M12: FetalCardiac Abnormalities Flashcards

1
Q

When does the heart begin to develop, when is it fully formed

A

5 wks

10 wks

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2
Q

Describe how the heart develops… when do the chambers of the heart develop

A

Paired heart tubes fuse to form a single heart

B/w 6-8 wks

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3
Q

When is a heart beat detected

A

5-6 wks

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4
Q

Describe the pathway of blood starting from the placenta

A

Placenta > umbilical vein > Lt portal vein > ductus venosus and some through the hepatic veins > IVC > RA > foramen of ovale > LA > LV > AO > iliacs > hypogastric A > umbilical A > placenta

Some blood also goes from the RA to the RV, through the PA, to the lungs, PV and to the left heart.

OR from the RV blood can go through the PA and ductus arteriosus to the AO

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5
Q

Do the umbilical V or A carry O2 rich blood

A

Veins

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6
Q

Number of umbilical artery and vein

A

2 arteries

1 vein

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7
Q

Most of the blood that does enter the RV will pass through which structure

A

The ductus arteriosus b/c blood is getting oxygenated from mom

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8
Q

What does the ductus venosus connect?

Ductus arteriosus?

A

DV: connects LPV to IVC

DA: PA to AO

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9
Q

indications for fetal echo

A

abnormal findings
fam HX of congenital heart disease
previous prog w/ cardiac abnormality
maternal disease associated w/ heart defects (type 1 diabetes)

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10
Q

1 reason for fetal echo

A

type 1 maternal diabetes

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11
Q

other findings associated w/ heart defects

A
2 vessel cord
CDH
omphalocele
thick nuchal fold or NT (> 3.5 mm will do echo)
hydrops
chromo abnorm
bradycardia
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12
Q

what % of T21 babies have heart defects

A

50%

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13
Q

fetal echo routine

which are done at detailed, which are fetal echo only

A
detailed:
find situs w/ stomach and heart
4CH
LVOT/RVOT
3 Vv
echo only:
AO arch and ductal arch
short axis of ventricles and atria
SVC/IVC (long horn view)
pulmonary veins
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14
Q

which chamber of the heart is most anterior

A

RV

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15
Q

how should the RVOT and LVOT cross

A

90 degrees

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16
Q

size of the structures in 3 vV

A

PA>AO>SVC

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17
Q

appearance of the AO arch and ductus venosus

A

AO: candy cane w/ great vessels

DA: hockey stick, no branches

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18
Q

in which views may you do doppler in a fetal echo

A

inflow
outflow
ductus arteriosus
foramen ovale

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19
Q

how do we do Mmode of the heart

why

A

insinuating through both the atria and ventricles

to rule out arrhythmias and heart block

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20
Q

when in wks is a fetal echo best performed

A

20 or 22 2ks to term

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21
Q

4CH view R/O what amount of cardiac defects

how about if we included outflows?

A

1/3

2/3

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22
Q

norm HR

what is considered bradycardia
tachy?

A

120-160… up to 180 in first trimester

Brady: <100 bpm
tachy: > 200 bpm (reduced SV)

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23
Q

what usually causes Bradycardia in fetuses

A

heart block

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24
Q

how is tachycardia of the fetus treated

A

digoxin to mom… moms heart will respond also

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25
Q

most common arrhythmia in a fetus

are they worrisome

A

PACs

not usually

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26
Q

describe an ASD

why is it hard to diagnose

A

partial or complete absence of the IAS

due to norm foramen ovale

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27
Q

how large should the foramen of ovale be

A

no larger than the AO root

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28
Q

how do you want the septum placed on the screen when looking for an ASD

A

horizontal

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29
Q

describe a VSD

A

partial or complete absence of the IVS, usually associated w/ other cardiac anomalies

MOST COMMON CARDIAC ANOMALY

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30
Q

best view to asses a VSD

A

subcostal/horizontal 4 CH and short axis of ventricles is best

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31
Q

prognosis for VSD

A

good, many close on their own if they’re small

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32
Q

how does blood move through the Foramen ovale

A

from RA to LA in the fetus

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33
Q

when does an atrioventricular septal defect (AVSD) occur

describe the abnormality

A

when the endocardial cushions fail to fuse early in embryology

1 common valve w/ 5 leaflets (combo of TV and MV)

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34
Q

describe the anatomy of the heart ear in embryology

A

starts as a common ventricle and common atria that communicate through the AV canal

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35
Q

another name for a AVSD

A

AV canal

endocardial cushion defect

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36
Q

what % of fetuses w/ T21 have an AVSD

37
Q

describe ebstein’s anomaly

US appearance

A

apical displacement of the TV into the RV

large RA
apical displacement of TV
sm/dysplastic RV

38
Q

ebstein’s anomaly is associated w/ which other anomalies

A

hydrops

pulmonary stenosis

39
Q

ebstein’s anomaly is associated w/ the ingestion of which medication

40
Q

why does a hypoplastic Right ventricle occur

A

secondary to pulmonary atresia w/ no VSD.. theres no blood flow getting into the RV which makes it small

41
Q

Us appearance of hypoplastic Right ventricle

A

difficult to see inner chamber and sm or absent pulmonary artery

42
Q

why does a hypoplastic left ventricle occur

US appearance

A

due to decreased flow into or out of the LV

sm LV
AO stenosis or atresia
MV atresia

43
Q

hypoplastic left ventricle is associated w/ which other anomalies

A
coarctation of the AO
endocardial fibroelastosis (EFE) as preg progresses
44
Q

RVOT, LVOT ratio

45
Q

describe endocardial fibroelastosis (EFE)

cause

A

myocardium is replaced by collagen and elastic tissue which causes decreased cardiac function and congestive HF

muscle hypertrophy

46
Q

when is endocardial fibroelastosis (EFE) seen

A

w/ hypoplastic heart syndromes

47
Q

US appearance of endocardial fibroelastosis (EFE)

