Sie sind bereits registriert?
Loggen Sie sich mit Ihrem Universimed-Benutzerkonto ein:
Sie sind noch nicht registriert?
Registrieren Sie sich jetzt kostenlos auf universimed.com und erhalten Sie Zugang zu allen Artikeln, bewerten Sie Inhalte und speichern Sie interessante Beiträge in Ihrem persönlichen Bereich
zum späteren Lesen. Ihre Registrierung ist für alle Unversimed-Portale gültig. (inkl. allgemeineplus.at & med-Diplom.at)
Sepsis-Induced Coagulopathy and Disseminated Intravascular Coagulopathy
Sponsoring Organizations: The Scientific and Standardization Committee on Disseminated Intravascular Coagulopathy and the Scientific and Standardization Committee on Perioperative and Critical Care of the International Society on Thrombosis and Haemostasis
Background and Objective
Hematologists are frequently called upon to interpret coagulation tests and manage coagulopathy in critically ill patients. Mainstays of managing disseminated intravascular coagulopathy (DIC) include treatment of the underlying cause and support with guided blood product transfusions. Anticoagulation is controversial, but subgroups of critically ill patients with coagulopathy may benefit from anticoagulation. As such, an international expert panel emphasizes the importance of early identification of coagulopathy, proposes “sepsis-induced coagulopathy” (SIC) as a preceding phase, and offers diagnostic and management strategies.
Key Points
- Suspect SIC with an International Society of Thrombosis and Haemostasis scoring system score ≥4, based on abnormalities of the platelet count: 1 point if 100–150×109/L, 2 points if <100×109/L; prothrombin time/international normalized ratio (PT/INR): 1 point if 1.2–1.4, 2 points if >1.4; and the sequential organ failure assessment (SOFA) scoring system, which assesses organ (respiratory, hepatic, cardiovascular, and renal) dysfunction: 1 point if 1, 2 points if ≥2
- If SIC is diagnosed, calculate an overt DIC score based on severity of thrombocytopenia, increase in d-dimer/fibrin degradation products, prolongation of the PT/INR, and decrease in fibrinogen.
- Consider low-molecular-weight heparin over unfractionated heparin in hope of preventing evolution of coagulopathy to overt DIC.
- Symmetrical peripheral gangrene is discussed as a consequence of DIC, but panelists acknowledge the uncertain efficacy of using anticoagulation for prevention.
Comment
This guidance statement is useful in its emphasis of a prodromal phase of DIC, during which an intervention may be helpful. However, there is not yet strong evidence to uniformly offer therapeutic anticoagulation in sepsis-induced coagulopathy. Although antithrombin and thrombomodulin are discussed, the panelists rightly acknowledge they are seldomly used in DIC. Establishing proper definitions and terminology will be useful for future studies, and reconsideration of study endpoints — such as a decrease in the rate of overt DIC progression or development of symmetrical peripheral gangrene —may be worthwhile in this population.
Bio
Note to readers: At the time we reviewed this paper, its publisher noted that it was not in final form and that subsequent changes might be made.
Citation(s)
Author:
Iba T et al.
Title:
Diagnosis and management of sepsisinduced coagulopathy and disseminated intravascular coagulation.
Source:
J Thromb Haemost
2019
Jul
20; [e-pub].
(Abstract/FREE Full Text)
Empfohlen von
Brady L. Stein, MD, MHS