Cardiology Flashcards

1
Q

Main causes of L to R shunts, and main presenting symptom…

A

L to R shunts (acyanotic heart disease):

  • VSD (most common)
  • PDA
  • ASD

Main symptom = breathlessness

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2
Q

Main causes of R to L shunts, and main presenting symptom…

A

R to L shunts (cyanotic heart disease) 1-5:

  1. Truncus Arteriosus (vessel joins to make 1)
  2. Transposition of Great Arteries (2 major vessels switch)
  3. Tricuspid atresia (3=tri)
  4. Tetralogy of Fallot (4 defects)
  5. Total Anomolous Pulmonary Vascular Return (TAPVR = 5 letters)

Main symptom = cyanosis

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3
Q

What kind of heart defects cause breathlessnesss AND cyanosis ?

A

Common mixing defect = AVSD - combination of both types of mixing.

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4
Q

What are some common causes of congenital heart defects?

A
Maternal disorders:
 - Rubella infection
 - SLE 
 - Diabetes
Teratogens: 
 - Warfarin 
 - Alcohol 
Genetic syndromes:
 - Down Syndrome 
 - Turner's Syndrome
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5
Q

What is an innocent murmur?

A

Benign, physiological murmur heard in up to 50% of children.
Key features:
- Soft, always well after first heart sound
- Always systolic
- Heard at L sternal edge
- Heart sounds are normal

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6
Q

What is the pathophysiology of hypoplastic left heart syndrome?

A
  1. Left ventricle is very underdeveloped
  2. LV is not able to pump blood adequately around the heart
  3. This causes increased afterload for the L atrium as very little blood can be transported via LV
  4. Hypertension of L atrium occurs leading to back up of pressure in the pulmonary veins into the pulmonary vasculature causing pulmonary hypertension and so pulmonary oedema
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7
Q

What are the different causes of heart failure in children?

A

Neonates - caused by obstruction:

  • Hypoplastic left heart
  • Aortic stenosis

Infants - high pulmonary bloodflow :

  • VSD
  • ASD
  • PDA

Children:

  • Esenmenger syndrome
  • Cardiomyopathy
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8
Q

What is Eisenmenger’s Syndrome and how is it treated?

A

Reversal of a L to R shunt in a congenital heart defect due to compensatory increase in pulmonary vascular resistance causing significant pulmonary hypertension leading to later development of a R to L shunt.

Only definitive treatment = heart and lung transplant

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9
Q

How does a VSD present?

A

Symptoms:

  • Breathlessness = key symptom
  • Failure to thrive (due to breathlessness cannot feed)
  • Recurrent respiratory infections

Signs:

  • Pansystolic murmur - heard near L sternal edge- the smaller the VSD, the harsher the murmur
  • Signs of heart failure in large VSD: gallop rhythm, cardiomegaly, hepatomegaly
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10
Q

Management of VSD…

A
- 50% will close spontaneously 
Medical management up to 3-4 months age: 
- Diuretics
- Fluid restriction  
- ACEi

Surgery at 3-4 months if no response to medications:
- PA banding (band around pulmonary artery to increase RV pressure therefore decrease shunt flow)

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11
Q

Presentation of ASD…

A
  • Most likely heart defect to be found in adulthood
  • Breathlessness

Signs:
- Ejection systolic murmur - fixed splitting of S2

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12
Q

Investigation findings of ASD…

A
  • ECG: RBBB

- CXR: cardiomegaly

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13
Q

Management of ASD…

A

Surgical repair at 3 - 5 years’ old - via cardiac catheterisation

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14
Q

How is the ductus arteriosus closed in neoneates?

A

When neonates take their first breaths, this causes an increase in pulmonary blood flow leading to increased clearance of prostaglandins.
Prostaglandins normally act as smooth muscle dilators which keeps the DA patent - but when they are removed, this allows the DA to close.

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15
Q

What is a PDA?

A

An acyanotic congenital heart defect where the DA remains patent after birth which allows blood to flow from the high pressure descending aorta into the lower pressure pulmonary artery.

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16
Q

Presentation of PDA …

A

*Most children are asymptomatic- normally picked up on screening

Signs:

  • Left subclavicular thrill
  • Continuous machinery murmur
  • Large volume - bounding, collapsing pulse
17
Q

Management of PDA…

A
  • Indomethacin - inhibits prostaglandin release which allows DA to close
  • Surgical repair at 12 months via coil or occlusion device
18
Q

What condition is most commonly associated to AVSD?

A

Down Syndrome

19
Q

How is AVSD managed ?

A

Surgical repair at around 3 months

Managed with heart failure medical management before this.

20
Q

What is coarctation of the aorta?

A

Narrowing of the aorta caused by duct tissue encircling the aorta at the point of insertion of the duct - as the DA closes, the aorta will constrict leading to LV outflow obstruction

21
Q

Presentation of coarctation of aorta?

A
  • Femoral pulses are absent
  • Delayed cap refill
  • Feeding problems
  • Severe metabolic acidosis
22
Q

Why are prostaglandins used for acutely managing coarctation?

A

Prostaglandins will keep the DA patent which allows blood to flow into descending aorta so lower part of the body can be supplied

23
Q

What is the hyperoxia test and what does it show?

A

100% oxygen given to neonate for 10 minutes, then ABG taken: pO2 <15kPa indicates cyanotic congenital heart disease as this shows that the oxygenated blood is not circulating properly through the heart.

24
Q

Management of cyanotic heart disease…

A
  • Prostaglandins - to keep DA open which allows some oxygenated blood to reach systemic circulation
  • Surgery = definitive treatment, dependent on the problem
25
Q

What are the features of TOF?

A

4 features:

  • Ventricular septal defect
  • Overriding aorta
  • Right ventricular outflow tract obstruction
  • Right ventricular hypertrophy
26
Q

Presentation of TOF…

A

Symptoms:

  • Cyanosis
  • Dyspnoea
  • Failure to thrive

Signs:
- Ejection systolic murmur - due to RVOT (pulmonary stenosis)

27
Q

Investigation findings for TOF…

A
  • ECG: right ventricular hypertrophy - R axis deviation
  • CXR: boot shaped heart
  • Echo: VSD, overriding aorta
28
Q

Management of TOF…

A
  • Closure of VSD

- Graft between right ventricle and pulmonary artery

29
Q

What is a cyanotic spell, and why does it occur?

A

Acute spells of hypoxia causing severe cyanosis, shortness of breath and loss of consciousness.

  1. Infundibulum = muscle around the pulmonary artery - there is infundibular spasm leading to increased pulmonary resistance which causes hypoxia.
  2. The child then becomes irritable and cries leading to increased intrathoracic pressure which increases pulmonary pressure causing increased R to L shunting
30
Q

How is a cyanotic spell managed?

A
  • B blockers to relax infundibular muscle
  • Morphine - reduce ventilatory drive
  • Give O2 - potent pulmonary vasodilator
  • Adrenaline - increase systemic vascular resistance
  • Manoeuvres: press on the liver and knees-to-chest
31
Q

What are the anatomical changes seen in TGA?

A
  • Aorta leaving the right ventricle : deoxygenated blood in systemic circulation
  • Pulmonary trunk leaving the left ventricle: oxygenated blood in pulmonary circulation
32
Q

Presentation of TGA…

A

Symptoms:

  • Cyanosis
  • Tachypnoea

Signs:

  • Loud single S2 sound - no S1
  • Prominent ventricular impulse on palpation
33
Q

Management of TGA…

A
  • Prostaglandins to keep DA open - allowing some mixing of oxygenated blood into systemic circulation
  • Surgery for correction of defect - arterial switch