Antenatal Care Flashcards

(393 cards)

1
Q

Triad of symptoms - vasa praevia

A

Painless vaginal bleeding
Foetal bradycardia
Rupture of membranes

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2
Q

What is vasa praevia and why is it dangerous?

A

Condition where the feotal blood vessels (not protected by the umbilical cord) run close or across the cervical os.

Rupture of membranes can cause rupture of feotal vessels and subsequent feotal haemorrhage

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3
Q

What should be done if a placenta is found to be low lying at the 20 week abnormality scan?

A

Repeat at 32 and 36 weeks (if still not moved at 32)

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4
Q

Social history considerations in pregnancy?

A

Planned vs unplanned
Safety issues
Home situation
Smoking and alcohol use
Risk factors for mental health problems - perinatal mental health team

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5
Q

What would a community midwife risk assess a pregnant patient for?

A

Small for gestational age
Pre eclampsia
Preterm labour
Gestational diabetes
VTE

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6
Q

Within how long is it reccomended a pregnant woman has a booking appointment with a midwife?

A

10 weeks

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7
Q

What might intractable vomiting lead to?

A

Thiamine deficiency leading to Wernickes encepalopathy leading to feotal death

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8
Q

What is 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

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9
Q

After how many weeks gestation does pre eclampsia occur?

A

20 weeks

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10
Q

What is the basic cause of pre eclampsia?

A

Spiral arteries of the placenta form abnormally, leading to a high vascular resistance in these vessels

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11
Q

Pre-eclampsia is a significant cause of maternal and fetal morbidity and mortality - what can it lead to?

A

Without treatment, it can lead to maternal organ damage, fetal growth restriction, seizures, early labour and in a small proportion, death.

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12
Q

Triad of signs in preeclampsia

A

Hypertension
Proteinuria
Oedema

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13
Q

What is chronic HTN in pregnancy, how does it compare to pre eclampsia?

A

Chronic hypertension is high blood pressure that exists before 20 weeks gestation and is longstanding (Pre-eclampsia is pregnancy-induced hypertension associated with organ damage, occuring after 20 weeks gestation)

This is not caused by dysfunction in the placenta and is not classed as pre-eclampsia.

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14
Q

What is pregnancy induced hypertension, how does it compare to pre eclampsia?

A

Pregnancy-induced hypertension or gestational hypertension is hypertension occurring after 20 weeks gestation, without proteinuria (pre eclampsia involves proteinuria)

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15
Q

What is eclampsia?

A

Eclampsia is when seizures occur as a result of pre-eclampsia (HTN oedema and proteinuria occurring from 20 weeks gestation)

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16
Q

Pathophysiology of pre eclampsia?

A

When the blastocyst implants on the endometrium, the outermost layer, called the syncytiotrophoblast, grows into the endometrium.

It forms finger-like projections called chorionic villi. The chorionic villi contain fetal blood vessels.

Trophoblast invasion of the endometrium sends signals to the spiral arteries in that area of the endometrium, reducing their vascular resistance and making them more fragile.

The blood flow to these arteries increases, and eventually they break down, leaving pools of blood called lacunae (lakes).

Maternal blood flows from the uterine arteries, into these lacunae, and back out through the uterine veins.

Lacunae form at around 20 weeks gestation.

When the process of forming lacunae is inadequate, the woman can develop pre-eclampsia.

Pre-eclampsia is caused by high vascular resistance in the spiral arteries and poor perfusion of the placenta.

This causes oxidative stress in the placenta, and the release of inflammatory chemicals into the systemic circulation, leading to systemic inflammation and impaired endothelial function in the blood vessels.

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17
Q

Pre eclampsia - high risk factors

A

Pre-existing hypertension
Previous hypertension in pregnancy
Existing autoimmune conditions (e.g. systemic lupus erythematosus)
Diabetes
Chronic kidney disease

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18
Q

Pre eclampsia moderate risk factors

A

Older than 40
BMI > 35
More than 10 years since previous pregnancy
Multiple pregnancy
First pregnancy
Family history of pre-eclampsia

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19
Q

Which women are offered aspirin as prophylaxis against pre-eclampsia and from when?

A

Women are offered aspirin from 12 weeks gestation until birth if they have one high-risk factor or more than one moderate-risk factors.

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20
Q

Symptoms of pre eclampsia

A

Headache
Visual disturbance or blurriness
Nausea and vomiting
Upper abdominal or epigastric pain (this is due to liver swelling)
Oedema - pitting
Reduced urine output
(Brisk reflexes, HTN>140)

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21
Q

How can pre eclampsia be diagnosed?

A

Systolic blood pressure above 140 mmHg
Diastolic blood pressure above 90 mmHg

PLUS any of:

Proteinuria (1+ or more on urine dipstick)
Organ dysfunction (e.g. raised creatinine, elevated liver enzymes, seizures, thrombocytopenia or haemolytic anaemia)
Placental dysfunction (e.g. fetal growth restriction or abnormal Doppler studies)

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22
Q

How is proteinuria quantified?

A

Urine protein:creatinine ratio (above 30mg/mmol is significant)
Urine albumin:creatinine ratio (above 8mg/mmol is significant)

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23
Q

PlGF - pre eclampsia

A

The NICE guidelines (2019) recommend the use of placental growth factor (PlGF) testing on one occasion during pregnancy in women suspected of having pre-eclampsia.

Placental growth factor is a protein released by the placenta that functions to stimulate the development of new blood vessels.

In pre-eclampsia, the levels of PlGF are LOW.

NICE recommends using PlGF between 20 and 35 weeks gestation to rule-out pre-eclampsia.

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24
Q

What blood test can rule out pre eclampsia between 20 and 35 weeks?

A

NICE recommends using PlGF (placental growth factor) between 20 and 35 weeks gestation to rule-out pre-eclampsia (low in pre eclampsia)

