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. 2015 Sep 21;9(1):15–20. doi: 10.1177/1753495X15601937

Table 3.

Comparison of features of disorders with thrombocytopenia and microangiopathy in pregnancy.7,19,3236,38,39

Pre-eclampsia HELLP syndrome Catastrophic antiphospholipid antibody syndrome Acquired ADAMTS13 deficiency-mediated TMA Complement-mediated TMA
Timing After 20 weeks’ gestation Predominantly third trimester and within 48 hours postpartum Anytime, may be precipitated by infections and medications Frequently in the second trimester and third trimester Predominantly postpartum
Hypertension Present Predominantly present Present/absent Present/absent Present/absent
Proteinuria Predominantly present Predominantly present Absent Absent Present/absent
Abdominal Pain Present in severe disease Often present Absent Absent Absent
Neurologic symptoms Present in severe disease Present/absent Present/absent Present/absent Uncommon
Renal involvement Present/absent Present/absent Present/absent Present/absent Present
Liver enzymes Elevated/normal Elevated Normal Elevated/normal Normal
Haemolysis Present or absent Present Present/absent Present/absent Present
Treatment Delivery Delivery Heparin corticosteroids ± IVIG ± plasma exchange Plasma exchange/plasma infusion and immune suppression Anticomplement agent and plasma infusion/exchange

Note: ADAMTS13: A disintegrin and metalloproteinase with thrombospondin motifs 13; DIC: disseminated intravascular coagulation; HELLP: haemolysis, elevated liver enzymes and low platelets; IVIG: intravenous immune globulin; TMA: thrombotic microangiopathy.