Haematology in Pregnancy Flashcards

1
Q

What are the immunological changes in pregnancy?

A
  • rise in neutrophils and monocytes
  • no changes in immunoglobulins and lymphocyte subsets
  • BUT some infections are more common or severe in pregnancy
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2
Q

What is immune tolerance and how does the body establish this during pregnancy?

A
  • immune tolerance is how the body responds to the foetus and placenta during pregnancy
  • counters the body’s usual natural response (rejection) to the presence of foreign material
  • as the trophoblast invades the decidua there is an increase in uterine NK and dendritic cells allowing the remodelling of the uterine wall rather than cytotoxic or antigen presenting function
  • infrequent lymphatic changes and minimal lymphoid tissue
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3
Q

What are the physiological changes in pregnancy?

A
  • Hb declines to 110-100g/l (anaemia common)
  • increase in red cells, bigger increase in plasma volume
  • rise in WBC (mainly neutrophils)
  • fall in platelets (gestational thrombocytopenia)
  • rise in mean cell volume
  • rise in fibrinogen and factors VIII, IX and X (coagulation factors)
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4
Q

Describe immune thrombocytopenic purpura (ITP)

A
  • autoimmune disease
  • triggered by infection/drug/pregnancy
  • formation of autoantibodies against platelets
  • if pregnant risk of neonatal thrombocytopenia due to IgG antibodies crossing placenta
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5
Q

What is the treatment for ITP?

A
  • watch and wait
  • steroids
  • immunoglobulins
  • splenectomy
  • drugs to mimic thrombopoietin
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6
Q

Describe thrombotic thrombocytopenic purpura (TTP)

A
  • life-threatening thrombotic microangiopathy
  • can be associated with autoimmune disease/HIV/pregnancy
  • enzyme that prevents large Von Willebrands polymers (ADAMS13) becomes deficient and causes platelets to aggregate
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7
Q

What is the clinical presentation and treatment of TTP?

A

Presentation:

  • fever
  • neurological disease
  • renal disease
  • low platelets
  • fragmented red cells
  • normal coagulation screen
  • treated with plasma exchange to replace the enzyme
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8
Q

What factors put you at risk of thromboembolic disease?

A
  • pregnant
  • 6 weeks post partum
  • age
  • previous clot
  • smoking
  • twins
  • obesity
  • thombophilia
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9
Q

What are some signs of thromboembolic disease in pregnant women?

A
  • leg swelling (due to compression of pelvic veins)
  • causes progressive pain, tenderness
  • unilateral swelling
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10
Q

What imaging can you use to look for thromboembolic disease in pregnant women?

A
  • doppler exam on swollen leg
  • chest X-ray
  • if abnormal then do a CT pulmonary angiogram
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11
Q

What is the treatment and future management of thromboembolic disease in pregnant women?

A
  • LMW heparin
  • due to increased rate of clearance and volume of distribution will need twice the daily dose
  • need to monitor anti Xa levels 3-4 hrs after dose to see if it is effective
  • for future pregnancies will need prophylactic anticoagulation
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12
Q

What are the signs of pre-eclampsia, its major complication and treatment?

A

Signs of pre-eclampsia:

  • hypertension
  • fluid retention
  • proteinuria
  • headache
  • high urate
  • major complication is HELLP syndrome (haemolytic anaemia, red cell fragmentation, raised LDH, liver enzymes, low platelets)
  • treatment: prompt delivery of baby and supportive care
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13
Q

What is disseminated intravascular coagulation, how it manifests and its treatment?

A

it is an acute and serious complication from:

  • placental abruption
  • amniotic fluid embolism
  • dead foetus
  • haemorrhagic, organ failure, depletion of coagulation factors, low platelets and red cell fragments
  • treatment: treat cause, coagulation factors and platelets
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14
Q

What are the risk factors for haemorrhage?

A
  • placenta praevia (placenta sits lower, over cervix)
  • placental abruption
  • retained products of conception
  • poor uterine contraction after delivery
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15
Q

Describe the WIlson and Jungner screening criteria

A
  • there should be a recognisable latent or early symptomatic stage
  • it should be a simple test with high sensitivity and specificity
  • the test should be acceptable to the population
  • early effective treatment needs to be of clear benefit
  • there should be an agreement as to who should be treated
  • condition is important health problem
  • diagnosis and treatment should be cost effective
  • case finding should be continuous process
  • natural history understood
  • should be cost effective overall
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16
Q

How would you detect a haemoglobinopathy/thalassaemia carriers?

A
  • ethnic origin questionnaire
  • take bloods and look at MCV (<80 microcytic) and MCH (<27)
  • do a blood film
  • do cellulose acetate or agarose gel Hb electrophoresis
  • do high performance liquid chromatopgraphy
  • gene copy number/sequencing
17
Q

How is pre-natal screening in low prevalence areas carried out?

A
  • FBC and family origin questionnaire is carried out for both partners
  • if either is positive then HPLC is used to look for thalassaemia/haemoglobinopathy
  • may need confirmatory tests
  • may need partner’s FBC
18
Q

What action is taken for positive tests for prenatal screening of thalassaemia/haemoglobinopathies?

A
  • card and letter issued to mum/dad and GP

- if foetus is at risk of serious Hb disorder then considers CVS or amniocentesis