OB-GYN Revision 3 Flashcards

1
Q
A
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2
Q

What nutritional supplements should be given and when? [2]

A

Folic acid - 400mcg
- before conception until 12 weeks

Folic acid 5mg if:
- Maternal coeliac or DM, obese, relative w/ NTD or epilepsy

Vitamin D
- daily supplement containing 10micrograms of vitamin

NB cases with need higher Folic acid: MORE - Maternal disease, Obese, Relative w/ NTD; Epilpesy

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3
Q

What advise would you give about air travel during pregnancy? [3]

A
  • women > 37 weeks with singleton pregnancy and no additional risk factors should avoid air travel
  • women with uncomplicated, multiple pregnancies should avoid travel by air once >32 weeks
  • associated with increased risk of venous thromboembolism
  • wearing correctly fitted compression stockings is effective at reducing the risk
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4
Q

Why are NSAIDs generally not prescribed in pregnancy? [2]

A

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

Therefore
- They are particularly avoided in the third trimester, as they can cause premature closure of the ductus arteriosus in the fetus.
- They can also delay labour.

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5
Q

What affect can beta blockers have if given during pregnancy? [3]
Which beta-blockers are used if neeed? [1]

A

Beta-blockers can cause:
* Fetal growth restriction
* Hypoglycaemia in the neonate
* Bradycardia in the neonate

Labetalol is the most frequently used beta-blocker in pregnancy, and is first-line for high blood pressure caused by pre-eclampsia.

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6
Q

What is the affect of of ACEin or ARBs in pregnancy? [4]

A
  • Oligohydramnios (reduced amniotic fluid)
  • The other notably effect is hypocalvaria, which is an incomplete formation of the skull bones.
  • Renal failure in the neonate
  • Hypotension in the neonate
  • Miscarriage or fetal death
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7
Q

What affect can opiates cause if given during pregnancy? [1]

A

The use of opiates during pregnancy can cause withdrawal symptoms in the neonate after birth. This is called neonatal abstinence syndrome (NAS).

NAS presents between 3 – 72 hours after birth with irritability, tachypnoea (fast breathing), high temperatures and poor feeding.

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8
Q

Warfarin is considered teratogenic in pregnancy, therefore it is avoided in pregnant women. Warfarin can cause [3]

A
  • Fetal loss
  • Congenital malformations, particularly craniofacial problems
  • Bleeding during pregnancy, postpartum haemorrhage, fetal haemorrhage and intracranial bleeding
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9
Q

The use of sodium valproate in pregnancy causes [] and []

A

The use of sodium valproate in pregnancy causes neural tube defects and developmental delay.

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10
Q

Lithium is particularly avoided in the [] trimester, as this is linked with congenital [] abnormalities.
- In particular, it is associated with [] anomaly

A

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

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11
Q

Lithium is associated with Ebstei’s anomaly.

Describe what this is [1]

A

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.

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12
Q

Women need to be aware of the potential risks of SSRIs in pregnancy.

What are they? [4]

A

First-trimester use has a link with congenital heart defects
* First-trimester use of paroxetine has a stronger link with congenital malformations

Third-trimester use has a link with persistent pulmonary hypertension in the neonate

Neonates can experience withdrawal symptoms, usually only mild and not requiring medical management

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13
Q

Describe in detail the first stage of labour
Include the different phases of the first stage of labour [3]

A

First stage: from the onset of labour until the cervix is fully dilated to 10cm

It involves cervical dilation (opening up) and effacement (getting thinner from front to back)

The “show” refers to the mucus plug in the cervix, that prevents bacteria from entering the uterus during pregnancy, falling out and creating space for the baby to pass through.

Phases of the first stage:
Latent phase:
- From 0 to 3cm dilation of the cervix.
- This progresses at around 0.5cm per hour. There are irregular contractions.

Active phase::
- From 3cm to 7cm dilation of the cervix.
- This progresses at around 1cm per hour, and there are regular contractions.

