Exam #4 Flashcards

1
Q

What are the landmarks for the 2nd trimester fetal biometry?

A
  • BOD
  • HC
  • AC
  • FL
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2
Q

BPD

A

*biparietal diameter
-most reliable for predicting fetal age

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3
Q

HC

A
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4
Q

AC

A
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5
Q

FL

A
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6
Q

What are the landmarks for the posterior fossa?

A
  • arnold chiarri (banana sign)
  • spina bifida
  • cisterna magna
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7
Q

Why is it important to image the posterior fossa?

A

to monitor if fluid increases, nuchal fold thickens

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8
Q

IUGR
- what is it?
- list some causes?

A

*Intrauterine Growth Restriction
- fetal birth weight AT or BELOW 10% for gestational age
- causes:
- HTN
- smoking
- previous IUGR
- UT anomaly (bicorn or fibroid)
- placenta hemorrhage/insufficiency

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9
Q

Symmetric IUGR occurs in the __ trimester and is generally caused by _____.

A
  • 1st
  • severe insult:
    • intrauterine infection
    • maternal malnutrition
    • fetal alcohol syndrome
    • chromosomal anomaly
    • severe congenital anomaly
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10
Q

Asymmetric IUGR occurs in the __ trimester and is often caused by _____.

A
  • 2nd
  • placental insufficiency
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11
Q

What tests are included in the biophysical profile?

A
  • cardiac non stress test (NST)
    • Doppler: heart rate & UT contractions
  • fetal breathing movements
  • fetal movements
  • fetal tone
  • AFV
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12
Q

Biophysical profile is used to determine __.

A

fetal well-being

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13
Q

AFI
- what is it?
- what is the normal range?

A
  • Amniotic Fluid Index
  • normal range:
    • four quadrant (total): 5-22 cm
    • single pocket: 2-8 cm
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14
Q

AFI: Polyhydroamnios

A
  • four quadrant (total): >22 cm
  • single pocket: >8 cm
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15
Q

AFI: Oligohydroamnios

A
  • four quadrant (total): <5 cm
  • single pocket: <2 cm
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16
Q

List the dangers of Maternal Diabetes:

A
  • polyhydramnios
  • macrosomic baby
  • very severe vascular disease can cause IUGR
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17
Q

Macrosomic baby

A

a birth weight AT or ABOVE the 90th percentile

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18
Q

It is important not to confuse IUGR with a baby who is just ___.

A

SGA

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19
Q

SGA
- what factors result in this type of baby?

A

*
- AT or BELOW 10th percentile
- factors
- genetics
- poor maternal weight gain & nutrition
- intrauterine infections
- chromosomal anomaly
- placental insufficiency

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20
Q

What are the functions of the placenta?
(HINT: P.H.E.R.N.)

A
  • protection
  • hormone production
  • excretion
  • respiration
  • nutrition
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21
Q

TORCH
- what is it?
- what can it lead to?

A
  • Toxoplasmosis
  • Ruebella
  • Cytomegalovirus
  • Herpes
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22
Q

What are the abnormal umbilical cord insertion types?

A
  • Battledore (Marginal)
  • Succenturiate
  • Velamatous
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23
Q

Describe the normal central insertion type of the umbilical cord.

A
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24
Q

Vasa Previa
*what is it?
- what does it result from?

A

*
- Velamatous

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25
Q

What are the types of abnormal placental attachment?

A
  • placenta accreta
  • placenta increta
  • placenta percreta
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26
Q

Placenta Accreta

A

invades 50% through the myometrium

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27
Q

Placenta Increta

A

invades <50% through the myometrium

28
Q

Placenta Percreta

A

extends through UT into the bladder and adjacent pelvic structures

29
Q

Name the four grades of placenta previa from least to most severe?

A
  • Low Lying
  • Marginal
  • Partial
  • Complete
30
Q

What are the dangers of nuchal cord?

31
Q

The dangers of nuchal cord to the fetus may result in…

32
Q

Mid Gut Herniation
*what is it?
- why it happens
- when it happens
- when it should resolve

A

  • happens around 8 wks; resolve by 12 wks
33
Q

Omphalocele

A

when the midgut herniation fails to resolve

34
Q

Gastroschisis

A

an abdominal defect (more likely RT-sided) where intestines spill out into the amniotic fluid

35
Q

Why is there an increase in AFP in association with ____?