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25
Management of pre eclampsia - preventative
Aspirin is used for prophylaxis against the development of pre-eclampsia. It is given from 12 weeks gestation until birth to women with: A single high-risk factor or Two or more moderate-risk factors All pregnant women are routinely monitored at every antenatal appointment for evidence of pre-eclampsia, with: Blood pressure, Symptoms, Urine dipstick for proteinuria
26
When gestational hypertension (without proteinuria) is identified, the general management involves what?
Treating to aim for a blood pressure below 135/85 mmHg Admission for women with a blood pressure above 160/110 mmHg Urine dipstick testing at least weekly Monitoring of blood tests weekly (full blood count, liver enzymes and renal profile) Monitoring fetal growth by serial growth scans PlGF testing on one occasion
27
General management of diagnosed pre eclampsia?
Treating to aim for a blood pressure below 135/85 mmHg Monitoring of blood tests weekly (full blood count, liver enzymes and renal profile) Scoring systems are used to determine whether to admit the woman (fullPIERS or PREP‑S) Blood pressure is monitored closely (at least every 48 hours) Urine dipstick testing is not routinely necessary (the diagnosis is already made) Ultrasound monitoring of the fetus, amniotic fluid and dopplers is performed two weekly
28
Medical management of pre eclampsia?
Labetolol is first-line as an antihypertensive Nifedipine (modified-release) is commonly used second-line Methyldopa is used third-line (needs to be stopped within two days of birth) Intravenous hydralazine may be used as an antihypertensive in critical care in severe pre-eclampsia or eclampsia IV magnesium sulphate is given during labour and in the 24 hours afterwards to prevent seizures Fluid restriction is used during labour in severe pre-eclampsia or eclampsia, to avoid fluid overload
29
Role of IV magnesium sulphate in a woman with pre eclampsia?
IV magnesium sulphate is given during labour and in the 24 hours afterwards to prevent seizures
30
What is eclampsia and how is it managed?
Eclampsia refers to the seizures associated with pre-eclampsia. IV magnesium sulphate is used to manage seizures associated with pre-eclampsia.
31
What is HELLP syndrome?
HELLP syndrome is a combination of features that occurs as a complication of pre-eclampsia and eclampsia. It is an acronym for the key characteristics: Haemolysis Elevated Liver enzymes Low Platelets
32
Define Last menstrual period (LMP)
Last menstrual period (LMP) refers to the date of the first day of the most recent menstrual period
33
Define Gestational age (GA)
Gestational age (GA) refers to the duration of the pregnancy starting from the date of the last menstrual period
34
Define Estimated date of delivery (EDD)
Estimated date of delivery (EDD) refers to the estimated date of delivery (40 weeks gestation)
35
Define Gravida (G)
Gravida (G) is the total number of pregnancies a woman has had
36
Define Primigravida
Primigravida refers to a patient that is pregnant for the first time
37
Define Multigravida
Multigravida refers to a patient that is pregnant for at least the second time
38
Define Para (P)
Para (P) refers to the number of times the woman has given birth after 24 weeks gestation, regardless of whether the fetus was alive or stillborn
39
Define Nulliparous (“nullip”)
Nulliparous (“nullip”) refers to a patient that has never given birth after 24 weeks gestation
40
Define Primiparous
Primiparous technically refers to a patient that has given birth after 24 weeks gestation once before
41
Define Multiparous
Multiparous (“multip”) refers to a patient that has given birth after 24 weeks gestation two or more times
42
How is gestational age described?
Weeks + Days e.g. 5 + 2 (5 weeks 2 days since first day of LMP)
43
When is the first trimester?
The first trimester is from the start of pregnancy until 12 weeks gestation.
44
When is the second trimester?
13 weeks to 26 weeks gestation
45
When is the third trimester?
The third trimester is from 27 weeks gestation until birth.
46
At how many weeks does fetal movement start?
Around 20 weeks gestation
47
When is booking clinic and what is the purpose?
Before 10 weeks Offer a baseline assessment and plan the pregnancy
48
When does a dating scan occur and what is the purpose?
Between 10 and 13 + 6 weeks An accurate gestational age is calculated from the crown rump length (CRL), and multiple pregnancies are identified
49
Purpose of 16 week antenatal appointment?
16 weeks Discuss results and plan future appointments
50
When does the anomaly scan occur and what is the purpose?
Between 18 and 20 + 6 weeks An ultrasound to identify any anomalies, such as heart conditions
51
At which points during a pregnancy should antenatal appointments be had?
Booking scan - before 10 weeks Dating scan - between 10 and 13+6 weeks 16 weeks (Discuss results and plan future appointments) Anomaly scan between 18 and 20+6 weeks 25, 28, 31, 34, 36, 38, 40, 41 and 42 weeks (monitor the pregnancy and discuss future plans)
52
What additional antenatal appointments may be required if the mother/pregnancy meet certain criteria?
Additional appointments for higher risk or complicated pregnancies Oral glucose tolerance test in women at risk of gestational diabetes (between 24 – 28 weeks) Anti-D injections in rhesus negative women (at 28 and 34 weeks) Ultrasound scan at 32 weeks for women with placenta praevia on the anomaly scan Serial growth scans are offered to women at increased risk of fetal growth restriction
53
Several things are covered at each routine antenatal appointment, including what?
Discuss plans for the remainder of the pregnancy and delivery Symphysis–fundal height measurement from 24 weeks onwards Fetal presentation assessment from 36 weeks onwards Urine dipstick for protein for pre-eclampsia Blood pressure for pre-eclampsia Urine for microscopy and culture for asymptomatic bacteriuria
54
Symphysis–fundal height measurement from how many weeks onwards?
24 weeks
55
Fetal presentation assessment from how many weeks onwards?
36 weeks
56
What vaccines should be offered to pregnant women?
Whooping cough (pertussis) from 16 weeks gestation Influenza (flu) when available in autumn or winter COVID 19
57
What vaccines should be avoided in pregnancy?
Live vaccines, such as the MMR vaccine, are avoided in pregnancy.
58
An ultrasound scan should be performed at how many weeks for women with placenta praevia on the anomaly scan?
32 weeks
59
What supplements are recommended in pregnancy?
Take folic acid 400mcg from before pregnancy to 12 weeks (reduces neural tube defects) Take vitamin D supplement (10 mcg or 400 IU daily) Avoid vitamin A supplements and eating liver or pate (vitamin A is teratogenic at high doses)
60
What should pregnant women avoid?
Avoid vitamin A supplements and eating liver or pate (vitamin A is teratogenic at high doses) Don’t drink alcohol when pregnant (risk of fetal alcohol syndrome) Don’t smoke (smoking has a long list of complications, see below) Avoid unpasteurised dairy or blue cheese (risk of listeriosis) Avoid undercooked or raw poultry (risk of salmonella) Continue moderate exercise but avoid contact sports
61
Advice for sexually active pregnant women?
Sex is safe STIs can be passed on to fetus/baby
62
Advice for travelling by car for pregnant women
Place car seatbelts above and below the bump (not across it)
63
Implications of drinking alcohol during pregnancy?
Alcohol can cross the placenta, enter the fetus, and disrupt fetal development. There is no safe level of alcohol in pregnancy. Pregnant women are encouraged not to drink alcohol at all. Small amounts are less likely to result in lasting effects. The effects are greatest in the first 3 months of pregnancy. Alcohol in early pregnancy can lead to: Miscarriage Small for dates Preterm delivery Fetal alcohol syndrome
64
What might alcohol in early pregnancy lead to?
Miscarriage Small for dates Preterm delivery Fetal alcohol syndrome
65
During which part of a pregnancy does drinking alcohol have the greatest effect on the fetus?
First 3 months
66
Features of fetal alcohol syndrome
Microcephaly (small head) Thin upper lip Smooth flat philtrum (the groove between the nose and upper lip) Short palpebral fissure (short horizontal distance from one side of the eye to the other) Learning disability Behavioural difficulties Hearing and vision problems Cerebral palsy
67
What are the risks of smoking during pregnancy?
Fetal growth restriction (FGR) Miscarriage Stillbirth Preterm labour and delivery Placental abruption Pre-eclampsia Cleft lip or palate Sudden infant death syndrome (SIDS)
68
Flying during pregnancy?
Flying increases the risk of venous thromboembolism (VTE) The RCOG advises flying is generally ok in uncomplicated healthy pregnancies up to: 37 weeks in a single pregnancy 32 weeks in a twin pregnancy After 28 weeks gestation, most airlines need a note from a midwife, GP or obstetrician to state the pregnancy is going well and there are no additional risks.
69
What pregnancy related topics are covered in booking clinic?
What to expect at different stages of pregnancy Lifestyle advice in pregnancy (e.g. not smoking) Supplements (e.g. folic acid and vitamin D) Plans for birth Screening tests (e.g. Downs screening) Antenatal classes Breastfeeding classes Discuss mental health Discuss female genital mutilation Discuss domestic violence
70
What bloods are taken at booking clinic?
Blood group, antibodies and rhesus D status Full blood count for anaemia Screening for thalassaemia (all women) and sickle cell disease (women at higher risk) Patients are also offered screening for infectious diseases, by testing antibodies for: - HIV - Hepatitis B - Syphilis Rubella immunity Screening for Down’s syndrome may be initiated depending on the gestational age. Bloods required for the combined test are taken from 11 weeks onwards.
71
''Bedside'' test and examinations at booking clinic
Weight, height and BMI Urine for protein and bacteria Blood pressure
72
At booking clinic women are assessed for risk factors for other conditions, and plans are put in place with additional appointments booked. What risk factors are screened for and what action might be taken?
Rhesus negative (book anti-D prophylaxis) Gestational diabetes (book oral glucose tolerance test) Fetal growth restriction (book additional growth scans) Venous thromboembolism (provide prophylactic LMWH if high risk) Pre-eclampsia (provide aspirin if high risk)
73
What condition is caused by three copies of chromosome 21, (also called trisomy 21)
Downs Syndrome
74
Downs Syndrome screening in pregnancy?
The screening tests involve taking measurements from the fetus using ultrasound, combining those measurements with the mother’s age and blood results and providing an indication of the risk of Down’s syndrome. Older mothers have a higher risk of Down’s syndrome. All women are offered screening for Down’s syndrome during pregnancy. The purpose of the screening test is to decide which women should receive more invasive tests to establish a definitive diagnosis. It is the choice of the woman whether to go ahead with screening.
75
When is the combined test (down syndrome screening performed)?
11 - 14 weeks
76
What is the first line and most accurate screening test for Downs Syndrome?
The combined test is the first line and the most accurate screening test.
77
How does the combined test screen for Downs Syndrome?
Ultrasound measures nuchal translucency, which is the thickness of the back of the neck of the fetus. Down’s syndrome is one cause of a nuchal thickness greater than 6mm. Maternal blood tests: Beta‑human chorionic gonadotrophin (beta-HCG) – a higher result indicates a greater risk Pregnancy‑associated plasma protein‑A (PAPPA) – a lower result indicates a greater risk
78
How does beta-HCG relate to risk of Downs Syndrome?
Beta‑human chorionic gonadotrophin (beta-HCG) – a HIGHER result indicates a greater risk
79
How does pregnancy-associated plasma protein-A (PAPPA) relate to risk of Downs Syndrome?
A LOWER result indicates a greater risk
80
How does USS at 11-14 weeks help to indicate risk of Downs Syndrome?
Down’s syndrome is one cause of a nuchal thickness greater than 6mm.
81
At what gestation can the triple test or quadruple for Downs Syndrome screening be performed?
14-20 weeks
82
What does the triple test involve?
It only involves maternal blood tests: Beta-HCG – a higher result indicates greater risk Alpha-fetoprotein (AFP) – a lower result indicates a greater risk Serum oestriol (female sex hormone) – a lower result indicates a greater risk
83
What does the quadruple test involve?
It only involves maternal blood tests: Beta-HCG – a higher result indicates greater risk Alpha-fetoprotein (AFP) – a lower result indicates a greater risk Serum oestriol (female sex hormone) – a lower result indicates a greater risk Inhibin-A - A higher inhibin-A indicates a greater risk.
84
Which women are offered amniocentesis or chorionic villus sampling for Downs Syndrome?
. When the risk of Down’s is greater than 1 in 150 (determined by combined, triple or quadruple assessment), the woman is offered amniocentesis or chorionic villus sampling.
85
What are CVS and amniocentesis (DS syndrome screening)
These tests involve taking a sample of the fetal cells to perform karyotyping for a definitive answer about Down’s: Chorionic villus sampling (CVS) involves an ultrasound-guided biopsy of the placental tissue. This is used when testing is done earlier in pregnancy (before 15 weeks). Amniocentesis involves ultrasound-guided aspiration of amniotic fluid using a needle and syringe. This is used later in pregnancy once there is enough amniotic fluid to make it safer to take a sample.
86
Chorionic villus sampling is the test of choice prior to what gestation?
15 weeks
87
Why is amniocentesis reserved for use later in pregnancy?
More amniotic fluid - safer sample
88
NIPT
Non-invasive prenatal testing (NIPT) is a relatively new test for detecting abnormalities in the fetus during pregnancy. It involves a simple blood test from the mother. The blood will contain fragments of DNA, some of which will come from the placental tissue and represent the fetal DNA. These fragments can be analysed to detect conditions such as Down’s.
89
Indications for Chorionic villus sampling?
Increased risk of abnormality identified through antenatal screening (risk >1:150) A previous child with chromosomal or genetic abnormality Known carrier status for a genetic condition A family history of a genetic condition Ultrasound scan evidence of fetal abnormalities that are associated with a chromosomal or genetic condition.
90
Chorionic villus sampling limitations and complications
Miscarriage: There is an additional risk of 0.5% following chorionic villus sampling. Vaginal bleeding: occurs in around 1 in 10 women (higher in transcervical approach). Other maternal complications include: pain, infection, amniotic fluid leakage and resus sensitisation (give anti-D) There is also a 1% risk of a mosaic result (where both normal and abnormal cells are found). Amniocentesis may then be offered to establish whether the baby has a mosaic karyotype or if mosaicism is just confined to the placenta (confined placental mosaicism). Chorionic Villus Sampling can be performed from 10 weeks’ gestation; however, this is technically challenging.
91
Amniocentesis limitations and complications
0.5% risk of miscarriage (RCOG). The risk is higher in a multiple pregnancy False reassurance – a “normal” result may make women feel their baby will be born completely healthy when this may not be the case. Risk of infection, as with most surgical procedures Pain from the procedure Rhesus sensitisation Increased risk of club foot
92
Untreated or under-treated hypothyroidism in pregnancy can lead to several adverse pregnancy outcomes, including what?
Miscarriage Anaemia Small for gestational age Pre-eclampsia.
93
Treatment of hypothyroidism in pregnancy?
Hypothyroidism is treated with levothyroxine (T4). Levothyroxine can cross the placenta and provide thyroid hormone to the developing fetus. The levothyroxine dose needs to be increased during pregnancy, usually by at least 25 – 50 mcg (30 – 50%). Treatment is titrated based on the TSH level, aiming for a low-normal TSH level.
94
What anti-hypertensive agents should be stopped during pregnancy?
ACE inhibitors (e.g. ramipril) Angiotensin receptor blockers (e.g. losartan) Thiazide and thiazide-like diuretics (e.g. indapamide)
