obs 2 Flashcards

1
Q

what is polyhydramnios?

A

when there is increased amniotic fluid

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2
Q

what are the causes of polyhydramnios?

A

increase in fetal urine production (maternal diabetes, TTTS, fetal hydrops)

Fetal inability to swallow or absorb amniotic fluid (GI obstruction e.g. duodenal atresia, trachea-oesophageal fistula, fetal neurological or muscular abnormalities, idiopathic)

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3
Q

what are the complications of polyhydramnios?

A

preterm delivery
complications of the cause - e.g. duodenal atresia is associated with trisomy 21
malpresentation at delivery because of increase room for fetus
maternal discomfort because of abdominal distension

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4
Q

what investigations would you perform for polyhydramnios?

A

exclude maternal diabetes with a GTT

USS for examination of fetus

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5
Q

how should you manage polyhydramnios?

A

if severe (AFI>40) -> amnioreduction or NSAIDs
if there is a fetal abnormality refer to a fetal medicine centre
TTTS - laser ablation of placental anastomoses
if preterm assess risk of delivery with cervical scan and or fibronectin assay and consider steroids
if unstable or transverse lie at term admit to hospital

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6
Q

what is oligohydramnios?

A

when amniotic fluid volume is reduced

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7
Q

what are the causes of oligohydramnios?

A
PPROM
IUGR
leakage of amniotic fluid - SROM
fetal renal failure or abnormalities 
post-dates pregnancy 
obstruction to fetal renal output
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8
Q

what are the complications of oligohydramnios?

A

lung hypoplasia if occurs <22 weeks
limb abnormalities e.g. clubbed foot
oligohydramnios before 22 weeks has a very poor prognosis

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9
Q

how do you manage oligohydramnios?

A

If SROM at 34-36 weeks - induce labour unless CS indicated for another reason

If SROM before 34-36 weeks: give prophylactic erythromycin, monitor for signs of infection, daily CTG, consider induction by 34-36 weeks

If IUGR: manage according to umbilical artery doppler and CTG

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10
Q

what are the principal functions of the placenta?

A

to anchor the fetus and establish fetoplacental unit
to act as an organ gaseous exchange
endocrine organ to bring the needed changes in pregnancy
transfer substances to the fetus
barrier against infection

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11
Q

what is breech presentation

A

the lie is longitudinal and the head is found in the fundus

the caudal end of the fetus occupies the lower segment

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12
Q

what are the three types of breech?

A

extended breech (frank breech 70%) - both legs extended with fee by head, presenting part is the buttock

Flexed breeches (15%)
- legs flexed at knees so that both buttocks and feet are presenting 

footling breeches (15%) - on leg flexed one leg extended

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13
Q

what are the risk factors/causes for breech presentation ?

A

most often idiopathic
is often associated with pre term delivery
previous breech presentation
uterine abnormalities
placenta praevia and obstruction to the pelvis
fetal abnormalities
multiple pregnancies

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14
Q

what are the consequences of breech presentation?

A

fetal complications - there is an increased risk of hypoxia and trauma in labour, there is an association with congenital abnormalities

cord prolapse is more common in breech presentations

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15
Q

what is the diagnosis of breech presentation ?

A

if diagnosed before 36 weeks It is not important unless in labour

breech presentation is commonly diagnosed before labour

on examination the lie is longitudinal and the head can be palpate at the fundus
the presenting part is not hard
the fetal heart is heard best high up on the uterus

USS can confirm the diagnosis

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16
Q

what can be used to change the presentation from breech to cephalic?

A

external cephalic version - manually turning a breech or transverse presentation into a cephalic one

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17
Q

after external cephalic version?

A

after the attempt, CTG is performed and anti-D given if the mother is rhesus -ve

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18
Q

what are some contraindications to external cephalic version?

A
  • if a C-section is already indicated
  • APH
  • fetal compromise
  • oligohydramnios
  • rhesus isoimmunization
  • pre-eclampsia

relative contraindications - one previous c section, fetal abnormality, maternal hypertension

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19
Q

other than breech presentation what are the other types?

