Final O&G II Flashcards

(55 cards)

1
Q

Which anti-epileptic drugs are safe in pregnancy? [3]

A

Levetiracetam, lamotrigine and carbamazepine are the safer anti-epileptic medication in pregnancy

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1
Q
A
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2
Q

Retinoids cause teratogenicity via which mechanism? [1]

A

Neural crest cell disruption

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3
Q

Describe the effect of using tobacco during pregnancy [+]

A

Low birthweight,
microcephaly, facial clefts

Increased risks of placenta previa, placental abruption, ectopic pregnancy, and PPROM

Reduced fetal oxygenation resulting in IUGR

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4
Q

Excessive alcohol consumption usually defined as >[]g/day during pregnancy [1]

A

Excessive alcohol consumption usually defined as >80g/day

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5
Q

Describe the effects / presentation of fetal alcohol syndrome [+]

A
  • short palpebral fissure
  • thin vermillion border/hypoplastic upper lip
  • smooth/absent filtrum
  • learning difficulties
  • microcephaly
  • growth retardation
  • epicanthic folds
  • cardiac malformations

Features can be remembered with ‘ALCOHOL’ :

Absent philtrum

Learning difficulties

Cardiac malformations

Ocular issues - short palpebral fissure/epicanthic folds

Hypoplastic upper lip

Overall growth ↓

Low head size (microcephaly)

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6
Q

Effects of cocaine during pregnancy? [5]

A
  • spontaneous miscarriage
  • Facial and skeletal anomalies
  • Intestinal atresia
  • Mental & growth retardation
  • Placental abruption
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7
Q

Describe the effects of heroin, methadone or opiates during pregnancy [3]

A
  • Placental vasoconstrictor so IUGR can occur
  • Mental & growth retardation
  • Placental abruption
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8
Q

Describe the treatment ladder for HG [4]

A

Hyperemesis gravidarum treatment dependent on severity: anti-emetics + thiamine 1.5mg od + Prednisolone 16mg od + Parental fluids + TPN1

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9
Q

Which of the following causes NTD and facial clefts during pregnancy

Rifampicin
Isoniazide
Ethambutol
Trimethoprim
Streptomycin

A

Which of the following causes NTD and facial clefts during pregnancy

Rifampicin
Isoniazide
Ethambutol
Trimethoprim
Streptomycin

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10
Q

Which of the following causes ototoxicty during pregnancy

Rifampicin
Isoniazide
Ethambutol
Trimethoprim
Streptomycin

A

Which of the following causes ototoxicty during pregnancy

Rifampicin
Isoniazide
Ethambutol
Trimethoprim
Streptomycin & other aminoglycosides

NB: Erythromycin safe

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11
Q

Which antibiotix drug class can cause dysplasia of bones if given during pregnancy? [1]

A

Tetracyclines

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12
Q

What is the a potential risk of when give levothyroxine during pregnancy? [1]

A

Some suggested association with
unilateral kidney agenesis

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13
Q

Describe the cART rec. for pregnancy [3]

Which drug should be given during labour? [1]

A

tenofovir DF or abacavir with emtricitabine or lamivudine as a nucleoside backbone.

During labour, zidovudine should be administered intravenously until the umbilical cord is clamped.

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14
Q

How do you manage obstetric cholestatis? [4]

A
  • induction of labour at 37 weeks is common practice but may not be evidence based
  • Emollients (i.e. calamine lotion) to soothe the skin
  • ursodeoxycholic acid - again widely used but evidence base not clear
  • vitamin K supplementation if clotting deranged (A lack of bile acids can lead to vitamin K deficiency, which lead to impaited clotting)
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15
Q

What are the symptoms of polymorphic eruption of pregnancy? [4]

A

Lesions are pruritic but spare the periumbilical region, face, and mucosal surfaces:
* Urticarial papules (raised itchy lumps)
* Wheals (raised itchy areas of skin)
* Plaques (larger inflamed areas of skin)

Systemic symptoms are absent.

