Women’s Health - Obestetrics Flashcards

1
Q

What are the steps (5 key ones) to the examination of the pregnant abdomen?

A

SLeeP EAsy
- introduction, consent and pain?
- GI - previous ECS scar?

Palpation:

  • symphyseal-fundal height
  • the lie - how many poles can you feel in the fundus
    • 1 - longitudinal - most common
    • 2 - transverse (-) or oblique (\ /)
  • the presentation- FACE FEET, ballot each pole, cephalic or breech
    • head feels boney vs bottom feel softer
  • the engagement - how many fifths?
  • fetal back → auscultation anterior shoulder (110-160bpm)
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2
Q

Define antepartum haemorrhage and outline the main causes of it

A

Antepartum haemorrhage (APH) is defined as bleeding from or in to the genital tract, occurring from 24+0 weeks of pregnancy and prior to the birth of the baby.

  • Occurs in 5% of pregnancies

Causes:
- No Identifiable cause in 40%
3 important causes:
- placenta praevia - painless bleeding
- placental abruption - painful bleeding
- Vasa praevia

  • Infection
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3
Q

What is low lying placenta vs placenta praevia

A

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. This is subdivided into partial and complete praevia (placenta completely covers the internal os)

Delivery of the placenta before baby is incompatible with survival.

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4
Q

How is placenta praevia diagnosed

A

Diagnosed at the routine 20-week anomaly scan - used to assess the position of the placenta and diagnose placenta praevia.

The scan is then repeated at 32 weeks (and 36 weeks) because the lower segment of the womb can stretch, if more than 2cm away from the internal os can avoid caesarian section

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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5
Q

Management of low lying placenta

A

Caesarian section - Planned delivery is considered between 36 and 37 weeks gestation. It is planned early to reduce the risk of spontaneous labour and bleeding. Planned cesarean section is required with placenta praevia and low-lying placenta (<20mm from the internal os).

Corticosteroids are given between 34 and 35 + 6 weeks gestation to mature the fetal lungs, given the risk of preterm delivery.

Advice:
- present if bleeding/pain
-avoid intercourse
- recurrent bleeding may require admission until delivery (remeber that lady in kings)
- anti-D if bleeding

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6
Q

KEY understanding - When is instrumental delivery indicated?

A

ONLY USED IN THE SECOND STAGE - if there is failure to progress (malpositioning, maternal exhuastion) or fetal distress

(failure to progress is after 2 hours in nulliparous women (one hour for decent, one hour pushing) or 1 hour pushing in multiparous.

If there is failure to progress or fetal compromise before 10cm then emergency CS is used. OMG this is key hun!

In general, the pre-requisites for performing an instrumental delivery are:

Fully dilated
Ruptured membranes
Cephalic presentation
Fetal head at least at the level of the ischial spines, and no more than 1/5 palpable per abdomen

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7
Q

What is vasa praevia? What are the two types?

A

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.

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.

There are two types of vasa praevia:

Type I vasa praevia – the fetal vessels are exposed as a velamentous umbilical cord (the umbilical cord inserts into the chorioamniotic membranes, and the fetal vessels travel unprotected through the membranes before joining the placenta)

Type II vasa praevia – the fetal vessels are exposed as they travel to an accessory placental lobe

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8
Q

Diagnosis of Vasa praevia

A

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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9
Q

Management of Vasa praevia

A

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.

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10
Q

What are the three types of morbidly adherent placenta?

A

Placenta accreta spectrum refers to when the placenta implants deeper, through and past the endometrium, making it difficult to separate the placenta after delivery of the baby.

There are three distinctions:
- placenta accreta is where the placenta implants at 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

mnemonic: accreta - placenta is at the myometrium, intreat - placenta is in the myometrium, percreta is past the myometrium

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11
Q

Diagnosis and management of morbidly adherent placenta?

A

Ideally it is diagnosed on antenatal ultrasound scans -> Mx w/ early delivery by caesarian (35-37 weeks + antenatal steroids)

It may be diagnosed at birth, when it becomes difficult to deliver the placenta. It is a cause of significant postpartum haemorrhage

The options during caesarean are:
1. Hysterectomy with the placenta remaining in the uterus (recommended)
2. Uterus preserving surgery, with resection of part of the myometrium along with the placenta
3. Expectant management, leaving the placenta in place to be reabsorbed over time. Expectant management comes with significant risks, particularly bleeding and infection.

What happens if undiagnosed and not a caesarian?

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12
Q

What is placental abruption? how does it present?

A

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.

Don’t confuse this with uterine rupture

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.

The typical presentation of placental abruption is with:

  • 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
  • remember concealed abruption - cervical os remains closed and any haemorrhage remains in the uterus - maternal shock and pain appears disproportionate to the amount of bleeding

There is no test- US only rules out placenta praevia as a cause of bleeding.

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13
Q

Management of placental abruption

A

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.

Any woman presenting with a significant antepartum haemorrhage should be resuscitated using an ABCDE approach. Do not delay maternal resuscitation in order to determine fetal viability. IV access, fluids, tranfusion. CTG monitoring.

The ongoing management of placental abruption is dependent on the health of the fetus:

Emergency delivery – indicated in the presence of maternal and/or fetal compromise and usually this is by caesarean section unless spontaneous delivery is imminent or instrumental vaginal birth is achievable.

Antenatal steroids are offered between 24 and 34 + 6 weeks gestation to mature the fetal lungs in anticipation of preterm delivery.

Induction of labour – for haemorrhage at term without maternal or fetal compromise, induction of labour is usually recommended to avoid further bleeding.

Conservative management – for some partial or marginal abruptions not associated with maternal or fetal compromise (dependant on the gestation and amount of bleeding).

In all cases, give anti-D within 72 hours of the onset of bleeding if the woman is rhesus D negative. 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.

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14
Q

Pre-eclampsia - Define:
- chronic hypertension
- pregnancy-induced hypertension
- pre-eclampsia
- severe pre-eclampsia
- eclampsia

A

Chronic hypertension is high blood pressure that exists before 20 weeks gestation and is longstanding. This is not caused by dysfunction in the placenta and is not classed as pre-eclampsia.

Pregnancy-induced hypertension or gestational hypertension is hypertension occurring after 20 weeks gestation, without proteinuria.

Pre-eclampsia is pregnancy-induced hypertension associated with organ damage, notably proteinuria.

Severe pre-eclampsia is pregnancy induced hypertension + proteinuria + neurological (headache, visual dirsturbance, clonus), hepatorenal (deranged LFTs, hepatomegaly, reduced platelets - HELLP), clotting

Eclampsia is when seizures occur as a result of pre-eclampsia.

