Women's health - Obstetrics Flashcards

1
Q

How many ANC visits are recommended in pregnancy?

A

10 antenatal visits in the first pregnancy if uncomplicated
7 antenatal visits in subsequent pregnancies if uncomplicated
women do not need to be seen by a consultant if the pregnancy is uncomplicated

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2
Q

What happens at a booking visit? When should this occur?

A

8 - 12 weeks (ideally < 10 weeks)

Booking visit
general information e.g. diet, alcohol, smoking, folic acid, vitamin D, antenatal classes
BP, urine dipstick, check BMI

Booking bloods/urine
FBC, blood group, rhesus status, red cell alloantibodies, haemoglobinopathies
hepatitis B, syphilis
HIV test is offered to all women
urine culture to detect asymptomatic bacteriuria

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3
Q

When does Early scan to confirm dates, exclude multiple pregnancy occur?

A

10-13+6 weeks

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4
Q

When does down’s syndrome screening including nuchal scan occur?

A

11-13+6 weeks

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5
Q

What happens at ANC at 16 weeks?

A

Information on the anomaly and the blood results. If Hb < 11 g/dl consider iron
Routine care: BP and urine dipstick

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6
Q

When is the anomaly scan?

A

18 - 20+6 weeks

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7
Q

What happens at ANC at 25 weeks if primip?

A

Routine care: BP, urine dipstick, symphysis-fundal height (SFH)

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8
Q

What happens at ANC at 28 weeks?

A

Routine care: BP, urine dipstick, SFH
Second screen for anaemia and atypical red cell alloantibodies. If Hb < 10.5 g/dl consider iron
First dose of anti-D prophylaxis to rhesus negative women

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9
Q

What happens at ANC at 31 weeks if primip?

A

Routine care: BP, urine dipstick, SFH

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10
Q

What happens at ANC at 34 weeks?

A

Routine care: BP, urine dipstick, SFH
Second dose of anti-D prophylaxis to rhesus negative women*
Information on labour and birth plan

*the evidence base suggests that there is little difference in the efficacy of single-dose (at 28 weeks) and double-dose regimes (at 28 & 34 weeks). For this reason the RCOG in 2011 advised that either regime could be used ‘depending on local factors’

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11
Q

What happens at ANC at 36 weeks?

A

Routine care: BP, urine dipstick, SFH
Check presentation - offer external cephalic version if indicated
Information on breast feeding, vitamin K, ‘baby-blues

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12
Q

What happens at ANC at 38 weeks?

A

Routine care: BP, urine dipstick, SFH

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13
Q

What happens at ANC at 40 weeks if primip?

A

Routine care: BP, urine dipstick, SFH
Discussion about options for prolonged pregnancy

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14
Q

What happens at ANC at 41 weeks?

A

Routine care: BP, urine dip, SFH
Discuss labour plans and possibility of induction

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15
Q

What test is done if there is a potential rhesus sensitisation situation in rhesus negative mothers in the 2nd/3rd trimester?

A

if event is in 2nd/3rd trimester give large dose of anti-D and perform Kleihauer test - determines proportion of fetal RBCs present

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16
Q

In which 8 situations should anti-D be given to rhesus -ve mothers?

A

-delivery of a Rh +ve infant, whether live or stillborn
-any termination of pregnancy
-miscarriage if gestation is > 12 weeks
-ectopic pregnancy (if managed surgically, if managed medically with methotrexate anti-D is not required)
-external cephalic version
-antepartum haemorrhage
-amniocentesis, chorionic villus sampling, fetal blood sampling
-abdominal trauma

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17
Q

What are the clinical features seen in baby and what is the treatment of haemolysis due to haemolytic disease of the foetus and newborn (HDFN) in rhesus disease?

A

-oedematous (hydrops fetalis, as liver devoted to RBC production albumin falls)
-jaundice, anaemia, hepatosplenomegaly
-heart failure
-kernicterus

treatment: transfusions, UV phototherapy

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18
Q

Who will get blood glucose tested in pregnancy?

A

Surprisingly perhaps, NICE now recommends that blood glucose is only checked to those considered at risk (e.g. obesity, previous macrosomic baby, family history, Asian ethnicity)

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19
Q

What does increased AFP indicate?

A

Neural tube defects (meningocele, myelomeningocele and anencephaly)
Abdominal wall defects (omphalocele and gastroschisis)
Multiple pregnancy

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20
Q

What does decreased AFP indicate?

A

Down’s syndrome
Trisomy 18
Maternal diabetes mellitus

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21
Q

What options are there for nausea and vomiting in pregnancy?

A

natural remedies - ginger and acupuncture on the ‘p6’ point (by the wrist) are recommended by NICE
antihistamines should be used first-line (BNF suggests promethazine as first-line)

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22
Q

Is vitamin D supplementation given in pregnancy?

A

NICE recommend ‘All women should be informed at the booking appointment about the importance for their own and their baby’s health of maintaining adequate vitamin D stores during pregnancy and whilst breastfeeding’
‘women may choose to take 10 micrograms of vitamin D per day, as found in the Healthy Start multivitamin supplement’. This was confirmed in 2012 when the Chief Medical Officer advised: ‘All pregnant and breastfeeding women should take a daily supplement containing 10micrograms of vitamin D, to ensure the mothers requirements for vitamin D are met and to build adequate fetal stores for early infancy’
particular care should be taken with women at risk (e.g. Asian, obese, poor diet)

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23
Q

What is the current advice on alcohol use in pregnancy?

A

in 2016 the Chief Medical Officer proposed new guidelines in relation to the safe consumption of alcohol following an expert group report.
the government now recommend pregnant women should not drink. The wording of the official advice is ‘If you are pregnant or planning a pregnancy, the safest approach is not to drink alcohol at all, to keep risks to your baby to a minimum. Drinking in pregnancy can lead to long-term harm to the baby, with the more you drink the greater the risk.’

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24
Q

what 10 things are all women screened for in pregnancy?

A

Anaemia
Bacteriuria
Blood group, Rhesus status and anti-red cell antibodies
Down’s syndrome
Fetal anomalies
Hepatitis B
HIV
Neural tube defects
Risk factors for pre-eclampsia
Syphilis

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25
Q

Is Placenta praevia screened for in pregnancy?

A

only in high risk women

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26
Q

Is Psychiatric illness screened for in pregnanacy?

A

only in high risk women

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27
Q

Is Sickle cell disease screened for in pregnancy?

A

only in high risk women

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28
Q

Is Tay-Sachs disease screened for in pregnancy?

A

only in high risk women

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29
Q

Is Thalassaemia screened for in pregnancy?

A

Only in high risk women

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30
Q

Is Bacterial vaginosis routinely screened for in pregnancy?

A

No

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31
Q

Is chlamydia routinely screened for in pregnancy?

A

No

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32
Q

Is Cytomegalovirus routinely screened for in pregnancy?

