obstetrics Flashcards
Name the urine and blood tests at booking
MSU - dipstick for blood and protein
Hb, blood group and antibody screen
BBV - syphilis, rubella, HIV
Consider sickle cell test, Hb electrophoresis for haemoglobinopathy, 25-hydroxyvitamin D if relevant.
At what gestation do you screen for chromosomal and structural abnormalities?
Booking (11-13+6)
What investigations should be performed at every antenatal visit?
Urine dipstick for protein, BP, fundal height.
When are Hb and Rh antibodies tested and what is administered?
Test all Rh- mothers for antibodies at booking
give anti-D if needed at 28 and 34 weeks
From what gestation should a Kleihauer test be performed to determine foetal RBC leak?
20+0
Anti-D should be given within 72h of which situations
Delivery of a Rh+ infant Any TOP or miscarriage after 12wks Surgical mx of miscarriage/ectopic at any gestation ECV APH or abdo trauma Amniocentesis/CVS/Foetal blood sampling
What measurements are used to date pregnancy?
Crown-rump length at 6-12wks
Biparietal diameter 14-34wks (peaks in accuracy at 20wks)
Causes of increased nuchal translucency
Down’s syndrome
congenital heart defect
abdominal wall defect
What is the underlying aneuploidy in Edward’s syndrome, describe the clinical presentation
trisomy 18
rarely survive 1yr, micrognathia, low set ears, rocker bottom feet, overlapping fingers
What is the underlying aneuploidy in Patau’s syndrome and describe the clinical presentation
trisomy 13
die soon after birth, microcephalic, cleft lip/palate, exomphalos, holoprosencephaly, polydactyly.
What does the combined test consist of and when should it be performed?
11-13+6 weeks
NT + serum b-hcg + Pregnancy Associated Plasma Protein A.
You are in antenatal clinic with a 37 year old woman, G6P4 who is 15 weeks gestation and missed her booking appointment. She has stated she would like screening for Down’s syndrome and other trisomy. What test is used?
15-20wks
triple/quadruple test - AFP + unconjugated estradiol + hCG (± inhibin-A)
In antenatal clinic you are counselling a lady who is currently 12+2 and has just been informed that the combined test indicates the foetus to have T21. You have mentioned invasive testing to confirm the diagnosis.
Describe what is involved in each test and what gestational periods can they be performed in?
Chorionic Villus Sampling - 11-14/40 - transabdominal (rarely transcervical) needle to retrieve cell sample from placenta. Not recommended in dichorionic pregnancy
Amniocentesis - 15-18/40 - US guided needle aspirates amniotic fluid to analyse foetal cells shed by skin/gut.
Both yield results in 3 working days (few weeks in rarer disease needing enzyme/gene probe analysis). Risks - increased rates miscarriage (less so in amniocentesis), BBV transmission.
Define hyperemesis gravidarum, at what gestation would you expect it to occur?
Persistent vomiting in pregnancy causing dehydration, electrolyte imbalance and weightloss (>5% from pre-pregnancy weight). Most common between 8 and 12 weeks, can persist up to 20wks.
Risk factors for hyperemesis gravidarum
multiple pregnancy, trophoblastic disease, previous Hyperemesis Gravidarum, primiparity, obesity, hyperthyroidism
How might someone with hyperemesis gravidarum present?
Persistent vomiting, unable to keep food/fluid down, weightloss, dehydration, tachycardia, postural hypotension, hypovolaemia, hyponatraemia, hypokalaemia, ketoacidosis, polyneuritis (vit B deficiency)
When should you consider admission for someone with hyperemesis gravidarum?
If they are on oral anti-emetics but still have persistent vomiting and are:
- Unable to keep fluid/anti-emetics down
- still displaying ketonuria/weightloss/severe electrolyte imbalance
- confirmed or suspected co-morbidity e.g. UTI
Ix in suspected hyperemesis gravidarum
Urine - MSU for infection and ketones
Blood - FBC (increased haematocrit), U+Es (hypo-natraemia/kalaemia)
How would you manage hyperemesis gravidarum?
Admission if needed to correct electrolyte imbalance/dehydration
IV fluids - 0.9% saline, Na+ and K+ guided by daily U+;Es
Anti-emetics - antihistamine (promethazine)/cyclizine, consider corticosteroids if intractable.
Additional - 5mg folic acid, thiamine/pabrinex for Wernicke encephalopathy, if in hospital thromboprophylaxis (e.g. enoxaparin) and TEDs
What inheritance pattern does sickle cell disease show?
Autosomal recessive
What is sickle cell disease?
Haemoglobinopathy which predisposes to sickling of RBCs in low O2 conditions leading to vaso-occlusion in small vessels and a tendency to haemolytic
Give 5 risks associated with sickle cell disease in pregnancy
Increased risk of perinatal mortality, premature labour, IUGR, painful crises inc acute chest syndrome, increased risk of haemolytic disease of newborn
How does acute chest syndrome present?
Cough, tachypnoea, chest pain and CXR shows new infiltrates.
A 27 year old woman with known sickle cell disease comes to the GP to discuss getting pregnant, what are some investigations/interventions which should be performed prenatally?
Assess current disease:
- ECHO less than 1yr old for pulm htn
- BP and urinalysis
- U+Es and LFTs
- retinal screening
Prophylactic abx and update vaccines (HBV, HiB, MenC, pneumococcal, influenza) due to increased risk infection
Start 5mg folic acid and stop ACEi/A2A drugs and hydroxycarbimide >3/12 pre-conception