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16
Q

How do you manage PMEP? [1]

A

Topical emollients
Topical steroids
Oral antihistamines
Oral steroids may be used in severe cases

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17
Q

What are the two main causes of SGA? [2]

A

Constitutionally small, matching the mother and others in the family, and growing appropriately on the growth chart

Fetal growth restriction (FGR), also known as intrauterine growth restriction (IUGR)

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18
Q

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

What are they? [2]

A

Placenta mediated growth restriction

Non-placenta mediated growth restriction, where the baby is small due to a genetic or structural abnormality

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19
Q

What are 4 causes of non-placental mediated growth restriction? [4]

A

Non-placenta medicated growth restriction refers to pathology of the fetus, such as:
* Genetic abnormalities
* Structural abnormalities
* Fetal infection
* Errors of metabolism

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20
Q

What are causes of placental mediated growth restriction? [+]

A

Placenta mediated growth restriction refers to conditions that affect the transfer of nutrients across the placenta:
* Idiopathic
* Pre-eclampsia
* Maternal smoking
* Maternal alcohol
* Anaemia
* Malnutrition
* Infection
* Maternal health conditions

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21
Q

Short term complications of fetal growth restriction include: [4]

A

Fetal death or stillbirth
Birth asphyxia
Neonatal hypothermia
Neonatal hypoglycaemia

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22
Q

How do you monitor for SGA? [2]

A

RCOG green-top guidelines on SGA (2013) lists major and minor risk factors. At the booking clinic, women are assessed for risk factors for SGA.

Low risk women:
- monitoring of the symphysis fundal height (SFH) at every appointment from 24 weeks. If < 10th centile - booked for serial growth scans with umbilical artery doppler

23
Q

How do you monitor SGA for those who are deemed high risk? [3]