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15
Q

severities of antepartum haemorrhage

A

The RCOG guideline (2011) defines the severity of antepartum haemorrhage as:

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 shoc

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16
Q

Diagnosis of pre-eclampsia

A

The NICE guidelines (2019) advise a diagnosis can be made with 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)

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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17
Q

Pathophysiology - by what mechanism does pre-eclampsia lead to eclampsia

A

This is a me card
Third spacing!!!

Third-spacing occurs when too much fluid moves from the intravascular space (blood vessels) into the interstitial or “third” space—the nonfunctional area between cells . This can cause potentially serious problems such as oedema, reduced cardiac output, and hypotension. Hypertension -> cerebral oedema -> seizure

yes interstitial fluid usually isn’t a problem, but here there is high pressure leading to too much interstitial fluid -> oedema

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18
Q

Pathophysiology of pre-eclampsia. How does pregnancy lead to hypertension?

A

Occurs after 20 weeks gestation - lacunae form in the placenta for exchange with chronic villi. 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.

Background:
Trophoblast invades endometrium -> Endometrial spiral arteries break down and form lacunae (lakes) in the intervillous space. Maternal blood flows from the uterine arteries, into these lacunae, and back out through the uterine veins. Lacunae form at around 20 weeks gestation. These lacunae surround the chorionic villi (a bit like alveoli knots of fetal vessels) , separated by the placental membrane. Oxygen, carbon dioxide and other substances can diffuse across the placental membrane between the maternal and fetal blood.

Look at a diagram xx

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19
Q

Medical Management of pre-eclampsia, including prophylaxes

A

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 - chronic hypertension, previous pregnancy induced hypertension, autoimmune disease, diabetes, CKD
Two or more moderate-risk factors - maternal age over 40, BMI over 35, 10+ since previous pregnancy, first pregnancy, family history, multiple pregnancy

Medical management of pre-eclampsia is with:

  • Labetolol is first-line as an antihypertensive
  • Nifedipine (modified-release) is commonly used second-line
  • methyldopa is third line
  • 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

Treating to aim for a blood pressure below 135/85 mmHg. Admission for women with a blood pressure above 160/110 mmHg. IV hydralazine may be used in severe pre-eclampsia

Planned early birth may be necessary if the blood pressure cannot be controlled or complications occur. (remember Lisa- birth is the only cure) Corticosteroids should be given to women having a premature birth to help mature the fetal lungs.

In women with pre-exsitng/chronic hypertension - management is the same as pregnancy induced hypertension. They need aspirin prophylaxis, treatment with labetalol -> nifedipine -> methyldopa. Treatment target is 135/85mmHg. Remeber ACE inhibitors are contraindicated, as are ARBs, thiazides.

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20
Q

Mx of eclampsia

A

Eclampsia refers to the seizures associated with pre-eclampsia. IV magnesium sulphate is used to manage seizures associated with pre-eclampsia.

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21
Q

What is maternal sepsis? What is septic shock?

What are the two causes of sepsis in pregnancy?

A

Sepsis is a condition where the body launches a large immune response to an infection, causing systemic inflammation and affecting the functioning of the organs of the body. It is still the leading cause of maternal death!

Severe sepsis is when sepsis results in organ dysfunction, such as hypoxia, oliguria or raised lactate. Septic shock is defined when arterial blood pressure drops (inflammation -> vasodilation) and results in organ hypo-perfusion.

Two key causes of sepsis in pregnancy are:

Chorioamnionitis
Urinary tract infections

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22
Q

Signs of sepsis, Signs of Chorio, Signs of UTI

A

The non-specific signs of sepsis include:

Fever
Tachycardia
Raised respiratory rate (often an early sign)
Reduced oxygen saturations
Low blood pressure
Altered consciousness
Reduced urine output
Raised white blood cells on a full blood count
Evidence of fetal compromise on a CTG

MEOWS - maternaity early obstetric warning sustem monitors for the signs of sepsis.

Additional signs and symptoms related to chorioamnionitis include:

Abdominal pain
Uterine tenderness - why Tess did the abdo examine on women with PROM
Vaginal discharge

Additional signs and symptoms related to a urinary tract infection include:

Dysuria
Urinary frequency
Suprapubic pain or discomfort
Renal angle pain (with pyelonephritis)
Vomiting (with pyelonephritis)

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23
Q

Management of maternal sepsis

A

Septic Six- BUFALO!

B- Blood cultures
U - Urine output
F- IV fluids
A - Empirical broad-spectrum antibiotics
L - Blood lactate level
O - oxygen to maintain sats 94-98%

Continous maternal and fetal monitoring (CTG) is required. Emergency C-section is indicated for signs of fetal distress.

Antibiotics used for maternal sepsis:
- piperacillin and tazobactam (tazocin) + gentamicin
- amoxicillin, clindamycin and genatimicin.

amoxicillin - gram positive coverage
Clinda - gram positive coverage
Gent - gram negative coverage.

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24
Q

Fetal compromise on CTG - what are early, late and prolonged decellarations? What is one significantly worrying sign on CTG

A

Early- vagus stimulation, these are normal
Late- hypoxia, fetus not coping
prolonged - compression of the cord

Early decelerations are gradual dips and recoveries in heart rate that correspond with uterine contractions. The lowest point of the declaration corresponds to the peak of the contraction. Early decelerations are normal and not considered pathological. They are caused by the uterus compressing the head the fetus, stimulating the vagus nerve of the fetus, slowing the heart rate.

Late decelerations are gradual falls in heart rate that starts after the uterine contraction has already begun. There is a delay between the uterine contraction and the deceleration. The lowest point of the declaration occurs after the peak of the contraction (they don’t line up!). Late decelerations are caused by hypoxia in the fetus, and are a more concerning finding. They may be caused by excessive uterine contractions, maternal hypotension or maternal hypoxia.

Prolonged decelerations 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.
A sinusoidal CTG is a rare pattern to be aware of, as it can indicate severe fetal compromise. It gives a pattern similar to a sine wave, with smooth regular waves up and down that have an amplitude of 5 – 15 bpm. It is usually associated with severe fetal anaemia, for example, caused by vasa praevia with fetal haemorrhage.

A sinusoidal CTG is a rare pattern to be aware of, as it can indicate severe fetal compromise. It gives a pattern similar to a sine wave, with smooth regular waves up and down that have an amplitude of 5 – 15 bpm. It is usually associated with severe fetal anaemia, for example, caused by vasa praevia with fetal haemorrhage.

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25
Q

What is cord prolaspe?

biggest risk factor?

management?

