Gen Preg Flashcards

1
Q

FGM

A

Counselling
Illegal - esp to reinfibulate

Obstetric - labour dystocia, tears/lacs, instrumental, epis, PPH, SB, infant resus

Sexual - dyspareunia, decreased satisfaction, anorgasmia

Gynae - chronic vulvodynia, vaginal discharge, UTI, dysmenorrhea

Psychological - PTSD, anxiety/depression

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2
Q

Stillbirth investigations

A

Gold standard: post mortem

MUM - hx of thrombosis, APS, bile salts, LFTs

Baby - autopsy,
if not, then clinical examination by paeds, MRI, babygram, minimally invasive autopsy

Placenta - macroscopic exam, histopath, cytogenetic, swabs

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3
Q

Anti D Isoimmnunisation

A

250IU first trimester
625IU if multiple
If 2nd tri incl amnio, TOP, APH, ECV = 625IU

If > 1 in 16, refer to MFM
Persisntent anaemia due to tranplacenta allo-antibody destruction of fetal blood cells

Titres
Test partner
MCA PSV
Consider cordocentesis - DAT, Hb + bilirubin levels

Neoate
-observe for jaundice/anaemia, feed regularly, consider phototherapy or plasma exchange

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4
Q

Hydrops

A

Isoimmunisation rhesus

Chromosomal - turners, Tri 18/13, molar
Autoimmune
U
Structural e.g. cardiac, thoracic, GI obsturction
Trauma - Fetal maternal haemorrhage, TWINS, TUMOUR
Infection - parvovirus, but also toxo/cmv
C

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5
Q

Differentials large for dates

A

Incorrect dates
Fibroid
Multiple gestation
Molar/gestational trophoblastic disease

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6
Q

Management hyperemesis

A
Admit
IV fluids
Anti emetics - cyclizine, metoclopramide, PRN ondans
Folic acid 5mg, Iodine
Thiamine
Pyridoxine
Regular ketone checks
Daily weight 
Dietician 
Regular small meals
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7
Q

Breech Delivery

A

Frank (extended knees most successful)

Offer ECV if intact membranes (primip from 36)
Analgesia, lithotomy

Ideally wait until breech reaches pelvic floor,
Commence pushing,
Fetus often deliveries spontaenously to the umbilicius
Maintain sacrum anteriorly
Grasp bony prominences only, if needed, SI joint, Ant sup iliac spines, avoid soft abdo
If legs do not deliver spontaneously, hook them anteriorly
Rotate body 90-180 degrees to deliver shoulders (Lovsetts)
MSV mauriceau-smelli-veit once occiput is visible, two fingers non dom hand on malar prominences, other hand neck/shoulders/middle finger occiput

Suprapubic pressure can increase flexion
Body rests on palm and forearm
Gentle downward traction + elevation

Forceps can be used for after coming head

RISKS - cord prolapse, nuchal arm, traumatic injuries

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8
Q

Parvovirus

A

C - DNA virus, maternal may be asym or slapped cheek, athralgia of large joints
May be detected as hydrops

R M-self limiting
F - <20 weeks, 10% excess fetal loss
9-20 weeks, 3% get hydrops (1/3 need IUT, 1/3 recover)
If no hydrops, v low risk congenital issue

Invx - confirm maternal serology, IgM can take 2-3 weeks to become positive, MFM USS, 1-2 weekly MCA PSV, if elevated, IUT, amnio not needed, repeat MCA PSV until 12 weeks post infection

T - TOP not offered as no long term sequalae

O

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9
Q

CMV

A

C - DNA virus, self limiting in parents, can be re-activated

R
M-low risk
F - early = structural, later in preg = visceral (hepatitis/pneumonia)
Growth
N- FU 2 years, seizures, developmental delay, microcephaly, chorioretinitis, SNHL within first 2 years.

