Cardiology Flashcards

1
Q

What is an ASD?

A

ASD occurs when the septum between the left and right atrium is not formed properly - oxygenated blood from the left atrium goes into the right atrium

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2
Q

What are some risk factors for ASD?

A

Maternal smoking in 1st trimester, maternal diabetes, maternal rubella, maternal drug use, Treacher Collins syndrome

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3
Q

What is found on auscultation of an ASD?

A

Soft systolic ejection murmur best heard over pulmonary valve region (2nd ICS)

Wife, fixed split S2

Diastolic rumble in lower left sternal edge in patients with large ASD

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4
Q

How is an ASD investigated?

A

ECG - tall P wave, right BBB, right axis deviation

Tranthoracic echocardiogram

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5
Q

How is an ASD managed?

A

If ASD <5mm, spontaneous closure should occur within 12 months of birth

If ASD >1cm - surgery

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6
Q

What are some complications of an untreated large ASD?

A

Arrhythmias, pulmonary hypertension, Eisenmenger syndrome, peripheral oedema, TIA/stroke

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7
Q

What is Tetralogy of Fallot?

A

Cyanotic congenital heart disease - tetrad of:

  • VSD
  • Pulmonary stenosis
  • Right ventricular hypertrophy
  • Overriding aorta
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8
Q

What are some risk factors for TOF?

A
Male
Family history
Teratogens (alcohol, warfarin, trimethadione)
CHARGE syndrome
Di George syndrome
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9
Q

What can be seen on CXR for Tetralogy of Fallot?

A

Boot shaped heart and reduced pulmonary vascular marking

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10
Q

What are the 3 categories of TOF?

A

1) Mild (Pink TOF) - mild PS/RVH and usually asymptomatic but disease progresses as the child grows so cyanotic by age 1-3 years
2) Moderate-severe (cyanotic TOF) - moderate-sever PS may present in the first few weeks of life with cyanosis and respiratory distress - prone to developing recurrent chest infections and or fail to thrive
3) Extreme - duct dependent lesions where the only way deoxygenated blood can flow to the lungs is through a PDA

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11
Q

What are hypoxic (‘tet’) spells?

A

Paroxysm of hyperpnoea

Irritability

Increasing cyanosis

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12
Q

What can be heard of auscultation of TOF?

A

Loud, single S2 (closure of aortic valve in diastole with absent/reduced pulmonary valve closure

Pansystolic murmur - best osculated either mid or upper left sternal edge (the smaller the VSD, the louder the murmur)

Ejection click - due to presence of dilated aorta

Continuous machinery murmur best heard at upper left sternal edge - occurs in the presence of PDA with extreme forms of TOF, especially those on prostaglandin infusion

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13
Q

What is the management of TOF?

A

Medical

  • Squatting
  • Prostaglandin infusion - maintains PDA
  • Beta blockers
  • Morphine
  • Saline 0.9% bolus

Surgical - definitive repair

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14
Q

What are some complications of untreated TOF?

A

Polycythaemia, stroke, cerebral abscess, infective endocarditis, congestive cardiac failure, death

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15
Q

What is transposition of the great arteries?

A

Ventriculoarterial discordance in which the aorta rises from the morphologic right ventricle and the pulmonary artery arises from the morphologic left ventricle

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16
Q

What is the most common cause of cyanosis in the newborn?

A

Transposition of the great arteries

17
Q

What are the 3 common anatomical sites for mixing of oxygenated and deoxygenated blood in TGA to allow life to be sustained?

A
  • Patent foramen ovale/ASD
  • VSD
  • PDA
18
Q

What are the clinical features of TGA?

A

Cyanosis appears in first 24 hours

Mild cyanosis particular when crying

Signs of CHF - tachypnoea, tachycardia, diaphoresis, failure to gain weight

Prominent right ventricular heave

Single second heart sound, loud A2

Systolic murmur potentially if VSD present

19
Q

What is the management of TGA?

A

Emergency prostaglandin E1 infusion to keep PDA patent

Correct metabolic acidosis

Atrial balloon septostomy

Surgical correction before the age of 4 weeks

20
Q

What are the long term consequences of TGA?

A
Neopulmonary stenosis
Neoaortic regurgitation
Neoaortic root dilatation
Coronary artery disease
Sudden cardiac death
Higher incidence of Neurodevelopmental abnormalities
21
Q

Which is the most common congenital heart defect?

A

VSD - hole in the septum separating the left and right ventricles

22
Q

What is Eisenmenger’s syndrome?

A

A condition where the pressure in the right ventricle exceeds that of the left and is caused by a significant gradual increase in the pulmonary vascular resistance

Results in a shunt reversal with deoxygenated blood flowing from the right ventricle into the left and entering the systemic circulation

This causes decreased systemic oxygen saturation and these patients become cyanotic

23
Q

What are some risk factors for VSD?

A

Maternal diabetes, maternal rubella, fetal alcohol syndrome, family history, Down’s syndrome, trisomy 13 and 18

24
Q

How would a baby with a moderate VSD present?

A

Excessive sweating, easily fatigued, tachypnoea

Usually obvious by 2-3 months of age

25
Q

How would a baby with a large VSD present?

A

Dyspnoea, problems with feeding, developmental issues, frequent chest infections

26
Q

Which is the most likely type of murmur to be heard with VSD?

A

Holosystolic (pan systolic) murmur - lower left sternal border

27
Q

What is the management of VSD?

A

Diuretics, ACE inhibitors, digoxin

Surgical repair

28
Q

What are the complications of untreated VSD?

A

CHF, growth failure, aortic valve regurgitation, pulmonary vascular disease, frequent chest infections, infective endocarditis, arrhythmias, sudden death