A

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

24
What are the risks to baby if they are LGA? [4]
**The risks to the baby include**: * **Birth injury** (Erbs palsy, clavicular fracture, fetal distress and hypoxia) * **Neonatal** **hypoglycaemia** * **Obesity** in **childhood and later life** * **Type 2 diabetes in adulthood**
25
# Lecture: How do determine if the baby is small because the placenta is not formed properly? [3]
**Check** **history** and **consider all risk factors for placental dysfunction** + measure **serum PAPP-A at 11-14 weeks: if < 0.4 placenta** may not have formed properly + **Doppler studies**
26
Describe the the process of hypoxia causing stillbirth [4] Describe how this would be detected on dopplers [4]
**Hypoxia --> acidemia --> CNS damage --> stillbirth:** * **Placental dysfunction** would be indicated by **abnormal uterine artery dopplers (UtA)** * Leads to **abnormal umbilical artery** * Leads to **brain sparing effect** - causing an **abnormal MCA Doppler** * Leads to **reduced cardiac compliance** and **abnormal venous doppler** * Leads to **fetal movements reduced** and **abnormal cCTG.** * Leads to still birth
27
# Lecture Difference between LGA and macrosomia? [1]
**LGA**= **EFW>90th centile** or **EFW>4000g** **Macrosomia**= **EFW>4.500g**
28
# Lecture Name a genetic syndrome which might cause LGA/macrosomia [1] What is the triad seen with it? [3]
**Beckwith Wiedemann** – macroglossia, exomphalos, organomegaly ## Footnote NB: comes up a couple of times in lecture
29
Describe how you manage placental abruption
**Placental abruption is an obstetric emergency**: * Urgent involvement of a senior obstetrician, midwife and anaesthetist * 2 x grey cannula * Bloods include FBC, UE, LFT and coagulation studies * Crossmatch 4 units of blood * Fluid and blood resuscitation as required * CTG monitoring of the fetus * Close monitoring of the mother * **Active management of stage 3 labour** * **Corticosteroids** for baby between **24th and 34th weeks of getation** ## Footnote **NB**: It is important to consider concealed haemorrhage, where the vaginal bleeding may be disproportionate to the uterine bleeding.
30
How do you decide whether to deliver baby if has placental abruption? [4]
Women with **antepartum** **haemorrhage** and **associated maternal and/or fetal compromise** are required to be **delivered immediately**. While **RCOG** **does** **not** **recommend** **premature delivery of fetus** in women with **less than 37 weeks of gestation** with **no fetal and maternal compromise**. **If gestational age** is **equal to or more than 37 weeks** and the **bleeding** presents as **spotting** or **mucus** streaks of blood, **active intervention is unlikely needed.** **Minor or major antepartum bleeding**, RCOG suggests **inducing** **labour** with the **aim of achieving vaginal delivery** to avoid serious complications related to placental abruption
31
How do you manage placenta praevia?
**Diagnosed** **early** in pregnancy (e.g. at the 20-week anomaly scan): - Repeat scan at **32**. If still present.. - Repeat at **36** weeks gestation **Corticosteroids** are given **between 34 and 35 + 6 weeks** gestation to mature the fetal lungs, given the risk of preterm delivery. **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 p**lacenta praevia and low-lying placenta** (< 20mm from the internal os).
32
Describe the pathophysiology of vasa praevia (describe normal vs abnormal formations)
**Normally**: - **umbilical** **cord** containing the **fetal vessels** (umbilical arteries and vein) **inserts directly into the central portion of the placenta**. - The fetal vessels are always **protected**, either by the **umbilical cord or by the placenta.** - The **umbilical cord contains Wharton’s jelly.** Wharton’s jelly is a layer of soft connective tissue that surrounds the blood vessels in the umbilical cord, offering protection. **Vasa praevia:** - Eccentric or marginal insertion of the umbilical cord. Get either: - **Velamentous cord insertion**: umbilical cord inserts into the chorioamniotic membranes rather than centrally into the placental mass. The blood vessels branch out from this point and travel within these membranes before reaching their connection with the placenta. OR - **Bilobed or succenturiate-lobed placentas**: variations in placental morphology where there's more than one lobe to a placenta. If a blood vessel connects two lobes across fetal membranes that traverse overlying cervical os, it can lead to vasa praevia.
33
Further subclassification of vasa praevia can be made based on clinical presentation: What are they? [2]
**Ramified Vasa Praevia**: - Also known as **branching vasa praevia**, it involves **multiple small-calibre vessels crossing over the internal os**. **Funic Presentation Vasa Praevia:** - Characterised by a **single large vessel running over or near the internal os**, often associated with a **funic presentation of umbilical cord.**
34
Describe the clinical features of vasa praevia [5]