36
Q

How many vessels are in the umbilical cord?
How long is the umbilical cord (in cm)?

A

3– 1 vein, 2 arteries
- 40-60 cm

37
Q

What are two ways to image the umbilical cord vessels?

38
Q

The umbilical cord is covered in ___. What is the purpose?

A
  • ## Wharton’s jelly
39
Q

What is placental abruption?

40
Q

What type of placental abruption presents with NO vaginal bleeding?

41
Q

Dizygotic

A

two zygotes (fertilized eggs)

42
Q

Monozygotic

A

one fertilized egg (which divides)

43
Q

Chorion refers to the…

44
Q

What are the types of twins?

A
  • MA/MC (monoamniotic/monochorionic)
  • DA/DC (diamniotic/dichorionic)
  • DA/MC (diamniotic/monochorionic)
  • conjoined
45
Q

What is the most dangerous twinning?

46
Q

The ‘Twin Peak” or ‘Lambda Sign’ indicates what type of twinning?

47
Q

The ‘T-sign’ indicates what type of twinning?

A

Diamniotic/Monochorionic

48
Q

TRAP

A

*Twin Reversed Arterial Perfusion
- 1 twin is acardiac (receives ALL bl. supply from pump twin)

49
Q

TTTS

A

*Twin Twin Transfusion Syndrome
- 1 twin recieves majority of blood over the other due to an AV shunt w/in placenta

50
Q

What is a vanishing twin?

A

a twin that dies early in 1st trimester and the mother’s body absorbs the remains

51
Q

What is a “stuck twin”?

A

*diamniotic pregnancy
- polyhydramnios in one sac
- severe oligohydramnios in other sac
- manifests 16-26 wks

52
Q

What are the tests in the Quadruple screen?

A
  • AFP
  • Elevated neural tube defects/anencephaly & spina bifida
53
Q

Trisomy 21

A

*aka Down Syndrome
- very common chromosomal defects
- adv. maternal age
- nuchal translucency (>3mm) & nuchal fold (>6mm)
- mental retardation
- hygroma
- duodenal atresia (double bubble)
- echogenic bowel
- mild ventriculomegaly

54
Q

Trisomy 18

A

*aka Edwards Syndrome
- 2nd most common chromosomal defect
- abnormal quad screen
- heart defects
- clenched hands
- rocker bottom foot
- cleft lip & palate
- omphalocele
- congenital diaphragmatic hernia
- cerebellar hypoplasia
- profoundly retarded w/ 90% dying in 1st year of life

55
Q

Trisomy 13

A

*aka Patau’s Syndrome
- extremely severe w/ multiple brain anomalies
- holoprosencephaly
- cyclopia & proboscis
- polydactyly, omphalocele
- micrognathia
- meningomyecele
- 80% die in 1st month

56
Q

Micrognathia

A

small chin

57
Q

Talipes Equinovarus

A

clubfoot (abnormal medial rotation of foot)

58
Q

Syndactyly

A

same, or all of the fingers/toes, partly or wholly united

59
Q

Polydactyly

A

extra fingers/toes

60
Q

Proboscis

A

a rare fetal anomaly
- appendage-like structure projecting from the ML fetal face/forehead.

61
Q

Cyclopia

A

prosencephalon fails to properly divide the orbits into two cavities
(often with a proboscis)

62
Q

Turner’s Syndrome

A

*45X
- genetic abnormality
- absence of an X or Y chromosome

63
Q

Cystic Hygroma

A

*
- infants CAN survive
- physical ft:
- short stature
- webbed neck

64
Q

Triploidy

A
  • extra set of chromosomes
  • physical/mental ft:
    • head defects
    • cranial & renal anomalies
    • omphalocele
    • mental retardation
65
Q

Dominant disorder

A

*autosomal dominant
- caused by a single defective gene

66
Q

Recessive disorder

A

*autosomal recessive
- caused by a PAIR of defective genes
- one from each parent