Atrioventricular septal defect Flashcards

1
Q

What is an atrioventricular septal defect?

A

Spectrum of congenital heart malformations that share a defect in the atrioventricular septum and abnormalities in the AV valves (mitral and tricuspid)

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2
Q

How can AVSDs be classified?

A

Complete

Partial

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3
Q

What percentage of all congenital heart defects do AVSDs account for?

A

5%

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4
Q

Which syndrome is strongly associated with AVSDs?

A

Downs syndrome (trisomy 21)

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5
Q

When does the AV septum form?

A

4-5 weeks

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6
Q

What do AVSD defects arise from?

A

Failure of superior and inferior endocardial cushions to fuse correctly leading to displacement of AV valves and causing the inlet portion of ventricular septum to be scooped out

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7
Q

Describe the pathophysiology in complete AVSD

A

Increased shunting of blood from left to right occurring at both atrial and ventricular levels

Pulmonary vascular resistance decreases normally over first 6 weeks of life and patient develops a large left to right shunt through both atrial and ventricular defects

Causes excessive pulmonary blood flow leading to heart failure and elevated pulmonary vascular resistance AV valves are usually abnormal and incompetent resulting in regurgitation

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8
Q

Describe the pathophysiology of partial AVSD

A

Left to right shunting at the level of atrial septal defect
Causes volume overload of both right atrium and right ventricle and pulmonary over circulation but pulmonary pressures are usually normal to mildly elevated therefore symptoms may be minimal until adulthood or may present in late childhood

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9
Q

Give some clinical features of AVSD

A
Tachypnoea
Tachycardia
Poor feeding
Sweating
Failure to thrive
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10
Q

What does the severity of clinical symptoms of AVSD depend on?

A

The degree of pulmonary overload and heart failure

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11
Q

When do virtually all AVSD patients have symptoms?

A

By 1 year of age

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12
Q

Give some examination findings of AVSD

A

Undernourished child - shows characteristics of downs syndrome, signs of congestive heart failure, hepatomegaly, gallop rhythm, generalised oedema and crackles may be present

Hyperactive precordium
Prominent systolic heave along the left sternal border
Palpable apical thrill

Auscultation -ejection systolic murmur or mid diastolic murmur. Wide and fixed splitting of S2

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13
Q

What investigations would you do for AVSD

A

Bloods - karyotopying for trisomy 21
ECG
CXR
Echo

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14
Q

What ECG changes occur with AVSD?

A

Superior QRS axis
Prolonged PR interval
P wave morphology
Right ventricular hypertrophy

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15
Q

What is shown on CXR in AVSD?

A

Cardiomegaly
Prominent pulmonary artery
Pulmonary vascular markings

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16
Q

Describe the management of AVSD

A

Medical - diuretics, ACEi, digoxin, adequate caloric intake

Surgical - between 3-6 months - palliative or corrective