Haematology

Category A
Local Expertise
Category B
Consider discussion with Maternal Medicine Centre (MMC)
Category C
Care led by Maternal Medicine Centre
Sickle cell traitSickle cell disease
Alpha/beta thalassaemia traitBeta thalassaemia major
Other complex thalassaemia: .
• iron overload
• Endocrine disease
Current VTE / previous single VTERecurrent VTECurrent VTE requiring anti Xa monitoring without same-day turnaround of result
Antiphospholipid syndrome with early pregnancy loss with no thrombotic
history
Antiphospholipid syndrome with history of second or third trimester loss, with no
thrombosis history
Antiphospholipid syndrome with any maternal arterial or venous thrombosis OR any evidence of active disease OR therapeutically anticoagulated when not pregnant
Inherited thrombophilia (no VTE, not antithrombin deficiency)Inherited thrombophilia with previous VTEAntithrombin deficiency
Gestational thrombocytopeni documented normal pit count in firs
trimester)
Plt count 75-150 x109/L not gestational or related to a pregnancy-specific causePits <75 x109/L with no acute/transienUpregnancy-specific cause identified AND no urgent local haematolooy review available
Mild platelet function disorder (e g storage pool disease, signalling or ADF eceptor defects)Moderate/severe
platelet
function disorder
(e.g.
thrombasthenia,
Benard Souis syndrome)
History of treated haematological malignancyStable myeloproliferative/myelodysplastic diseaseActive haematological malignancy
B 12/folate deficiencyWhite cell disordersTransfusion-dependent disease
Thrombocytosis (pits >450 x109/L on two
occasions) without evidence of iron
deficiency or other underlvina cause
Mild, isolated clotting factor deficiency
• Factor II, V, VII, XI or XIII > 0.2iu/ml
• Factor X > 0.3iu/ml|
Clotting factor deficiency:
• Factor II, V, VII, XI or XIII ≤ 0.2iu/ml
• Factor X ≤ 0.3iu/ml
• Combined deficiencies
Carriers of haemophilia with known female fetus AND normal maternal factor VIII/IX levelsCartiers of haemophila with male or unknown gender of fetus
Type 1 Von-Willebrand disease/low VWF where VWF activity normalised in
pregnancy
Von-Willebrand disease:
Type 1 /low VWF if WWF not normalised, Type 2,
Type 3, platelet-type VWD
Therapeutic anticoagulation
when
not pregnant for mechanical heart valve /
APLS /VTE with antithrombin deficiency
Previous or current TTP/HUS

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