A

No

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33
Q

Is fragile x routinely screened for in pregnancy?
s

A

No

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34
Q

Is Hep C routinely screened for in pregnancy?

A

No

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35
Q

Is Group B strep routinely screened for in pregnancy?

A

No

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36
Q

Is toxoplasmosis routinely screened for in pregnancy?

A

No

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37
Q

How to define APH

A

Antepartum haemorrhage is defined as bleeding from the genital tract after 24 weeks pregnancy, prior to delivery of the fetus

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38
Q

Placental abruption - describe
visible blood loss?
Pain?
Uterus examination?
Lie and presentation?
Fetal heart?
Coagulation problems?

A

shock out of keeping with visible loss
pain constant
tender, tense uterus
normal lie and presentation
fetal heart: absent/distressed
coagulation problems
beware pre-eclampsia, DIC, anuria

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39
Q

Placental praevia - describe
visible blood loss?
Pain?
Uterus examination?
Lie and presentation?
Fetal heart?
Coagulation problems?

A

shock in proportion to visible loss
no pain
uterus not tender
lie and presentation may be abnormal
fetal heart usually normal
coagulation problems rare
small bleeds before large

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40
Q

3 main causes of bleeding in first trimester pregnancy?

A

Spontaneous abortion
Ectopic pregnancy
Hydatidiform mole

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41
Q

3 main causes of bleeding in second trimester pregnancy?

A

Spontaneous abortion
Hydatidiform mole
Placental abruption

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42
Q

4 main causes of bleeding in third trimester pregnancy?

A

Bloody show
Placental abruption
Placenta praevia
Vasa praevia

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43
Q

Spontaneous abortion, describe:
-Threatened miscarriage
-Missed miscarriage
-Inevitable miscarriage
-Incomplete miscarriage
-Complete miscarriage

A

Threatened miscarriage - painless vaginal bleeding typically around 6-9 weeks
Missed (delayed) miscarriage - light vaginal bleeding and symptoms of pregnancy disappear
Inevitable miscarriage - complete or incomplete depending or whether all fetal and placental tissue has been expelled. Incomplete miscarriage - heavy bleeding and crampy, lower abdo pain. Complete miscarriage - little bleeding

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44
Q

What is the typical history and symptoms of ectopic pregnancy?

A

Typically history of 6-8 weeks amenorrhoea with lower abdominal pain (usually unilateral) initially and vaginal bleeding later. Shoulder tip pain and cervical excitation may be present

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45
Q

what is the typical history and findings of a Hydatidiform mole

A

Typically bleeding in first or early second trimester associated with exaggerated symptoms of pregnancy e.g. hyperemesis. The uterus may be large for dates and serum hCG is very high

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46
Q

What is the typical history and examinatoin of placental abruption?

A

Constant lower abdominal pain and, woman may be more shocked than is expected by visible blood loss. Tender, tense uterus* with normal lie and presentation. Fetal heart may be distressed

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47
Q

What is the typical history and examination of placenta praevia?

A

Vaginal bleeding, no pain. Non-tender uterus* but lie and presentation may be abnormal

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48
Q

what is the typical history and findings of vasa praevia?

A

Rupture of membranes followed immediately by vaginal bleeding. Fetal bradycardia is classically seen

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49
Q

Describe maternal advantages of breastfeeding

A

bonding
involution of uterus
protection against breast and ovarian cancer
cheap, no need to sterilise bottle
contraceptive effect (unreliable)

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50
Q

Describe immunological advantages of breastfeeding and medical

A

IgA (protects mucosal surfaces), lysozyme (bacteriolytic enzyme) and lactoferrin (ensures rapid absorption of iron so not available to bacteria)
reduced incidence of ear, chest and gastro-intestinal infections
reduced incidence of eczema and asthma
reduced incidence of type 1 diabetes mellitus

Reduced incidence of sudden infant death syndrome

Baby is in control of how much milk it takes

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51
Q

what are the disadvantages of breastfeeding?

A

Transmission of drugs

Transmission of infection (e.g. HIV) - advised to exclusively formula feed if have HIV, additionally to infant PEP and maternal antiretrovirals

Nutrient inadequacies (prolonged breast feeding may lead to vitamin D deficiency)

Vitamin K deficiency

Breast milk jaundice

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52
Q

What antibiotics should be avoided in breastfeeding?

A

ciprofloxacin, tetracycline, chloramphenicol, sulphonamides

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53
Q

What psychiatric drugs should be avoided in breastfeeding?

A

lithium, benzodiazepines

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54
Q

Which of these drugs should be avoided whilst breast feeding - amoxicillin or aspirin?

A

Aspirin

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55
Q

Which of these drugs should be avoided whilst breast feeding - Levothyroxine or carbimazole?

A

Carbimazole

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56
Q

Which of these drugs should be avoided whilst breast feeding - Methotrexate or prednisolone?

A

Methotrexate

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57
Q

Which of these drugs should be avoided whilst breast feeding - Sulfonylureas or metformin?

A

Sulfonylurea (gliclazide)

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58
Q

Which of these drugs should be avoided whilst breast feeding - cytotoxic drugs or amitriptyline?

A

Cytotoxic drugs

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59
Q

Which of these drugs should be avoided whilst breast feeding - amiodarone or digoxin?

A

Amiodarone (hypothyroidism or hyperthyroidism in baby)

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60
Q

What is a galactocele? When does this occur?

A

Galactocele typically occurs in women who have recently stopped breastfeeding and is due to occlusion of a lactiferous duct. A build up of milk creates a cystic lesion in the breast.

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61
Q

Does galactocele require further investigation?

A

No

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62
Q

What is lactation mastitis? what percentage of women does it affect? when does this most commonly occur?

A

Lactation mastitis is inflammation in the interlobular connective tissue of the breast, which may or may not be associated with infection. It occurs in around 10% on breast feeding women and is most common six weeks post-partum.

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63
Q

How does lactation mastitis present?

A

Clinically this presents as a painful breast, with fever, malaise and a tender, red, swollen and hard area of the breast, usually in a wedge-shaped distribution.

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64
Q

When should you suspect infectious mastitis over lactation mastitis?

A

Symptoms do not improve or are worsening after 12-24 hours despite effective milk removal.
The woman has a nipple fissure that is infected.
Bacterial culture is positive (breast milk culture is not routinely required unless mastitis is severe, there has been no response to antibiotics, or this is recurrent mastitis).

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65
Q

How is lactation mastitis managed? When to give antibiotics?

A

Management of mastitis focuses on relieving pain with simple analgesia and warm compresses, and encouraging complete emptying of the breast after feeding (this may require the woman to express the remaining milk by hand or by using a breast pump).

The BNF advises to treat ‘if systemically unwell, if nipple fissure present, if symptoms do not improve after 12-24 hours of effective milk removal of if culture indicates infection’. The first-line antibiotic is flucloxacillin for 10-14 days. Breastfeeding or expressing should continue during treatment.

If left untreated, mastitis may develop into a breast abscess. This generally requires incision and drainage.

