Cardiac Disease Of The Newborn Flashcards

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1
Q

3 important shunts in the newborn

A

PFO
Aterial ductus
Venous ductus liver

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2
Q

What changes take place at birth and the timing

Cardiac

A

Breathing
Pulmonary vascular resistance PVR decreases (drops 4-8/52)/ more with oxygen decreases resistance
Systemic vascular resistance increases
Closure of shunts PFO, Ductus arteriosis , ductus venosis

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3
Q

Syndromes association with congenital cardiac problems

A

Down’s syndrome AVSD
Turners Sx CoA/ bicuspid aorta
Velocardial Facial syndrome VSD, T of F/ Ca++ levels

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4
Q

Congenital Cardiac disease how does it present

A

1 cyanosis OR

2 CCF tachyponea/ increased WOB
Poor feeding HMG, Tachycardia

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5
Q

Incidence of Congenital heart disease

A

6-8/1000

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6
Q

VSD features

A

Commonest type of CHD
VSD many different points and this effects outcome
Eg high assoc with valvular disease and rarely close
Peri membranous rarely close

VSD presents about 6/52 Left to right shunt
Murmur not present at birth the pressures are the same no mumrmur
As time goes on the PVR decreases and the pressure gradient increases across the right and left ventricle and therefore you get murmur
don’t give O2 as this decreases the PVR and makes the murmur worse
long term untreated VSD pulmonary a damage
If CCF treat with diuretics

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7
Q

CoA of aorta

A

Presentation varies greatly
Poor feeding
Poor weight gain
Metabolic collapse
Decrease femoral pulses BP can be different in the upper and lower limbs
Ductus closes 3-7 days and that shows the CoA symptoms
TREAT PROSTIN reopens the ductus

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8
Q

Tetralogy of Fallot

A
Cyanotic heart disease 
2 things 
1 large VSD right to left shunt 
2 tight/narrowing of right vent outflow/pulmonary a stenosis and all the blood mixes and goes into the aorta 
Cyanosis 
If they do have increased Pulmonary flow  CCF and increased WOB
Tet spells 
Murmurs
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9
Q

Aortic stenosis

A

Too little systemic blood flow
Treat with PROSTIN keeps the ductus open and this helps flow
Otherwise catheter
Surgery

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10
Q

Transposition of the great vessels TGA

A
Aorta comes out of the right ventricle
Pulmonary a comes out of the left V
End up with parallel circulation 
CYANOSIS at birth
USS 18-20/52 may pick up
TREAT make the PDA larger
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11
Q

Murmurs that would concern

A
Loud 
Diastolic 
Continuous 
Associate with other abnormalities eg cyanosis FTT poor feeding 
HMG
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12
Q

CXR changes in CHD

A

Increased Pul blood flow
Large heart size
Abnormal cardiac contour

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13
Q

Blood test are helpful in CHD

A

ABG
Ca++ LOW in VCFS
Genetic Down’s syndrome, Turners VCFD

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14
Q

Management principals
LARGE VSD
Cyanosis

A

Large VSD too much blood flow to lungs wet lungs Diurectics
Avoid Oxygen and may need pulmonary a banding ( prevents the increased pressure that damages the pulmonary a
Cyanosis too little blood flow to lungs PROSTIN PGE1
Catheter
Surgery

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15
Q

Arrhythmias in new born

A
SVT
Atrial Flutter
Complete heart block 
Prolonged QT 
VT
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16
Q

SVT

A

Accessory short circuit leads to increased rate
Treat a gal maneuvers iced cold water
2 adenosine AV node blocked - SR
3 often further episodes
4 long term 2/3 resolve by 12/12 age
5 cease anti arrhythmia meds 6/23
6 1/3 will need ablation of the accessory pathway

17
Q

Long QT

A
1/2500
Inherited autosomal dominant 
Abnormal K+/Na+ channels
Risk of VF/VT
10% SIDS 

If parents have prolonged qt ECG and if neonatal QT b blocker

18
Q

Innocent murmur features

A
Murmur found in a very normal child completely normal examination 
Systolic murmur 
Ejection murmur 
Musical 
Grade 2-3/6
Changes with body position sitting /standing may go away
Varies with review 
Augmented by illness 

Ix. May do nothing
ECG don’t forget paed population different standards RHS dominant
CXR ?CCF
ECHO needs a paed cardiologist doing it

19
Q

Clues of a congenital heart murmur /problem

A

Appearance of the child eg Down’s syndrome other facial changes
FTT
Cyanosis ( pO2 <85%) periph vs central ( look in the mouth)
Symptoms of CCF. Tachyponea/ poor feeding/ poor exercise tolerance
Clubbing ( late sign) BP ( CoA of A)
Pulses UL/LL. Hepatomegally

20
Q

Commonest lesions CHD

A
VSD
Persistent Ductus Arteriosis 
ASD
Pulmonary valve stenosis 
Aortic stenosis 
CoA of Aorta 
Tetralogy of fallout Cyanotic 
Transposition of the great vessels. Cyanotic
21
Q

Long term consequences of Cyanotic heart disease

A

Hypoxia
Myocardial dysfunction
Increased risk of thromobisis infection embolus
Neurological effects CVA/ plagia/ abscess

22
Q

ANC 18-20 week uss normal does not rule out significant congenital heart disease

A

It will pick about 35-40% but some are normal
Eg ASD and patent ductus arteriosis so wont be commented on
Don’t be lulled into a false sense of security

23
Q

Prophlaxisis antibiotics

What is and what lesions do you use if for

A

1 cyanotic heart disease
2 6/12 post cardiac surgery
3 prosthetic valves
4 Rh heart disease

Big thing is to have regular dental check ups avoid dental caries

24
Q

General care of CHD

A
1 growth/nutrition 
2 CVS risk factors 
3 exercise 
4 antibiotic prophlaxisis 
5 dental care 
6 general infections 
7 immunizations 
8 psychological well-being  support the families /stressors