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Measurement of Factor V Activity in Human Plasma Using a Microplate Coagulation Assay
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Thrombotic Thrombocytopenic Purpura, Heparin-Induced Thrombocytopenia, and Disseminated Intravascular Coagulation

Ram Kalpatthi1, Joseph E Kiss2

  • 1Division of Pediatric Hematology Oncology, Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, 4401 Penn Avenue, Suite 501A, Pittsburgh, PA 15224, USA.

Critical Care Clinics
|March 17, 2020
PubMed

Hemostatic abnormalities are common among critically ill patients and are associated with a high risk of bleeding. The abnormalities range from isolated thrombocytopenia or prolongation of global coagulation assays to complex disease states, such as thrombotic microangiopathic syndromes, and can be associated with a wide range of conditions, including trauma, surgery, acute disease processes, cardiopulmonary bypass, and exposure to drugs and blood products. Prompt identification of underlying causes is important because treatment strategies vary. Moreover, prompt initiation of both supportive and specific treatments is vital to decrease the morbidity and mortality in the intensive care unit.

Keywords:
CaplacizumabHeparinICUMicroangiopathic hemolytic anemiaPlasmapheresisRituximabThrombocytopeniaThrombotic microangiopathy

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