A

Cord prolapse is when the umbilical cord descends below the presenting part of the fetus and through the cervix into the vagina, after rupture of the fetal membranes. There is a significant danger of the presenting part compressing the cord, resulting in fetal hypoxia.

The most significant risk factor for cord prolapse is when the fetus is in an abnormal lie after 37 weeks gestation (i.e. unstable, transverse or oblique). Being in an abnormal lie provides space for the cord to prolapse below the presenting part. In a cephalic lie, the head typically descends into the pelvis, without room for the cord to descend.

Management:
Emergency caesarean section is indicated where cord prolapse occurs. A normal vaginal delivery has a high risk of cord compression and significant hypoxia to the baby.

Pushing the cord back in is not recommended -> (handling causes vasospasm).

When the baby is compressing a prolapsed cord, the presenting part can be pushed upwards to prevent it compressing the cord. Woman lies in the left lateral position and Tocolytic medication (e.g. terbutaline) can be used to minimise contractions

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26
Q

What is a post-partum haemorrhage. What are the two types? What are the main causes?

A

Postpartum haemorrhage (PPH) refers to bleeding after delivery of the baby and placenta. It is the most common cause of significant obstetric haemorrhage, and a potential cause of maternal death (but not baby- antepartum with praevias and abruption…)

500ml after a vaginal delivery
1000ml after a caesarean section

It can also be categorised as:
Primary PPH: bleeding within 24 hours of birth
Secondary PPH: from 24 hours to 12 weeks after birth

There are four causes of postpartum haemorrhage, remembered using the “Four Ts” mnemonic:

T – Tone (uterine atony – the most common cause)
T – Trauma (e.g. perineal tear)
T – Tissue (retained placenta) - this is the secondary cause, the others are primary usually
T – Thrombin (bleeding disorder)

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27
Q

Management of post-partum haemorrhage

A

Treat the Cause - 4 Ts:

Stopping the bleeding:

  • mechanical stimulation (rubbing) the uterus
  • catheritisation (full bladder prevents contraction)

Medical:
- syntocinon
- Ergometrine - stimulates smooth muscle contraction
- carboprost (haemobate- prostoglandin analogue -> contraction)
-tranexamic acid (anti-fibrinolytic)
- Misoprostol

Surgical treatment options involve:

Intrauterine balloon tamponade – inserting an inflatable balloon into the uterus to press against the bleeding
B-Lynch suture – putting a suture around the uterus to compress it
Uterine artery ligation – ligation of one or more of the arteries supplying the uterus to reduce the blood flow
Hysterectomy is the “last resort” but will stop the bleeding and may save the woman’s life

Secondary post-partum haemorrhage:
Secondary postpartum haemorrhage is where bleeding occurs from 24 hours to 12 weeks postpartum. This is more likely to be due to retained products of conception (RPOC) or infection (i.e. endometritis).

Investigations involve:
Ultrasound for retained products of conception
Endocervical and high vaginal swabs for infection

Management depends on the cause:
Surgical evaluation of retained products of conception
Antibiotics for infection

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28
Q

What is the only known cause of shoulder dystocia? 4 complications?

A

1% of vaginal births

Shoulder dystocia is when the anterior shoulder of the baby becomes stuck behind the pubic symphysis of the pelvis, after the head has been delivered. This requires additional obstetric manoeuvres to enable delivery of the rest of the body.

Shoulder dystocia is an obstetric emergency:
The key complications of shoulder dystocia are:

Fetal hypoxia (and subsequent cerebral palsy)
Brachial plexus injury and Erb’s palsy
Perineal tears
Postpartum haemorrhage

Shoulder dystocia is often caused by macrosomia secondary to gestational diabetes.

presentation - not testing just a reminder:
Shoulder dystocia presents with difficulty delivering the face and head, and obstruction in delivering the shoulders after delivery of the head. There may be failure of restitution, where the head remains face downwards (occipito-anterior) and does not turn sideways as expected after delivery of the head. The turtle-neck sign is where the head is delivered but then retracts back into the vagina.

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29
Q

Management of Shoulder dystocia (5 steps)

A

External manoeuvres:
1. McRoberts manoeuvre involves hyperflexion of the mother at the hip (bringing her knees to her abdomen). This provides a posterior pelvic tilt, lifting the pubic symphysis up and out of the way - 90% resolve here

  1. Pressure to the anterior shoulder involves pressing on the suprapubic region of the abdomen. This puts pressure on the posterior aspect of the baby’s anterior shoulder, to encourage it down and under the pubic symphysis. (backs to maternal right/left - want to push on the back of the sholder)

Then internal manoeuvres:
3. rotational manoeuvre (rubins) - hands inside vagine push posterior aspect of anterior sholder and anterior aspect of posterior cholder to twist shoulders under the pubic synthesis
4. remove the posterior arm

  1. If internal manoeuvres fail - Zavanelli manoeuver involves pushing the baby’s head back into the vagina so that the baby can be delivered by emergency caesarean section.
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30
Q

What are the three stages of labour? What is partogram used for?

A

First stage (until 10cm dilation of the cervix) - subdivided into:
- latent first stage (up until 4cm)
-active first stage (active labour) (from 4cm-10cm)

Second stage - 10cm to delivery of the fetus

Third stage - from delivery of the fetus to delivery of the placenta

Partogram is for the First stage only! (remember second stage- pushing takes 1/2 hours)

Women are monitored for their progress in the first stage of labour using a partogram - cervical dilation nd fetal head dissent recorded amongst other things. Crossing the alert line is an indication for amniotomy (artificially rupturing the membranes) and a repeat examination in 2 hours. Crossing the action line means care needs to be escalated to obstetric-led care and senior decision-makers for appropriate action.

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31
Q

What is the main complication of placenta praevia and how is it managed? (5 Mx options)

A

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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32
Q

How long should the second stage of labour last?

A

The success of the second stage depends on “the three Ps”: power, passenger and passage. Delay in the second stage is when the active second stage (pushing) lasts over:

2 hours in a nulliparous woman
1 hour in a multiparous woman

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33
Q

What is involved in active management of the third stage of labour?

A

Active management involves intramuscular oxytocin and controlled cord traction.

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34
Q

Management of Failure to Progress (4 options)

A

The main options for managing failure to progress are:

  • Amniotomy, also known as artificial rupture of membranes (ARM) for women with intact membranes
  • Oxytocin infusion
  • Instrumental delivery
  • Caesarean section

remember this is both first and second stage

Oxytocin is used first-line to stimulate uterine contractions during labour. It is started at a low rate and titrated up at intervals of at least 30 minutes as required. The aim is for 4 – 5 contractions per 10 minutes. Too few contractions will mean that labour does not progress. Too many contractions can result in fetal compromise, as the fetus does not have the opportunity to recover between contractions.

