Diagnostic approach to thrombocytopenia in pregnancy
1. History | Bleeding symptoms Infectious symptoms Prior platelet counts: pregnant and nonpregnant Family history of thrombocytopenia Autoimmune disorders Medications Headache | ||
2. Physical examination | Bleeding: bruising, petechiae, purpura, oral mucosal blood blisters, conjunctival hemorrhages Blood pressure Lymphadenopathy, hepatomegaly, splenomegaly Abdominal tenderness Lower extremity edema Rashes or synovitis | ||
3. Timing | Categorize by onset and severity of thrombocytopenia (Figure 2) | ||
4. Peripheral smear examination | Platelet clumping (Pseudothrombocytopenia)![]() | Normal morphology of all 3 cell lines ![]() | Schistocytes (TMA)![]() |
Laboratory assessment | None indicated![]() | Investigate potential contributors Infection Screen for HIV, HBV, HCV, H pylori Thorough assessment of any current infectious symptoms Liver injury LFTs Coagulation profile Autoimmune processes APLA panel ANA ![]() | Hemolytic panel LDH Reticulocyte count Haptoglobin LFTs (bilirubin) Urinalysis Renal function ADAMTS13 activity Coagulation profile ![]() |
Management | Standard obstetric care | Trend platelet count Reserve treatment for clinically significant processes/bleeding or as needed to prepare for delivery | Initiate therapy for the most likely TMA Revisit the diagnosis and escalate or redirect therapies pending clinical course |
1. History | Bleeding symptoms Infectious symptoms Prior platelet counts: pregnant and nonpregnant Family history of thrombocytopenia Autoimmune disorders Medications Headache | ||
2. Physical examination | Bleeding: bruising, petechiae, purpura, oral mucosal blood blisters, conjunctival hemorrhages Blood pressure Lymphadenopathy, hepatomegaly, splenomegaly Abdominal tenderness Lower extremity edema Rashes or synovitis | ||
3. Timing | Categorize by onset and severity of thrombocytopenia (Figure 2) | ||
4. Peripheral smear examination | Platelet clumping (Pseudothrombocytopenia)![]() | Normal morphology of all 3 cell lines ![]() | Schistocytes (TMA)![]() |
Laboratory assessment | None indicated![]() | Investigate potential contributors Infection Screen for HIV, HBV, HCV, H pylori Thorough assessment of any current infectious symptoms Liver injury LFTs Coagulation profile Autoimmune processes APLA panel ANA ![]() | Hemolytic panel LDH Reticulocyte count Haptoglobin LFTs (bilirubin) Urinalysis Renal function ADAMTS13 activity Coagulation profile ![]() |
Management | Standard obstetric care | Trend platelet count Reserve treatment for clinically significant processes/bleeding or as needed to prepare for delivery | Initiate therapy for the most likely TMA Revisit the diagnosis and escalate or redirect therapies pending clinical course |
ANA, antinuclear antibody; APLA, antiphospholipid antibody antibodies; LDH, lactate dehydrogenase.