95
What anti-hypertensive agents are considered safe during pregnancy?
Labetalol (a beta-blocker – although other beta-blockers may have adverse effects) Calcium channel blockers (e.g. nifedipine) Alpha-blockers (e.g. doxazosin)
96
Women with epilepsy should take how much folic acid daily from before conception to reduce the risk of neural tube defects?
5mg
97
How much folic acid should be taken during pregnancy and at what dose?
400mcg (usually) Ideally start 3 months prior to conception Carry on to 12 weeks gestation
98
How do pregnancy and epilepsy affect eachother?
Pregnancy may worsen seizure control due to the additional stress, lack of sleep, hormonal changes and altered medication regimes. Seizures are not known to be harmful to the pregnancy, other than the risk of physical injury.
99
Why should sodium valproate be avoided during pregnancy?
Sodium valproate is avoided as it causes neural tube defects and developmental delay There are a lot of warnings about the teratogenic effects of sodium valproate, and NICE updated their guidelines in 2018 to reflect this. It must be avoided in girls or women unless there are no suitable alternatives and strict criteria are met to ensure they do not get pregnant. There is a specific program for this, called Prevent (valproate pregnancy prevention programme).
100
Why should phenytoin be avoided during pregnancy?
Phenytoin is avoided as it causes cleft lip and palate
101
What anti-epileptic drugs are considered the safe options during pregnancy?
Levetiracetam Lamotrigine Carbamazepine
102
Ideally, rheumatoid arthritis should be well controlled for how long before becoming pregnant?
At least 3 months
103
How does pregnancy affect RA?
Often the symptoms of rheumatoid arthritis will improve during pregnancy, and may flare up after delivery.
104
What treatments used for autoimmune conditions are considered safe in pregnancy?
Hydroxychloroquine is considered safe during pregnancy and is often the first-line choice Sulfasalazine is considered safe during pregnancy Corticosteroids may be used during flare-ups
105
Which DMARD should NOT be used in pregnancy?
Methotrexate is contraindicated, and is teratogenic, causing miscarriage and congenital abnormalities
106
NSAIDS are generally avoided in pregnancy unless really necessary (e.g. in rheumatoid arthritis), when in particular and why?
Particularly in third trimester Can cause premature closure of the ductus arteriosus in the fetus. They can also delay labour.
107
Why can NSAIDs cause problems in pregnancy?
They work by blocking prostaglandins. Prostaglandins are important in maintaining the ductus arteriosus in the fetus and neonate. Prostaglandins also soften the cervix and stimulate uterine contractions at the time of delivery.
108
What problems can beta blockers cause in pregnancy?
Fetal growth restriction Hypoglycaemia in the neonate Bradycardia in the neonate
109
What is the most commonly used beta blocker in pregnancy and what is it used for?
Labetalol is the most frequently used beta-blocker in pregnancy, and is first-line for high blood pressure caused by pre-eclampsia.
110
What can ARBs and ACEi cause if used in pregnancy?
Oligohydramnios (reduced amniotic fluid) Miscarriage or fetal death Hypocalvaria (incomplete formation of the skull bones) Renal failure in the neonate Hypotension in the neonate
111
How can ACEi and ARBs cause Oligohydramnios if used in pregnancy?
Medications that block the renin-angiotensin system (ACE inhibitors and ARBs) can cross the placenta and enter the fetus. In the fetus, they mainly affect the kidneys, and reduce the production of urine (and therefore amniotic fluid).
112
Warfarin crosses the placenta and is considered teratogenic in pregnancy, therefore it is avoided in pregnant women. What can it cause?
Fetal loss Congenital malformations, particularly craniofacial problems Bleeding during pregnancy Postpartum haemorrhage Fetal haemorrhage Intracranial bleeding
113
Lithium is avoided in pregnant women, breastfeeding women, or those planning pregnancy unless other options (i.e. antipsychotics) have failed - why?
Lithium is particularly avoided in the first trimester, as this is linked with congenital cardiac abnormalities in particular, it is associated with Ebstein’s anomaly When lithium is used, levels need to be monitored closely (NICE says every four weeks, then weekly from 36 weeks). Lithium also enters breast milk and is toxic to the infant, so should be avoided in breastfeeding.
114
What congenital abnormality is Lithium particularly associated with in the first trimester of pregnancy?
Ebstein’s anomaly, where the tricuspid valve is set lower on the right side of the heart (towards the apex), causing a bigger right atrium and a smaller right ventricle.
115
Use of SSRIs in pregnancy
Selective serotonin reuptake inhibitors (SSRIs) are the most commonly used antidepressants in pregnancy. SSRIs can cross the placenta into the fetus. The risks need to be balanced against the benefits of treatment. The risks associated with untreated depression can be very significant. Women need to be aware of the potential risks of SSRIs in pregnancy:
116
What is the risk of first trimester use of SSRIs?
First-trimester use has a link with congenital heart defects In particular, paroxetine has a stronger link with congenital malformations
117
What is the risk of third trimester use of SSRIs?
Third-trimester use has a link with persistent pulmonary hypertension in the neonate
118
Implications of taking SSRIs during pregnancy on the neonate?
Neonates can experience withdrawal symptoms, usually only mild and not requiring medical management
119
What common drug used to treat acne is considered dangerous to take during pregnancy?
Isotretinoin is a retinoid medication (relating to vitamin A) that is used to treat severe acne. It should be prescribed and monitored by a specialist dermatologist. Isotretinoin is highly teratogenic, causing miscarriage and congenital defects. Women need very reliable contraception before, during and for one month after taking isotretinoin.
120
Family planning considerations for women taking isotretinoin?
Women need very reliable contraception before, during and for one month after taking isotretinoin.
121
What is neonatal abstinence syndrome (NAS) and when and how does it present?
The use of opiates during pregnancy can cause withdrawal symptoms in the neonate after birth. NAS presents between 3 – 72 hours after birth with: Irritability Tachypnoea (fast breathing) High temperatures Poor feeding
122
Why do autoimmune conditions improve during pregnancy?
The anterior pituitary gland produces more ACTH in pregnancy. Higher ACTH levels cause a rise in steroid hormones, particularly cortisol and aldosterone. Higher steroid levels lead to an improvement in most autoimmune conditions.
123
Why does susceptibility to diabetes and infections increase during pregnancy?
The anterior pituitary gland produces more ACTH in pregnancy. Higher ACTH levels cause a rise in steroid hormones, particularly cortisol and aldosterone. Higher steroid levels lead to a susceptibility to diabetes and infections.
124
Why are pregnant women at increased risk of thromboembolism?
Clotting factors such as fibrinogen and factor VII, VIII and X increase in pregnancy, making women hyper-coagulable.
125
Why do pregnant women have a higher requirement for B12, iron and folate?
There is increased red blood cell production in pregnancy, leading to higher iron, folate and B12 requirements.
126
Why might pregnant women become anaemic?
Plasma volume increases more than red blood cell volume, leading to a lower concentration of red blood cells. High plasma volume means the haemoglobin concentration and red cell concentration (haematocrit) fall in pregnancy, resulting in anaemia.
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Will a pregnant woman with HSV pass protection on to her fetous?
The mother’s antibodies can transfer across the placenta to the fetus during pregnancy. These antibodies allow the fetus to benefit from the long term immunity of the mother during the pregnancy and shortly after birth. The mother’s antibodies to the herpes virus cross the placenta and protect the baby during labour and delivery, preventing infection during birth. This protection does not occur during an initial episode of genital herpes, as the mother has not yet started producing sufficient antibodies against the herpes virus to offer the fetus protection.
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Nageles Rule of EDD
1. Regular periods 2. No hormonal contraception in last 3 months 3. Not lactation EDD=LMP + 9 months and 7 days
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Women at moderate or high risk pre eclampsia should take what, and when?
A woman at moderate or high risk of pre-eclampsia should take aspirin 75-150mg daily from 12 weeks gestation until the birth
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NIPT
NOn invasive prenatal screening test - analyses small DNA fragments that circulate in the blood of a pregnant woman (cell tree 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
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What can the quadruple test suggest risk of?
Down's syndrome Edward's syndrome Neural tube defects
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Edward's syndrome: quadruple test result
↓ AFP ↓ oestriol ↓ hCG ↔ inhibin A
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Patau syndrome: quadruple test result
↑ AFP, ↔ oestriol, ↔ hCG, ↔ inhibin A
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Patau syndrome characteristics
small eyes, cleft lip and polydactyly
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Edwards syndrome characteristics
overlapping fingers and low-set ears
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Why is trace glucosuria not usually and concern in pregnancy?
Trace glycosuria is common in pregnancy due to the increased GFR and reduction in tubular reabsorption of filtered glucose
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Factors associated with miscarriage
Increased maternal age Smoking in pregnancy Consuming alcohol Recreational drug use High caffeine intake Obesity Infections and food poisoning Health conditions, e.g. thyroid problems, severe hypertension, uncontrolled diabetes Medicines, such as ibuprofen, methotrexate and retinoids Unusual shape or structure of womb Cervical incompetence
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Factors commonly mistaken as being associated with miscarriage
Heavy lifting Bumping your tummy Having sex Air travel Being stressed
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Risk factors for breech presentation
uterine malformations, fibroids placenta praevia polyhydramnios or oligohydramnios fetal abnormality (e.g. CNS malformation, chromosomal disorders) prematurity (due to increased incidence earlier in gestation)
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Women with autoimmune conditions such as SLE or antiphospholipid syndrome are at high risk of what?
Pre eclampsia
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When should iron replacement be considered in the first trimester of pregnancy?
A cut-off of 110 g/Lshould be used in the first trimester to determine if iron supplementation should be taken
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Down’s syndrome quadruple test result
↓ AFP ↓ oestriol ↑ hCG ↑ inhibin A
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At what gestation would a referral to the maternal fetal medicine unit for a presentation of absence of feotal movements?
24 weeks
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Risks of ondansetron use in first trimester
Ondansetron during pregnancy is associated with a small increased risk of cleft palate/lip - the MHRA advise that these risks need to be discussed with the pregnant woman before use
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Metoclopramide is an option for nausea and vomiting in pregnancy, but it should not be used for more than a given period? How long is this period and what is the reason!?
5 days, due to risk of extrapyramidal effects
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What should be done in gestational diabetes, if blood glucose targets are not met with diet/metformin?
insulin should be added
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Plasma glucose targets in pregnancy?
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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Why are pregnant women more susceptible to thyrotoxicosis?
The biochemical structure of beta hCG is very similar to that of luteinizing hormone (LH), follicle-stimulating hormone (FSH), and thyroid-stimulating hormone (TSH). That being said, high levels of beta hCG can stimulate the thyroid gland to produce thyroxine (T4), and then triiodothyronine (T3). This can result in signs and symptoms of thyrotoxicosis. High levels of T4 and T3 have a negative feedback effect on the pituitary gland to stop secretion of TSH, causing and overall reduction in TSH levels.
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Ovarian cysts in pregnancy?
In early pregnancy, ovarian cysts are usually physiological - known as a corpus luteum. They will usually resolve from the second trimester on wards.
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What sign of pre eclampsia is particularly specific to the condition?
Brisk reflexes
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Formal definition of pre eclampsia
new-onset blood pressure ≥ 140/90 mmHg after 20 weeks of pregnancy, AND 1 or more of the following: - proteinuria - other organ involvement: e.g. renal insufficiency (creatinine ≥ 90 umol/L), liver, neurological, haematological, uteroplacental dysfunction
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Features of severe pre eclampsia
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
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For patients with intrauterine fibroids, what can be given while surgery is awaited.
For patients with uterine fibroids, GnRH agonists may reduce the size of the fibroid but are typically useful for short-term treatment E.g. Triptorelin
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Acute fatty liver of pregnancy typical presentation
jaundice, mild pyrexia, hepatitic LFTs, raised WBC, coagulopathy and steatosis on imaging Clinically, acute fatty liver of pregnancy has predominantly non-specific symptoms (e.g. malaise, fatigue, nausea)
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If low-lying placenta is found at the 20-week scan what should be done?
Rescan at 32 weeks to assess
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Haemoglobin lower than what is the cut-off level to prescribe iron replacement therapy in women during the second and third trimesters?
105 g/L
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What should be done for all pregnant women regardless of station following abdominal trauma?
A pregnant woman with abdominal trauma should have Rhesus testing asap because women who are Rhesus-negative should be given anti-D to prevent Rhesus isoimmunization.
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Managing pregnant women at high risk of VTE
Low molecular weight heparin (LMWH) antenatally + 6 weeks postpartum
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Suspected cases of rubella in pregnancy should be discussed with who?
the local Health Protection Unit
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Fibroid degeneration may develop during pregnancy, presenting how?
Presenting with low-grade fever, pain and vomiting.
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Pregnant women > 20 weeks presenting with symptoms of chicken pox
Pregnant women ≥ 20 weeks who develop chickenpox are generally treated with oral aciclovir if they present within 24 hours of the rash
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What is a Kleihauer test and when is it required?
A Kleihauer test is a test for FMH (fetomaternal haemorrhage) which detects fetal cells in the maternal circulation and, if present, estimates the volume of FMH to allow calculation of additional anti-D immunoglobulin. According to BCSH guidelines, it is required for any sensitising event after 20 weeks gestation.
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What food acquired infections should pregnant women be warned about?