The condition of the fetus needs to be monitored throughout labour and delivery. Fetal compromise may mean delivery needs to be expedited, or example, with emergency caesarean section.

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35
Q

Physiology of the second stage of labour -
- the 7 cardinal movements?
Why these movements - key understanding

A

There are seven cardinal movements of labour:

Engagement
Descent
Flexion
Internal Rotation
Extension
Restitution and external rotation
Expulsion

Explanation
- the pelvic inlet is widest side to side, the pelvic outlet is widest front to back
- the fetal skull is widest front to back (sagittally)
- enters the pelvic inlet Occiput tranverse so that the widest part of the skull aligns with the widest part of the pelvis, then internally rotates to exit at the pelvis outlet
- flexion of the head (chin to chest) - reduces the diameter of the head, if baby is OP this also increases diameter because baby can’t flex
- extend head around the pubic synthesis
-external rotation because shoulders are wider (not as long as the head sagittally, but wider than it coronally)

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36
Q

Diagnosing the onset of labour - 4 signs?

A

The signs of labour are:

  • Show (mucus plug from the cervix)
  • Rupture of membranes
  • Regular, painful contractions (vs Braxton hicks which are irregular)
  • Dilating cervix on examination
37
Q

How is a pregnancy of unknown location monitored?

A

Serum human chorionic gonadotropin (hCG) can be tracked over time to help monitor a pregnancy of unknown location. The serum hGC level is repeated after 48 hours, to measure the change from baseline.

The developing syncytiotrophoblast of the pregnancy produces hCG. In an intrauterine pregnancy, the hCG will roughly double every 48 hours. This will not be the case in a miscarriage or ectopic pregnancy.

A rise of more than 63% after 48 hours is likely to indicate an intrauterine pregnancy. A repeat ultrasound scan is required after 1 – 2 weeks to confirm an intrauterine pregnancy. A pregnancy should be visible on an ultrasound scan once the hCG level is above 1500 IU / l.

A rise of less than 63% after 48 hours may indicate an ectopic pregnancy. When this happens the patient needs close monitoring and review.

A fall of more than 50% is likely to indicate a miscarriage. A urine pregnancy test should be performed after 2 weeks to confirm the miscarriage is complete.

Monitoring the clinical signs and symptoms is more important than tracking the hCG level, and any change in symptoms needs careful assessment.

38
Q

Summary of intrahepatic cholestasis of pregnancy
- what is it
- when does it present
- pathophysiology and presentation
- complication
- Ix
- Mx

A

Obstetric cholestasis is characterised by the reduced outflow of bile acids from the liver.

Occours in roughly 1% of pregnancies and usually presents with the third trimester

Bile acids are produced from the breakdown of cholesterol in the liver. In obstetric cholestasis the processing and outflow of bile acids is reduced and meaning that they build up in the blood. This causes pruritis (particularly in the palms of the hands and soles of the feet).

Complication - Bile acids are fetotoxic and OC is is associated with increased risk of stillbirth

LFTs and bile are used for monitoring- weekly. (if substantially elevated delivery is brough foward). Remeber ALP normally rises in pregnancy due to placental production. Other Ix - OC is a diagnosis of exclusion so other cause of raised LFTs are ecluded - hepititis bloods, US liver.

Management:
- The condition resolves after delivery of the baby - if LFTs deranged this needs to be brought forward to reduced risk of stillbirth
- emollients, topical menthol
- anti-histmamine help with sleeping, not itching (bile acids not histmaine causing the itch)
- vitamin K if PT is deranged
- Formerly used ursodeoxycholic acid - no longer advised

39
Q

Premature labour - definition

A

Birth before 37 weeks gestation. The more premature, the worse the outcomes.

Babies born before 24 weeks are not concidered viable.

40
Q

HERE IS WHERE THE EDITING SHOULD START

A
41
Q

A key card
What is a PROM and P-PROM?
Ix?
Management of Both?

A

Different to a SROM (spontanoeus)

PROM - prelabour rupture of memebranes - when fetal membranes rupture (waters break but contractions don’t occour) past 37 weeks gestation.

P-PROM - Preterm prelabour rupture of membranes is where the amniotic sac ruptures, releasing amniotic fluid, before the onset of labour and in a preterm pregnancy (under 37 weeks gestation).

Ix:
- speculum examination to assess for pooling of amniotic fluid in the vagina
- If there is doubt then tests can be performed to confirm that the fluid isn’t just physiological discharge - ILGFBP-1 or PAMG-1.

Management of PROM and P-PROM
>36 weeks (PROM) - monitor for signs of choria and induction of labour if not in labour within 24 hours

P-PROM:
- 34-36 weeks then ertythromycin for chorio prophalaxis, before 34+6 cortiosteroids and IOL recommended (historically people wated until 36 weeks unless evidence of chorio but now management has shifter to IOL at 34 weeks).
- if before 34 weeks monitor for chorio, prophalactic erthyromcyin and wait until 34 weeks

42
Q

Prophalaxis of preterm labour

A

Vaginal progesterone:
cervical legnth <25mm between 16-24 weeks -> vaginal progesterone to decrease mymoetrium actvitiy and cervic remodelling

Prophalactic cervical cerclage - cervical legnth <25mm between 16-24 weeks + a previous premature birth or cervical traima (colposcopy + cone biopsy)

Rescue cervical cerclage - between 16-28 weeks where Painless cervical dilation occours without ROM to prevent progression and premature delivery. Contractions (painful tightenings), signs of chorio and ROM are absolute contraindications.

43
Q

how is ROM diagnased

A

Clinically- amniotic fluid pooling in the vagina on speculum examination

If doubt - test the fluid for Insulin-like growth factor-binding protein-1 (IGFBP-1) or Placental alpha-microglobin-1 (PAMG-1).

44
Q

Key Card:
What is preterm labour with intact membranes?

Management of PLWIM vs P-PROM

A

Preterm labour with intact membranes involves regular painful contraction and cervical dilatation, without rupture of the amniotic sac.

Diangosis:
<30 weeks - clinical
>30 weeks - TV USS shows cervical legnth less than 15mm (above this preterm labour is unlikely)

Key understadning point
Unlike with P-PROM, in PLWIM the labour process has started so the goal of management is steroids and IV mag sulf for prematurity. P-Prom Mx is all about preventing chorio and waiting until labour starts. Mag sulfate isnt used because they arent in labour, steroids are used once at 34 weeks before induction.