Transition phase:
- From 7cm to 10cm dilation of the cervix.
- This progresses at around 1cm per hour, and there are strong and regular contractions.

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14
Q

Describe the second stage of labour [+]

A

The second stage of labour lasts from 10cm dilatation of the cervix to delivery of the baby.

The success of the second stage depends on “the three Ps”: power, passenger and passage.

1. Power:
- the strength of the uterine contractions.

2. Passenger: the four descriptive qualities of the fetus:
- Size: particularly the size of the head as this is the largest part.
- Attitude: the posture of the fetus. For example, how the back is rounded and how the head and limbs are flexed.
- Lie: the position of the fetus in relation to the mother’s body: Longitudinal lie – the fetus is straight up and down; Transverse lie – the fetus is straight side to side; Oblique lie– the fetus is at an angle.
- Presentation: the part of the fetus closest to the cervix: Cephalic (head first); Shoulder presentation (shoulder first); Breech presentation (legs first)

3. Passage: the size and shape of the passageway, mainly the pelvis.

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15
Q

What are the signs of labour? [4]

A

Abdominal pains – regular, initial frequency 2-3 in 10 minutes

Passage of show – mucous plug, brownish or blood stained (not always)

Water leak (often) – but typically waters should break in labour

Others (nausea, vomiting, general malaise…)

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16
Q

Describe the monitoring given in labour for the fetus [1] and mother [5]

A

Fetus:
* FHR monitored every 15min (or continuously via CTG)

Maternal:
* Maternal pulse rate assessed every 60min
* Maternal BP and temp should be checked every 4 hours
* VE should be offered every 4 hours to check progression of labour
* Maternal urine should be checked for ketones and protein every 4 hours
* Contractions assessed every 30min

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17
Q

Average labour duration:
[] hours for a primipara
[] hours for a multipara

A

Average labour duration:
8 hours for a primipara
5 hours for a multipara

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18
Q

A partogram is used to monitor the active phase of the first stage of labour.

Describe what you would measure on the partogram and what it would indicate if these were atypical [+]

A

A tool for monitoring maternal and foetal wellbeing during the active phase of labour, and a decision-making aid when abnormalities are detected

Fetal HR
- Normal is 110-160

Maternal pulse, BP, temperature
- raised if chorioamnionitis, UTI, group B streptococcal infection)

Maternal urianalysis
- protein = pre-eclampsia/liquor contamination; glucose = diabetes; ketones = starvation; blood = UTI/obstructed labour

Contractions:
- Frequency per 10 mins: 2nd stage of labour aim is 1min contractions in 10 mins, 3-5 strong)
- Strength
- Regularity

Cervical dilatation:
- PV exam performed every 4hrs: aim is 1cm/hr primiparous, 2cm/hr multiparous
- Alert line: 1cm/2hrs if primiparous or 1cm/hr if multiparous

Head descent:
- PV exam every 4 hrs
- Assess: Fifths palpable per abdomen; station of presenting part (measured in relation to ischial spine); position (orientation of fetal head - feel for fontanelles/sutures); moulding (extent of overlapping fetal skull bones); caput: swelling of presenting part

Liquor:
- Noted every hour
- Assess if intact: clear (membrane rupture), bloody (placental abruption) or meconium present (fetal distress)

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19
Q

Which medical devices would you use for HR in 1st or 2nd stage if there were no concerns? [2]

During 1st and 2nd stage how often would you check? [2]

What would you move to next if you were concerned? [1]

A

Intermittant ascultations: Pinard stethoscope or Doppler ultrasound

1st stage:
- Every 15 minutes, after a contraction, for 1 minute; record maternal pulse hourly

2nd stage: Every 5 minutes, after a contraction, for 1 minute; record maternal pulse every 15 min

Record accelerations and decelerations !!!

