RT Journal Article
SR Electronic
T1 Laboratory Findings in Hematology, Clinical Chemistry, and Urinalysis for Patients With Thrombotic Thrombocytopenic Purpura
JF American Society for Clinical Laboratory Science
JO Clin Lab Sci
FD American Society of Chemistry and Laboratory Science
DO 10.29074/ascls.2020002279
A1 Doig, Kathy
A1 McQuiston, Susan
YR 2020
UL http://hwmaint.clsjournal.ascls.org/content/early/2023/04/10/ascls.2020002279.abstract
AB Laboratory diagnosis of thrombotic thrombocytopenic purpura (TTP) often begins with routine laboratory tests; a complete blood count, clinical chemistry panel, and urinalysis. The classical findings may include anemia with schistocytes, thrombocytopenia, reticulocytosis or polychromasia, bilirubinemia, dark urine, and hemoglobinuria without red blood cells in the sediment. Additional findings, including decreased haptoglobin, can identify fragmentation as the cause for the hemolysis. The hemolysis in TTP arises from increased shear stress on red blood cells in arterioles and capillaries narrowed by microthrombi. Hemoglobinemia and schistocytes may generate spurious results in hematology analyzers that require correction before results can be released to the patient chart.