Obstetric Haem Flashcards

1
Q

Normal blood count changes in pregnancy

A

o Mild anaemia
 Red cell mass rises (120-130%)
 Plasma volume rises (150%)Net Dilution

o Macrocytosis

o Neutrophilia

o Thrombocytopenia (increased platelet size from increase in turnover of platelets)

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2
Q

Iron and Folate requirement for pregnancy

A

RDA of 30mg of iron- 60mg supplement given

Folate- 200mcg/day- 400mcg given supplement

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3
Q

What does IDA cause in pregnancy

A

IUGR, prematurity and PPH

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4
Q

Defining IDA in pregnancy

A

<110 in 1st
<105 2nd
<100 3rd

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5
Q

Causes of thrombocytopenia in pregnancy

A

1) Physiological (gestational or incidental thrombocytopenia)
(2) Pre-eclampsia (HELLP – Haemolysis, Elevated Liver enzymes, Low Platelets)
(3) Immune thrombocytopenia (ITP) – BM creates lots of platelets but there is peripheral destruction
(4) MAHA syndromes

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6
Q

Coagulation changes in pregnancy

A

Increase in factor 8, VWF, fibrinogen- pro-thrombotic

Decrease in protein S, increase in plasminogen activator inhibitor - less fibrinolysis

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7
Q

Risk factors for PE

A

High BMI >25- largest factor
Post-partum- most likely time for Thrombotic event
1st trimester

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8
Q

Treatment of ITP in pregnancy

A

o IVIG + steroids
o Anti-D (in RhD +ve mothers with spleen) – the anti-D coats the RBCs and is preferentially removed by the reticuloendothelial system in preference to the AB-covered platelets, thus conserving platelet levels

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9
Q

Treatment of Thromboembolic disease in pregnancy

A

 LMWH (OD or BD) does not cross placenta

 No Warfarin DOES CROSS PLACENTA (teratogenic), avoid weeks 6-12

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10
Q

Diagnosis of APLS

A

 Miscarriages (≥3) + lupus anticoagulant or anticardiolipin antibodies

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11
Q

Treatment of APLS

A

 Treat with (unfractionated) heparin and aspirin → dramatically improved outcomes

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12
Q

4 main causes of PPH

A

Tone, trauma, tissue, thrombin

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13
Q

Which leg do DVTs mainly occur in and why

A

Left due to compression

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14
Q

How DIC manifests in pregnancy

A

• Coagulation changes in pregnancy predispose to DIC (TF and factor 7a can come into contact and start the cascade)

With amniotic embolism and Pe-eclampsia precipitating decomposition

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15
Q

Haemoglobinopathy screening aims

A

o Alpha 0 thalassaemia / Hb Barts (4 gamma chains) - death in utero, hydrops fetalis

o Beta 0 thalassemia (transfusion dependent)

o HbSS / SCD (life expectancy 43yo)

o Other compound HbS syndromes – symptomatic, stroke

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16
Q

Complications of sickle cell in pregnancy

A

FGR, miscarriage, preterm, pre-eclampsia, VTE

17
Q

Mx of sickle cell in pregnancy

A

Red cell transfusion, prophylactic treatment to reduce vaso-occlusive events

18
Q

IDA vs thalassaemia trait

A

RBC low in Ida, high in thalassaemia

19
Q

Put count in ITP after delivery

A

o Platelet count may fall following delivery in babies born to mothers with ITP