A

thick, echogenic myocardium

48
Q

in general, what causes hypoplastic heart syndromes

A

lack of blood flow into or out of either of the ventricles, which doesn’t allow them to develop normally

49
Q

4 abnormalities w/ tetralogy of fallot

A

VSD
AO overriding ventricular septum (too big)
hypertrophy of RV
pulmonary stenosis

50
Q

describe truncus arteriosis

A

single large vessel arising from the base of the heart (PA and AO start as one didnt separate)

51
Q

the single vessel w/ truncus arteriosis supplies which vessels/circulation

A

coronary arteries
pulmonary circulation
systemic circulation

52
Q

US appearance of truncus arteriosis

A

VSD
larger overriding AO
pulm A origins will vary off the AO

53
Q

will you have a separate ductal and AO arch w/ truncus arteriosis

A

no, only one vessel

54
Q

describe double outlet RV

common anomaly w/ this condition

A

when the Ao & PA both arise form the RV

VSD

55
Q

double outlet RV is associated w/ what maternal factors

A

maternal diabetes

alcohol abue

56
Q

describe transposition of the great vessels

A

when the AO arises from the RV and the PA arises from the LV and both outflow vessels are parallel/dont cross at 90 degrees

57
Q

2 types of transposition of the great vessels

A

complete/D loop:
D for dextro

corrected/L loop:
L for levo

58
Q

describe a D loop/complete transposition

A

closed circuit where blood flows from RA to RV

not compatible with life

59
Q

US appearance of D loop/complete transposition

A

great vessels parallel instead of crossing

maybe VSD

60
Q

describe the direction/flow of blood w/ a complete transposition

A

De02 > RV > AO > body/head

02 > LV > PA > lungs

61
Q

describe a L loop/corrected transposition

what to look for to identify the RV

A

when the RV is attached to the LA

moderator band

62
Q

is pulmonary and systemic circulation normal with corrected transposition

63
Q

US appearance of corrected transposition

A

parallel great vessels

morphologic RV to LA

64
Q

can people w/ corrected transposition be asymp

when might they start to show symptoms

A

yes

mid life, they might show signs of heart failure b/c the RV can’t cope w/ the pressure

65
Q

describe the morphology of the PA and AO w/ corrected transposition

A

PA comes off the LV and de02 goes to lungs

AO off the RV and 02 goes to body…

basically the LV and the RV switch spots and everything else is normal

66
Q

describe coarctation of the AO

A

narrowing of the AO lumen, usually at the isthmus (area b/w the Lt subcla A and the descending AO)

67
Q

US appearance of coarctation of the AO

A

prominent RV
sm LV (not enough flow into/out of the LV and AO)
narrowing of the AO

68
Q

coarctation of the AO is associated w/ which conditions

A

AVSD
VSD
maternal diabetes

69
Q

when does coarctation of the AO often occur

A

after birth due to tissue from the ductus arteriosus entering the AO as it seals off

70
Q

2 locations for coarctation of the AO

A

pre ductal and post ductal

71
Q

most common cardiac tumor

A

Rhabdomyoma (cardiac hamartoma)

72
Q

US appearance of Rhabdomyoma

A

solid echogenic tumors usually on the ventricular septum… may obstruct outflows

73
Q

DDX for Rhabdomyoma

A

cardiac fibroma
hemangioma
myxoma
teratoma

74
Q

describe cardiomyopathy

A

muscle damage that results in altered cardiac function

75
Q

causes of cardiomyopathy

A

viral infection
bacterial infection
metabolic disease
maternal type 1 diabetes

76
Q

what is ectopic cordis

associated w/ which condition

A

heart outside the chest cavity

pentalogy of central

77
Q

describe cardiosplenic syndromes

which organs are affected

A

symmetrical development of normally asymmetric organs or organ systems…. fetus either has 2 left sides or 2 right sides

liver
lungs
stomach
heart

78
Q

another name for cardiosplenic syndrome

A

isomerism
situ ambiguous
heterotaxia

79
Q

describe polysplenia

US appearance

A

bilateral left sidedness…

multiple spleens (polysplenia)
LA isomerism (2 LAs)
2 left lungs
midline liver
IVC interruption
dextro or mesocardia
80
Q

what happens to the IVC w/ polysplenia

A

IVC doesnt course through the liver and the HV empty into the RA… the renal and subhepatic segments drain into the azygous veins which drain into the IVC

81
Q

describe dextro and mesocardia

A

dextrocardia: heart points to R side
mesocardia: heart in the middle of the chest

82
Q

is Lt or RT isomerism better

83
Q

other names for bilateral right sidedness

A

asplenia

ivenmark’s syndrome

84
Q

describe the anomalies of asplenia

A
no spleen
right atrial isomerism (2 RAs)
2 right lungs
midline liver
bilateral SVC
85
Q

possible heat defects seen w/ cardiosplenic syndromes.

asplenia/right isomerism

A
  • transposition of great arteries
  • pulm stenosis or atresia
  • total anomalous pulmonary venous return (2 RA, normal LA)
  • complete heart block

heart defect are much worse w/ asplenia
-AVSD is common w/ asplenia

86
Q

which defects are associated w/ heterotaxia

A

almost any heart defects can be associated w/ it

87
Q

diagnosing cardiosplenic syndrome on US

A

hard to diagnose

clues may be:

  • interrupted IVC
  • large azygous vein
  • abnormal liver, stomach or heart position
88
Q

which type of transposition is more common

A

D loop/complete