A

transverse or oblique occurs when the axis of the uterus - common before term but uncommon after 37 weeks

unstable lie occurs when the lie is still changing, usually several times a day and may be transverse or longitudinal lie, and cephalic or breech presentation

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20
Q

how do you manage an abnormal lie?

A

admission to hospital at 37 weeks is usually recommended with unstable lie that that a c section can be carried out if labour starts or membranes rupture

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21
Q

why is there increased risk of anaemia in pregnancy?

A

because normal pregnancy has 2-3 fold increase in iron requirements and 10-20 fold increase in folate requirements in pregnancy

plasma volume expansion (50%) greater than red cell mass - this leads to physiological dilution with decreased Hb and haematocrit

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22
Q

what is the most common cause of anaemia in pregnancy?

A

iron deficiency anaemia

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23
Q

how should iron deficiency anaemia be treated?

A

oral iron supplementation - if not tolerated parenteral iron

*in situations such as multiple pregnancy with high risk then prophylactic iron should be given

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24
Q

what are risk factors for folate deficiency anaemia in pregnancy?

A

poor nutritional status
haematological problems with rapid turnover of blood cells e.g. haemolytic anaemia and haemoglobinopathies
drug interaction with folate metabolism e.g. antiepileptics

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25
Q

why is folic acid given pre-conception?

A

also given in early pregnancy

given to reduce risk of neural tube defect

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26
Q

who should be given high dose folic acid?

A
high dose = 5mg 
those on anticonvulsants 
a previous child with neural tube defects 
with demonstrated deficiency 
with diabetes 
with a BMI >35
with sickle cell disease
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27
Q

what ae the risks of sickle cell disease in pregnancy?

A

crisis are more common during pregnancy
increased risk of pre-eclampsia
increase risk of delivery by c section secondary to fetal distres

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28
Q

what are the fetal risk of sickle cell disease during pregnancy~?

A

miscarriage
IUGR
prematurity
still birth

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29
Q

how should sickle cell disease be managed during pregnancy?

A

MDT care with obstetrician and haematologist
pre pregnancy counselling should involve screening of the partner
stop iron-chelating agents before pregnancy
screen for urine infection during each visit
regular assessment of fetal growth

30
Q

what is obstetric cholestasis?

A

Intrahepatic cholestasis of pregnancy (ICP) is a pruritic condition during pregnancy caused by impaired bile flow allowing bile salts to be deposited in the skin and the placenta

31
Q

what are the risk factors for obstetric cholestasis?

A

previous history of intrahepatic cholestasis of pregnancy
hep c
fam history
age >35 years

32
Q

what are the symptoms of obstetric cholestasis?

A

pruritus of the trunk and limbs sparing the face, without the presence of a rash
anorexia and malaise
epigastric discomfort, steatorrhoea and dark urine

33
Q

what are the complications of obstetric cholestasis?

A

maternal risks - vitamin K deficiency = PPH risk

fetal risks - preterm labour, still birth, resp distress syndrome in pre-term infants due to insufficient levels of surfactant

34
Q

what investigation would you perform to diagnose obstetric cholestasis?

A

bile acids and LFTs should be sent for all woman itching without a rash

coagulation profile
fasting serum, cholesterol
hep c virology

35
Q

how do you manage obstetric cholestasis?

A

antihistamine (hydroxyzine) for symptomatic relief
cholestyramine plus vitamin K
ursodeoxycholic acid (improves itching and liver function)

36
Q

what makes UTI more common in pregnancy?

A

dilatation of upper renal tract and urinary stasis

37
Q

what are the risk factors for UTI in pregnancy?

A
previous infections 
renal stones 
DM 
immunosuppression 
polycystic kidneys 
congenital anomalies of renal tract 
neuropathic bladder
38
Q

what are the symptoms of cystitis and pyelonephritis in pregnancy?