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66
Q

If a breastfed infant is frequently feeding, is this a sign of low milk supply?

A

frequent feeding in a breastfed infant is not alone a sign of low milk supply

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67
Q

What can nipple pain in breastfeeding indicate? How are each of these treated?

A

nipple pain: may be caused by a poor latch
blocked duct (‘milk bleb’)
nipple candidiasis
Engorgement
Raynauds disease of the nipple

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68
Q

What is a blocked duct in breastfeeding? how is this managed?

A

blocked duct (‘milk bleb’): causes nipple pain when breastfeeding. Breastfeeding should continue. Advice should be sought regarding the positioning of the baby. Breast massage may also be tried

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69
Q

How is nipple candidiasis treated?

A

nipple candidiasis: treatment for nipple candidiasis whilst breastfeeding should involve miconazole cream for the mother and nystatin suspension for the baby

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70
Q

what is breast engorgement and how may this present?

A

Breast engorgement is one of the causes of breast pain in breastfeeding women. It usually occurs in the first few days after the infant is born and almost always affects both breasts. The pain or discomfort is typically worse just before a feed. Milk tends to not flow well from an engorged breast and the infant may find it difficult to attach and suckle. Fever may be present but usually settles within 24 hours. The breasts may appear red.

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71
Q

How is breast engorgement managed?

A

Although it may initially be painful, hand expression of milk may help relieve the discomfort of engorgement.

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72
Q

What are the complications of breast engorgement?

A

Complications include blocked milk ducts, mastitis and difficulties with breastfeeding and, subsequently, milk supply

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73
Q

Describe the pain experienced and clinical signs in Raynauds disease of the nipple?

A

In Raynaud’s disease of the nipple, pain is often intermittent and present during and immediately after feeding. Blanching of the nipple may be followed by cyanosis and/or erythema. Nipple pain resolves when nipples return to normal colour.

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74
Q

What are the treatment options of Raynaud’s disease of the nipple?

A

Options of treatment for Raynaud’s disease of the nipple include advice on minimising exposure to cold, use of heat packs following a breastfeed, avoiding caffeine and stopping smoking. If symptoms persist consider specialist referral for a trial of oral nifedipine (off-license).

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75
Q

What is the threshold cut off for weight loss in babies in the first week of life? How often does this occur in breastfed infants?

A

Around 1 in 10 breastfed babies lose more than the ‘cut-off’ 10% threshold in the first week of life. The infant should also be examined to look for any underlying problems. NICE recommends an ‘expert’ review of feeding if this occurs (e.g. midwife-led breastfeeding clinics) and monitoring of weight until weight gain is satisfactory

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76
Q
A
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77
Q

Gestational diabetes
What are the target glucose levels in pregnancy - fasting, 1 hour post-meal, 2 hours post-meal

A

Plasma glucose Target value
Fasting 5.3 mmol/L
One hour after a meal 7.8 mmol/L
Two hours after a meal 6.4 mmol/L

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78
Q

How many pregnancies are complicated by diabetes?
Of these what proportion are gestational / type 1 / type 2

A

It complicates up to 1 in 20 pregnancies.
87.5% have gestational diabetes
7.5% have type 1 diabetes
5% have type 2 diabetes

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79
Q

What percentage of pregnancies are affecting by gestational diabetes?

A

4%

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80
Q

What are 5 risk factors for gestational diabetes?

A

BMI of > 30 kg/m²
previous macrosomic baby weighing 4.5 kg or above
previous gestational diabetes
first-degree relative with diabetes
family origin with a high prevalence of diabetes (South Asian, black Caribbean and Middle Eastern)

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81
Q

What is the screening tool used for gestational diabetes and who is offered screening?

A

the oral glucose tolerance test (OGTT) is the test of choice
women who’ve previously had gestational diabetes: OGTT should be performed as soon as possible after booking and at 24-28 weeks if the first test is normal. NICE also recommend that early self-monitoring of blood glucose is an alternative to the OGTTs
women with any of the other risk factors should be offered an OGTT at 24-28 weeks

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82
Q

What are the threshold glucose levels for diagnosis of gestational diabetes?

A

these have recently been updated by NICE, gestational diabetes is diagnosed if either:
fasting glucose is >= 5.6 mmol/L
2-hour glucose is >= 7.8 mmol/L

(5678)

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83
Q

Management of gestational diabetes:
-What kind of clinic should they be reviewed in and when?

A

newly diagnosed women should be seen in a joint diabetes and antenatal clinic within a week

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84
Q

Management of gestational diabetes:
-What advice and patient teaching do patients recieve?

A

women should be taught about self-monitoring of blood glucose
advice about diet (including eating foods with a low glycaemic index) and exercise should be given

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85
Q

Management of gestational diabetes:
-What is given if the fasting plasma glucose level is >7

A

if the fasting plasma glucose level is < 7 mmol/l a trial of diet and exercise should be offered

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86
Q

Management of gestational diabetes:
-When is metformin started?

A

if glucose targets are not met within 1-2 weeks of altering diet/exercise metformin should be started

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87
Q

Management of gestational diabetes:
-When is insulin started?

A

if glucose targets are still not met insulin should be added to diet/exercise/metformin
gestational diabetes is treated with short-acting, not long-acting, insulin
if at the time of diagnosis the fasting glucose level is >= 7 mmol/l insulin should be started
if the plasma glucose level is between 6-6.9 mmol/l, and there is evidence of complications such as macrosomia or hydramnios, insulin should be offered

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88
Q

Management of gestational diabetes:
-When is glibenclamide offered?

A

glibenclamide should only be offered for women who cannot tolerate metformin or those who fail to meet the glucose targets with metformin but decline insulin treatment

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89
Q

When should patients who have had gestational diabetes be offered a fasting plasma glucose level after birth? Should they be tested thereafter?

A

In women with gestational diabetes, offer a fasting plasma glucose at 6 weeks after birth to exclude diabetes
After 13 weeks, HbA1c testing can be performed instead of fasting plasma glucose
offering an annual HbA1c test is recommended for all women without type 2 diabetes who have a history of gestational diabetes.

90
Q

Management of pre-existing diabetes in pregnancy
-what is advised?
-what medications are used?
-What is treated as it can worsen during pregnancy?

A

weight loss for women with BMI of > 27 kg/m^2
stop oral hypoglycaemic agents, apart from metformin, and commence insulin
folic acid 5 mg/day from pre-conception to 12 weeks gestation and aspirin
treat retinopathy as can worsen during pregnancy

91
Q

What scan is offered to women with pre-existing diabetes in pregnancy?

A

detailed anomaly scan at 20 weeks including four-chamber view of the heart and outflow tracts

92
Q

What reduced complication rates in women with pre-existing diabetes?

A

tight glycaemic control reduces complication rates

93
Q

What are the two maternal complications of diabetes in pregnancy?

A
  1. polyhydramnios - 25%, possibly due to fetal polyuria
  2. preterm labour - 15%, associated with polyhydramnios
94
Q

What are the neonatal complications of diabetes in pregnancy?

