Hemolytic Uremic Syndrome, Post-diarrheal (HUS)
Hemolytic uremic syndrome (HUS) is characterized by the acute onset of microangiopathic hemolytic anemia, renal injury, and low platelet count. Thrombotic thrombocytopenic purpura (TTP) is also characterized by these features but also can include central nervous system involvement and fever, and may have a more gradual onset. Most cases of HUS (but few cases of TTP) occur after an acute gastrointestinal illness (usually diarrheal). Only HUS or TTP occurring after an acute diarrheal illness is reportable.
The following are present at some time during the illness:
Anemia (acute onset) with microangiopathic changes (i.e., schistocytes, burr cells, or helmet cells) on peripheral blood smear
Renal injury (acute onset), evidenced by either
Note: A low platelet count can usually, but not always, be detected early in the illness, but it may then become normal or even high. If a platelet count obtained within 7 days after onset of the acute gastrointestinal illness is not less than 150,000/mm 3, other diagnoses should be considered.
Probable:
Confirmed: An acute illness diagnosed as HUS or TTP, that both meets the laboratory criteria and began within 3 weeks of onset of an acute or bloody diarrhea
Some investigators consider HUS and TTP to be part of a continuum of disease. Therefore, criteria for diagnosing TTP on the basis of central nervous system involvement and fever are not provided because cases diagnosed clinically as postdiarrheal TTP should also meet the criteria for HUS. These cases are reported as postdiarrheal HUS.