Management of Preterm labour (with or without intact membranes
- CTG monitoring
- tocolysis with nifedipine (CCB) - only for 48 hours to buy time for steroids and IV magnesium sulfate
- maternal corticosteroids (before 36 weeks) - reduce repsiratory distress sydrome (2 doses 24 hours apart)
- IV magnesium suphate (before 34 weeks) - neuroprotection (cerebral palsy)
- delayed cord clamping - increase circulating blood volume in the baby

P-PROM (before the onset of labour) Mx:
- prophalactic erthromycin for chrioamnionitis
- if <34 weeks then just prophalaxis and delivery at 34 weeks.
- if >36 weeks delivery
- steroid and mag sulfate as required
- THIS IS ANOTHER CARD.

45
Q

What is baby blues and how is it managed

A

Baby blues affect more than 50% of women in the first week or so after birth, particularly first-time mothers. It presents with symptoms such as:

  • Mood swings
  • Low mood
  • Anxiety
  • Irritability
  • Tearfulness

Baby blues may be the result of a combination of:

  • Significant hormonal changes
  • Recovery from birth
  • Fatigue and sleep deprivation
  • The responsibility of caring for the neonate
  • Establishing feeding
  • All the other changes and events around this time

Symptoms are usually mild, only last a few days and resolve within two weeks of delivery. No treatment is required.

46
Q

What is postnatal depression and how is it managed (3)

A

Postnatal depression is similar to depression that occurs outside of pregnancy, with the classic triad of:

  • Low mood
  • Anhedonia(lack of pleasure in activities)
  • Low energy

Typically, women are affected around three months after birth. Symptoms should last at least two weeks before postnatal depression is diagnosed.

Treatment is similar to depression at other times:

  • Mild casesmay be managed with additional support, self-help and follow up with their GP
  • Moderate casesmay be managed withantidepressant medications(e.g. SSRIs) andcognitive behavioural therapy
  • Severe casesmay need input from specialist psychiatry services, and rarely inpatient care on themother and baby unit

Note- different to baby blues (huge hormonal and life change for a few weeks after birth)

47
Q

What screening tool is used for post natal depression

A

The Edinburgh postnatal depression scale can be used to assess how the mother has felt over the past week, as a screening tool for postnatal depression.

There are ten questions, with a total score out of 30 points. A score of 10 or more suggests postnatal depression.

48
Q

What is puerperal psychosis? How is it managed?

A

puerperal - 6 weeks after birth whilst body reverts to non-pregnant condition

Puerperal psychosis is a rare (1 in 1000) but severe illness that typically has an onset between two to three weeks after delivery. Women experience full psychotic symptoms, such as:

  • Delusions
  • Hallucinations
  • Depression
  • Mania
  • Confusion
  • Thought disorder

Women with puerperal psychosis need urgent assessment and input from specialist mental health services.

Treatment is directed by specialist services, and may involve:

  • Admission to themother and baby unit
  • Cognitive behavioural therapy
  • Medications (antidepressants,antipsychoticsormood stabilisers)
  • Electroconvulsive therapy(ECT)
49
Q

What is the most common cause of polyhydramnios

A

Gestational diabetes - polyurea

Also unlinking about oesophageal atresia - baby not swallowing

50
Q

What is the biggest risk factor for abnormally adherent placenta

A

Main risk is multip with previous section. If low lying placenta at 20 weeks rescan at 30 weeks. If still low lying then MRI to see if there is a clear boundry between placenta (just a praevia) and uterus or if placenta acreta spectrum.

Can be a cause of antepartum haemorrage, also diagnosed with difficulty delivering the placenta.

51
Q

When Triaging a pregnant lady what 3 key Sx do the midwives ask - useful things for your history

A

Movements
Pain
Bleeding or fluid loss from down below

52
Q

NOT ON THE LIST, What is hyperemesis gravidarum?

A

The severe form of nausea and vomiting in pregnancy is called hyperemesis gravidarum. Hyper- refers to lots, -emesis refers to vomiting and gravida- relates to pregnancy.

Plus 5% weight loss, dehyrdation or electrolyte imbalance

Management is with anti-emetics
- prochlorperazine
- cyclizine
- ondansetron
-metoclopramide

Nausea and vomiting are normal during early pregnancy. Symptoms usually start from 4 – 7 weeks, are worst around 10 – 12 weeks and resolve by 16 – 20 weeks. Symptoms can persist throughout pregnancy. It is thought to be caused by placental production of hCG

53
Q

NOT ON THE LIST

9 classes of drugs that are best avoided in pregnancy. all but 2 are contraindicated. Not on the list but i recon very helpful to know.

A

Not an exhuastive list!

NSAIDs - gnerally avoided because they block prostaglandins (important in maintaining the ductus arteriosus) and delay labour (prostaglandins stimulate uterine contractions). Aspirin works differently.

Beta blockers (except labetalol) - can cause fetal growth restriction, hypoglycemia and bradycardia in the neonate

ACE inhibitors - cross the placenta and cause oligohydramnios (reduced perfusion of foetal kidneys), hypocalvaria (incomplete formation of skill bones), Interuterine death

Opiates - OKAY - can cause neonatal abstinence syndrome after birth (withdrawal). NAS presents between 3 – 72 hours after birth with irritability, tachypnoea (fast breathing), high temperatures and poor feeding.

Warfarin - teratogenic

Sodium valproate - teratogenic

isotretinoin (severe acne) - teratogenic

lithium (mania Rx) - cardiac abnormalities if used in the first trimester. other antipsychotics are preferred

SSRIs - OKAY - are the most commonly used antidepressants in pregnancy. Untreated depression can be significant in pregnancy so needs to be balanced with the risks. Main risk is persistent pulmonary hypertension in the neonate.

54
Q

Gestational diabetes - what are the 2 most significant complications?

A

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.

The other is neonatal hypoglycaemia. Babies become accustomed to the high glucose levels during pregnancy and struggle to maintain their blood glucose afar birth.

Longer-term, women are at higher risk of developing type 2 diabetes after pregnancy.

55
Q

What is the screening test for gestational diabetes? Which women are screened? What are the results?

A

OGTT around25 weeks is the screening test

Woman with previous gestational diabetes are offered screening shortly after booking clinic and again around 25 weeks gestation

Risk factors that warrent 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) - not gestational just tyoe 1 or 2

OGTT is also used when there are features that suggest gestational diabetes:

  • Large for dates fetus
  • Polyhydramnios (increased amniotic fluid)
  • Glucose on urine dipstick

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.

TOM TIP: It is really easy to remember the cutoff for gestational diabetes as simply 5 – 6 – 7 – 8.

