Diagnosis:
- Microangiopathic haemolytic anemia (>=5% fragments) with normal INR/aPTT
- Classic pentad:
- Fever
- Altered mental status
- Renal failure
- Microangiopathic haemolytic anemia
- Thrombocytopenia
- Few people present with the classic pentad unless left untreated for a long time. Most present with MAHA thrombocytopenia alone.
- Needs to be contrasted with Haemolytic Uremic Syndrome in children with diarrhea (E. coli 0157:H7)
- Need to exclude DIC from sepsis or malignancy, malignant hypertension, scleroderma renal crisis, HELLP syndrome
Causes:
- HIV
- Drugs (ticlodipine, clopidogrel, quinine, valacyclovir, cyclosporin A, tacrolimus, others)
- Idiopathic/genetic
- Pregnancy associated
Management:
- Arrange transfer to specialized centre for PLEX
- In interim add steroids for idiopathic TTP
- In interim add FFP infusions (i.e. 1u q2h)
I have previously blogged about
TTP here and
anemia (including haemolytic anemia) and
thrombocytopenia.
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