Move to CTG if any concerns

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20
Q

CTG:
- What is baseline tachycardia [1] and bradycardia [1]

  • What are potential causes of fetal tachycardia? [4]
  • What are potential causes of fetal bradycardia? [2]
A

Baseline bradycardia: HR < 100
- Increased fetal vagal tone
- Maternal beta blocker use

Baseline tachycardia: HR > 160:
- Maternal pyrexia
- chorioamnionitis
- fetal hypoxia
- fetal or maternal anaemia
- prematurity
- hyperthyroidism

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21
Q

Describe what is meant by an early deceleration in CTG? [1]
What are the causes of early deceleration in CTG? [1]

A

Deceleration of the heart rate which commences with the onset of a contraction and returns to normal on completion of the contraction
- They are caused by the uterus compressing the head the fetus, stimulating the vagus nerve of the fetus, slowing the heart rate

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22
Q

CTG:
- What is fetal bradycardia? [1]
- What are two common causes for fetal bradycardia? [2]
- Severe prolonged bradycardia count as less than [] bpm for more than 3mins. What are the causes? [4]

A

Fetal bradycardia is defined as a baseline heart rate of less than 110 bpm.

Fetal bradycardia is common in postdate gestation or OP or transverse presentations

Severe prolonged bradycardia (less than 80 bpm for more than 3 minutes) indicates severe hypoxia:
* Prolonged cord compression
* Cord prolapse
* Epidural and spinal anaesthesia
* Maternal seizures
* Rapid fetal descent

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23
Q

Why does variability occur in CTGs? [3]

What is normal / reassuring variability? [1]

A

Variability occurs as a result of the interaction between the nervous system, chemoreceptors, baroreceptors and cardiac responsiveness.
- Normal variability is between 5-25 bpm

24
Q

What reassuring [1], non-reassuring [2] and abnormal [3] fetal HR variability?

A

Reassuring:
- 5 – 25 bpm

Non-reassuring:
* less than 5 bpm for between 30-50 minutes
* more than 25 bpm for 15-25 minutes

Abnormal:
* less than 5 bpm for more than 50 minutes
* more than 25 bpm for more than 25 minutes
* sinusoidal

25
Q

What can caused reduced variability in CTGs? [6]

A

Fetal sleeping: this should last no longer than 40 minutes (this is the most common cause)

Fetal acidosis (due to hypoxia): more likely if late decelerations are also present

Fetal tachycardia

Drugs: opiates, benzodiazepines, methyldopa and magnesium sulphate

Prematurity: variability is reduced at earlier gestation (< 28 weeks)

Congenital heart abnormalities

26
Q

Define what decelerations are on CTGs [1]

A

Decelerations are an abrupt decrease in the baseline fetal heart rate of greater than 15 bpm for greater than 15 seconds.
- The fetal heart rate is controlled by the autonomic and somatic nervous system. In response to hypoxic stress, the fetus reduces its heart rate to preserve myocardial oxygenation and perfusion. Unlike an adult, a fetus cannot increase its respiration depth and rate. This reduction in heart rate to reduce myocardial demand is referred to as a deceleration.

27
Q

Describe the difference in causes between early, late and prolonged decelerations [3]

A

Early decelerations start when the uterine contraction begins and recover when uterine contraction stops
- This is due to increased fetal intracranial pressure causing increased vagal tone.
- It therefore quickly resolves once the uterine contraction ends and intracranial pressure reduces
- considered to be physiological and not pathological.

Late decelerations
- begin at the peak of the uterine contraction and recover after the contraction ends
- This type of deceleration indicates there is insufficient blood flow to the uterus and placenta. As a result, blood flow to the fetus is significantly reduced causing fetal hypoxia and acidosis.

Prolonged deceleration:
* A prolonged deceleration is defined as a deceleration that lasts more than 2 minutes:
* If it lasts between 2-3 minutes it is classed as non-reassuring.
If it lasts longer than 3 minutes it is immediately classed as abnormal.