listeriosis: avoid unpasteurised milk, ripened soft cheeses (Camembert, Brie, blue-veined cheeses), pate or undercooked meat salmonella: avoid raw or partially cooked eggs and meat, especially poultry
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What food should be avoided due to concerns re teratogenicity?
Liver - contains high levels of vitamin A (a teratogen)
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First line management of NVP/hyperemesis gravidarum?
Antihistamines e.g. CYCLIZINE are first-line in the management of nausea & vomiting in pregnancy/hyperemesis gravidarum
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Second line management of NVP/hyperemesis gravidarum?
Ondansetron (a 5-HT3 reception antagonist) and domperidone (dopamine receptor antagonist) are second-line antiemetic.
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RCOG guidance on monitoring of women on LMWH for treatment of acute VTE in pregnancy
'Routine measurement of peak anti-Xa activity for patients on LMWH for treatment of acute VTE in pregnancy or postpartum is not recommended except in women at extremes of body weight (less than 50 kg and 90 kg or more) or with other complicating factors (for example, with renal impairment or recurrent VTE).' 'Routine platelet count monitoring should not be carried out.'
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First dose of anti-D prophylaxis to rhesus negative women should be given when
28 weeks
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When should the anomaly scan occur
18 - 20+6 weeks
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When should the dating scan occur
10 - 13+6 weeks
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When gestation diabetes is diagnosed, when should insulin be commenced immediately?
Gestational diabetes - insulin should be commenced if fasting glucose level is >= 7 mmol/l insulin at the time of diagnosis
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If a pregnant woman reports reduced fetal movements what is the first line investigation?
handheld Doppler should be used to confirm fetal heartbeat as a first step (CTG is incorrect in this situation as it is only used to assess reduced foetal movement once viability has been confirmed. The viability must be initially confirmed with a handheld doppler to detect a foetal heartbeat.)
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Which pregnant women should be screened for gestational diabetes with an oral glucose tolerance test (OGTT) at 24-28 weeks?
Women who have a first degree relative with diabetes History of a previous macrosomic baby weight of 4.5kg or more BMI above 30 kg/m² Ethnicity with high prevalence of diabetes Previous gestational diabetes
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If after 28/40 weeks, if a woman reports reduced fetal movements and no heart is detected with handheld Doppler then what should be offered
Immediate ultrasound
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GDM blood sugar targets
Pregnant women with GDM should be advised to maintain their CBGs below the following target levels: fasting: 5.3mmol/L AND 1 hour postprandial: 7.8 mmol/L or 2 hours postprandial: 6.4 mmol/L
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Alternatives to antihistamines as first line to treat NVP/hyperemesis gravidarum
oral prochlorperazine is an alternative
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Previous pregnancy Risk factors for consultant lead care
Unexplained stillbirth/neonatal death or previous death related to intrapartum difficulty Previous baby with neonatal encephalopathy Pre-eclampsia requiring preterm birth Placental abruption with adverse outcome Eclampsia Uterine rupture Primary postpartum hemorrhage requiring additional treatment or blood transfusion Retained placenta requiring manual removal in theatre Caesarean section Shoulder dystocia
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Why should bimanual examination be avoided in women with placenta praevia
risk of causing worsening bleeding, which can lead to hypovolaemic shock in severe cases.
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Risk of vertical transmission in pregnant women with hep B
Without intervention the vertical transmission rate is around 20%, which increases to 90% if the woman is positive for HBeAg.
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Pregnant women with blood pressure above what are likely to be admitted and observed, regardLess of symptoms of proteinuria?
≥ 160/110 mmHg
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Definitive treatment for obstetric cholestasis
ursodeoxycholic acid
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How is placental abruptiom characterised
Placental abruption is characterised by constant pain, shock out of keeping with the visible loss, tender and tense uterus
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Increased BMI implications on pregnancy and birth
BMI>30 screen for GDM Increased risk PPH INcreased risk of still birth Increased risk of vit D def Increased risk of intra+PP VTE Increased risk of HTN and pre eclampsia SFH less likely to be accurate, BMI > 35 refer for serial fetal growth USS
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Normal fundal height increase after 24 weeks
After 24 weeks you would only expect the fundal height to increase by 1cm a week.
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Raised AFP in pregnancy
AFP - raised with fetal abdominal wall defects (e.g. omphalocele)
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Risk factors for placental abruption
A for Abruption previously; B for Blood pressure (i.e. hypertension or pre-eclampsia); R for Ruptured membranes, either premature or prolonged; U for Uterine injury (i.e. trauma to the abdomen); P for Polyhydramnios; T for Twins or multiple gestation; I for Infection in the uterus, especially chorioamnionitis; O for Older age (i.e. aged over 35 years old); N for Narcotic use (i.e. cocaine and amphetamines, as well as smoking)
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In which stage of pregnancy is rubella most harmful to the fetus
During the first 10 weeks
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When can congenital rubella syndrome occur
When mother is infected by rubella virus within first 20 weeks of pregnancy
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Pregnancy and MMR vaccine
Women planning to become pregnant should ensure they have had the MMR vaccine. When in doubt, they can be tested for rubella immunity. If they do not have antibodies to rubella, they can be vaccinated with two doses of the MMR, three months apart. Pregnant women should not receive the MMR vaccination, as this is a live vaccine. Non-immune women should be offered the vaccine after giving birth.
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What are the features of congenital rubella syndrome
Congenital deafness Congenital cataracts Congenital heart disease (PDA and pulmonary stenosis) Learning disability
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Why is chickenpox dangerous in pregnancy?
Chickenpox is caused by the varicella zoster virus (VZV). It is dangerous in pregnancy because it can lead to: More severe cases in the mother, such as varicella pneumonitis, hepatitis or encephalitis Fetal varicella syndrome Severe neonatal varicella infection (if infected around delivery)
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Chicken pox exposure during pregnancy?
Mothers that have previously had chickenpox are immune and safe. When in doubt, IgG levels for VZV can be tested. A positive IgG for VZV indicates immunity. Women that are not immune to varicella may be offered the varicella vaccine before or after pregnancy. Exposure to chickenpox in pregnancy: When the pregnant woman has previously had chickenpox, they are safe When they are not sure about their immunity, test the VZV IgG levels. If positive, they are safe. When they are not immune, they can be treated with IV varicella immunoglobulins as prophylaxis against developing chickenpox. This should be given within ten days of exposure.
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If a woman who is pregnant develops a chickenpox rash during pregnancy, when can she be treated?
When the chickenpox rash starts in pregnancy, they may be treated with oral aciclovir if they present within 24 hours and are more than 20 weeks gestation.
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What is congenital varicella syndrome
Congenital varicella syndrome occurs in around 1% of cases of chickenpox in pregnancy. It occurs when infection occurs in the first 28 weeks of gestation. The typical features include: Fetal growth restriction Microcephaly, hydrocephalus and learning disability Scars and significant skin changes located in specific dermatomes Limb hypoplasia (underdeveloped limbs) Cataracts and inflammation in the eye (chorioretinitis)
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What is listeria and why is it a concern in pregnancy?
Listeria is an infectious gram-positive bacteria that causes listeriosis. Listeriosis is many times more likely in pregnant women compared with non-pregnant individuals. Infection in the mother may be asymptomatic, cause a flu-like illness, or less commonly cause pneumonia or meningoencephalitis. Listeriosis in pregnant women has a high rate of miscarriage or fetal death. It can also cause severe neonatal infection. Listeria is typically transmitted by unpasteurised dairy products, processed meats and contaminated foods. Pregnant women are advised to avoid high-risk foods (e.g. blue cheese) and practice good food hygiene.
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Congenital cytomegalovirus infection
Congenital cytomegalovirus infection occurs due to a cytomegalovirus (CMV) infection in the mother during pregnancy. The virus is mostly spread via the infected saliva or urine of asymptomatic children. Most cases of CMV in pregnancy do not cause congenital CMV.
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What are the features of congenital cytomegalovirus infection
Fetal growth restriction Microcephaly Hearing loss Vision loss Learning disability Seizures
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Toxoplasmosis in pregnancy
Infection with the Toxoplasma gondii parasite is usually asymptomatic. It is primarily spread by contamination with faeces from a cat that is a host of the parasite. When infection occurs during pregnancy, it can lead to congenital toxoplasmosis. The risk is higher later in the pregnancy.
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Triad of features of toxoplasmosis
Intracranial calcification Hydrocephalus Chorioretinitis (inflammation of the choroid and retina in the eye)
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Fifth disease in pregnancy
Parvovirus B19 infection typically affects children. It is also known as fifth disease, slapped cheek syndrome and erythema infectiosum. It is caused by the parvovirus B19 virus. The illness is self-limiting, and the rash and symptoms usually fade over 1 – 2 weeks. Parvovirus infection starts with non-specific viral symptoms. After 2 – 5 days, the rash appears quite rapidly as a diffuse bright red rash on both cheeks, as though they have “slapped cheeks”. A few days later a reticular mildly erythematous rash affecting the trunk and limbs appears, which can be raised and itchy. Reticular means net-like. Healthy children and adults have a low risk of any complications, and management is supportive. They are infectious 7 – 10 days before the rash appears. They are not infectious once the rash has appeared. Significant exposure to parvovirus is classed as 15 minutes in the same room, or face-to-face contact, with someone that has the virus. Infections with parvovirus B19 in pregnancy can lead to several complications, particularly in the first and second trimesters.
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When is parvovirus 19 most dangerous in pregnancy
First two trimesters
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Infections with parvovirus B19 in pregnancy can lead to several complications, particularly in the first and second trimesters, such as what?
Miscarriage or fetal death Severe fetal anaemia Hydrops fetalis (fetal heart failure) Maternal pre-eclampsia-like syndrome
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How can maternal parvovirus 19 infection cause fetal anaemia +/- hydrops fetalis?
Fetal anaemia is caused by parvovirus infection of the erythroid progenitor cells in the fetal bone marrow and liver. These cells produce red blood cells, and the infection causes them to produce faulty red blood cells that have a shorter life span. Less red blood cells results in anaemia. This anaemia leads to heart failure, referred to as hydrops fetalis.
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What is maternal pre-eclampsia-like syndrome and what are the features
Maternal pre-eclampsia-like syndrome is also known as mirror syndrome. It can be a rare complication of severe fetal heart failure (hydrops fetalis). It involves a triad of hydrops fetalis, placental oedema and oedema in the mother. It also features hypertension and proteinuria.
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Suspected parvovirus infection in pregnancy
IgM to parvovirus, which tests for acute infection within the past four weeks IgG to parvovirus, which tests for long term immunity to the virus after a previous infection Rubella antibodies (as a differential diagnosis)
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Management of parvovirus 19 in pregnancy?
Treatment is supportive. Women with parvovirus B19 infection need a referral to fetal medicine to monitor for complications and malformations.
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What is Zika virus and why is it a concern in pregnancy
The zika virus is spread by host Aedes mosquitos in areas of the world where the virus is prevalent. It can also be spread by sex with someone infected with the virus. It can cause no symptoms, minimal symptoms, or a mild flu-like illness. In pregnancy, it can lead to congenital Zika syndrome,
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Features of congenital zika syndrome
Microcephaly Fetal growth restriction Other intracranial abnormalities, such as ventriculomegaly and cerebellar atrophy
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Management of suspected Zika virus in pregnancy
Pregnant women that may have contracted the Zika virus should be tested with viral PCR and antibodies to the Zika virus. Women with a positive result should be referred to fetal medicine for close monitoring of the pregnancy. There is no treatment for the virus.
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What is meant by rhesus negative/positive
Within the rhesus group, many different types of antigens can be present or absent, depending on the person’s blood type. The most relevant antigen within the rhesus blood group system is the rhesus-D antigen. When we refer to someone’s rhesus status in relation to pregnancy (e.g. “she is rhesus-negative”), we are usually referring to whether they have the rhesus-D antigen present on their red blood cell surface.
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When a woman that is rhesus-D negative becomes pregnant, we have to consider the possibility that her child will be rhesus positive - why?
It is likely at some point in the pregnancy (i.e. childbirth) that the blood from the baby will find a way into the mother’s bloodstream. When this happens, the baby’s red blood cells display the rhesus-D antigen. The mother’s immune system will recognise this rhesus-D antigen as foreign, and produce antibodies to the rhesus-D antigen. The mother has then become sensitised to rhesus-D antigens. Usually, this sensitisation process does not cause problems during the first pregnancy. During subsequent pregnancies, the mother’s anti-rhesus-D antibodies can cross the placenta into the fetus. If that fetus is rhesus-D positive, these antibodies attach themselves to the red blood cells of the fetus and causes the immune system of the fetus to attack them, causing the destruction of the red blood cells (haemolysis). The red blood cell destruction caused by antibodies from the mother is called haemolytic disease of the newborn.