56
Q

Management of gestational diabetes

A

Diet and exercise -> metformin -> insulin

Insulin needs to be used if there is a fasting glucose >7, or >6 with macrosomia

woman are managed in joint diabetes and antenatal clinics and need to monitor their blood glucose several times a day.

57
Q

How are women with pre-existing diabetes managed in pregnancy? 4 key points

A

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.

Planned delivery between 37-39 weeks is recommended (gestational is up to 41 weeks)

Type 1 diabetes - sliding scale insulin regime during labour.

58
Q

Anaemia in pregnancy - what are the normal Hb levels? What tests are used? when are women screened for anaemia?

A

Women are routinely screened for anaemia twice during pregnancy:

Booking clinic
28 weeks gestation

Ix
FBC- (Hb level):

Normal Hb levels are 110, 105 and 100 in the 1st, 2nd, 3rd trimester (usually in women 120, men 136)

The mean cell volume (MCV) can indicate the cause of the anaemia:

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

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 severe anaemia in pregnancy - managed with folic acid and transfusions.

Additional investigations are not routinely performed, by may help establish the cause of the anaemia. They may include: Ferritin, B12, Folate

Background:
Defined as low concentration of haemoglobin. 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.

Also just makes women feel SOB, fatigue, dizzyness like normal.

59
Q

Management of anaemia in pregnancy

A

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 deficiency is treated with IM hydroxocobalamin. Often it is physiological (increased plasma volume and B12 requirements) but women with B12 deficiency should have testing for intrinsic factor antibodies (pernicious)

Folate - already on 400mcg. women should go onto 5 mg if folate deficient.

thalassemia and sickle cell - managed with folic acid and transfusions as required.

60
Q

What is oligohydramnios? what causes it - 3 key things?

A

Oligohydramnios occurs when the amniotic fluid index is < 5th centile for gestational age. Amniotic fluid is usually recorded as the amniotic fluid index (Amniotic fluid index is calculated by measuring maximum cord-free vertical pocket of fluid in four quadrants of the uterus and adding them together.

Amniotic fluid is primary comprised of foetal urine output. As such the most common causes of oligohydramnios are:

  • premature ROM (amniotic fluid leaks)
  • placental insufficiency (blood flow to the brain is prioritised so poor blood flow to foetal kidneys)
  • structural problems with the renal kidneys - renal agenesis
  • there are toehrs but these are the main ones.

Management then follows a SROM (delivery after 34 weeks, steroids IV magnesium sulfate, erhtyromycin) or a placetnal insufficiency pathway (early delivery, usually ebfore 36 weeks.

61
Q

What is polyhydramnios? Cause?

A

It is defined by an amniotic fluid index that is above the 95th centile for gestational age.

The main cause for this is idiopathic, but structural (oesophageal or duodenal atresia, down’s syndrome), viral and diabetes (OGTT) as causes must be investigated for.

Reading made it seem like diabetes was a minor cause but i thought it was the main one.

In contrast to oligohydramnious, if the fetus has no abnormalities then prognosis is good and no management is required. If the maternal symptoms are severe (e.g breathlessness), an aminoreduction can be considered

62
Q

What is small for gestational age

A

Small for gestational age is defined as a fetus that measures below the 10th centile for their gestational age (i think nationally universal growth chart).Severe SGA is when the fetus is below the 3rd centile for their gestational age. Low birth weight is defined as a birth weight of less than 2500g.

Two measurements on ultrasound are used to assess the fetal size:

Estimated fetal weight (EFW)
Fetal abdominal circumference (AC)

63
Q

What is the difference between small for gestational age and interuterine growth restriction

A

The causes of SGA can be divided into two categories:

SGA - can just be constitutional small (matching the mothers size) and growing steadily on the growth chart

Inter-uterine growth restriction - when the foetus is failing to meet their growth potential (plateau on the foetal growth chart) due to a pathology reducing the amount of nutrients and oxygen being delivered to the foetus through the placenta

Extra…

The causes of fetal growth restriction can be divided into two categories:

Placenta mediated growth restriction - pre-eclampsia, maternal smoking, anaemia, malnutrition
Non-placenta mediated growth restriction, where the baby is small due to a genetic or structural abnormality

64
Q

Signs of fetal growth restriction

A
  • small for gestational age on scan
  • reduced liquor volume
  • reduced fetal movements
65
Q

Management of Small for gestational age

A

If there is foetal growth restriction rather than constitutionally small, the babies are at increased risk of stillbirth.

Serial growth scans with umbilical artery doppler

Early delivery is considered when growth is static on the growth charts, or other problems are identified (e.g. abnormal Doppler results). This reduces the risk of stillbirth. Corticosteroids are given when delivery is planned early, particularly when delivered by caesarean section. Paediatricians should be involved at birth to help with neonatal resuscitation and management if required.

A cause of IUG restriction is investigated for- BP and urine for pre-eclampsia, uterine artery doppler scanning, fetal anomaly scan, karyotyping

66
Q

Which way round - umbilical arteries and veins

A

The backwards bit is the oxygenation status (bit like the pulmonary system) - the artereis still come after the fetal heart. Remember the palcenta and cord and fetal organs not maternal.

So the 2 umbilical arteries are branches of the fetal iliac arteries carrying deoxygenated blood and waste to the placenta

The umbilical vein carries OXYGENATED blood (the backwards bit) from the placenta to the ductus venosus.

67
Q

When is a foetus considered large for gestational age babies (macrosomnia)? Main cause? Main risk?

A

When the weight of the newborn is more than 4.5kg at birth. During pregnancy, an estimated fetal weight above the 90th centile is considered large for gestational age.

Main causes:
- constitutional
- gestational diabetes
- maternal obesity
- overdue
- male baby

Complication
- shoulder dystocia -> birth injury (Erbs palsy, clavicular fracture, fetal distress, hypoxia)

68
Q

Ix for large for gestational age babies? Management

A

USS - exclude polyhydramnios and estimate fetal weight

OGGT - for gestational diabetes

When the weight of the new-born is more than 4.5kg at birth. During pregnancy, an estimated foetal weight above the 90th centile is considered large for gestational age. (Although gestational diabetes 41 weeks is the cut off).

Risk of shoulder dystocia can be reduced by delivery on a consultant led unit.