A

-macrosomia (although diabetes may also cause small for gestational age babies)
-hypoglycaemia (secondary to beta cell hyperplasia)
-respiratory distress syndrome: surfactant production is delayed
-polycythaemia: therefore more neonatal jaundice
-malformation rates increase 3-4 fold e.g. sacral agenesis, CNS and CVS malformations (hypertrophic cardiomyopathy)
-stillbirth
-hypomagnesaemia
-hypocalcaemia
-shoulder dystocia (may cause Erb’s palsy)

95
Q

Anaemia in pregnancy - what are the cut off values for 1st, 2nd and 3rd trimester

A

First trimester < 110 g/L
Second/third trimester < 105 g/L
Postpartum < 100 g/L

96
Q

Anaemia in pregnancy - when are pregnant women screened for anaemia?

A

the booking visit (often done at 8-10 weeks), and at
28 weeks

97
Q

how is anaemia in pregnancy treated? how long for?

A

oral ferrous sulfate or ferrous fumarate
treatment should be continued for 3 months after iron deficiency is corrected to allow iron stores to be replenished

98
Q

Hepatitis B in pregnancy
What should be given if a mother has chronic hep B and her latest results are:
HBsAg Positive
HBeAg Positive

A

Give the newborn hepatitis B vaccine + hepatitis B immunoglobulin

99
Q

Hepatitis B in pregnancy
What should be given if a mother has chronic hep B and her latest results are:
HBsAg Positive
Anti- HBe Positive

A

Give the newborn hepatitis B vaccine

100
Q

What should be given to babies born to mothers who are chronically infected with hepatitis B or to mothers who’ve had acute hepatitis B during pregnancy

A

babies born to mothers who are chronically infected with hepatitis B or to mothers who’ve had acute hepatitis B during pregnancy should receive a complete course of vaccination + hepatitis B immunoglobulin

unless the mother is anti-HBe positive, if so they dont need the immunoglobulin

101
Q

Hepatitis B in pregnancy
-Does CS reduce vertical transmission?
-Can hep B be transmitted via breastfeeding?

A

here is little evidence to suggest caesarean section reduces vertical transmission rates
hepatitis B cannot be transmitted via breastfeeding (in contrast to HIV)

102
Q

What is used to screen for depression in pregnancy?
-what does this consist of and what time scale is this assessment?
-what score indicated depressive illness?
-is this sensitive/specific?
-Does this ask about self harm?

A

Edinburgh Postnatal Depression Scale
10-item questionnaire, with a maximum score of 30
indicates how the mother has felt over the previous week
score > 13 indicates a ‘depressive illness of varying severity’
sensitivity and specificity > 90%
includes a question about self-harm

103
Q

Baby blues
-How common is this?
-When is this seen and which ladies is this most common in?
-What are the symptoms?

A

Seen in around 60-70% of women

Typically seen 3-7 days following birth and is more common in primips

Mothers are characteristically anxious, tearful and irritable

104
Q

Baby blues
-What is the main management

A

Reassurance and support, the health visitor has a key role

105
Q

Post-natal depression
-How common is this
-When is this seen
-What features are seen?

A

Affects around 10% of women

Most cases start within a month and typically peaks at 3 months

Features are similar to depression seen in other circumstances

106
Q

What is the management of post-natal depression?

A

As with the baby blues reassurance and support are important

NICE CKS state ‘Most women with the baby blues will not require specific treatment other than reassurance’

Cognitive behavioural therapy may be beneficial. Certain SSRIs such as sertraline and paroxetine* may be used if symptoms are severe** - whilst they are secreted in breast milk it is not thought to be harmful to the infant

107
Q

Which SSRI should be avoided for post-natal depression?

A

fluoxetine is best avoided due to a long half-life

108
Q

Puerperal psychosis
-How common is this?
-When is this seen
-What are the features?

A

Affects approximately 0.2% of women

Onset usually within the first 2-3 weeks following birth

Features include severe swings in mood (similar to bipolar disorder) and disordered perception (e.g. auditory hallucinations)

109
Q

Puerperal psychosis
-What is the management?

A

Admission to hospital is usually required, ideally in a Mother & Baby Unit

There is around a 25-50% risk of recurrence following future pregnancies

110
Q

What are the risk factors for couples of conceiving a child with a neural tube defect (NTD)

A

Either partner has a NTD, they have had a previous pregnancy affected by a NTD, or they have a family history of a NTD
The woman is taking antiepileptic drugs or has coeliac disease, diabetes, or thalassaemia trait
The woman is obese (defined as a body mass index [BMI] of 30 kg/m2 or more)

111
Q

What is folic acid converted to once ingested?

A

Folic acid is converted to tetrahydrofolate (THF). Green, leafy vegetables are a good source of folic acid.

112
Q

what is the function of THF?

A

THF plays a key role in the transfer of 1-carbon units (e.g. methyl, methylene, and formyl groups) to the essential substrates involved in the synthesis of DNA & RNA

113
Q

What are 4 causes of folic acid deficiency?

A

phenytoin
methotrexate
pregnancy
alcohol excess

114
Q

What can folic acid deficiency cause?

A

macrocytic, megaloblastic anaemia
neural tube defects

115
Q

How are neural tube defects prevented in pregnancy?

A

all women should take 400mcg of folic acid until the 12th week of pregnancy
women at higher risk of conceiving a child with a NTD should take 5mg of folic acid from before conception until the 12th week of pregnancy

116
Q

What can reduced fetal movements represent and why?

A

Reduced fetal movements can represent fetal distress, as a method of fetal compensation to reduce oxygen consumption as a response to chronic hypoxia in utero. This is concerning, as it reflects risk of stillbirth and fetal growth restriction. It is believed that there may also be a link between reduced fetal movements and placental insufficiency.

117
Q

When does the first onset of fetal movement occur? what is this called? What happens to fetal movements throughout pregnancy and when do they plateau? When should fetal movements be established?

A

The first onset of recognised fetal movements is known as quickening. This usually occurs between 18-20 weeks gestation, and increase until 32 weeks gestation at which point the frequency of movement tends to plateau. Multiparous women will usually experience fetal movements sooner, from 16-18 weeks gestation. Towards the end of pregnancy, fetal movements should not reduce.

Fetal movements should be established by 24 weeks gestation.

118
Q

What defines reduced fetal movements?

A

There is no established definition for what constitutes reduced fetal movements (RFM), but the RCOG considers less than 10 movements within 2 hours (in pregnancies past 28 weeks gestation) an indication for further assessment.

119
Q

what percentage of pregnancies are affected by reduced fetal movements?

A

Reduced fetal movements is a fairly common presentation, affecting up to 15% of pregnancies. 3-5% of pregnant women will have recurrent presentations with RFM.

120
Q

What are 8 risk factors for reduced fetal movement in pregnancy?