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What is the mainstay of rhesus-D negative management during pregnancy and why is it important
Prevention of sensitisation is the mainstay of management. This involves giving intramuscular anti-D injections to rhesus-D negative women. There is no way to reverse the sensitisation process once it has occurred, which is why prophylaxis is so essential.
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When is anti d given in pregnancy
28 weeks gestation Birth (if the baby’s blood group is found to be rhesus-positive)
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How does anti D work to prevent sensitisation
The anti-D medication works by attaching itself to the rhesus-D antigens on the fetal red blood cells in the mothers circulation, causing them to be destroyed. This prevents the mother’s immune system recognising the antigen and creating it’s own antibodies to the antigen. It acts as a prevention for the mother becoming sensitised to the rhesus-D antigen.
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Other than at 28 weeks gestation and at birth, when should rhesus negative women be given anti-D
Anti-D injections should also be given at any time where sensitisation may occur, such as: Antepartum haemorrhage Amniocentesis procedures Abdominal trauma
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Within what time period should anti D be given after a sensitisation event has occured
Anti-D is given within 72 hours of a sensitisation event
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What is The Kleihauer test and when is it done?
The Kleihauer test checks how much fetal blood has passed into the mother’s blood during a sensitisation event. This test is used after any sensitising event past 20 weeks gestation, to assess whether further doses of anti-D is required. The Kleihauer test involves adding acid to a sample of the mother’s blood. Fetal haemoglobin is naturally more resistant to acid, so that they are protected against the acidosis that occurs around childbirth. Therefore, fetal haemoglobin persists in response to the added acid, while the mothers haemoglobin is destroyed. The number of cells still containing haemoglobin (the remaining fetal cells) can then be calculated.
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What is small for gestational age defined as?
Small for gestational age is defined as a fetus that measures below the 10th centile for their gestational age.
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What measurements on USS are used to measure fetal size?
Estimated fetal weight (EFW) Fetal abdominal circumference (AC)
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Customised growth charts are used to assess the size of the fetus, based on what?
Customised growth charts are used to assess the size of the fetus, based on the mother’s: Ethnic group Weight Height Parity
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What is severe SGA
Severe SGA is when the fetus is below the 3rd centile for their gestational age
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What are the two categories of causes of SGA
Constitutionally small, matching the mother and others in the family, and growing appropriately on the growth chart Fetal growth restriction (FGR), also known as intrauterine growth restriction (IUGR)
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What is FGR
Fetal growth restriction (FGR), also known as intrauterine growth restriction (IUGR), is when there is a small fetus (or a fetus that is not growing as expected) due to a pathology reducing the amount of nutrients and oxygen being delivered to the fetus through the placenta. Higher risk of morbidity and mortality
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What are the two categories of FGR
Placenta mediated growth restriction Non-placenta mediated growth restriction, where the baby is small due to a genetic or structural abnormality
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Placenta mediated growth restriction refers to conditions that affect the transfer of nutrients across the placenta, such as what?
Idiopathic Pre-eclampsia Maternal smoking Maternal alcohol Anaemia Malnutrition Infection Maternal health conditions
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Non-placenta medicated growth restriction refers to pathology of the fetus, such as?
Genetic abnormalities Structural abnormalities Fetal infection Errors of metabolism
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Signs of FGR
SGA Reduced amniotic fluid volume Abnormal Doppler studies Reduced fetal movements Abnormal CTGs
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Short term complications of FGA?
Fetal death or stillbirth Birth asphyxia Neonatal hypothermia Neonatal hypoglycaemia
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What are babies with growth restriction at increased risk of long term?
Cardiovascular disease, particularly hypertension Type 2 diabetes Obesity Mood and behavioural problems
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Risk factors for SGA
Previous SGA baby Obesity Smoking Diabetes Existing hypertension Pre-eclampsia Older mother (over 35 years) Multiple pregnancy Low pregnancy‑associated plasma protein‑A (PAPPA) Antepartum haemorrhage Antiphospholipid syndrome
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At the booking clinic, women are assessed for risk factors for SGA. How are low risk women subsequently monitored?
Low-risk women have monitoring of the symphysis fundal height (SFH) at every antenatal appointment from 24 weeks onwards to identify potential SGA. The SFH is plotted on a customised growth chart to assess the appropriate size for the individual woman. If the symphysis fundal height is less than the 10th centile, women are booked for serial growth scans with umbilical artery doppler. Women are booked for serial growth scans with umbilical artery doppler if they have: Three or more minor risk factors One or more major risk factors Issues with measuring the symphysis fundal height (e.g. large fibroids or BMI > 35)
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At the booking clinic, women are assessed for risk factors for SGA. How are high risk women subsequently monitored?
Women at risk or with SGA are monitored closely with serial ultrasound scans measuring: Estimated fetal weight (EFW) and abdominal circumference (AC) to determine the growth velocity Umbilical arterial pulsatility index (UA-PI) to measure flow through the umbilical artery Amniotic fluid volume The local guidelines for the initiation and frequency of ultrasound scans may vary. An example regime is a growth scan every four weeks from 28 weeks gestation. Ultrasound frequency is increased where there is reduced growth velocity or problems with umbilical flow.
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At the booking clinic, women are assessed for risk factors for SGA. How are low risk women subsequently monitored?
Women at risk or with SGA are monitored closely with serial ultrasound scans measuring: Estimated fetal weight (EFW) and abdominal circumference (AC) to determine the growth velocity Umbilical arterial pulsatility index (UA-PI) to measure flow through the umbilical artery Amniotic fluid volume The local guidelines for the initiation and frequency of ultrasound scans may vary. An example regime is a growth scan every four weeks from 28 weeks gestation. Ultrasound frequency is increased where there is reduced growth velocity or problems with umbilical flow.
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What does increased ultrasound frequency suggest?
reduced growth velocity or problems with umbilical flow.
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What is large for gestation age
During pregnancy, an estimated fetal weight above the 90th centile is considered large for gestational age.
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Causes of macrosomia
Constitutional Maternal diabetes Previous macrosomia Maternal obesity or rapid weight gain Overdue Male baby
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Macrosomia risks to the baby
Shoulder dystocia Failure to progress Perineal tears Instrumental delivery or caesarean Postpartum haemorrhage Uterine rupture (rare)
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Macrosomia - risk to the baby
Birth injury (Erbs palsy, clavicular fracture, fetal distress and hypoxia) Neonatal hypoglycaemia Obesity in childhood and later life Type 2 diabetes in adulthood
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Investigations for LGA
Ultrasound to exclude polyhydramnios and estimate the fetal weight Oral glucose tolerance test for gestational diabetes
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The main risk with a large for gestational age baby is shoulder dystocia. The risks at delivery can be reduced how?
The main risk with a large for gestational age baby is shoulder dystocia. The risks at delivery can be reduced by: Delivery on a consultant lead unit Delivery by an experienced midwife or obstetrician Access to an obstetrician and theatre if required Active management of the third stage (delivery of the placenta) Early decision for caesarean section if required Paediatrician attending the birth
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Monozygotic twins
Monozygotic: identical twins (from a single zygote)
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Dizygotic twins
Dizygotic: non-identical (from two different zygotes)
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Monoamniotic twins
Monoamniotic: single amniotic sac
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Diamniotic twins
Diamniotic: two separate amniotic sacs
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Monochorionic twins
Monochorionic: share a single placenta
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Dichorionic: two separate placentas
Dichorionic twins
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What types of twins have the best outcomes and why
The best outcomes are with diamniotic, dichorionic twin pregnancies, as each fetus has their own nutrient supply.
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When is multiple pregnancy diagnosed
Multiple pregnancy is usually diagnosed on the booking ultrasound scan. Number of placentas (chorionicity) and amniotic sacs (amnionicity)
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Dichorionic diamniotic twins USS
Dichorionic diamniotic twins have a membrane between the twins, with a lambda sign or twin peak sign
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Monochorionic diamniotic twins USS
Monochorionic diamniotic twins have a membrane between the twins, with a T sign
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Monochorionic monoamniotic twins USS
Monochorionic monoamniotic twins have no membrane separating the twins
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What is the lambda sign on USS
The lambda sign, or twin peak sign, refers to a triangular appearance where the membrane between the twins meets the chorion, as the chorion blends partially into the membrane. This indicates a dichorionic twin pregnancy (separate placentas).
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What is the T sign on USS
The T sign refers to where the membrane between the twins abruptly meets the chorion, giving a T appearance. This indicates a monochorionic twin pregnancy (single placenta).
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Multiple pregnancies - risks to mother
Anaemia Polyhydramnios Hypertension Malpresentation Spontaneous preterm birth Instrumental delivery or caesarean Postpartum haemorrhage
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Multiple pregnancies - risk to fetuses/neonates
Miscarriage Stillbirth Fetal growth restriction Prematurity Twin-twin transfusion syndrome Twin anaemia polycythaemia sequence Congenital abnormalities
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What is twin to twin transfusion syndrome
Twin-twin transfusion syndrome occurs when the fetuses share a placenta. It is called feto-fetal transfusion syndrome in pregnancies with more than two fetuses. When there is a connection between the blood supplies of the two fetuses, one fetus (the recipient) may receive the majority of the blood from the placenta, while the other fetus (the donor) is starved of blood. The recipient gets the majority of the blood, and can become fluid overloaded, with heart failure and polyhydramnios. The donor has growth restriction, anaemia and oligohydramnios. There will be a discrepancy between the size of the fetuses. Women with twin-twin transfusion syndrome need to be referred to a tertiary specialist fetal medicine centre. In severe cases, laser treatment may be used to destroy the connection between the two blood supplies.
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What is twin anaemia polycythaemia sequence
Twin anaemia polycythaemia sequence is similar to twin-twin transfusion syndrome, but less acute. One twin becomes anaemic whilst the other develops polycythaemia (raised haemoglobin).
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Monitoring in twin pregnancies
Women with multiple pregnancies require additional monitoring for anaemia, with a full blood count at: Booking clinic: 20 weeks gestation 28 weeks gestation Additional ultrasound scans are required in multiple pregnancy to monitor for fetal growth restriction, unequal growth and twin-twin transfusion syndrome: 2 weekly scans from 16 weeks for monochorionic twins 4 weekly scans from 20 weeks for dichorionic twins
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What type of twins require 2 weekly scans and from when
2 weekly scans from 16 weeks for monochorionic twins
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What type of twins require 4 weekly scans and from when
4 weekly scans from 20 weeks for dichorionic twins
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Planned birth is offered when for uncomplicated monochorionic monoamniotic twins
32-33+6 weeks
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Planned birth is offered when for uncomplicated monochorionic diamniotic twins
36 and 36+6 weeks
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Planned birth is offered when for uncomplicated dichorionic diamniotic twins
37 and 37+6 weeks
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Planned birth is offered when for triplets
Before 35 + 6 weeks for triplets
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Pregnant women are at higher risk of developing lower urinary tract infections (cystitis) and pyelonephritis (infection of kidneys). Why is this a problem?
Urinary tract infections in pregnant women increase the risk of preterm delivery. They may also increase the risk of other adverse pregnancy outcomes, such as low birth weight and pre-eclampsia.
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What is asymptomatic bacterium in and why is it a problem in pregnancy?
Asymptomatic bacteriuria refers to bacteria present in the urine, without symptoms of infection. Pregnant women with asymptomatic bacteriuria are at higher risk of developing lower urinary tract infections and pyelonephritis, and subsequently at risk of preterm birth.
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Monitoring of urine in pregnancy
Pregnant women are tested for asymptomatic bacteriuria and other abnormalities at booking and routinely throughout pregnancy. This involves sending a urine sample to the lab for microscopy, culture and sensitivities (MC&S). Testing for bacteria in the urine of asymptomatic patients is not recommended as it may lead to unnecessary antibiotics. Pregnant women are an exception to this rule, due to the adverse outcomes associated with infection.
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How might a lower urinary tract infection present
Dysuria (pain, stinging or burning when passing urine) Suprapubic pain or discomfort Increased frequency of urination Urgency Incontinence Haematuria
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How might an upper urinary tract infection (pyelonephritis) present
Fever (more prominent than in lower urinary tract infections) Loin, suprapubic or back pain (this may be bilateral or unilateral) Looking and feeling generally unwell Vomiting Loss of appetite Haematuria Renal angle tenderness on examination