69
Q

What is a normal fetal heart rate

A

110-160 bpm

70
Q

Me - management of reduced fetal movements

A

Reduced fetal movements are usually nothing serious but occassionally they are a sign of fetal death. A Hx needs to consider risk factors for IUD such as FGR, congential abnormalities and placental insufficiency

  1. Auscultate the fetal heart to exclude fetal death
  2. CTG to exclude fetal compromise if the pregnancy is over 28+0 weeks of gestation.
  3. Ultrasound scan assessment should be undertaken as part of the preliminary investigations of a woman presenting with RFM after 28+0 weeks of gestation if the perception of RFM persists despite a normal CTG or if there are any additional risk factors for FGR/stillbirth.

Ultrasound scan assessment should include the assessment of abdominal circumference and/or estimated fetal weight to detect the SGA fetus, and the assessment of amniotic fluid volume.

SUMMARY CTG and USS

71
Q

What is the bishop score and when is it used?

A

The bishop score is an assessment of ‘cervical ripeness‘ based on measurements taken during vaginal examination. It is checked to prior to iduction to determine whether or not to induce and during induction to assess progress (24 hours post-pessary).

A score of 8 or more predicts a successful induction of labour. A score below this suggests cervical ripening may be required to prepare the cervix. Failure of a cervix to ripen despite use of prostaglandins may result in the need for a caesarean section.

Five things are assessed and given a score based on different criteria (minimum score is 0 and maximum is 13):

Fetal station (scored 0 – 3)
Cervical position (scored 0 – 2) - posterior (hard to reach), mid/anterioir - look at a diagram
Cervical dilatation (scored 0 – 3)
Cervical effacement/legnth (scored 0 – 3)
Cervical consistency (scored 0 – 2) - firm, average or soft

72
Q

Indications for induction of labour

A

Induction of labour can be used where patients go over the due date. IOL is offered between 41 and 42 weeks gestation.

Induction of labour is also offered in situations where it is beneficial to start labour early, such as:

Prelabour rupture of membranes
Fetal growth restriction
Pre-eclampsia
Obstetric cholestasis
Existing diabetes
Intrauterine fetal death - mifepristone and misoprostol

73
Q

Methods of induction of labour

A

Membrane sweep involves inserting a finger into the cervix to stimulate the cervix and begin the process of labour. It can be performed in antenatal clinic, and if successful, should produce the onset of labour within 48 hours. A membrane sweep is not considered a full method of inducing labour, and is more of an assistance before full induction of labour. It is used from 40 weeks gestation to attempt to initiate labour in women over their EDD.

Vaginal Prostaglandins - stimulates the cervix and the uterus to cause the onset of labour. Usually done in hospital so that wmen can be monitored before being allowed home to await the full onset of labour. (Jessops get prostglandin and then once cervix is ripe and they are ARMable they get sent home until labour ward has space to ARM)

Cervical ripening balloon - applies pressure about and blow the cervix which softens and dilates the cervix so that amniotomy can then be used. It is used when vaginal prostoglandins are not prefered. Previous C-section (scar dihence risk), multiparous women or postoglanins have failed.

ARM/amniotomy - Artificial rupture of membranes with an oxytocin infusion can also be used to induce labour, although this would only be used where there are reasons not to use vaginal prostaglandins - it should NOT be the primary method of inducing labour but to progress labour when there is no or slow progress with vaginal prostaglandins.The aim is to start low and titrate upwards until there are 4 contractions every 10 minutes.

CTG monitoring and the biscop score are used to monitor induction of labour.

74
Q

What is the main complication of induction of labour and how is it managed

A

Uterine hyperstimulation is the main complication of induction of labour with vaginal prostaglandins. This is where the contraction of the uterus is prolonged and frequent. Uterine hyperstimulation can lead to:

Fetal compromise, with hypoxia and acidosis
Emergency caesarean section
Uterine rupture

The two criteria often given are:

Individual uterine contractions lasting more than 2 minutes in duration
More than five uterine contractions every 10 minutes

Management of uterine hyperstimulation involves:

Removing the vaginal prostaglandins, or stopping the oxytocin infusion
Tocolysis with terbutaline

75
Q

SGA babies are monitored with serial ultrasound scans (growth scans). What three things are measured on scan.

A

REALLY DONT KNOW IF YOU NEED THIS CARD BUT I FOUND IT INTERESTING.

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

FAR BEYOND MED SCHOOL BUT USEFUL:
A raised pulsatility index suggests impaired placental perfusion. NOTE THIS- IT IS INVERSELY PROPORTIONAL TO PERFUSION. In normal pregnancies, umbilical PI starts at high values and then decreases progressively toward term. This indicates that normal placental development entails a progressive decrease in the impedance of the umbilical vascular bed to blood flow.

My understanding - it is the difference in blood flow in the umbilical artery (from fetus to placenta) between the peak systolic flow (fetal heart beating) and end diastolic flow. if the placental resistance is high then there is a big difference because when the fetal heart is in diastoly the flow is massively reduced.

76
Q

Retained products of conception:
- definition
- presentation
- diagnosis
- management

A

Retained products of conception refers to when pregnancy-related tissue (e.g. placental tissue or fetal membranes) remain in the uterus after delivery. It can also occur after miscarriage or termination of pregnancy.

Sx:
- vaginal bleeding that doesnt improve with time
- abnormal vaginal discharge
- pelvic pain
- fever - infection

Diagnosis is with Ultrasound

Management:
Surgical! ERPC -evacuation of RPC under GA.

Key complications are endometritis and ashermans syndrome (damaged endometrium leads to adhesions).

77
Q

What is postpartum endometritis?

A

Endometritis refers to inflammation of the endometrium, usually caused by infection. It can occur in the postpartum period, as infection is introduced during or after labour and delivery. The process of delivery opens the uterus to allow bacteria from the vagina to travel upwards and infect the endometrium.

Endometritis occurs more commonly after caesarean section compared with vaginal delivery. Prophylactic antibiotics are given during a caesarean to reduce the risk of infection.

Endometritis can be caused by a large variety of gram-negative, gram-positive and anaerobic bacteria.

Endometritis can also be caused by sexually transmitted infections such as chlamydia and gonorrhoea. When endometritis occurs unrelated to pregnancy and delivery, it is usually part of pelvic inflammatory disease, which is covered elsewhere.

78
Q

Post partum endometritis

  • Presentation
  • Diagnosis and managment
A

Sx:
Foul-smelling discharge or lochia
Bleeding that gets heavier or does not improve with time
Lower abdominal or pelvic pain
Fever
Sepsis

Mx:
- vaginal swabs
- urine culture and sensativities
- US to rule out RPOC
Rx:
- Sepsis - sepsis six, inc IV antibiotics
- milder symptoms - oral antibiotics

79
Q

Failure to progress - what are the criteria for delay in labour for the first stage?
Second stage?
What might be causing a delay in labour?