A

Posture
Distraction
Placental position
Medication
Fetal position
Body habitus
Amniotic fluid volume
Fetal size

121
Q

Why is posture a risk factor for reduced fetal movements in pregnancy?

A

Posture
There can be positional changes in fetal movement awareness, generally being more prominent during lying down and less when sitting and standing

122
Q

Why is distraction a risk factor for reduced fetal movements in pregnancy?

A

Distraction
Awareness of fetal movements can be distractable, and if a woman is busy or concentrating on something else, these can be less prominent
§

123
Q

Why is placental position a risk factor for reduced fetal movements in pregnancy?

A

Placental position
Patient with anterior placentas prior to 28 weeks gestation may have lesser awareness of fetal movements

124
Q

What medications can increase the risk of reduced fetal movements in pregnancy?

A

Medication
Both alcohol and sedative medications like opiates or benzodiazepines can temporarily cause reduced fetal movements

125
Q

Why can fetal position increase the risk of reduced fetal movements in pregnancy?

A

Fetal position
Anterior fetal position means movements are less noticeable

126
Q

Why does body habitus increase the risk of reduced fetal movements in pregnancy?

A

Body habitus
Obese patients are less likely to feel prominent fetal movements

127
Q

How does amniotic fluid volume increase the risk of reduced fetal movements in pregnancy?

A

Amniotic fluid volume
Both oligohydramnios and polyhydramnios can cause reduction in fetal movements

128
Q

How does fetal size increase the risk of reduced fetal movements in pregnancy?

A

Fetal size
Up to 29% of women presenting with RFM have a SGA fetus

129
Q

Describe the investigations of reduced fetal movements in pregnancy if past 28 weeks?

A

Initially, handheld Doppler should be used to confirm fetal heartbeat.
If no fetal heartbeat detectable, immediate ultrasound should be offered.
If fetal heartbeat present, CTG should be used for at least 20 minutes to monitor fetal heart rate which can assist in excluding fetal compromise.
If concern remains, despite normal CTG, urgent (within 24 hours) ultrasound can be used. Ultrasound assessment should include abdominal circumference or estimated fetal weight (to exclude SGA), and amniotic fluid volume measurement

130
Q

Describe the investigations of reduced fetal movements in pregnancy if between 24-28 weeks?

A

If between 24 and 28 weeks gestation, a handheld Doppler should be used to confirm presence of fetal heartbeat

131
Q

Describe the investigations of reduced fetal movements in pregnancy if below 24 weeks?

A

If below 24 weeks gestation, and fetal movements have previously been felt, a handheld Doppler should be used.

132
Q

What should be done if fetal movements have not been felt by 24weeks?

A

If fetal movements have not yet been felt by 24 weeks, onward referral should be made to a maternal fetal medicine unit.

133
Q

What percentage of women who suffer from stillbirth experience reduced fetal movements?

A

Between 40-55% of women who suffer from stillbirth experience reduced fetal movements prior to diagnosis

134
Q

What percentage of women who have a single episode of reduced fetal movements have no onward complications?

A

However, in 70% of pregnancies with a single episode of reduced fetal movement, there is no onward complication.

135
Q

What is chicken pox caused by? what is shingles caused by?

A

Chickenpox is caused by primary infection with varicella-zoster virus. Shingles is caused by the reactivation of dormant virus in dorsal root ganglion.

136
Q

What is the term for fetal risks in chicken pox

A

a syndrome now termed fetal varicella syndrome

137
Q

what is the maternal risk of chicken pox in pregnancy?

A

Risks to the mother - 5 times greater risk of pneumonitis

138
Q

What is the risk of FVS following maternal varicella exposure?

A

risk of FVS following maternal varicella exposure is around 1% if occurs before 20 weeks gestation
studies have shown a very small number of cases occurring between 20-28 weeks gestation and none following 28 weeks

139
Q

what are the features of fetal varicella syndrome?

A

features of FVS include skin scarring, eye defects (microphthalmia), limb hypoplasia, microcephaly and learning disabilities

140
Q

What is the risk of shingles in infancy if there is maternal exposure?

A

shingles in infancy: 1-2% risk if maternal exposure in the second or third trimester

141
Q

When is there a risk of neonatal varicella? how can this affect the newborn child?

A

severe neonatal varicella: if the mother develops rash between 5 days before and 2 days after birth there is a risk of neonatal varicella, which may be fatal to the newborn child in around 20% of cases

142
Q

Management of chickenpox exposure in pregnancy
-What should be done if there is any doubt if the Mum had previous chickenpox?

A

if there is any doubt about the mother previously having chickenpox maternal blood should be urgently checked for varicella antibodies

143
Q

Management of chickenpox exposure in pregnancy
-What should be done if the pregnant lady is not immune to varicella and she is <=20 weeks?

A

if the pregnant woman <= 20 weeks gestation is not immune to varicella she should be given varicella-zoster immunoglobulin (VZIG) as soon as possible

A second dose of VZIG may be required if a further exposure is reported and 3 weeks have elapsed since the last dose.

144
Q

Management of chickenpox exposure in pregnancy
-What should be done if the pregnant lady is not immune to varicella and she is >20 weeks?

A

if the pregnant woman > 20 weeks gestation is not immune to varicella then either VZIG or antivirals (aciclovir or valaciclovir) should be given days 7 to 14 after exposure

145
Q

Management of chicken pox exposure in pregnancy
-How many days is VZIG effective up to?

A

RCOG and Greenbook guidelines suggest VZIG is effective up to 10 days post exposure

146
Q

How is a pregnant lady managed if they develop chicken pox in pregnancy and they are <20 weeks gest? what if they are >=20 weeks?

A

if a pregnant woman develops chickenpox in pregnancy then specialist advice should be sought
there is an increased risk of serious chickenpox infection (i.e. maternal risk) and fetal varicella risk (i.e. fetal risk) balanced against theoretical concerns about the safety of aciclovir in pregnancy
consensus guidelines (Health Protection Authority and RCOG) suggest oral aciclovir should be given if the pregnant women is ≥ 20 weeks and she presents within 24 hours of onset of the rash
if the woman is < 20 weeks the aciclovir should be ‘considered with caution’

147
Q

What are the three stages of postpartum thyroiditis?

A

Three stages
1. Thyrotoxicosis
2. Hypothyroidism
3. Normal thyroid function (but high recurrence rate in future pregnancies)

148
Q

How is post-partum thyroiditis diagnosed?

A

Postpartum thyroiditis can be definitively diagnosed based on three criteria:
1) Patient is within 12 months of giving birth
2) Clinical manifestations are suggestive of hypothyroidism
3) Thyroid function tests support diagnosis

149
Q

Are TPO antibodies found in post-partum thyroiditis?

A

Thyroid peroxidase antibodies are found in 90% of patient

150
Q

Describe the management of post-partum thyroiditis?

A

thyrotoxic phase
propranolol is typically used for symptom control
not usually treated with anti-thyroid drugs as the thyroid is not overactive.
hypothyroid phase
usually treated with thyroxine

151
Q

What happens to BP in normal pregnancy?