**Painless PV Bleeding:** - Most common - Often sudden and can be heavy **Abnormal Fetal Heart Rate Patterns**: - Due to compromise in fetal blood supply - Most commonly bradycardia **Rupture of membranes**: - The membrane rupture exposes the unprotected vessels causing them to tear and bleed. **Fetal Anemia** - In cases where there has been chronic slow leakage from the vasa praevia, fetal anemia may occur due to gradual loss of fetal blood. **Fetal Distress or Death**: - If not promptly diagnosed and managed, vasa praevia can lead to severe fetal distress due to hypoxemia and even intrauterine death.
35
Describe the management of suspect vasa praevia [3] and emergency vasa praevia [2]
**Suspected vasa praevia**: hospital admission between 28-32w, antenatal steroids, elective CS between 35-37w **Undiagnosed vasa praevia**: emergency cat 1 CS and aggressive fetal resuscitation
36
A pregnant patient presents with breathlessness and a swollen leg. What are key differentials? What are key differentials?
If not above knee and presents with no other symptoms / signs - think **physiological dyspnea of pregnancy** If unilateral leg swelling - Think **VTE** If bilateral & hypertension (w/ proteinuira) - Think **pre-eclampsia** - also ask about **headache and visual changes** -
37
Describe the risk of infection of chickenpox during pregnancy [+]
Risk of **Fetal varicella syndrome (FVS)**: - skin scarring - eye defects (microphthalmia) and cataracts - scars and significant skin changes located in **dermatomes** - **limb** **hypoplasia** - microcephaly - learning disabilities **Lecture notes:** - soft-tissue calcification * polyhydramnios, * limb defects and dermatomal skin scarring (due to fetal herpes zoster), * soft-tissue calcification * damage to the eyes and CNS. Neurological defects include cortical atrophy, microcephaly, limb paresis, spinal cord atrophy, encephalitis, seizures and Horner’s syndrome.
38
**severe neonatal varicella:** * if the mother develops **rash** between **[] days before and [] days** after birth there is a risk of **neonatal** **varicella**, which may be fatal to the newborn child in around 20% of cases
**severe neonatal varicella**: - if the mother develops rash **between 5 days before and 2 days** after birth there is a risk of neonatal varicella, which may be fatal to the newborn child in around 20% of cases
39
Describe how you manage chickenpox **exposure** during pregnancy [1] Describe how you manage chickenpox **infection** during pregnancy [1]
**oral aciclovir (or valaciclovir**) is now the first choice of **PEP** for **pregnant women at any stage of pregnancy** who are **exposed** to **chickenpox** - antivirals should be **given at day 7 to day 14 after exposure**, **NOT immediately** **Infection**: - consensus guidelines (Health Protection Authority and RCOG) suggest **oral aciclovir should** be given if the **pregnant women is ≥ 20 weeks and she presents within 24 hours of onset of the rash** - if the woman is **< 20 weeks the aciclovir should be 'considered with caution'** ## Footnote -Unknown exposure--> Antibodies test -NOT immune --> Oral aciclovir from day 7-14 after exposure -Aciclovir C.I? --> VZIG -Developed chickenpox--> Oral aciclovir if >20 weeks + present within 24 hours of onset of rash
40
Rubella infection causing congenital rubella sydnrome is caused by maternal infection within the **first [] weeks of pregancy.** **When is there the highest risk? [1]** **What is the clinical significance of this? [1]**
**First 20 weeks** - but first **10 weeks poses highest risk** When **primary infection occurs before 12weeks’ gestation**, given the **risk of fetal infection and the risk of an infected fetus developing severe abnormalities**, it is reasonable to consider **termination** of **pregnancy** when appropriate
41
The features of congenital CMV are [5]
The features of congenital CMV are: * **'Blueberry muffin rash'** * **Petachial rash** * **Fetal growth restriction** * **Microcephaly** * **Hearing loss** - this is the key one to remember * **Vision loss** * **Learning disability** * **Seizures** ## Footnote **NB**: With approximately 40,000 infected children per year, **congenital CMV infection is the most common cause of congenital non-genetic hearing loss**
42
A baby born with congenital Zika syndrome which would [2]
**Microcephaly** **Fetal growth restriction** Other intracranial abnormalities, such as **ventriculomegaly and cerebellar atrophy**
43
Causes of polyhydramnios can be due to excessive production of amniotic fluid or insufficient removal of amniotic fluid . Excess production can be due? [4] Insufficient removal can be due to reduced foetal swallowing. Due to: [4]
**Excess production can be due to increased foetal urination:** * **Maternal** **diabetes** **mellitus** * **Foetal** **renal disorders** * **Foetal** **anaemia** * **Twin-to-twin transfusion** syndrome **Insufficient removal can be due to reduced foetal swallowing**. Due to: [4] * **Oesophageal or duodenal atresia** * **Diaphragmatic** **hernia** * **Anencephaly** * **Chromosomal** **disorders**
44
What are the maternal [4] complications of polyhydramnios?
