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Sepsis and thrombosis.

Abstract
Activation of coagulation frequently occurs in severe infection and sepsis and may contribute to the development of thrombosis. Coagulation abnormalities in sepsis range from a small decrease in platelet count and subclinical prolongation of global clotting times to fulminant disseminated intravascular coagulation (DIC), characterized by simultaneous widespread microvascular thrombosis and profuse bleeding from various sites. Septic patients with severe forms of DIC may present with manifest thromboembolic disease or clinically less apparent microvascular fibrin deposition, which predominantly presents as multiple organ dysfunction. Thrombophilia is associated with a prohemostatic state and consequently with an increased tendency to develop thrombosis. Hypothetically, patients with thrombophilia may suffer from more severe coagulopathy in case of severe infection or sepsis, which may result in a more serious clinical course and an unfavorable outcome. On the basis of the knowledge of the pathogenesis of thrombosis in severe inflammation and sepsis, strategies aimed at the inhibition of coagulation activation have been developed and have been found favorable in experimental and clinical studies.
AuthorsMarcel Levi, Marcus Schultz, Tom van der Poll
JournalSeminars in thrombosis and hemostasis (Semin Thromb Hemost) Vol. 39 Issue 5 Pg. 559-66 (Jul 2013) ISSN: 1098-9064 [Electronic] United States
PMID23625756 (Publication Type: Journal Article, Review)
CopyrightThieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.
Chemical References
  • Anticoagulants
Topics
  • Anticoagulants (therapeutic use)
  • Blood Coagulation (drug effects)
  • Disseminated Intravascular Coagulation (diagnosis, etiology, prevention & control)
  • Humans
  • Multiple Organ Failure (diagnosis, etiology, prevention & control)
  • Sepsis (blood, complications)
  • Thrombophilia (diagnosis, etiology, prevention & control)
  • Thrombosis (diagnosis, etiology, prevention & control)
  • Treatment Outcome

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