A

blood pressure usually falls in the first trimester (particularly the diastolic), and continues to fall until 20-24 weeks
after this time the blood pressure usually increases to pre-pregnancy levels by term

152
Q

Define hypertension in pregnancy

A

Hypertension in pregnancy in usually defined as:
systolic > 140 mmHg or diastolic > 90 mmHg
or an increase above booking readings of > 30 mmHg systolic or > 15 mmHg diastolic

153
Q

What medication should women who are at high risk of developing PET take and for how long?

A

Women who are at high risk of developing pre-eclampsia should take aspirin 75mg od from 12 weeks until the birth of the baby.

154
Q

What are the three different groups of hypertension in pregnancy?

A

Pre-existing hypertension
Gestational hypertension/ Pregnancy induced hypertension
Pre-eclampsia

155
Q

Define pre-existing hypertension in pregnancy?

A

A history of hypertension before pregnancy or an elevated blood pressure > 140/90 mmHg before 20 weeks gestation

No proteinuria, no oedema

156
Q

How common is pre-existing hypertension in pregnancy?

A

Occurs in 3-5% of pregnancies and is more common in older women

157
Q

Can women take ACEI or ARB in pregnancy?

A

If a pregnant woman takes an ACE inhibitor or angiotensin II receptor blocker (ARB) for pre-existing hypertension this should be stopped immediately and alternative antihypertensives started (e.g. labetalol) whilst awaiting specialist review

158
Q

Define Pregnancy induced hypertension / gestational hypertension

A

Hypertension (as defined above) occurring in the second half of pregnancy (i.e. after 20 weeks)

No proteinuria, no oedema

159
Q

How often does pregnancy induced hypertension occur?

A

Occurs in around 5-7% of pregnancies

160
Q

What happens to BP following birth in pregnancy induced hypertension

A

Resolves following birth (typically after one month). Women with PIH are at increased risk of future pre-eclampsia or hypertension later in life

161
Q

Define pre-eclampsia

A

new-onset blood pressure ≥ 140/90 mmHg after 20 weeks of pregnancy, AND 1 or more of the following:
proteinuria
other organ involvement (see list below for examples): e.g. renal insufficiency (creatinine ≥ 90 umol/L), liver, neurological, haematological, uteroplacental dysfunction

162
Q

What are 8 consequences of pre-eclampsia?

A

-eclampsia
-other neurological complications include altered mental status, blindness, stroke, clonus, severe headaches or persistent visual scotomata
-fetal complications
-intrauterine growth retardation
-prematurity
-liver involvement (elevated transaminases)
-haemorrhage: placental abruption, intra-abdominal, intra-cerebral
-cardiac failure

163
Q

Give 8 features of pre-eclampsia

A

-hypertension: typically > 160/110 mmHg and –proteinuria as above
-proteinuria: dipstick ++/+++
-headache
-visual disturbance
-papilloedema
-RUQ/epigastric pain
-hyperreflexia
-platelet count < 100 * 106/l, abnormal liver enzymes or HELLP syndrome

164
Q

Give 5 high risk risk factors for pre-eclampsia

A

-hypertensive disease in a previous pregnancy
-chronic kidney disease
-autoimmune disease, such as systemic lupus erythematosus or antiphospholipid syndrome
-type 1 or type 2 diabetes
-chronic hypertension

165
Q

Give 6 moderate risk risk factors for pre-eclampsia

A

-first pregnancy
-age 40 years or older
-pregnancy interval of more than 10 years
-body mass index (BMI) of 35 kg/m² or more at first visit
-family history of pre-eclampsia
-multiple pregnancy

166
Q

Which women need to take medication to reduce the risk of pre-eclampsia and what medication should they take?

A

Reducing the risk of hypertensive disorders in pregnancy
women with the following should take aspirin 75-150mg daily from 12 weeks gestation until the birth
≥ 1 high risk factors
≥ 2 moderate factors

167
Q

HOw often does pre-eclampsia occur?

A

Occurs in around 5% of pregnancies

168
Q

Describe the initial assessment of women with suspected pre-eclampsia?

A

NICE recommend arranging emergency secondary care assessment for any woman in whom pre-eclampsia is suspected
women with blood pressure ≥ 160/110 mmHg are likely to be admitted and observed

169
Q

What is the management of pre-eclampsia?

A

oral labetalol is now first-line following the 2010 NICE guidelines. Nifedipine (e.g. if asthmatic) and hydralazine may also be used
delivery of the baby is the most important and definitive management step. The timing depends on the individual clinical scenario

170
Q

What percentage of newborns born to non-epileptic mother have congenital defects? What does this percentage rise to if the mother takes antiepileptic meds?

A

Around 1-2% of newborns born to non-epileptic mothers have congenital defects. This rises to 3-4% if the mother takes antiepileptic medication.

171
Q

How many drugs should epileptic patients be taking in pregnancy? should drug levels be monitored?

A

aim for monotherapy
there is no indication to monitor antiepileptic drug levels

172
Q

What are the risks associated with each drug:
-Sodium valproate
-Carbamazepine
-Phenytoin
-Lamotrigine

A

sodium valproate: associated with neural tube defects
carbamazepine: often considered the least teratogenic of the older antiepileptics
phenytoin: associated with cleft palate. It is advised that pregnant women taking phenytoin are given vitamin K in the last month of pregnancy to prevent clotting disorders in the newborn
lamotrigine: studies to date suggest the rate of congenital malformations may be low. The dose of lamotrigine may need to be increased in pregnancy

The November 2013 issue of the Drug Safety Update also carried a warning about new evidence showing a significant risk of neurodevelopmental delay in children following maternal use of sodium valproate.

The update concludes that sodium valproate should not be used during pregnancy and in women of childbearing age unless clearly necessary. Women of childbearing age should not start treatment without specialist neurological or psychiatric advice

173
Q

Is breastfeeding safe on antiepileptics?

A

Breast feeding is generally considered safe for mothers taking antiepileptics with the possible exception of the barbiturates

174
Q

Down’s syndrome screening
-When should this be done?
-What does the test consist of?
-What results indicate high chance of downs syndrome?
-How does this compare with trisomy 18 (edward syndrome) and 13 (patau syndrome)?

A

Combined test is standard
these tests should be done between 11 - 13+6 weeks
nuchal translucency measurement + serum B-HCG + pregnancy-associated plasma protein A (PAPP-A)
Down’s syndrome is suggested by ↑ HCG, ↓ PAPP-A, thickened nuchal translucency
trisomy 18 (Edward syndrome) and 13 (Patau syndrome) give similar results but the hCG tends to lower

175
Q

HOw is Down’s syndrome screened for if women book later than 11-13+6?