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Causative organisms of UTI
Most common cause of urinary tract infection is Escherichia coli (E. coli). This is a gram-negative, anaerobic, rod-shaped bacteria that is part of the normal lower intestinal microbiome. It is found in faeces, and can easily spread to the bladder. Other causes: Klebsiella pneumoniae (gram-negative anaerobic rod) Enterococcus Pseudomonas aeruginosa Staphylococcus saprophyticus Candida albicans (fungal)
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Managing uti in pregnancy
Urinary tract infection in pregnancy requires 7 days of antibiotics. The antibiotic options are: Nitrofurantoin (avoid in the third trimester) Amoxicillin (only after sensitivities are known) Cefalexin
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Which antibiotic used to treat UTIs must be avoided in the first trimester and why
Trimethoprim needs to be avoided in the first trimester as it is works as a folate antagonist. Folate is important in early pregnancy for the normal development of the fetus. Trimethoprim in early pregnancy can cause congenital malformations, particularly neural tube defects (i.e. spina bifida). It is not known to be harmful later in pregnancy, but is generally avoided unless necessary.
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What antibiotic may be used to treat UTI IN pregnancy but must be avoided in the third trimester and why
Nitrofurantoin needs to be avoided in the third trimester as there is a risk of neonatal haemolysis (destruction of the neonatal red blood cells).
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When are women routinely tested for anaemia in pregnancy
Booking clinic 28 weeks gestation
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Why does pregnancy increase the risk of anaemia and why is this significant
During pregnancy, the plasma volume increases. This results in a reduction in the haemoglobin concentration. The blood is diluted due to the higher plasma volume. It is important to optimise the treatment of anaemia during pregnancy so that the woman has reasonable reserves, in case there is significant blood loss during delivery.
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How might pregnant women with anaemia present
Asymptomatic Shortness of breath Fatigue Dizziness Pallor
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The mean cell volume (MCV) can indicate the cause of the anaemia - how?
Low MCV may indicate iron deficiency Normal MCV may indicate a physiological anaemia due to the increased plasma volume of pregnancy Raised MCV may indicate B12 or folate deficiency
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What haematological screening is performed at booking clinic
Women are offered haemoglobinopathy screening at the booking clinic for thalassaemia (all women) and sickle cell disease (women at higher risk). Both are causes of significant anaemia in pregnancy.
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What additional investigations other than MCV may help establish the cause of anaemia
Additional investigations are not routinely performed, by may help establish the cause of the anaemia. They may include: Ferritin B12 Folate
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Management of anaemia in pregnancy
IRON Women with anaemia in pregnancy are started on iron replacement (e.g. ferrous sulphate 200mg three times daily). When women are not anaemic, but have a low ferritin (indicating low iron stores), they may be started on supplementary iron. B12 The increased plasma volume and B12 requirements often result in a low B12 in pregnancy. Women with low B12 should be tested for pernicious anaemia (checking for intrinsic factor antibodies). Advice should be sought from a haematologist regarding further investigations and treatment of low B12 in pregnancy. Treatment options for low B12 are: Intramuscular hydroxocobalamin injections Oral cyanocobalamin tablets FOLATE All women should already be taking folic acid 400mcg per day. Women with folate deficiency are started on folic acid 5mg daily. THALASSAEMIA AND SICKLE CELL ANAEMIA Women with a haemoglobinopathy will be managed jointly with a specialist haematologist. They require high dose folic acid (5mg), close monitoring and transfusions when required.
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What risk factors increase the risk of VTE in pregnancy
Smoking Parity ≥ 3 Age > 35 years BMI > 30 Reduced mobility Multiple pregnancy Pre-eclampsia Gross varicose veins Immobility Family history of VTE Thrombophilia IVF pregnancy
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When do the RCOG reccomend VTE prophylaxis be started in pregnancy
28 weeks if there are three risk factors First trimester if there are four or more of these risk factors
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Scenarios where VTE prophylaxis may be indicated in pregnancy despite lack of the risk factors given by RCOG
Hospital admission Surgical procedures Previous VTE Medical conditions such as cancer or arthritis High-risk thrombophilias Ovarian hyperstimulation syndrome
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When are pregnant women assessed for risk of VTE
All pregnant women should have a risk assessment for their risk of venous thromboembolism (VTE) at booking. A risk assessment is performed again after birth. Additional risk assessments are necessary at other times, such as if they are admitted to hospital, undergo a procedure or develop significant immobility Each unit will have a policy and protocol for assessing risk and starting prophylaxis in pregnancy.
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What prophylaxis is given against VTE in pregnancy
Women at increased risk of VTE should receive prophylaxis with low molecular weight heparin (LMWH) unless contraindicated. Examples of LMWH are enoxaparin, dalteparin and tinzaparin. Prophylaxis is started as soon as possible in very high risk patients and at 28 weeks in those at high risk. It is continued throughout the antenatal period and for six weeks postnatally. Prophylaxis is temporarily stopped when the woman goes into labour, and can be started immediately after delivery (except with postpartum haemorrhage, spinal anaesthesia and epidurals).
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Mechanical prophylaxis may be considered in women with contraindications to LMWH. The options for mechanical prophylaxis are what?
Intermittent pneumatic compression with equipment that inflates and deflates to massage the legs Anti-embolic compression stockings
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DVT presentation
Deep vein thrombosis is almost always unilateral. Bilateral DVTs are rare, and bilateral symptoms are more likely due to an alternative diagnosis such as chronic venous insufficiency or heart failure. DVTs present with: Calf or leg swelling Dilated superficial veins Tenderness to the calf (particularly over the deep veins) Oedema Colour changes to the leg To examine for leg swelling measure the circumference of the calf 10cm below the tibial tuberosity. More than 3cm difference between calves is significant.
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PE PRESENTATION
Pulmonary embolism can present with subtle signs and symptoms. In patients with potential features of a PE, risk factors for PE, and no other explanation for their symptoms, have a low threshold for suspecting a PE. Presenting features include: Shortness of breath Cough with or without blood (haemoptysis) Pleuritic chest pain Hypoxia Tachycardia (this can be difficult to distinguish from the normal physiological changes in pregnancy) Raised respiratory rate Low-grade fever Haemodynamic instability causing hypotension
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Diagnosing DVT/PE in pregnancy
Doppler ultrasound is the investigation of choice for patients with suspected deep vein thrombosis. The RCOG guideline (2015) recommends repeating negative ultrasound scans on day 3 and 7 in patients with a high index of suspicion for DVT. Women with suspected pulmonary embolism require: Chest xray ECG There are two main options for establishing a definitive diagnosis: CT pulmonary angiogram (CTPA) or ventilation-perfusion (VQ) scan. CT pulmonary angiogram involves a chest CT scan with an intravenous contrast that highlights the pulmonary arteries to demonstrate any blood clots. This is usually the first choice for investigating a pulmonary embolism, as it tends to be more readily available, provides a more definitive assessment and gives information about alternative diagnoses such as pneumonia or malignancy. Ventilation-perfusion (VQ) scan involves using radioactive isotopes and a gamma camera, to compare the ventilation with the perfusion of the lungs. First, the isotopes are inhaled to fill the lungs, and a picture is taken to demonstrate ventilation. Next, a contrast containing isotopes is injected, and a picture is taken to demonstrate perfusion. The two images are compared. With a pulmonary embolism, there will be a deficit in perfusion, as the thrombus blocks blood flow to the lung tissue. This area of lung tissue will be ventilated but not perfused. When considering the choice between CTPA and VQ scan: CTPA is the test for choice for patients with an abnormal chest xray CTPA carries a higher risk of breast cancer for the mother (minimal absolute risk) VQ scan carriers a higher risk of childhood cancer for the fetus (minimal absolute risk) Patients with a suspected deep vein thrombosis and pulmonary embolism should have a Doppler ultrasound initially, and if a DVT is present, they do not require a VQ scan or CTPA to confirm a PE. The treatment for DVT and PE are the same.
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What tests/screening associated with VTE are not used in pregnant women
The Wells score is not validated for use in pregnant women. D-dimers are not helpful in pregnant patients, as pregnancy is a cause of a raised D-dimer.
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Management of VTE in pregnancy
Management of venous thromboembolism in pregnancy is with low molecular weight heparin (LMWH). Examples of LMWH are enoxaparin, dalteparin and tinzaparin. The dose is based on the woman’s weight at the booking clinic, or from early pregnancy. LMWH should be started immediately, before confirming the diagnosis in patients where DVT or PE is suspected and there is a delay in getting the scan. Treatment can be stopped when the investigations exclude the diagnosis. When the diagnosis is confirmed, LMWH is continued for the remained of pregnancy, plus six weeks postnatally, or three months in total (whichever is longer). There is an option to switch to oral anticoagulation (e.g. warfarin or a DOAC) after delivery. An individual risk assessment is performed before stopping anticoagulation, with advice from a haematologist if necessary. Women with a massive PE and haemodynamic compromise need immediate management by an experienced team of medical doctors, obstetricians, radiologists and others. This is a life-threatening scenario. Treatment options are: Unfractionated heparin Thrombolysis Surgical embolectomy
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Why does gestational diabetes occur
Gestational diabetes refers to diabetes triggered by pregnancy. It is caused by reduced insulin sensitivity during pregnancy, and resolves after birth.
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Complications of gestation diabetes?
The most significant immediate complication of gestational diabetes is a large for dates fetus and macrosomia. This has implications for birth, mainly posing a risk of shoulder dystocia. Longer-term, women are at higher risk of developing type 2 diabetes after pregnancy. P
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Screening for gestational diabetes
Anyone with risk factors should be screened with an oral glucose tolerance test at 24 – 28 weeks gestation. Women with previous gestational diabetes also have an OGTT soon after the booking clinic.
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Risk factors that warrant testing for gestational diabetes
Previous gestational diabetes Previous macrosomic baby (≥ 4.5kg) BMI > 30 Ethnic origin (black Caribbean, Middle Eastern and South Asian) Family history of diabetes (first-degree relative)
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Features other than maternal risk factors that may be suggestive of gestational diabetes that therefore warrant OGGT
Large for dates fetus Polyhydramnios (increased amniotic fluid) Glucose on urine dipstick
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How should an OGTT be performed
An OGTT should be performed in the morning after a fast (they can drink plain water). The patient drinks a 75g glucose drink at the start of the test. The blood sugar level is measured before the sugar drink (fasting) and then at 2 hours.
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OGGT results
Normal results are: Fasting: < 5.6 mmol/l At 2 hours: < 7.8 mmol/l Results higher than these values are used to diagnose gestational diabetes. (5 6 7 8]
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Management of gestational diabetes
Patients with gestational diabetes are managed in joint diabetes and antenatal clinics, with input from a dietician. Women need careful explanation about the condition, and to learn how to monitor and track their blood sugar levels. Four weekly ultrasound scans to monitor the fetal growth and amniotic fluid volume from 28 to 36 weeks gestation. The initial management suggested by the NICE guidelines (2015) is: Fasting glucose less than 7 mmol/l: trial of diet and exercise for 1-2 weeks, followed by metformin, then insulin Fasting glucose above 7 mmol/l: start insulin ± metformin Fasting glucose above 6 mmol/l plus macrosomia (or other complications): start insulin ± metformin Glibenclamide (a sulfonylurea) is suggested as an option for women who decline insulin or cannot tolerate metformin. Women need to monitor their blood sugar levels several times a day. The NICE (2015) target levels are: Fasting: 5.3 mmol/l 1 hour post-meal: 7.8 mmol/l 2 hours post-meal: 6.4 mmol/l Avoiding levels of 4 mmol/l or below
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What is a suggested option for women with gestational diabetes who decline insulin and cannot tolerate metformin
Glibenclamide (a sulfonylurea) is suggested as an option for women who decline insulin or cannot tolerate metformin.
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Gestational diabetes - monitoring for fetal growth and amniotic fluid volume
four weekly ultrasound scans to monitor the fetal growth and amniotic fluid volume from 28 to 36 weeks gestation.
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Pregnancy with pre existing diabetes
Before becoming pregnant, women with existing diabetes should aim for good glucose control. They should take 5mg folic acid from preconception until 12 weeks gestation. Women with existing type 1 and type 2 diabetes should aim for the same target insulin levels as with gestational diabetes. Women with type 2 diabetes are managed using metformin and insulin, and other oral diabetic medications should be stopped. Retinopathy screening should be performed shortly after booking and at 28 weeks gestation. This involves referral to an ophthalmologist to check for diabetic retinopathy. Diabetes carries a risk of rapid progression of retinopathy, and interventions may be required. NICE (2015) advise a planned delivery between 37 and 38 + 6 weeks for women with pre-existing diabetes. (Women with gestational diabetes can give birth up to 40 + 6). A sliding-scale insulin regime is considered during labour for women with type 1 diabetes. A dextrose and insulin infusion is titrated to blood sugar levels, according to the local protocol. This is also considered for women with poorly controlled blood sugars with gestational or type 2 diabetes.
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When should women with pre existing diabetes have retinopathy screening
Shortly after booking clinic And at 28 weeks gestation
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Maternal diabetes risks to baby