28
Q

Name 3 causes of late deceleration CTGs [3]

A

Causes of reduced uteroplacental blood flow include:
* Maternal hypotension
* Pre-eclampsia
* Uterine hyperstimulation
* asphyxia
* placental insufficiency

29
Q

Describe what causes variable decelerations

A

Variable decelerations are usually caused by umbilical cord compression. The mechanism is as follows:
1. The umbilical vein is often occluded first causing an acceleration of the fetal heart rate in response.
2. Then the umbilical artery is occluded causing a subsequent rapid deceleration.
3. When pressure on the cord is reduced another acceleration occurs and then the baseline rate returns.

30
Q

The accelerations before and after a variable deceleration are known as the [] of deceleration. What do they indicate? [1]

A

The accelerations before and after a variable deceleration are known as the shoulders of deceleration
- Their presence indicates the fetus is not yet hypoxic and is adapting to the reduced blood flow.
- Variable decelerations without the shoulders are more worrying, as it suggests the fetus is becoming hypoxic.

31
Q

What does a sinusoidal CTG patten indicate? [3]

A

A sinusoidal pattern usually indicates one or more of the following:
* Severe fetal hypoxia
* Severe fetal anaemia
* Fetal/maternal haemorrhage

32
Q

Describe how you would present a CTG

A

DRDefine Risk (define the risk based on the individual woman and pregnancy before assessing the CTG)
C – Contractions
BRa – Baseline Rate
V – Variability
A – Accelerations
D – Decelerations
O – Overall impression (given an overall impression of the CTG and clinical picture)

33
Q

Describe how you go through each of the following:

DR C BRaVADO

A

DR:
- Maternal medical illness: Gestational DM; HTN: Asthma
- Obstetric complications: pre-eclampsia; oxytocin induced; post-date gestation; previous c section; IUGR
- Others: smoking, drug abuse

Contractions:
- Record no per 10 minute period
- Each big square is 1 minute
- How long?
- How strong?

BRa: Baseline rate:
- A normal fetal heart rate is between 110-160 bpm
- Fetal tachycardia?
- Fetal bradycardia?

V: Variability:
- Baseline variability refers to the variation of fetal heart rate from one beat to the next.
- Reassuring: 5 – 25 bpm
- Non-reassuring: < 5 bpm for 30-50 mins; > 25bpm for 15-25 mins
- Abnormal: < 5 bpm for 50+ mins; > 25bpm for 25+ mins

A: Accelerations:
- abrupt increase in the baseline fetal heart rate of greater than 15 bpm for greater than 15 seconds
- The presence of accelerations is reassuring.

D: Decelerations
- abrupt decrease in the baseline fetal heart rate of greater than 15 bpm for greater than 15 seconds
- Early: physiological
- Variable: There is a fall of more than 15 bpm from the baseline. Variable decelerations often indicate intermittent compression of the umbilical cord, causing fetal hypoxia. Brief accelerations before and after the deceleration are known as shoulders, and are a reassuring sign that the fetus is coping
- Late: gradual falls in heart rate that starts after the uterine contraction has already begun. They may be caused by excessive uterine contractions, maternal hypotension or maternal hypoxia
- Prolonged: last between 2 and 10 minutes with a drop of more than 15 bpm from baseline. This often indicates compression of the umbilical cord, causing fetal hypoxia. These are abnormal and concerning.

O: Overall impression:
- The overall impression can be described as either reassuring, suspicious or abnormal

34
Q

What’s a mneumonic for remembering what the causes of decelerations / acelerations are? [4]

A

VEAL CHOP

Variable decelerations –> Cord compression
Early decelerations –> Head compression
Accelerations –> Okay!
Late decelerations –> Placental Insufficiency

35
Q

What is the ‘rule of 3’s’ for fetal bradycardia when they are prolonged? [4]

A

3 minutes – call for help
6 minutes – move to theatre
9 minutes – prepare for delivery
12 minutes – deliver the baby (by 15 minutes)

36
Q

Describe the different positions of the baby’s head during labour (and which ones are problematic) [4]

A

Occipito-anterior (OA):
- optimal position
- baby is head down with his or her face looking at spine

occipito-posterior (OP):
- baby is head down, facing naval

Occiput Transverse (OT) - R or L
- This is when the baby is lying at a right angle across the parent’s abdomen.