A

if women book later in pregnancy the quadruple test should be offered between 15 - 20 weeks
quadruple test: alpha-fetoprotein, unconjugated oestriol, human chorionic gonadotrophin and inhibin A

176
Q

What results of the below markers would indicate high chance down’s syndrome?
alpha-fetoprotein,
unconjugated oestriol,
human chorionic gonadotrophin
inhibin A

A

alpha-fetoprotein: low
unconjugated oestriol: low
human chorionic gonadotrophin : high
inhibin A: high

177
Q

What results of the below markers would indicate high chance edwards syndrome (tri 18) syndrome?
alpha-fetoprotein,
unconjugated oestriol,
human chorionic gonadotrophin
inhibin A

A

alpha-fetoprotein: low
unconjugated oestriol: low
human chorionic gonadotrophin : low
inhibin A: normal

178
Q

What results of the below markers would indicate high chance neural tube defects?
alpha-fetoprotein,
unconjugated oestriol,
human chorionic gonadotrophin
inhibin A

A

alpha-fetoprotein: high
unconjugated oestriol: normal
human chorionic gonadotrophin : normal
inhibin A: normal

179
Q

What result do both the combined and quadruple tests return for down’s syndrome in pregnancy?

A

Both the combined and quadruple tests return either a ‘lower chance’ or ‘higher chance’ result
‘lower chance’: 1 in 150 chance or more e.g. 1 in 300
‘higher chance’: 1 in 150 chance or less e.g. 1 in 100

180
Q

What will a woman be offered if they have a higher chance result from down’s syndrom screening?

A

If a woman has a ‘higher chance’ results she will be offered a second screening test (NIPT) or a diagnostic test (e.g. amniocentesis or chorionic villus sampling (CVS). Given the non-invasive nature of NIPT and extremely high sensitivity and specificity, it is likely this will be the preferred choice for the vast majority of women.

181
Q

describe Non-invasive prenatal screening test (NIPT)
-How does this work?
-is this sensitive/specific?

A

analyses small DNA fragments that circulate in the blood of a pregnant woman (cell free fetal DNA, cffDNA)
cffDNA derives from placental cells and is usually identical to fetal DNA
analysis of cffDNA allows for the early detection of certain chromosomal abnormalities
sensitivity and specificity are very high for trisomy 21 (>99%) and similarly high for other chromosomal abnormalities
private companies (e.g. Harmony) offer NIPT screening from 10 weeks gestation

182
Q

What are 3 causes of increased nuchal translucency on fetal US?

A

Down’s syndrome
congenital heart defects
abdominal wall defects

183
Q

What are three causes of hyperechogenic bowel on fetal US?

A

cystic fibrosis
Down’s syndrome
cytomegalovirus infection

184
Q

How much folic acid should pregnant women with a BMI >=30 take? and how long for?

A

Pregnant women with a BMI >= 30 kg/m² should receive 5 mg folic acid daily until the 13th week of pregnancy

185
Q

Which patients groups should recieve a 5mg folic acid daily? (8)

A

In addition to patients with a BMI of more than 30 kg/m², folic acid should also be prescribed at a 5mg daily dose for those with diabetes, sickle cell disease (SCD), thalassaemia trait, coeliac disease, on anti-epileptic medication, personal or family history of NTD, or who have previously given birth to a baby with an NTD. Ideally, folic acid should be commenced whilst trying to conceive as this will further minimise NTD risk.

186
Q

what are the maternal risks of obesity? (BMI 30+)

A

Maternal risks
-miscarriage
-venous thromboembolism
-gestational diabetes
-pre-eclampsia
-dysfunctional labour, induced labour
-postpartum haemorrhage
-wound infections

187
Q

What are the fetal risks of obesity? (BMI 30+)

A

Fetal risks
-congenital anomaly
-prematurity
-macrosomia
-stillbirth
-increased risk of developing obesity and metabolic disorders in childhood
-neonatal death

188
Q

Should obese women try and lose weight whilst pregnant?

A

Explain to women with a BMI of 30 or more at the booking appointment how this poses a risk, both to their health and the health of the unborn child. Explain that they should not try to reduce this risk by dieting while pregnant and that the risk will be managed by the health professionals caring for them during their pregnancy

189
Q

What is the management of obesity in pregnancy?

A

obese women should take 5mg of folic acid, rather than 400mcg
all obese women should be screened for gestational diabetes with an oral glucose tolerance test (OGTT) at 24-28 weeks
if the BMI >= 35 kg/m² women should give birth in a consultant-led obstetric unit
if the BMI >= 40 kg/m² should have an antenatal consultation with an obstetric anaesthetist and a plan made

190
Q

What percentage of pregnancies are affected by intrahepatic cholestasis of pregnancy?

A

Intrahepatic cholestasis of pregnancy (also known as obstetric cholestasis) affects around 1% of pregnancies in the UK. It is associated with an increased risk of premature birth.

191
Q

What are the clinical features of intrahepatic cholestasis of pregnancy?

A

pruritus - may be intense - typical worse palms, soles and abdomen
clinically detectable jaundice occurs in around 20% of patients
raised bilirubin is seen in > 90% of cases

192
Q

What is the management of intrahepatic cholestasis of pregnancy?

A

induction of labour at 37-38 weeks is common practice but may not be evidence based
ursodeoxycholic acid - again widely used but evidence base not clear
vitamin K supplementation

193
Q

what is the recurrence rate of intrahepatic cholestasis of pregnancy?

A

Recurrence of intrahepatic cholestasis of pregnancy is 45-90% in subsequent pregnancies.

194
Q

What is the most common cause of early-onset severe infection in the neonatal period?
How common is this found in bowel flora?

A

Group B Streptococcus (GBS) is the most common cause of early-onset severe infection in the neonatal period. It is thought around 20-40% of mothers have GBS present in their bowel flora and may therefore be thought of as ‘carriers’ of GBS. Infants may be exposed to maternal GBS during labour and subsequently develop potentially serious infections.

195
Q

What are 4 risk factors for GB strep infection?

A

Risk factors for Group B Streptococcus (GBS) infection:
-prematurity
-prolonged rupture of the membranes
-previous sibling GBS infection
-maternal pyrexia e.g. secondary to chorioamnionitis

196
Q

Does universal screening for GBS in pregnancy take place?

A

universal screening for GBS should not be offered to all women
the guidelines also state a maternal request is not an indication for screening

197
Q

How should women who have had GBS detected in a previous pregnancy be managed?

A

-women who’ve had GBS detected in a previous pregnancy should be informed that their risk of maternal GBS carriage in this pregnancy is 50%. -They should be offered intrapartum antibiotic prophylaxis (IAP) OR testing in late pregnancy and then antibiotics if still positive
-if women are to have swabs for GBS this should be offered at 35-37 weeks or 3-5 weeks prior to the anticipated delivery date

198
Q

Which women recieve intrapartum antibiotic prophylaxis for GBS?

A

-IAP should be offered to women with a previous baby with early- or late-onset GBS disease
-IAP should be offered to women in preterm labour regardless of their GBS status
-women with a pyrexia during labour (>38ºC) should also be given IAP
-benzylpenicillin is the antibiotic of choice for GBS prophylaxis

199
Q

Where is the symphysis fundal height measured?
What should this match after 20 weeks?

