Cardiology Flashcards

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1
Q

Egg on a String

A

CXR for TGA

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2
Q

Boot

A

TOF (RVH)

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3
Q

Snowman

A

TAPVR

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4
Q

Giant heart

A

Ebstein’s Anomaly

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5
Q

Two tests for cyanotic heart lesions

A

Pre-post ductal saturations

Hyperoxia test

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6
Q

Hyperoxia test

A

ABG in room air, then repeated after placed on 100% FiO2 for 10 min - if PaO2 >80, unlikely to be cyanotic congenital heart disease

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7
Q

3 sign

A

Coarctation of Aorta on CXR

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8
Q

Signs of PDA

A

Continuous murmur
Pulmonary edema
Wide pulse pressure
Bounding pulses

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9
Q

Risks of PDA in preterm infants

A

NEC
Renal injury
Myocardial ischemia

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10
Q

Components required for PDA closure

A

Absence of Prostaglandins
Smooth muscle
Platelets

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11
Q

Murmur of PDA

A

Continuous murmur
LUSB
Machine like

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12
Q

Treatment of PDAs

A

Indomethacin - risk of NEC, SIP, bleeding (do not use in thrombocytopenia, IVH, intracranial hypertension)
Ibuprofen - monitor renal function
Acetaminophen -monitor liver function

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13
Q

ASD murmur

A

Systolic ejection murmur
LUSB
Wide fixed split S2

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14
Q

Commonest type of ASD

A

Secundum

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15
Q

Natural history of ASD

A

Most will close spontaneously by 8 years of age

5-10% of patients will develop pulmonary hypertension over time due to increased pulmonary blood flow

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16
Q

Types of VSDs

A

Membranous/peri-membranous (70%)
Muscular (5-20%)
Inlet/AV canal type VSD (5-8%)
Supracristal/infundibular (5-7%)

17
Q

Most common congenital heart disease

A

Bicuspid aortic valve

18
Q

Most common cyanotic congenital heart disease

A

TOF

19
Q

VSD murmur

A

Holosystolic, LLSB

If defect close to aortic or tricuspid valves, can lead to insufficiency and other murmurs

20
Q

Bicuspid aortic valve auscultation

A

Midsystolic ejection click +/- murmur if stenosis/insufficiency present

21
Q

Late sequelae of BAV (2)

A

Aortic root dilatation

Aortic dissection

22
Q

Natural history of BAV

A

Valvular calcification and stenosis
Valvular degradation and insufficiency
Aortic root dilatation/dissection

23
Q

Important long term management/surveillance of BAV

A

Serial echo - assess aortic root, function of valve

Strict hypertension control

24
Q

Genetic association with CoA

A

Turner syndrome (30%)

25
Q

Genetic association with TOF

A
Trisomy 21
22q11
Trisomy 18
Trisomy 13
Alagille syndrome
Holt Oram
26
Q

Developmental problem in TOF

A

Anterior deviation of infundibular septum

27
Q

Lesions in TOF (4)

A

Overriding aorta
VSD
RV outflow tract obstruction
RVH

28
Q

Medication options for management of hyper cyanotic spell

A

Morphine (calm baby)
Propranolol
Phenylephrine (increase SVR and reverse shunt)
Paralysis (last option)

29
Q

Non-medication options for management of hyper cyanotic spell

A

Comfort
Knee to chest (baby)
Squat (child)
Fluid bolus