A

cystitis: urinary frequency, urgency, dysuria, haematuria, proteinuria and suprapubic pain

pyelonephritis - fever, rigors, vomiting, loin and abdominal pain

39
Q

what investigations should you perform for UTI?

A

urinalysis (nitrites and leukocytes)
MSU
bloods - cultures, FBC, U&E, CRP in a pyrexial patient
renal USS

40
Q

how should UTI in pregnancy be treated?

A

oral Abx are recommended in asymptomatic bacteria and cystitis to prevent pre term labour and pyelonephritis

pyelonephritis should be treated with IV Abx until pyrexia and vomiting stops

41
Q

what is the duration of treatment for UTI in pregnancy ?

A

NICE recommends 7 day course in all cases of bacteriuria

may require longer if pyeloniphritis

42
Q

what antibiotics should be used in UTI in pregnancy?

A

amoxicillin
cephalosporin
gentamicin - however needs monitoring

Trimethoprim should be avoided in first trimester - folate antagonist
Nitrofurantoin - avoid in 3rd trimester as risk of haemolytic anaemia in the neonate with G6PD deficiency
sulphonamides - avoid in 3rd trimester as risk of kernicterus in the neonate due to displacement of protein binding to bilirubin

43
Q

what antibiotics are contraindicated in pregnancy?

A

tetracyclines - causes staining of teeth and problems with skeletal development

Ciprofloxacin - causes skeletal problems

44
Q

what are the differential diagnosis for a first seizure during pregnancy?

A

eclampsia
epilepsy
infection (meningitis, encephalitis, abscess)
metabolic (drug/alcohol, drug toxicity, hypoglycaemia, electrolyte imbalance)
severe hypoxia
space-occupying lesion
vascular

45
Q

what are the fetal risks of epilepsy during pregnancy?

A

congenita abnormalities

risks of anticonvulsant therapy - teratogenicity, neonatal withdrawal, VK deficiency, developmental delay and behavioural problems

46
Q

what are the main teratogenic risks of commonly used anticonvulsants?

A

valproate - neural tube defect, GU abnormalities, cardiac abnormalities, facial clefts, neurodevelopmental delay

carbamazepine - neural tube defects, cardiac anomalies, facial clefts

Phenytoin - facial clefts, cardiac anomalies

47
Q

what screening would you perform for pregnant woman on anticonvulsants?

A

prenatal screening

  • alpha fetoprotein (neural tube defects)
  • detailed anomaly scan (facial clefts and cardiac abnormalities)
48
Q

what is the postnatal care for women with epilepsy?

A

neonatal vitamin K to decrease the risk of haemorrhagic disease of new-born

49
Q

what is antiphospholipid antibody syndrome?

A

Antiphospholipid syndrome is an acquired disorder characterised by a predisposition to both venous and arterial thromboses, recurrent fetal loss and thrombocytopenia.

50
Q

what are the maternal risk s of antiphospholipid antibody syndrome?

A

placenta abruption and pre-eclampsia

51
Q

what are the fetal risks of antiphospholipid antibody syndrome?

A

early and late miscarriage
in utero death
IUGR

52
Q

how should antiphospholipid antibody syndrome be managed in pregnancy?

A

if no previous thrombosis or pregnancy loss - no treatment of aspirin

previous thrombosis - aspirin and LMWH

53
Q

what are the effects of diabetes on pregnancy?

A

maternal hyperglycaemia leads to fetal hyperglycaemia
fetal hyperglycaemia leads to hyperinsulinemia
insulin acts aa growth promotor
this leads to macrosomia, organomegaly increased erythropoiesis and fetal polyuria (polyhydramnios)

neonatal hypoglycaemia due to removal of mothers glucose at birth

54
Q

what are the maternal complications of diabetes in pregnancy?

A
UTI
recurrent vulvovaginal candidiasis 
pregnancy induced hypertension/pre-eclampsia 
obstructed labour 
operative deliveries 
increase retinopathy 
increased nephropathy 
cardiac disease
55
Q

what are the fetal complication of diabetes during pregnancy?