90% of transmission = asymptomatic
OVERALL risk of long term sequalae in a congenitally infected infant is 10-20%

(30% risk of transmission, 10% of those = infected, 50% of those = long term sequalae, OVERALL 10-20% of INFECTED babies have issues)

Invx - Maternal serology, if IgG positive, then avidity, if LOW avidity = RECENT infection

  • USS - cns (microcephaly, calcifications), oligo/poly, hydrops, echogenic bowel, iugr
  • Amnio >20/40 + 6/52 after primary
  • MRI: microcephaly

T - no maternal treatment
-Consider TOP if affected, infected fetus may not be affected

O

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10
Q

Day care worker/parent of toddler

A

CMV

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11
Q

School aged parent

A

Parvovirus

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12
Q

MCDA twins

A

Single embryo
Chorionicity determined by 14 weeks
Oral iron, 5mg folate, detailed anomalie + cardiac scans

Fortnightly from 16 weeks
Detailed anoamlie + cardiac as increased risk (uneven distribution inner cell mass)

TTTS -15%, quintero
SFGR - 15% , refer >20% discrep, gratacos (1,2,3)
TAPS - post laser, small anastomseis (anaemia/polycythaemia)
TRAP - acardiac twin
Co twin demise - 15% demise, 26% abnormality , MRI to assess surviving twin neuro

Advise Mum symptoms of TTTS, increased girth, SOB, decreased movements

Mode of delivery, if >32 weeks, consider vaginal if cephalic

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13
Q

Increased risks in twins

A

GESTATION based
1 in 90
Slightly higher >35, therefore more anomalies

Hyperemesis
Anaemia
GDM
PTB
VTE
APH
Poly
operative delivery
PPH
PND
Maternal mortality
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14
Q

Fetal risks of prematurity/PPROM

A
PREMATURITY 
Hyaline membrane disease
Intraventricular haemorrhage
Periventricular leukomalacia
Infection - sepsis, pneumonia, meningitis
NEC
Retinopathy 

Pulm hypoplasia
MSK/facial deformities as reduced amniotic fluid + restricted mvmt
Malpresentation
Abruption
Umbilical cord issues - compression/prolapse

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15
Q

Lithium

A

Antipyschotic/mood stabiliser (alternatives lamotrigine, quetiapine, risperidone)

Risks
Ebstein anomaly
Polyhydramnios

Associated with thyroid issues

Consider: weaning if stable (DONT stop abruptly), switching to another anti-pyschotic
-4 weekly levels
-Weekly from 36 weeks
Stop in labour due to fluctuations, risks and signs of toxicity

NOT breastfeeding, therefore dostinex, extended stay postnatally

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16
Q

HSV

A

Congenital infection rare, vertical tranmission at delivery

Suppressive from 36/40

Recurrent, risk is 1-3%
15% type 1
<0.1 % for type 2

Neonatal observation, if active lesions, swab for HSV and consider antivirals

17
Q

FU after molar pregnancy

A

Complete
-if normal HCG within 56 days, = 6/12 from ERPOC
if >56 days.8 weeks, then 6/12 from negative HCG

Partial
x2 negative HCG, 4 weeks apart

Do not need repeat HCG 6 weeks unless had chemo

18
Q

Complete molar

A

1 egg, 2 sperm (either dispermy or replicate)

Presents, hyperemesis, irregular vaginal bleeding, uterine enlargement, hyperthyroidism, early onset PET, (RARE = haemoptysis/headache due to mets)

Assoc w theca lutein cysts
More likely to get chorangiocarcinoma

No fetal parts, therefore evacuation of uterus is treatment, irrespective of uterine size. Avoid medical and oxytocin (potential to embolise, similar to AFE)

19
Q

Balanced translocation

A

Same amount of genetic material
Usually phenotypically normal
Can have implications if at critical break point

Recommend

  • check parental chromosomes
  • refer to geneticist
  • could consider micro-array
20
Q

Vit K

A

IM injection
Babies are deficient, 1-2% have risk of sig bleeding
Early or LATE (up to 12 weeks)
Increased risk: mum on AED, ptb, instrumental
IM injection much more effective than PO, but PO option
Low risk, some studies some assoc w solid tumours but largely disproven and thought to be safe

21
Q

Rubella

A

1st trimester = offer TOP
2nd trimester = offer amnio >20/40, 6 weeks from infection, ideally not cvs

Delivery
-all vaccinated, PPE,
FU for 9 months

22
Q

Vomiting in 1st tri

A
Hyperemesis
Thyrotoxicosis
Multiple
Molar
INfection