A

Delay in active phase labour (4-10cm) is considered when there is either:

Less than 2cm of cervical dilatation in 4 hours
Slowing of progress in a multiparous women

The things that might be causing this- the 3 Ps (another card)

From further reading. Latent phase can take days before reaching established labour, but i think less than 4cm dilated after 12 hours of PAINFUL contractions can be considered a delay?. Also the 2cm in 4 criteria apply for induction with amniotomy below 4cm.

The second stage of labour lasts from 10cm dilatation of the cervix to delivery of the baby. Delay in the second stage is when the active second stage (pushing) lasts over:

2 hours in a nulliparous woman
1 hour in a multiparous woman

Progress in labour is influenced by the three P’s:

Power (uterine contractions)
Passenger (size, presentation and position of the baby)
Passage (the shape and size of the pelvis and soft tissues)

80
Q

PARTOGRAM - what is a partogram and what does it record. What does crossing the alert line indicate.

A

Partograms are used to monitor progress in the first stage of labour

81
Q

Define delay in the third stage of labour,

A

The third stage of labour is from delivery of the baby to delivery of the placenta. Delay in the third stage is defined by the NICE guidelines (2017) as:

More than 30 minutes with active management - involves intramuscular oxytocin and controlled cord traction

More than 60 minutes with physiological management - after 60 minutes of physiological management, or if there is PPH then active management is used.

Sidenote: After delivery of the plancenta the uterus is massaged until it is contracted and firm. The placenta is examined to ensure it is complete and no tissue remains in the uterus.

82
Q

Management of Failure to Progress (4)

A

The main options for managing failure to progress are:

Amniotomy, also known as artificial rupture of membranes (ARM) for women with intact membranes
Oxytocin infusion
Instrumental delivery
Caesarean section

sidenote: changing positions might also be helpful for delay in the second stage

Oxytocin is used first-line to stimulate uterine contractions during labour. It is started at a low rate and titrated up at intervals of at least 30 minutes as required. The aim is for 4 – 5 contractions per 10 minutes. Too few contractions will mean that labour does not progress. Too many contractions can result in fetal compromise, as the fetus does not have the opportunity to recover between contractions.

The condition of the fetus needs to be monitored throughout labour and delivery. Fetal compromise may mean delivery needs to be expedited, or example, with emergency caesarean section.

83
Q

What affects progress in labour

A

Progress in labour is influenced by the three P’s:

Power (uterine contractions)
Passenger (size, presentation and position of the baby)
Passage (the shape and size of the pelvis and soft tissues)

84
Q

Risk of Instrumental delivery? - baby (forceps vs ventous), mum - they are the same

A

The key risks to remember to the baby are:
- Cephalohaematoma with ventouse (blood between the skull and periosteum)
- Facial nerve palsy with forceps

Maternal risks:
- PPH
- episiotomy and perineal tears
- incontinence of bladder or bowel
- nerve injuries: obturator (weakness of hip adduction, medial thigh numbness - makes sense) or femoral nerve (weakeness of knee extension, numbness of anteroir thigh and medial leg) - THESE DISTRUBUTIONS MAKE SENSE WHEN YOU THINK ABOUT THE MUSCLES.

SEPERATE TOM TIP: It is worth remembering there is an increased risk of requiring an instrumental delivery when an epidural is in place for analgesia.

85
Q

VTE in pregancy - what prophalaxis is used and criteria for is offering it?

A

VTE - includes DVT and PE (potentially fatal). Oestrogen in pregnancy makes the blood hypercoagulable. thrombus also occours due to stagnation of blood.

PE is a significant cause of maternal death. The risk is highest in the postpartum period

Women should have their VTE risk assessed at booking and again at birth.

The RCOG guidelines (2015) advise starting prophylaxis with LMWH from:
- 28 weeks if there are three risk factors
- First trimester if there are four or more of these risk factors

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).

Don’t rote learn these - risk factors for VTE in pregnancy:
- smoking
- parity 3<
- age 35<
- BMI 30<
- pre-eclampsia
- gross varicose vains
- imobility
- IVF
- family history
- thrombophilia

86
Q

Management of Breech Presentation

A

Babies that are breech before 36 weeks often turn spontaneously, so no intervention is advised. External cephalic version (ECV) can be used at term (37 weeks) to attempt to turn the fetus. About 5% of pregnancies are breech presentation by 37 weeks

Where ECV fails, women are given a choice between vaginal delivery and** elective caesarean section**. Vaginal delivery needs to involve experienced midwives and obstetricians, with access to emergency theatre if required. There is about a 40% chance of requiring an emergency caesarean section when vaginal birth is attempted.

When the first baby in a twin pregnancy is breech, caesarean section is required.

87
Q

Types of Breech - probs low yield

A

Complete breech, where the legs are fully flexed at the hips and knees - tuck
Incomplete breech, with one leg flexed at the hip and extended at the knee
Extended breech, also known as frank breech, with both legs flexed at the hip and extended at the knee - pike
Footling breech, with a foot is presenting through the cervix with the leg extended

88
Q

What is the main prenancy-related complication of genital herpes? What is the managment?

A

The main issue with genital herpes during pregnancy is the risk of neonatal herpes simplex infection contracted during labour and delivery. Neonatal herpes simplex infection has high morbidity and mortality.

Management:
Management of genital herpes in pregnancy depends on whether it is the first episode of genital herpes (primary infection) or recurrent genital herpes.

Primary gential herpes contracted before 28 weeks:
- aciclovir during the inital infection
- prophalactic aciclovir from 36 weeks
- if asymptomatic they can have a normal delivery, if symptomatic then caesarean section.

Primary genital herpes contracted after 28 weeks gestation
- the same as above (inital and prophalactic aciclovir) however, Caesarean section is recommended in all cases to reduce the risk of neonatal infection.

Recurrent gential herpes (infected before pregnancy -> antibodies cross the placenta)
- low risk of neonatal infeciton even if symptomatic during delivery, so vaginal delivery is possible
- prophalactic aciclovir is considered from 36 weeks

89
Q

HIV in pregnancy

A

The mother’s viral load will determine the mode of delivery:

  • <50 - normal vedilvery
  • > 50 - consider a pre-labour caesarean section
  • > 400 - pre-labour caesarean section is recommended

Zidovudine:
IV zidovudine is given during labour and delivery if the viral load is >1000 or unknown

prophalatic zidovudine is given to baby regardless or viral load, with additonal drugs for high risk babies

Breast feeding:
HIV can be trasnmitted through breastfeeding so it is avoided. It can be attempted with monitoring if the viral load is undetectable.