A
miscarriage 
congenital abnormalities (neural tube defects, microcephaly, cardiac abnormalities, sacral agenesis, renal abnormalities)
preterm labour
polyhydramnios
macrosomia 
IUGR
unexplained IUD
56
Q

what are the neonatal abnormalities of diabetes in pregnancy?

A
polycythaemia
jaundice 
hypoglycaemia 
hypocalcaemia 
hypomagnesaemia 
hypothermia 
cardiomegaly 
birth trauma 
RDS
57
Q

what is puerperal pyrexia?

A

Puerperal pyrexia may be defined as a temperature of > 38ºC in the first 14 days following delivery.

58
Q

what are some causes of puerperal pyrexia?

A
endometritis - most common cause 
UTI
wound infections 
mastitis/breast abbcess 
venous thromboembolism
59
Q

what could increase the risks of endometritis?

A
c section
prelabour ROM
intrapartum chorioamnionitis 
prolonged labour
multiple pelvic examinations
internal fetal monitoring
anaemia
60
Q

what investigations would you perform for puerperal pyrexia?

A
FBC
blood cultures 
MSU 
swabs from cervix
wound swabs 
throat swabs
sputum culture and CXR
61
Q

how should puerperal pyrexia be managed?

A

analgesics and NSAIDS
wound care in cases of wound infection

ABx
if endometritis is suspected - the patient should be referred to the hospital and receive IV Abx (clindamycin and gentamycin)

62
Q

what are the fetal complications of shoulder dystocia?

A
hypoxia and neurological injury (cerebral palsy)
brachial plexus palsy 
fracture of clavicle or humerus 
intracranial haemorrhage 
cervical spine injury 
rarely, fetal death
63
Q

how should you treat uterine atony?

A

IV ergometrine
start oxytocin infusion
if bleeding still persists then give misoprostol
if still continues give carboprost IM into thigh or directly into myometrium

64
Q

why does pregnancy increase the risk of VTE?

A

because there is venous stasis in the lower limbs
possible trauma to the pelvic veins at the time of delivery
changes in the coagulation system

65
Q

what are the risk factors for VTE in pregnancy?

A
previous VTE
thrombophilia 
age>35 years 
obesity 
parity >3
gross varicose veins 
paraplegia 
sickle cell disease 
fam history of unprovoked VTE 
multiple pregnancy

new onset/transient risk factors - OHHS, hyperemesis, dehydration, long haul travel, severe infection, immobility (>4days bed rest), pre-eclampsia, prolonged labour

66
Q

how are VTE prevented in pregnancy?

A

LMWH is the gent of choice
should be given immediately if there are four or more risk factors and it should be continued until 6 weeks postnatal
if they have 3 risk factors it should be started at 28 weeks gestation

67
Q

what are the symptoms/signs of a DVT?

A
leg pain or discomfort 
swelling 
tenderness
pyrexia
erythema, increased skin temp and oedema
lower abdominal pain 
elevated WBC
68
Q

what are the symptoms/signs of a PE?

A
dyspnoea 
collapse 
chest pain 
haemoptysis 
faintness 
raised JVP 
focal signs in chest 
symptoms and signs associated with DVT
69
Q

how would you investigate VTE?

A
thrombophilia screen 
FBC
U&amp;E
LFTs 
coagulation screen 

compression duplex USS

If PE suspected - ECG, CXR, ABG, ventilation perfusion lung scanning, CT/MRI

*D-Dimer - not used in pregnancy as often gives a false positive, however if it is low then it would usually rule out VTE

70
Q

what considerations should be taken if a women is on LMWH during labour/delivery?

A

once she is in labour she is advised not to inject further heparin
avoid epidural haematoma - regional anaesthesia should be avoided until 12 hours after the last dose, LMWH should not be given until 4 hours after epidural catheter has been removed.
there is an increased risk of wound haematoma following C-section
there is a higher risk of haemorrhage

71
Q

what should women who are at risk of haemorrhage be put on for VTE?

A

unfractional heparin - has a shorter half life and is completely reversed with protamine sulphate