Neonatal hypoglycaemia Polycythaemia (raised haemoglobin) Jaundice (raised bilirubin) Congenital heart disease Cardiomyopathy
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Blood glucose in babies born to mothers with GD or DM
Babies need close monitoring for neonatal hypoglycaemia, with regular blood glucose checks and frequent feeds. The aim is to maintain their blood sugar above 2 mmol/l, and if it falls below this, they may need IV dextrose of nasogastric feeding. Babies become accustomed to a large supply of glucose during the pregnancy, and after birth they struggle to maintain the supply they are used to with oral feeding alone.
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What is obstetric choleostasis and when does it usualy develop
Obstetric cholestasis is characterised by the reduced outflow of bile acids from the liver. The condition resolves after delivery of the baby. Obstetric cholestasis is a relatively common complication of pregnancy, occurring in around 1% of pregnant women. It usually develops later in pregnancy (i.e. after 28 weeks)
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Why is obstetric cholestasis thought to occur and who is most at risk?
increased oestrogen and progesterone levels There seems to be a genetic component. It is more common in women of South Asian ethnicity.
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What happens in obstetric cholestasis
Bile acids are produced in the liver from the breakdown of cholesterol. Bile acids flow from liver to the hepatic ducts, past the gallbladder and out of the bile duct to the intestines. In obstetric cholestasis, the outflow of bile acids is reduced, causing them to build up in the blood, resulting in the classic symptoms of itching (pruritis).
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What is obstetric cholestasis associated with an increased risk of?
Still birth
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Presentation of obstetric cholestasis
Obstetric cholestasis typically present later in pregnancy, particularly in the third trimester. Itching (pruritis) is the main symptom, particularly affecting the palms of the hands and soles of the feet. Other symptoms are related to cholestasis and outflow obstruction in the bile ducts: Fatigue Dark urine Pale, greasy stools Jaundice Importantly, there is no rash associated with obstetric cholestasis
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Importantly, there is no rash associated with obstetric cholestasis. If a rash is present, an alternative diagnosis should be considered, such as what?
polymorphic eruption of pregnancy or pemphigoid gestationis
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Causes of pruritus and deranged LFTs in pregnancy
Obstetric cholestasis/intrahepatic cholestasis of pregnancy Gallstones Acute fatty liver Autoimmune hepatitis Viral hepatitis
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Investigating obstetric cholestasis (+what bloods show)
Women presenting with pruritus should have liver function tests and bile acids checked. Obstetric cholestasis will cause: Abnormal liver function tests (LFTs), mainly ALT, AST and GGT Raised bile acids (It is normal for alkaline phosphatase (ALP) to increase in pregnancy. This is because the placenta produces ALP. A rise in ALP without other abnormal LFT results is usually due to placental production of ALP, rather than liver pathology.)
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Management of obstetric cholestasis
Ursodeoxycholic acid is the primary treatment for obstetric cholestasis. It improves LFTs, bile acids and symptoms. Symptoms of itching can be managed with: Emollients (i.e. calamine lotion) to soothe the skin Antihistamines (e.g. chlorphenamine) can help sleeping (but does not improve itching) Water-soluble vitamin K can be given if clotting (prothrombin time) is deranged. Vitamin K is a fat-soluble vitamin. Bile acids are important in the absorption of fat-soluble vitamins in the intestines. A lack of bile acids can lead to vitamin K deficiency. Vitamin K is an important part of the clotting system, and deficiency can lead to impaired clotting of blood. Monitor of LFTs is required during pregnancy (weekly) and after delivery (after at least ten days), to ensure the condition does not worsen and resolves after birth. Planned delivery after 37 weeks may be considered, particularly when the LFTs and bile acids are severely deranged. Stillbirth in obstetric cholestasis is difficult to predict, and early delivery aims to reduce the risk.
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What is acute fatty liver of pregnancy, when does it occur and what are the implications
Acute fatty liver of pregnancy is a rare condition that occurs in the third trimester of pregnancy. There is a rapid accumulation of fat within the liver cells (hepatocytes), causing acute hepatitis. There is a high risk of liver failure and mortality, for both the mother and fetus.
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Pathophysiology of acute fatty liver of pregnancy
Acute fatty liver of pregnancy results from impaired processing of fatty acids in the placenta. This is the result of a genetic condition in the fetus that impairs fatty acid metabolism. The most common cause is long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency in the fetus, which is an autosomal recessive condition. This mode of inheritance means the mother will also have one defective copy of the gene. Th LCHAD enzyme is important in fatty acid oxidation, breaking down fatty acids to be used as fuel. The fetus and placenta are unable to break down fatty acids. These fatty acids enter the maternal circulation, and accumulate in the liver. The mother’s defective copy of the gene may also contribute to the accumulation of fatty acids. The accumulation of fatty acids in the mother’s liver leads to inflammation and liver failure.
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Presentation of acute fatty liver of pregnancy
The presentation is with vague symptoms associated with hepatitis : General malaise and fatigue Nausea and vomiting Jaundice Abdominal pain Anorexia (lack of appetite) Ascites
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Bloods in acute fatty liver of pregnancy
Liver function tests will show elevated liver enzymes (ALT and AST). Other bloods may be deranged, with: Raised bilirubin Raised WBC count Deranged clotting (raised prothrombin time and INR) Low platelets NOTE elevated liver enzymes and low platelets should make you think of HELLP syndrome rather than acute fatty liver of pregnancy. HELLP syndrome is much more common, but keep acute fatty liver of pregnancy in mind as a differential.
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Management of acute fatty liver of pregnancy
Acute fatty liver of pregnancy is an obstetric emergency and requires prompt admission and delivery of the baby. Most patients will recover after delivery. Management also involves treatment of acute liver failure if it occurs, including consideration of liver transplant.
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Polymorphic eruption of pregnancy presentation
Polymorphic eruption of pregnancy is also known as pruritic and urticarial papules and plaques of pregnancy. It is an itchy rash that tends to start in the third trimester. It usually begins on the abdomen, particularly associated with stretch marks (striae). It is characterised by: Urticarial papules (raised itchy lumps) Wheals (raised itchy areas of skin) Plaques (larger inflamed areas of skin)
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Polymorphic eruption of pregnancy
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The condition will get better towards the end of pregnancy and after delivery. Management is to control the symptoms, what can be used?
Topical emollients Topical steroids Oral antihistamines Oral steroids may be used in severe cases
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What is atopic eruption of pregnancy and what are the two types?
Atopic eruption of pregnancy essentially refers to eczema that flares up during pregnancy. This includes both women that have never suffered with eczema and those with pre-existing eczema. Atopic eruption of pregnancy presents in the first and second trimester of pregnancy. There are two types: E-type, or eczema-type: with eczematous, inflamed, red and itchy skin, typically affecting the insides of the elbows, back of knees, neck, face and chest. P-type, or prurigo-type: with intensely itchy papules (spots) typically affecting the abdomen, back and limbs.
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Atopic eruption of pregnancy will usually get better following delivery. How can symptoms be managed
Topical emollients Topical steroids Phototherapy with ultraviolet light (UVB) may be used in severe cases Oral steroids may be used in severe cases
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What is melasama and why does it occur
Melasma is also known as mask of pregnancy. It is characterised by increased pigmentation to patches of the skin on the face. This is usually symmetrical and flat, affecting sun-exposed areas. Melasma is thought to be partly related to the increased female sex hormones associated with pregnancy. It can also occur with the combined contraceptive pill and hormone replacement therapy. It is also associated with sun exposure, thyroid disease and family history.
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Management of melasama
No active treatment is required if the appearance is acceptable to the woman. Management is with: Avoiding sun exposure and using suncream Makeup (camouflage) Skin lightening cream (e.g. hydroquinone or retinoid creams), although not in pregnancy and only under specialist care Procedures such as chemical peels or laser treatment (not usually on the NHS)
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What is pyogenic granuloma and when might they occur
Pyogenic granuloma is also known as lobular capillary haemangioma. This is a benign, rapidly growing tumour of capillaries. It present as a discrete lump with a red or dark appearance. They occur more often in pregnancy, and can also be associated with hormonal contraceptives. They can also be triggered by minor trauma or infection.
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Presentation of pyogenic granuloma
Pyogenic granuloma present with a rapidly growing lump that develops over days up to 1-2 cm in size, (but can be larger). They often occur on fingers, or on the upper chest, back, neck or head. They may cause profuse bleeding and ulceration if injured.
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Management of pyogenic granuloma
Other differentials, such as malignancy, need to be excluded (particularly nodular melanoma). When they occur in pregnancy, they usually resolve without treatment after delivery. Treatment is with surgical removal with histology to confirm the diagnosis.
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What is phemigoid gestationis and why does it occur
Pemphigoid gestationis is a rare autoimmune skin condition that occurs in pregnancy. Autoantibodies are created that damage the connection between the epidermis and the dermis. The pregnant woman’s immune system may produce these antibodies in response to placental tissue. This causes the epidermis and dermis to separate, creating a space that can fill with fluid, resulting in large fluid-filled blisters (bullae).
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Presentation of phemigoid gestationis
Pemphigoid gestationis usually occurs in the second or third trimester. The typical presentation is initially with an itchy red papular or blistering rash around the umbilicus, that then spreads to other parts of the body. Over several weeks, large fluid-filled blisters form.
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Phemigoid gestationis
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Management of phemigoid gestationis
The rash usually resolves without treatment after delivery. It may go through stages of improvement and worsening during pregnancy and after birth. The blisters heal without scarring. Treatment is with: Topical emollients Topical steroids Oral steroids may be required in severe cases Immunosuppressants may be required where steroids are inadequate Antibiotics may be necessary if infection occurs
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What are the risks to the baby in maternal phemigoid gestationis
Fetal growth restriction Preterm delivery Blistering rash after delivery (as the maternal antibodies pass to the baby)
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Causes of cardiac arrest during pregnancy
The Resuscitation Council UK list the reversible causes of adult cardiac arrest as the 4 Ts and 4 Hs: 4 Ts: Thrombosis (i.e. PE or MI) Tension pneumothorax Toxins Tamponade (cardiac) 4 Hs: Hypoxia Hypovolaemia Hypothermia Hyperkalaemia, hypoglycaemia, and other metabolic abnormalities The RCOG guideline advises adding to the list: Eclampsia Intracranial haemorrhage
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What are the three major causes of cardiac arrest in pregnancy
Obstetric haemorrhage Pulmonary embolism Sepsis leading to metabolic acidosis and septic shock
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What are the causes of massive obstetric haemorrhage
Ectopic pregnancy (early pregnancy) Placental abruption (including concealed haemorrhage) Placenta praevia Placenta accreta Uterine rupture
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Why is resuscitation more complicated in pregnancy
Aortocaval compression Increased oxygen requirements Splinting of the diaphragm by the pregnant abdomen Difficulty with intubation Increased risk of aspiration Ongoing obstetric haemorrhage
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What is aortocaval compression and why does it occur. How can it be relieved?
After 20 weeks gestation, the uterus is a significant size. When a pregnant woman lies on her back (supine), the mass of the uterus can compress the inferior vena cava and aorta. The compression on the vena cava is most significant, as it reduces the blood returning to the heart (venous return). This reduces the cardiac output, leading to hypotension. In some instances, this can be enough to lead to the loss of cardiac output and cardiac arrest. The vena cava is slightly to the right side of the body. The solution to aortocaval compression is to place the woman in the left lateral position, lying on her left side, with the pregnant uterus positioned away from the inferior vena cava. This should relieve the compression on the inferior vena cava and improve venous return and cardiac output.
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Resuscitation in pregnancy follows the same principles as standard adult life support, except for what?
A 15 degree tilt to the left side for CPR, to relieve compression of the inferior vena cava and aorta Early intubation to protect the airway Early supplementary oxygen Aggressive fluid resuscitation (caution in pre-eclampsia) Delivery of the baby after 4 minutes, and within 5 minutes of starting CPR
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How should a pregnant woman be positioned in CPR and why
A 15 degree tilt to the left side for CPR, to relieve compression of the inferior vena cava and aorta
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In a cardiac arrest when should delivery happen
Delivery of the baby after 4 minutes, and within 5 minutes of starting CPR
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What is meant by placenta praevia
Placenta praevia is where the placenta is attached in the lower portion of the uterus, lower than the presenting part of the fetus.
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Low lying placenta vs placenta praevia
Low-lying placenta is used when the placenta is within 20mm of the internal cervical os Placenta praevia is used only when the placenta is over the internal cervical os
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Causes of antepartum haemorrhage
The three causes of antepartum haemorrhage to remember are placenta praevia, placental abruption and vasa praevia. These are serious causes with high morbidity and mortality. Causes of spotting or minor bleeding in pregnancy include cervical ectropion, infection and vaginal abrasions from intercourse or procedures.