Breech
- Breech is when the baby is lying bottom down in the womb.

37
Q

How can you determine which position the baby is during birth by feeling its head? [1]

A

Look at the fontanelles to determine position
- Posterior is triangular; hard;
- Anterior is a diamond; soft

  • Therefore if the posterior further up: OA

Can feel the sagitalle suture (long one) - follow along until other suture. If theres 3 its posterior; if 4 and anterior is soft

38
Q

The length of the first stage of labour varies widely:

First labour: an average of around [] hours may be expected, rarely would it last longer than 18 hours.

Subsequent labour: may last around [] hours on average and rarely longer than 12 hours.

A

The length of the first stage of labour varies widely:

First labour: an average of around 8 hours may be expected, rarely would it last longer than 18 hours.

Subsequent labour: may last around 5 hours on average and rarely longer than 12 hours.

39
Q

The length of the second stage varies widely:

Nulliparous (no previous births): normally will last less than [] hours
Multiparous (more than one previous birth): normally will last less than [] hours

A

Length

The length of the second stage varies widely:

Nulliparous (no previous births): normally will last less than 3 hours
Multiparous (more than one previous birth): normally will last less than 2 hours

40
Q

NICE guidelines on intrapartum care (2017) refer to the latent first stage and established first stage.

What is the difference between them? [1]

A

The latent first stage is when there are both:
* Painful contractions
* Changes to the cervix, with effacement and dilation up to 4cm

The established first stage of labour is when there are both:
* Regular, painful contractions
* Dilatation of the cervix from 4cm onwards

41
Q

Describe what is meant by a PMS [2]

A

Premenstrual syndrome (PMS) describes the psychological, emotional and physical symptoms that occur during the luteal phase of the menstrual cycle, particularly in the days prior to the onset of menstruation.

42
Q

How do you differentiate between PMS and menarche, pregnancy or after menopause? [1]

A

The symptoms of PMS resolve once menstruation begins

Symptoms are not present before menarche, during pregnancy or after menopause. These are key things to note when you take a history.

43
Q

How do you diagnose PMS? [2]

A

Diagnosis is made based on a symptom diary spanning two menstrual cycles.

The symptom diary should demonstrate cyclical symptoms that occur just before, and resolve after, the onset of menstruation.

A definitive diagnosis may be made, under the care of a specialist, by administering a GnRH analogues to halt the menstrual cycle and temporarily induce menopause, to see if the symptoms resolve.

44
Q

How do you treat PMS? [4]

A

RCOG recommends COCPs containing drospirenone first line (i.e. Yasmin)
- Drospironone as some antimineralocortioid effects, similar to spironolactone
- Continuous use of the pill, as opposed to cyclical use, may be more effective.

Continuous transdermal oestrogen (patches) can be used to improve symptoms
- Progestogens are required for endometrial protection against endometrial hyperplasia when using oestrogen. This can be in the form of low dose cyclical progestogens (e.g. norethisterone) to trigger a withdrawal bleed, or the Mirena coil.

GnRH analogues can be used to induce a menopausal state.
- reserved for severe cases due to the adverse effects (e.g. osteoporosis)

Hysterectomy and bilateral oophorectomy
- can be used to induce menopause where symptoms are severe and medical management has failed. Hormone replacement therapy will be required, particularly in women under 45 years.

45
Q

What can you use to treat breast pain in PMS? [2]

A

Danazole and tamoxifen are options for cyclical breast pain, initiated and monitored by a breast specialist.

46
Q

[] may be used to treat the physical symptoms of PMS, such as breast swelling, water retention and bloating.

