Congenital Heart Disease Flashcards

1
Q

What are the causes of cyanotic heart disease?

A

Tetrology of fallot
Transposition of the great arteries
Tricuspid atresia

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2
Q

What are causes of acyanotic CHD?

A

VSD
ASD
Coarctation of the aorta
PDA

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3
Q

What are the constituents of ToF?

A

VSD
Pulmonary stenosis causing right ventricular outflow obstruction
Overriding aorta
Right ventricular hypertrophy

Allows passage of blood from right to left side of the heart

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4
Q

What are clinical features of ToF?

A

If not diagnosed antenatally/birth then may present at 1-2 months postpartum

Cyanosis
Failure to thrive- poor feeding/weight gain
Tet spells- acute worsening of cyanosis often precipitated by exertion/crying
Tearful
Dyspnoeic

Ejection systolic murmur loudest in pulmonary area and on inspiration
Clubbing

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5
Q

What are the investigations/management of ToF?

A

CXR- boot shaped sign
ECHO= diagnostic

Treatment
- prostaglandin infusion in neonates to maintain PDA
- Will require surgical repair
- TET spells managed with beta blockers/morphine

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6
Q

What are features of transposition of great arteries?

A

Swapping of aorta and pulmonary artery leading to circulation of deoxygenated blood

Risk factor- maternal diabetes

CXR
- egg on side appearance

Treatment
- prostaglandin infusion to maintain PDA patency
- Surgery

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7
Q

What are features of tricuspid atresia?

A

Lack of tricuspid valve preventing blood flow from right atrium to ventricle

Leads to
- hypoplastic right ventricle
- ASD- can have right to left shunt leading to variations in oxygen levels
- VSD (to allow flow)
Pulmonary stenosis- restricting blood flow, often present
Left ventricular hypertrophy- increased workload

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8
Q

What are clinical features of tricuspid atresia?

A

Presents within first few days/weeks

Cyanosis
Dyspnoea
FTT
Fatigue

O/E
-Cyanosis
- Tachypnoea
- Murmurs either holosystolic if VSD or ejection systolic if pulmonary stenosis
- Clubbing- in chronic places

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9
Q

What is the management of tricuspid atresia?

A

Prostaglandin infusion- maintain ductal patency
Surgery- including Blalock Taussig shunt, Glenn Procedure, Fontan procedure

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10
Q

What are features of VSD?

A

OPening in interventricular septum allowing blood flow between left and right ventricles

Causes
- chromosomal disorders- downs/pataus
-post-MI

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11
Q

What are clinical features of VSD?

A

FT
HF
Hepatomegaly
Tachypnoea

O/E
- harsh pan systolic murmur loudest at lower left sternal edge

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12
Q

What are complications of VSD?

A

Eisenmenger syndrome
- initial left to right shunt causes pulmonary hypertension which causes RVH with increased pressures
-At some point pressure generated by the right exceeds the left leading to right to left shunt
- symptoms cyanosis, clubbing
- requires surgical management

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13
Q

What are features of ASD?

A

Commonly identified in adulthood

SoB esp on exertion
Right heart failure
Pulmonary hypertension
Arrythmias e.g. AF
Stroke following DVT
- clot passes through defect from RA to LA and into circulation

O/E
- ejection systolic murmur
- fixed splitting of S2

Holt-oram syndrome- ASD and triphalengeal thumbs

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14
Q

What are classification of ASD?

A

Ostium Primum
- defect of septum near AV valve
- associated with Downs

Ostium Secundum
- defects of superior atrial septum
- most common form

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15
Q

What are features of PDA?

A

Incomplete closure

Risk factors- maternal rubella, prematurity

O/E
- continuous machinery type murmur
- left subclavicular thrill
- bounding collapsing pulse

Manage with indomethacin or ibuprofen to inhibit prostaglandin production

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16
Q

What are features of patent Foramen Ovale?

A

Connects the atria usually 6 months-1 year post birth

Can mean DVT/PE travel to arterial circulation and cause stroke