kazuo
Wada, Hideo
Honda, Goichi
Kawano, Noriaki
Uchiyama, Toshimasa
Madoiwa, Seiji
Takezako, Naoki
Suzuki, Kei
Seki, Yoshinobu
Ikezoe, Takayuki
Iba, Toshiaki
Okamoto, Kohji
author_sort Kawasugi, Kazuo
collection PubMed
description BACKGROUND: In patients with infectious diseases, disseminated intravascular coagulation (DIC) is often diagnosed without the fibrinogen value. The relationship between hypofibrinogenemia and outcomes of DIC in infectious diseases has thus remained unclear. METHODS: We analyzed 3204 patients who received with thrombomodulin alfa (TM-α) for DIC and suspected DIC. Hypofibrinogenemia was defined by a fibrinogen level < 1.5 g/L. RESULTS: Hypofibrinogenemia was observed in 10.3% of patients with infectious diseases. The frequencies of both bleeding and organ failure symptoms, and the scores for organ failure or the DIC diagnostic criteria were significantly higher in infectious disease patients with hypofibrinogenemia, suggesting that in patients with infectious diseases, hypofibrinogenemia is associated with more progressive and severe DIC. Although the 28-day survival rate and the DIC resolution rate were both significantly lower for infectious disease patients with DIC with hypofibrinogenemia than for those without hypofibrinogenemia, this difference was not observed in DIC patients with hematological diseases. CONCLUSIONS: Hypofibrinogenemia among infectious disease patients with DIC may reflect increased consumption of fibrinogen due to accelerated coagulation reactions, while hypofibrinogenemia among hematological disease patients with DIC may be caused by fibrinogenolysis due to hyperfibrinolysis, and frequently results in bleeding and multiple-organ failure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12959-021-00264-z.
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spelling pubmed-79087292021-02-26 Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa Kawasugi, Kazuo Wada, Hideo Honda, Goichi Kawano, Noriaki Uchiyama, Toshimasa Madoiwa, Seiji Takezako, Naoki Suzuki, Kei Seki, Yoshinobu Ikezoe, Takayuki Iba, Toshiaki Okamoto, Kohji Thromb J Research BACKGROUND: In patients with infectious diseases, disseminated intravascular coagulation (DIC) is often diagnosed without the fibrinogen value. The relationship between hypofibrinogenemia and outcomes of DIC in infectious diseases has thus remained unclear. METHODS: We analyzed 3204 patients who received with thrombomodulin alfa (TM-α) for DIC and suspected DIC. Hypofibrinogenemia was defined by a fibrinogen level < 1.5 g/L. RESULTS: Hypofibrinogenemia was observed in 10.3% of patients with infectious diseases. The frequencies of both bleeding and organ failure symptoms, and the scores for organ failure or the DIC diagnostic criteria were significantly higher in infectious disease patients with hypofibrinogenemia, suggesting that in patients with infectious diseases, hypofibrinogenemia is associated with more progressive and severe DIC. Although the 28-day survival rate and the DIC resolution rate were both significantly lower for infectious disease patients with DIC with hypofibrinogenemia than for those without hypofibrinogenemia, this difference was not observed in DIC patients with hematological diseases. CONCLUSIONS: Hypofibrinogenemia among infectious disease patients with DIC may reflect increased consumption of fibrinogen due to accelerated coagulation reactions, while hypofibrinogenemia among hematological disease patients with DIC may be caused by fibrinogenolysis due to hyperfibrinolysis, and frequently results in bleeding and multiple-organ failure. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12959-021-00264-z. BioMed Central 2021-02-25 /pmc/articles/PMC7908729/ /pubmed/33632246 http://dx.doi.org/10.1186/s12959-021-00264-z Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Research
Kawasugi, Kazuo
Wada, Hideo
Honda, Goichi
Kawano, Noriaki
Uchiyama, Toshimasa
Madoiwa, Seiji
Takezako, Naoki
Suzuki, Kei
Seki, Yoshinobu
Ikezoe, Takayuki
Iba, Toshiaki
Okamoto, Kohji
Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa
title Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa
title_full Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa
title_fullStr Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa
title_full_unstemmed Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa
title_short Hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa
title_sort hypofibrinogenemia is associated with a high degree of risk in infectious diseases: a post-hoc analysis of post-marketing surveillance of patients with disseminated intravascular coagulation treated with thrombomodulin alfa
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908729/
https://www.ncbi.nlm.nih.gov/pubmed/33632246
http://dx.doi.org/10.1186/s12959-021-00264-z
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