A

Spironolactone may be used to treat the physical symptoms of PMS, such as breast swelling, water retention and bloating.

47
Q

How do you treat menorrhagia:
- if the patient does not want contraception? [2]
- accepts contraception [3]

A

When the woman does not want contraception; treatment can be used during menstruation for symptomatic relief, with:

  • Tranexamic acid when no associated pain (antifibrinolytic – reduces bleeding)
  • Mefenamic acid when there is associated pain (NSAID – reduces bleeding and pain)

Management when contraception is wanted or acceptable:
* Mirena coil (first line)
* Combined oral contraceptive pill
* Cyclical oral progestogens, such as norethisterone 5mg three times daily from day 5 – 26 (although this is associated with progestogenic side effects and an increased risk of venous thromboembolism)

48
Q

Describe the features of the perimenopause [+]

A

A lack of oestrogen in the perimenopausal period leads to symptoms of:
* Hot flushes
* Emotional lability or low mood
* Premenstrual syndrome
* Irregular periods
* Joint pains
* Heavier or lighter periods
* Vaginal dryness and atrophy
* Reduced libido

49
Q

HRT may be given as ‘unopposed’ oestrogen or as a combination of oestrogen and progesterone. They can be offered in an oral or transdermal form.

The choice is dictated by the presence or absence of a uterus.

What do you offer for women with [1] or without [1] a uterus?

A

Women with a uterus:
- combined oestrogen and progesterone HRT

Women with a without uterus:
- oestrogen-only HRT.

50
Q

TOM TIP: It is worth making a note and remembering two key side effects of the progesterone depot injection (e.g. Depo-Provera).

What are they? [2]

A

Weight gain and reduced bone mineral density (osteoporosis). These side effects are unique to the depot and do not occur with other forms of contraception. Reduced bone mineral density makes the depot unsuitable for women over 45 years.

51
Q

How can you manage vasomotor symptoms of menopause in without HRT? [2]

A

Exercise
Fluoxetine, citalopram or venlafaxine

52
Q

Define
premature ovarian insufficiency [1]

A

Premature ovarian insufficiency is defined as menopause before the age of 40 years. It is the result of a decline in the normal activity of the ovaries at an early age. It presents with early onset of the typical symptoms of the menopause.

53
Q

Describe the pathophysiology of POI [2]

What will hormonal analysis show?

A

Premature ovarian insufficiency is characterised by hypergonadotropic hypogonadism.

Under-activity of the gonads (hypogonadism) means there is a lack of negative feedback on the pituitary gland, resulting in an excess of the gonadotropins (hypergonadotropism).

Hormonal analysis will show:
* Raised LH and FSH levels (gonadotropins)
* Low oestradiol levels

54
Q

What is the the cause for 50% of POI? [1]
What are other causes? [4]

A
  • Idiopathic (the cause is unknown in more than 50% of cases)
  • Iatrogenic, due to interventions such as chemotherapy, radiotherapy or surgery (i.e. oophorectomy)
  • Autoimmune, possibly associated with coeliac disease, adrenal insufficiency, type 1 diabetes or thyroid disease
  • Genetic, with a positive family history or conditions such as Turner’s syndrome
  • Infections such as mumps, tuberculosis or cytomegalovirus
55
Q

NICE guidelines on menopause (2015) say premature ovarian insufficiency can be diagnosed if women have what [3]?

A

NICE guidelines on menopause (2015) say premature ovarian insufficiency can be diagnosed in women younger than 40 years with typical menopausal symptoms plus elevated FSH.
- The FSH level needs to be persistently raised (more than 25 IU/l) on two consecutive samples separated by more than four weeks to make a diagnosis.
- The results are difficult to interpret in women taking hormonal contraception.

56
Q

How do you manage POI? [2]

A

Management involves hormone replacement therapy (HRT) until at least the age at which women typically go through menopause
- associated with a lower blood pressure compared with the combined oral contraceptive pill

OR

Combined oral contraceptive pill