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Placenta praevia is associated with increased morbidity and mortality for the mother and fetus. The risks include what?
Antepartum haemorrhage Emergency caesarean section Emergency hysterectomy Maternal anaemia and transfusions Preterm birth and low birth weight Stillbirth
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Grading placenta praevia
Traditionally, there are four grades of placenta praevia: Minor praevia, or grade I – the placenta is in the lower uterus but not reaching the internal cervical os Marginal praevia, or grade II – the placenta is reaching, but not covering, the internal cervical os Partial praevia, or grade III – the placenta is partially covering the internal cervical os Complete praevia, or grade IV – the placenta is completely covering the internal cervical os The RCOG guidelines (2018) recommend against using this grading system, as it is considered outdated. The two descriptions used are low-lying placenta and placenta praevia.
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What are the risk factors for placenta praevia
Previous caesarean sections Previous placenta praevia Older maternal age Maternal smoking Structural uterine abnormalities (e.g. fibroids) Assisted reproduction (e.g. IVF)
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Presentation and diagnosis of placenta praevia
The 20-week anomaly scan is used to assess the position of the placenta and diagnose placenta praevia. Many women with placenta praevia are asymptomatic. It may present with painless vaginal bleeding in pregnancy (antepartum haemorrhage). Bleeding usually occurs later in pregnancy (around or after 36 weeks).
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For women with a low-lying placenta or placenta praevia diagnosed early in pregnancy (e.g. at the 20-week anomaly scan), when is repeat TVUSS reccomended
32 weeks gestation 36 weeks gestation (if present on the 32-week scan, to guide decisions about delivery)
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Given the risk of preterm delivery what is done towards the end of pregnancy in women with placenta praevia
Corticosteroids are given between 34 and 35 + 6 weeks gestation to mature the fetal lungs, given the risk of preterm delivery.
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What is the main complication of placenta praevia and what is done if this occurs
The main complication of placenta praevia is haemorrhage before, during and after delivery. When this occurs, urgent management is required and may involve: Emergency caesarean section Blood transfusions Intrauterine balloon tamponade Uterine artery occlusion Emergency hysterectomy
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Vasa praevia pathophysiology
Under normal circumstances, the umbilical cord containing the fetal vessels (umbilical arteries and vein) inserts directly into the placenta. The fetal vessels are always protected, either by the umbilical cord or by the placenta. The umbilical cord contains Wharton’s jelly. Wharton’s jelly is a layer of soft connective tissue that surrounds the blood vessels in the umbilical cord, offering protection. There are two instances when the fetal vessels can be exposed, outside the protection of the umbilical cord or placenta: Velamentous umbilical cord is where the umbilical cord inserts into the chorioamniotic membranes, and the fetal vessels travel unprotected through the membranes before joining the placenta. An accessory lobe of the placenta (also known as a succenturiate lobe) is connected by fetal vessels that travel through the chorioamniotic membranes between the placental lobes. In vasa praevia, the fetal vessels are exposed, outside the protection of the umbilical cord or the placenta. The fetal vessels travel through the chorioamniotic membranes, and pass across the internal cervical os (the inner opening of the cervix). These exposed vessels are prone to bleeding, particularly when the membranes are ruptured during labour and at birth. This can lead to dramatic fetal blood loss and death.
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Vasa praevia types
Type I vasa praevia – the fetal vessels are exposed as a velamentous umbilical cord Type II vasa praevia – the fetal vessels are exposed as they travel to an accessory placental lobe
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What is vasa praevia
Vasa praevia is a condition where the fetal vessels are within the fetal membranes (chorioamniotic membranes) and travel across the internal cervical os. The fetal membranes surround the amniotic cavity and developing fetus. The fetal vessels consist of the two umbilical arteries and single umbilical vein.
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Vasa praevia risk factors
Low lying placenta IVF pregnancy Multiple pregnancy
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How might vasa praaevia present
Vasa praevia may be diagnosed by ultrasound during pregnancy. This is the ideal scenario, as it allows a planned caesarean section to reduce the risk of haemorrhage. However, ultrasound is not reliable, and it is often not possible to diagnose antenatally. It may present with antepartum haemorrhage, with bleeding during the second or third trimester of pregnancy. It may be detected by vaginal examination during labour, when pulsating fetal vessels are seen in the membranes through the dilated cervix. Finally, it may be detected during labour when fetal distress and dark-red bleeding occur following rupture of the membranes. This carries a very high fetal mortality, even with emergency caesarean section.
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Management of vasa praevia
For asymptomatic women with vasa praevia, the RCOG guidelines (2018) recommend: Corticosteroids, given from 32 weeks gestation to mature the fetal lungs Elective caesarean section, planned for 34 – 36 weeks gestation Where antepartum haemorrhage occurs, emergency caesarean section is required to deliver the fetus before death occurs. After stillbirth or unexplained fetal compromise during delivery, the placenta is examined for evidence of vasa praevia as a possible cause.
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What is placental abruption
Placental abruption refers to when the placenta separates from the wall of the uterus during pregnancy. The site of attachment can bleed extensively after the placenta separates. Placental abruption is a significant cause of antepartum haemorrhage.
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Risk factors for placental abruption
Previous placental abruption Pre-eclampsia Bleeding early in pregnancy Trauma (consider domestic violence) Multiple pregnancy Fetal growth restriction Multigravida Increased maternal age Smoking Cocaine or amphetamine use
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Presentation of placental abruption
Sudden onset severe abdominal pain that is continuous Vaginal bleeding (antepartum haemorrhage) Shock (hypotension and tachycardia) Abnormalities on the CTG indicating fetal distress Characteristic “woody” abdomen on palpation, suggesting a large haemorrhage
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Severity of antepartum haemorrhage
Spotting: spots of blood noticed on underwear Minor haemorrhage: less than 50ml blood loss Major haemorrhage: 50 – 1000ml blood loss Massive haemorrhage: more than 1000 ml blood loss, or signs of shock
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What is concealed placental abruption
Concealed abruption is where the cervical os remains closed, and any bleeding that occurs remains within the uterine cavity. The severity of bleeding can be significantly underestimated with concealed haemorrhage. Concealed abruption is opposed to revealed abruption, where the blood loss is observed via the vagina.
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Management of placental abruption
There are no reliable tests for diagnosing placental abruption. It is a clinical diagnosis based on the presentation. Placental abruption is an obstetric emergency. The urgency depends on the amount of placental separation, extent of bleeding, haemodynamic stability of the mother and condition of the fetus. It is important to consider concealed haemorrhage, where the vaginal bleeding may be disproportionate to the uterine bleeding. The initial steps with major or massive haemorrhage are: Urgent involvement of a senior obstetrician, midwife and anaesthetist 2 x grey cannula Bloods include FBC, UE, LFT and coagulation studies Crossmatch 4 units of blood Fluid and blood resuscitation as required CTG monitoring of the fetus Close monitoring of the mother Ultrasound can be useful in excluding placenta praevia as a cause for antepartum haemorrhage, but is not very good at diagnosing or assessing abruption. Antenatal steroids are offered between 24 and 34 + 6 weeks gestation to mature the fetal lungs in anticipation of preterm delivery. Rhesus-D negative women require anti-D prophylaxis when bleeding occurs. A Kleihauer test is used to quantify how much fetal blood is mixed with the maternal blood, to determine the dose of anti-D that is required. Emergency caesarean section may be required where the mother is unstable, or there is fetal distress. There is an increased risk of postpartum haemorrhage after delivery in women with placental abruption. Active management of the third stage is recommended.
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What is placenta accreta
Placenta accreta refers to when the placenta implants deeper, through and past the endometrium, making it difficult to separate the placenta after delivery of the baby. It is referred to as placenta accreta spectrum, as there is a spectrum of severity in how deep and broad the abnormal implantation extends.
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Why might placenta accreta occur
With placenta accreta, the placenta embeds past the endometrium, into the myometrium and beyond. This may happen due to a defect in the endometrium. Imperfections may occur due to previous uterine surgery, such as a caesarean section or curettage procedure. The deep implantation makes it very difficult for the placenta to separate during delivery, leading to extensive bleeding (postpartum haemorrhage).
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Further definitions of placenta accreta
Depending on depth of insertion Superficial placenta accreta is where the placenta implants in the surface of the myometrium, but not beyond Placenta increta is where the placenta attaches deeply into the myometrium Placenta percreta is where the placenta invades past the myometrium and perimetrium, potentially reaching other organs such as the bladder
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Risk factors for placenta accreta
Previous placenta accreta Previous endometrial curettage procedures (e.g. for miscarriage or abortion) Previous caesarean section Multigravida Increased maternal age Low-lying placenta or placenta praevia
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Superficial placenta accreta
is where the placenta implants in the surface of the myometrium, but not beyond
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Placenta increta
is where the placenta attaches deeply into the myometrium
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Placenta percreta
is where the placenta invades past the myometrium and perimetrium, potentially reaching other organs such as the bladder
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Presentation of placenta accreta
Placenta accreta does not typically cause any symptoms during pregnancy. It can present with bleeding (antepartum haemorrhage) in the third trimester. It may be diagnosed on antenatal ultrasound scans, and particular attention is given to women with a previous placenta accreta or caesarean during scanning. It may be diagnosed at birth, when it becomes difficult to deliver the placenta. It is a cause of significant postpartum haemorrhage.
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Diagnosis of placenta accerta
Ideally, placenta accreta is diagnosed antenatally by ultrasound. This allows planning for birth. MRI scans may be used to assess the depth and width of the invasion.
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A specialist MDT should manage women with placenta accreta. Patients may require additional management at birth due to the risk of bleeding and difficulty separating the placenta. This may include what?
Complex uterine surgery Blood transfusions Intensive care for the mother Neonatal intensive care
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Diagnosis of intrauterine death
Ultrasound scan is the investigation of choice for diagnosing intrauterine fetal death (IUFD). It is used to visualise the fetal heartbeat to confirm the fetus is still alive. Passive fetal movements are possible after IUFD, and a repeat scan is offered to confirm the situation.
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What can be used to classsify the severity of vomiting in pregnancy
The Pregnancy-Unique Quantification of Emesis (PUQE) score can be used to classify the severity of nausea and vomiting in pregnancy
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At what stage does colostrum formations start
16 weeks gestation
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What supplements should be taken through pregnancy and for how long?
Vitamin D 400IU daily throughout the pregnancy, and folic acid 4-5mg (depending on risk factors) daily for the first 12 weeks of pregnancy
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Screening for Down's syndrome, Edwards' syndrome and Patau's syndrome is offered when?
between 10 and 14 weeks of pregnancy.
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What is placenta accreta and what problems can it causw
Placenta accreta describes the attachment of the placenta to the myometrium, due to a defective decidua basalis. As the placenta does not properly separate during labour there is a risk of postpartum haemorrhage.
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How often should a pregnant women with T1DM check her blood sugar
Daily fasting, pre-meal, 1-hour post-meal and bedtime tests.
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Bleeding in pregnancy - first trimester
Spontaneous abortion Ectopic pregnancy Hydatidiform mole
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Bleeding in pregnancy - second trimester
Spontaneous abortion Hydatidiform mole Placental abruption
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Bleeding in pregnancy - third trimester
Bloody show Placental abruption Placenta praevia Vasa praevia
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Placenta accreta vs increta vs percreta
accreta: chorionic villi attach to the myometrium, rather than being restricted within the decidua basalis increta: chorionic villi invade into the myometrium percreta: chorionic villi invade through the perimetrium
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Urine culture to detect asymptomatic bacteriuria should be performed when?
8-12 weeks
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Dextrose solutions for fluid replacement should be avoided in hyperemesis gravidarum - why?
They can precipitate Wernicke’s encephalopathy
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Where will the uterine fundus be at 12 weeks gestation?
pubic symphisis
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Where will the uterine fundus be at 20 weeks gestation?
umbilicus
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Where will the uterine fundus be at 36 weeks gestation?
The xiphoid process of the sternum
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What are the 3 types of fetal lie?
Longitudinal lie: the head and buttocks are palpable at each end of the uterus. Oblique lie: the head and buttocks are palpable in one of the iliac fossae. Transverse lie: the fetus is lying directly across the uterus.
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SFH after 20 weeks
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
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What type of insulin is used in gestational diabetes?
Gestational diabetes is treated with short-acting, but not longer-acting SC insulin