Screening + Monitoring Pregnancy Flashcards

1
Q

CTG: cardiotocography indications

A

Confidently used > 32 wks
Normal = reassuring, abnormal not always pathological
Mat indications: pre-eclampsia, DM, APH, prev c section)
Fetal indications: IUGR, prematurity, oligohydramnios, multip, breech
Intra partum: oxytocin, epidural, induction

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2
Q

CTG interpretation

A

Baseline: 110-160
Sustained tachy= hypoxia, fetal distress, mat pyrexia, exog B agonists
Sustained brady= severe fetal distress, mat sedation, hypoxia, post maturity, hypotension

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3
Q

10-14 wk USS

A

Date fetus using crown-rump length
EDD calculated from LMP retained unless USS differs by more than 1 wk
>14 wks bi parietal diameter/head circumference used instead

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4
Q

EDD

A

40 wks after first day of LMP

IF cycle is 28 days and regular

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5
Q

Reasons for 1st trimester USS -12wks

A

Establish viability
Detect multiple pregnancies and det chorionicity + amnioticity
Nuchal translucency test
Gross anatomical abnormalities

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6
Q

Chorionic villus sampling

A

Transabdo/transcervical under US guidance, rh -ve req anti D
Result in 48hrs
Risk of miscarriage 1-2%
11-14 wks
Not performed before 9-11 wks as fetal limb abnormalities can occur
Inconclusive (placental mosaicism) -> amnio

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7
Q

Nuchal translucency

A

11-14 wks during 1st trimester USS
Thickness of skin fold over neck of fetus measured
Risk determined by combining result with blood markers

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8
Q

Rhesus status

A

Blood group established at booking
15% rhesus -ve
Rhesus +ve fetus + sensitising event = anti D antibodies
Risk is to subsequent rhesus +ve pregnancy
HDN was 1% prior to introduction of prophylaxis

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9
Q

Rhesus prophylaxis

A

All rhesus -ve
500 IU anti D at 28wks
500 IU anti D at 34 wks
Regardless of sensitising events
Additional prophylaxis at sensitising events: 250 IU 20
No prophylaxis for threatened or spontaneous miscarriage

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10
Q

Sensitising events (rhesus disease)

A
APH
Closed abdo injury
ECV
Invasive procedures e.g. Amniocentesis, CVS, shunt
Intrauterine death
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11
Q

BHCG

A

Unlikely to visualise gestational sac on USS
Repeat BHCG should double in 48hr with continuing pregnancy
Repeat USS in one week

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12
Q

Triple test

A

Used if too late for combined
+ve = >1/250
15-16 wks

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13
Q

Amniocentesis

A

From 15 wks
Risk if miscarriage: 0.5-1%
Diagnostic test, antiD for rhesus -ve
Shed fetal cells extracted from amniotic fluid are analysed
Full karyotype 2-3 wks, PCR/FISH = more rapid

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14
Q

Reasons for second trimester USS -20 wks

A

Approx 2/3 Down’s syndrome babies appear normal at 1st scan
Purpose = detect abnormalities in structural anatomy, measure fetal growth, measure liquor volume, site placenta rescan at 34 wks if near or over os
Can also determine sex with 99% accuracy

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15
Q

Dating a pregnancy

A

EDD: from LMP
14 wks: bi parietal diameter
Discrepancy of > 14 days betw EDD derived from LMP and scan change to date indicated by scan
Accuracy of dating pregnacy decreases with gestation

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16
Q

Reasons for additional follow up scans

A

Measuring small or large for dates in 3rd trimester: serial scans 2 wks apart to measure: abdo circ, bi parietal diam, femur length
Follow up of structural abnormalities identified at 20 wk scan
Amniotic fluid vol
Real time USS: fetal wellbeing
Fetal Echo: may congenital heart disease, prev children with congenital heart disease, some with epilepsy, DM
Uterine artery Doppler: those at increased risk of pre-eclampsia, abruption, growth restriction
To confirm breech

17
Q

Combined test

A
10-13 wks
Nuchal translucency 
PAPP-A
BetaHCG
2.2% false positive
18
Q

Quadruple test

A
Unconjugated oestradiol
Total HCG
AFP 
inhibin A
4.4% false positive
19
Q

Integrated test

A

Combined test
Quadruple test
1% false positive

20
Q

Infection tests at booking

A

Syphyilis
HIV
Hepatitis B
Rubella