**Maternal**: - **respiratory** **compromise** due to **increased pressure on the diaphragm** - **Increased risk of urinary tract infections** due to **increased pressure on the urinary system** - **Worsening** of other symptoms associated with pregnancy such as **gastro-oesophageal reflux, constipation, peripheral oedema and stretch marks** * **Increased incidence** of **caesarean section delivery**
45
What are the foetal [4] complications of polyhydramnios?
* **Pre-term labour** and **delivery** * **Premature** **rupture** of **membranes** * **Placental** **abruption** * **Malpresentation** of the **foetus** (the foetus has more space to “move” within the uterus) * **Umbilical cord prolapse** (polyhydramnios can prevent the foetus from engaging with the pelvis, thus leaving room for the cord to prolapse out of the uterus before the presenting part)
46
*Lecture* When is the greatest risk of transmission of CMV in pregnancy? [1] When is the greatest risk of severe fetal infection? [1]
The risk of congenital infection appears to vary according to the point in gestation at which primary infection occurs, **increasing from around 30% in the first trimester to 47% in the third trimester.** **While the risk of viral transmission is lower in early pregnancy**, the proportion of cases with a prenatal diagnosis of **severe fetal infection is higher when infection occurs in the first compared with the third trimester of pregnancy.**
47
Lecture: **The main sequelae of congenital toxoplasma infection** involve the **CNS** and **eyes**, and typically include [**4**]
The main sequelae of congenital toxoplasma infection involve the CNS and eyes, and typically include **microcephaly, hydrocephalus, ventriculomegaly and chorioretinitis**. These may lead to developmental delay, epilepsy and blindness.
48
How do you treat TG infection: - to prevent vertical transmission after maternal infection [1] - If vertical transmission is confirmed [4]
**Spiramycin** (until the end of the pregnancy, in the absence of confirmed vertical transmission) **should be used to prevent vertical transmission after maternal toxoplasma infection during pregnancy** If **vertical transmission** is **confirmed**: - fetal infection should be treated by **spiramycin** **only for 1 week,** followed by **pyrimethamine** **plus** **sulfadiazine** **plus** **folinic** **acid** **throughout** the **pregnancy** and the **infant treated for 1further year.**
49
# Parvovirus Fetal anaemia and fetal hydrops both visible on ultrasound. Anaemia can be assessed measuring at the how exactly? [1]
Fetal anaemia and fetal hydrops both visible on ultrasound. Anaemia can be assessed measuring at the **Peak Systolic on Middle Cerebral artery (raised MCA-PSV).**
50
How do you treat HSV infection in pregnancy? [2]
Treatment should not be delayed. Management of the woman should be in line with her clinical condition and will usually involve the **use of oral** (or intravenous for disseminated HSV) **aciclovir** in **standard doses** (400 mg three times daily, usually for 5 days). **In the third trimester, treatment will usually continue with daily suppressive aciclovir 400 mg three times daily until delivery**. **Caesarean** **section** should be the **recommended mode of delivery** for all women developing **first episode genital herpes in the third trimester**, particularly those **developing symptoms within 6 weeks of expected delivery**, as the risk of neonatal transmission of HSV is very high at 41%
51
Describe how you would deliver a patient with polyhydramnios: - moderate [1] - severe [1] - what would do for baby afterwards birth [1]
Delivery: * Risk of malpresentation / cord prolapse/ pre term labour * Aim **delivery** around **37 weeks** for **severe polyhydramnios** * **38-40 weeks** for **moderate** **polyhydramnios** * **Nasogastric tube postnatally** to ensure there is **no blockage in oesophgus/ tracheoesophageal fistula**
52
Describe what the symptoms are like for someone who has undergone medical abortion < 10 / 12 weeks [5]
**Symptoms** typically start **2-3 hours** after starting **misoprostol** (second medication) * **Vaginal bleeding** - gestational age correlates to bleeding amount * **Heavy with clots** * Some **bleeding** up to **2-3 weeks** - normal * **Lower abdominal pain** - stronger than period pain **Bad period-like cramping pain** * Most **complete** within **6-8 hours**, almost all by **24 hours** Since telemedicine, EMA can be provided in many circumstances without the need for a scan
53
Describe the surgical process from 14+ plus [3]
**Dilatation and evacuation (D&E)** Typically from **14-24 weeks** * **Cervical** **preparation** with **mifepristone** / **misoprostol (or both) / osmotic dilators** inserted into cervical os; absorb fluid and then dilate cervix * **Cervical dilation and removal of fetus and placenta using forceps and vacuum aspiration**
54
Post-surgery, what medication do you need to consider / give? [2]
**Antibiotic prophylaxis** * Not required for early medical abortion * Surgical: **doxycycline 100mg bd for 3 days** (or Azithromycin 1g oral) **Anti-D** * Not required for early medical abortion * **Prophylactic anti-D for all Rh negative, non-sensitised women** undergoing surgical abortion * Administer within 72 hours of abortion