A

The symphysis-fundal height (SFH) is measured from the top of the pubic bone to the top of the uterus in centimetres

It should match the gestational age in weeks to within 2 cm after 20 weeks, e.g. if 24 weeks then the a normal SFH = 22 to 26 cm

200
Q

What is the definition of puerperal pyrexia? what are 5 causes?

What is the management if endometritis is suspected?

A

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

Causes:
endometritis: most common cause
urinary tract infection
wound infections (perineal tears + caesarean section)
mastitis
venous thromboembolism

Management
if endometritis is suspected the patient should be referred to hospital for intravenous antibiotics (clindamycin and gentamicin until afebrile for greater than 24 hours)

201
Q

What are the features of acute fatty liver of pregnancy?

A

Acute fatty liver of pregnancy is rare complication which may occur in the third trimester or the period immediately following delivery.

abdominal pain
nausea & vomiting
headache
jaundice
hypoglycaemia
severe disease may result in pre-eclampsia

202
Q

What is the investigation for acute fatty liver of pregnancy?

A

Investigations
ALT is typically elevated e.g. 500 u/l

203
Q

What is the management of acute fatty liver of pregnancy?

A

Management
support care
once stabilised delivery is the definitive management

204
Q

What is the incubation period of rubella?

A

the incubation period is 14-21 days and individuals are infectious from 7 days before symptoms appear to 4 days after the onset of the rash.

205
Q

What is the risk to the fetus if Mothers contract rubella?

A

in first 8-10 weeks risk of damage to fetus is as high as 90%
damage is rare after 16 weeks

206
Q

Give some features of congenital rubella syndrome? (9)

A

sensorineural deafness
congenital cataracts
congenital heart disease (e.g. patent ductus arteriosus)
growth retardation
hepatosplenomegaly
purpuric skin lesions
‘salt and pepper’ chorioretinitis
microphthalmia
cerebral palsy

207
Q

What is the diagnosis of rubella in pregnancy?

A

suspected cases should be discussed immediately with the local Health Protection Unit (HPU) as type/timing of investigations may vary
IgM antibodies are raised in women recently exposed to the virus
it should be noted that it is very difficult to distinguish rubella from parvovirus B19 clinically. It is therefore important to also check parvovirus B19 serology as there is a 30% risk of transplacental infection, with a 5-10% risk of fetal loss

208
Q

What is the management of suspected rubella in pregnancy?
-What should be advised to non-immune mothers?

A

suspected cases of rubella in pregnancy should be discussed with the local Health Protection Unit
since 2016, rubella immunity is no longer routinely checked at the booking visit
if a woman is however tested at any point and no immunity is demonstrated they should be advised to keep away from people who might have rubella
non-immune mothers should be offered the MMR vaccination in the post-natal period
MMR vaccines should not be administered to women known to be pregnant or attempting to become pregnant

209
Q

Give 5 risk factors for breech presentation

A

-uterine malformations, fibroids
-placenta praevia
-polyhydramnios or oligohydramnios
-fetal abnormality (e.g. CNS malformation, chromosomal disorders)
-prematurity (due to increased incidence earlier in gestation)

210
Q

What is the management of a breech baby?

A

-if < 36 weeks: many fetuses will turn spontaneously
-if still breech at 36 weeks NICE recommend external cephalic version (ECV)- this has a success rate of around 60%. The RCOG recommend ECV should be offered from 36 weeks in nulliparous women and from 37 weeks in multiparous women
-if the baby is still breech then delivery options include planned caesarean section or vaginal delivery

211
Q

What are 6 absolute contraindications to ECV?

A

-where caesarean delivery is required
-antepartum haemorrhage within the last 7 days
-abnormal cardiotocography
-major uterine anomaly
-ruptured membranes
-multiple pregnancy

212
Q

What is a complete hydatiform mole? What are the features?

A

Benign tumour of trophoblastic material. Occurs when an empty egg is fertilized by a single sperm that then duplicates its own DNA, hence the all 46 chromosomes are of paternal origin

Features
bleeding in first or early second trimester
exaggerated symptoms of pregnancy e.g. hyperemesis
uterus large for dates
very high serum levels of human chorionic gonadotropin (hCG)
hypertension and hyperthyroidism* may be seen

213
Q

What is the management of complete hydatiform mole?
What can this develop into and how often does this occur?

A

urgent referral to specialist centre - evacuation of the uterus is performed
effective contraception is recommended to avoid pregnancy in the next 12 months

Around 2-3% go on to develop choriocarcinoma

214
Q

What is a partial hydatiform mole?

A

In a partial mole a normal haploid egg may be fertilized by two sperms, or by one sperm with duplication of the paternal chromosomes. Therefore the DNA is both maternal and paternal in origin. Usually triploid - e.g. 69 XXX or 69 XXY. Fetal parts may be seen

215
Q

What factors reduce the risk of vertical transmission of HIV from mum to baby?

A

Factors which reduce vertical transmission (from 25-30% to 2%)
maternal antiretroviral therapy
mode of delivery (caesarean section)
neonatal antiretroviral therapy
infant feeding (bottle feeding)

216
Q

What is the mode of delivery to HIV positive mums

A

Mode of delivery
vaginal delivery is recommended if viral load is less than 50 copies/ml at 36 weeks, otherwise caesarian section is recommended
a zidovudine infusion should be started four hours before beginning the caesarean section

217
Q

What is given to the baby of HIV positive mums after birth? how long is this given for?

A

Neonatal antiretroviral therapy
zidovudine is usually administered orally to the neonate if maternal viral load is <50 copies/ml. Otherwise triple ART should be used. Therapy should be continued for 4-6 weeks.

218
Q

What is the incidence and associated factors of placenta praevia?

A

Epidemiology
5% will have low-lying placenta when scanned at 16-20 weeks gestation
incidence at delivery is only 0.5%, therefore most placentas rise away from the cervix

Associated factors
multiparity
multiple pregnancy
embryos are more likely to implant on a lower segment scar from previous caesarean section

219
Q

What is the diagnosis of placenta praevia?

A

digital vaginal examination should not be performed before an ultrasound as it may provoke a severe haemorrhage
placenta praevia is often picked up on the routine 20 week abdominal ultrasound
the RCOG recommend the use of transvaginal ultrasound as it improves the accuracy of placental localisation and is considered safe

220
Q

What is the grading of placenta praevia?

A

I - placenta reaches lower segment but not the internal os
II - placenta reaches internal os but doesn’t cover it
III - placenta covers the internal os before dilation but not when dilated
IV (‘major’) - placenta completely covers the internal os

221
Q

How often does placental abruption occur?
What are 5 assoc factors?

A

Epidemiology
occurs in approximately 1/200 pregnancies

Cause - not known but associated factors:
proteinuric hypertension
cocaine use
multiparity
maternal trauma
increasing maternal age