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

Author:

Wada Hideo1ORCID,Honda Goichi2,Kawano Noriaki3,Uchiyama Toshimasa4,Kawasugi Kazuo5,Madoiwa Seiji6,Takezako Naoki7,Suzuki Kei8,Seki Yoshinobu9,Ikezoe Takayuki10,Iba Toshiaki11,Okamoto Kohji12

Affiliation:

1. Department of General Medicine, Mie Prefectural General Medical Center, Mie, Japan

2. Department of Medical Affairs, Asahi Kasei Pharma Corporation, Tokyo, Japan

3. Department of Internal Medicine, Miyazaki Prefectural Miyazaki Hospital, Miyazaki, Japan

4. Department of Laboratory Medicine, National Hospital Organization Takasaki General Medical Center, Gunma, Japan

5. Faculty of Medical Technology, Teikyo University, Tokyo, Japan

6. Department of Clinical Laboratory Medicine, Tokyo Saiseikai Central Hospital, Tokyo, Japan

7. Department of Hematology, National Hospital Organization Disaster Medical Center, Tokyo, Japan

8. Emergency and Critical Care Center, Mie University Hospital, Mie, Japan

9. Department of Hematology, Uonuma Institute of Community Medicine, Niigata University Medical and Dental Hospital, Niigata, Japan

10. Department of Hematology, Fukushima Medical University, Fukushima, Japan

11. Department of Emergency and Disaster Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan

12. Department of Surgery, Center for Gastroenterology and Liver Disease, Kitakyushu City Yahata Hospital, Fukuoka, Japan

Abstract

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.

Funder

Asahi Kasei Pharma Corporation

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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