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Management of Thrombocytopenia in Advanced Liver Disease
Author(s) -
Venu Gopala Reddy Gangireddy,
PC Kanneganti,
Subbiah Sridhar,
Swathi Talla,
Teresa A. Coleman
Publication year - 2014
Publication title -
canadian journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.921
H-Index - 65
eISSN - 2291-2797
pISSN - 2291-2789
DOI - 10.1155/2014/532191
Subject(s) - medicine , cirrhosis , thrombopoietin , platelet , chronic liver disease , complication , gastroenterology , splenectomy , liver disease , bone marrow , disease , haematopoiesis , etiology , eltrombopag , thrombopoietin receptor , platelet transfusion , immunology , immune thrombocytopenia , spleen , stem cell , biology , genetics
Thrombocytopenia (defined as a platelet count <150×10(9)) is a well-known complication in patients with liver cirrhosis and has been observed in 76% to 85% of patients. Significant thrombocytopenia (platelet count <50×10(9) to 75×10(9)) occurs in approximately 13% of patients with cirrhosis. Thrombocytopenia can negatively impact the care of patients with severe liver disease by potentially interfering with diagnostic and therapeutic procedures. Multiple factors can contribute to the development of thrombocytopenia including splenic platelet sequestration, immunological processes, bone marrow suppression by chronic viral infection, and reduced levels or activity of the hematopoietic growth factor thrombopoietin. The present review focuses on the etiologies and management options for severe thrombocytopenia in the setting of advanced liver disease.

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