formative and wb Flashcards
(37 cards)
young woman with BMI 18.5, she is pregnant and her baby is smaller than the 3rd centile for gestational age. She has had herpes in the past and was treated for chlamydia. What is the most likely cause of her baby being small?
Given the facts:
History of HSV and chlamydia are less likely to be direct causes here.
BMI is 18.5: while at the low end of normal, it alone is unlikely to cause severe FGR (<3rd centile).
No mention of pre-eclampsia or hypertensive disease.
In practice, the most common cause of FGR in a structurally normal fetus is placental insufficiency.
➡️ Most likely cause: placental insufficiency.
If congenital infection screening was done and is negative, this is even more likely.
blood marker for a hyatidiform mole turned cancer
hCG levels are the gold standard for diagnosis, monitoring, and assessing the persistence or malignant transformation of a molar pregnancy.
Persistent elevated hCG levels after evacuation of a molar pregnancy indicate gestational trophoblastic neoplasia (GTN).
is oxygen used in delivery
Indications:
Maternal hypoxia: If the mother shows clinical signs of hypoxia (e.g., cyanosis, low oxygen saturation).
Not routinely recommended just for non-reassuring CTG unless there is evidence of maternal hypoxia or another clinical need. NICE advises against routine oxygen use solely to improve fetal status.
oxytocin indications in labour
Indications:
Delayed progress in labour:
In the first stage: If cervical dilatation is <2 cm in 4 hours in active labour.
In the second stage: If there is delayed descent after 1 hour of active pushing in nulliparous women (or 0.5 hours in multiparous women).
To correct uterine inertia (ineffective contractions).
Caution:
If CTG is abnormal, oxytocin should be used with care and only after correcting reversible causes of fetal compromise.
FBC - fetal scalp blood sampling indications
Indications:
When the CTG is suspicious or pathological and there is uncertainty about fetal wellbeing.
Cervix must be ≥3 cm dilated and membranes ruptured.
Contraindications (where FBS should NOT be done):
Maternal infection (HIV, Hepatitis B/C, herpes).
Known bleeding disorders or fetal bleeding disorders (e.g., hemophilia).
Non-vertex presentations.
NICE recommends avoiding FBS if there is an acute event (e.g., cord prolapse, prolonged deceleration).
electrode monitoring indications
Fetal Scalp Electrode Monitoring (FSE)
Indications:
Poor-quality external CTG: Difficulty in obtaining a reliable external fetal heart rate trace (e.g., maternal obesity, excessive maternal/fetal movements).
When continuous internal monitoring is needed for high-risk pregnancies.
To differentiate between maternal and fetal heart rate when the external trace is confusing.
Requires:
Cervix ≥2 cm dilated and ruptured membranes.
Contraindications:
Same as for FBS (infection risk, bleeding disorders).
main risk if a mother contracts chickenpox at 38 weeks
Key points from NICE and RCOG (Green-top Guideline No. 13):
Greatest risk: When maternal chickenpox occurs from 7 days before to 2 days after delivery.
At 38 weeks, if the mother develops chickenpox and delivers within this high-risk window, the newborn may not receive protective maternal antibodies in time.
This puts the neonate at risk of:
Severe disseminated varicella (neonatal varicella infection)—potentially life-threatening.
🔑 Immediate management implications:
If the mother is within 7 days pre-delivery to 2 days post-delivery:
The newborn should receive Varicella-Zoster Immunoglobulin (VZIG) (or intravenous immunoglobulin if VZIG unavailable) as soon as possible after birth.
If the neonate develops signs of infection, intravenous acyclovir is required.
If more than 7 days elapse between the maternal rash and delivery, the baby is usually protected by maternal antibodies.
combined smoking and alcohol effect on FBC
individual effects of smoking and alcohol on
placental abruption presentation
The classic presentation of placental abruption typically includes:
Severe abdominal pain,
Vaginal bleeding (which may or may not be present),
Uterine tenderness/rigidity,
Fetal heart rate abnormalities (indicating fetal distress),
Signs of maternal shock (if hemorrhage is significant).
vasa praevia vs placental abruption
Placental Abruption typically presents with painful abdominal bleeding, uterine rigidity, and fetal distress due to impaired placental function. It requires emergency management and can result in significant maternal and fetal morbidity and mortality, especially in severe cases.
Vasa Previa is a condition where fetal vessels are located near or across the cervix and are at risk of rupture during labor, leading to bright red vaginal bleeding and severe fetal bradycardia if rupture occurs. Immediate cesarean delivery is required to prevent fetal exsanguination.
vasa praevia causes
Velamentous cord insertion
- Low-lying placenta
- Multiple pregnancies (twins/triplets)
- In vitro fertilization (IVF)
causes of placental abruption
Trauma (e.g., abdominal injury)
- Hypertension
- Smoking
- Cocaine use
- Previous abruption
- Preeclampsia
- Advanced maternal age
fill out this table for placental abruption vs vasa praevia
fill out this table for placental abruption vs vasa praevia
what is a marginal bleed
A marginal bleed refers to bleeding near the edge of the placenta, often seen as a sign of minor placental separation or vascular issues with the placenta. While mild marginal bleeds may resolve on their own, close monitoring is required to assess the risk of progression to a more serious condition, such as placental abruption.
obstetric cholestasis implications for mother
pruritis, elevated LFTs, fatigue, gallstones, coagulopathy (affects Vit K absorption), liver failure,
PPH, preterm labour, higher risk of pre eclampsia,
management of obstetric cholestasis
obstetric cholestasis fetal implications
stillbirth, preterm birth, meconium stained liquor, fetal distress, IUGR
placental abruption maternal outcomes - immediate complications name 6
and death
3 long term outcomes of placental abruption
management of meconium stained liqor
postnatal monitoring after meconium stained amniotic fluid
lab findings in ICP