2.2 Cardiac Disease & Rhesus Isoimmunisation Flashcards

1
Q

Normal cardiovascular changes in pregnancy

A
  • Mild dyspnea especially upon exercise
  • Fatigue
  • Oedema
  • Occasional palpitations and dysrhythmia
  • Increased risk for thromboembolism
  • 3rd heart sound
  • Soft systolic murmur - due to increased flow through the valves
  • Reflux
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2
Q

Abnormal cardiovascular changes in pregnancy

A
  • Any diastolic or continuous murmur
  • Any systolic murmur with a thrill
  • Clubbing, cyanosis, jugular vein distention, dyspnea, orthopnea, palpitations
  • 4th heart sound - signs of diastolic failure
  • Unequivocal heart enlargement
  • Pulmonary hypertension
  • Nocturnal cough
  • Oedema beyond the ankles (upper limbs)
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3
Q

Midwifery care for women with cardiac disease

A

Medical management:
- ECGs, medication management, growth scans (heart and dopplers), foetal echo, anticoagulants

Labour:
- Shortened second stage is preferable (syntocinon and assisted deliveries), vaginal delivery preferred (due to lower blood loss, decreased risk of blood clots), continuous CTG, obs, 5-lead ECG (if indicated by cardiologist), FBC, just synt going slower - no CSL.

Third stage:
- active management (syntocinon - avoid syntometrine & ergometrine as this increases cardiac factors)

Postnatal:
- close monitoring in first 72 hours (haemodynamic shift), HDU or 1:1 in BS for 24 hours, stable 1:1 on ward, weary of blood clots (TEDs, clexane, recommencing anticoagulants), early mobilisation, analgesia for pain management

Cardiologist - women with cardiac conditions should consult with a cardiologist for a preconception evaluation and close follow-ups throughout pregnancy
Obstetrician, paediatrician (intrapartum/postnatal period), neonatologist (once baby is born, especially for congenital diseases)

Anaesthetist - recommend potentially early epidural

Education - explain the increased risk of pregnancy

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4
Q

Rh isoimmunisation - pathophysiology

A

Rh- mother (no Rhesus surface antigen on red blood cells) carries Rh+ foetus (Rhesus surface antigen on red blood cells) and develops antibodies which attack foetal RBC

Sensitising event → spill of foetal blood into maternal circulation → maternal blood recognises foetal Rh+ blood cells as foreign → production of Rh antibodies in response (wont affect first preg but will for second as antibodies still producing) → attacks foetal red blood cells → haemolysis

Future pregnancy implication - sensitisation causes memory cells which will rapidly respond in Rh+ blood cells in future pregnancies

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5
Q

Sensitising events of Rhesus Isoimmunisation

A

Trimester 1:
- Spontaneous abortion
- Pregnancy termination
- Ectopic pregnancy
- Chorionic villi sampling

Trimester 2:
- Amniocentesis
- Antepartum haemorrhage - placental
- Abdominal trauma - placental abruption

Trimester 3:
- External cephalic version
- Antepartum haemorrhage
- Abdominal trauma
- Birth of placenta

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6
Q

Care pathway - Prophylactic use of Rh D immunoglobin in pregnancy

A
  • Woman’s blood group and antibody screen in pregnancy confirms Rh D negative → at 11 weeks determine foetal RHD status via NIPT of maternal blood sample → foetus predicted RhD positive or uncertain → at 28 weeks retest antibody screen and administer first dose of Rh D IG 625 IU → at 34 weeks administer 2nd dose Rh D Ig

After birth:
- Cord blood or neonatal testing to determine foetal Rh D type → RhD positive foetus → immediately administer Rh D ig 625 IU (best within 72 hours but can be up to 10 days)
- Kleihaur Test - measures foetal blood spill in maternal circulation → More significant (6mls/625 IU) = more anti D doses to destroy foetal blood cells
- Indirect Coombes - determines any previous sensitisation to the Rh D antigen - important for second pregnancy w/ Rh+ child - memory cells recognise baby’s blood cells as foreign bodies and attacks foetus
- Anaemia, miscarriage, jaundice

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