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Updated: Jun 26, 2026

Measurement of Factor V Activity in Human Plasma Using a Microplate Coagulation Assay
Published on: September 9, 2012
[Severe sepsis and disseminated intravascular coagulation. Supplementation with antithrombin]
M Angstwurm1, J Hoffmann, H Ostermann
1Medizinische Klinik, Ziemssenstr. 1, 80336 München, Deutschland. matthias.angstwurm@med.uni-muenchen.de
Insights
High-dose antithrombin (AT) did not reduce mortality in severe sepsis overall. However, AT without heparin significantly lowered mortality in specific patient subgroups, including those with disseminated intravascular coagulation (DIC).
Area of Science:
- Critical Care Medicine
- Hematology
- Pharmacology
Context:
- Severe sepsis is a life-threatening condition associated with high mortality rates.
- Antithrombin (AT) is a protein crucial for regulating blood coagulation.
- Previous studies on AT in sepsis have yielded conflicting results.
Purpose:
- To evaluate the efficacy of high-dose antithrombin (AT) in patients with severe sepsis.
- To investigate the impact of AT administration, with or without concomitant heparin, on mortality rates.
- To explore potential benefits of AT in specific sepsis-related complications like disseminated intravascular coagulation (DIC).
Summary:
- The KyberSept study found no significant overall mortality reduction with high-dose AT in severe sepsis patients compared to placebo.
- A significant reduction in 90-day mortality was observed in patients receiving AT but not concurrent heparin.
- This benefit was particularly notable in high-risk patients (SAPS grade II) and those with sepsis-induced DIC.
Impact:
- Findings suggest a potential therapeutic role for AT in specific sepsis patient populations, particularly when heparin is contraindicated or avoided.
- Coagulation diagnostics are vital for identifying patients who may benefit from AT therapy.
- Results support the need for a dedicated randomized controlled trial to confirm AT efficacy in selected severe sepsis patients.
Abstract:
Administration of high-dose antithrombin (AT) was investigated on a large collective of patients with severe sepsis in the KyberSept study. In the total study the administration of AT resulted in no significant reduction of the mortality rate in comparison to a placebo. However, in the protocol of this study subgroups were predefined, which when analyzed revealed that the group of patients who received AT but not simultaneously heparin did show a reduction of the mortality rate in comparison to the placebo group. The reduction of the absolute mortality rate of 15% reached statistical significance on day 90. Even patients classified as risk group grade II according to the Simplified Acute Physiology Score (SAPS), showed a significant reduction of the mortality rate of approximately 22% after 90 days without simultaneous administration of heparin. Such a positive result for administration of AT without simultaneous heparin treatment can also be found when severe sepsis complicated by disseminated intravascular coagulation (DIC) is present. Coagulation diagnostic assists the recognition of latent or fulminant DIC and also in surveillance of the course and development. The results of AT supplementation for severe sepsis and DIC are in agreement with earlier studies on smaller patient collectives and suggest that a randomized controlled clinical study should be carried out on a subcollective of severely ill patients.
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