Cardiac Problems Flashcards

1
Q

What are the symptoms of cardiac disease in an infant?

A
Breathlessness
Difficulty feeding
Poor weight gain
Sweating with feeding
Cyanosis
Collapse
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the features of an innocent heart murmur?

A

Systolic (diastolic is never innocent)
Low intensity
Asymptomatic
Often loudest at left sternal edge but may be elsewhere (e.g. venous hum)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Which type of cardiac defects are more likely to present with neonatal collapse?

A

Duct-dependent lesions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is the difference between systemic and cyanotic duct dependent lesions?

A

Systemic:

  • severe obstruction of blood flow out of left side of heart
  • systemic circulation dependent on PDA

Cyanotic:
- obstruction to pulmonary blood flow OR lack of oxygenation of systemic blood

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Which conditions are systemic duct dependent lesions?

A

Hypoplastic left heart syndrome
Critical aortic stenosis
Interrupted aortic arch (or severe coarctation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Which conditions are cyanotic duct dependent lesions?

A

Transposition of the great arteries

Pulmonary atresia with intact septum

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the features of an atrial septal defect (ASD)?

A
SOB, cyanosis, haemoptysis
Chest pain
Ejection systolic murmur in pulmonary area
Split S1, wide fixed split S2
Pulmonary hypertension
Raised JVP
AF
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How is ASD diagnosed?

A

Echo

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What would be seen on ECG and CXR in ASD?

A

ECG: right axis deviation, RBBB
CXR: cardiomegaly, prominent pulmonary artery

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How is ASD managed?

A

Surgical closure - open or trans catheter

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the features of a VSD?

A

Harsh pan systolic murmur at left sternal edge
CHF: tachycardia, SOB, hepatomegaly
Systolic thrill
Parasternal heave

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How is a VSD diagnosed?

A

Echo

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What would be seen on ECG and CXR in VSD?

A

ECG: LVH signs
CXR: cardiomegaly, large pulmonary arteries

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How is a VSD managed?

A

Initially medical as may close spontaneously:
- diuretics for HF
- ACE inhibitors to reduce afterload
Surgical closure if unsuccessful/complications

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the complications of VSD?

A

Aortic regurgitation
Infective endocarditis
Eisenmenger’s –> shunt reversal + cyanosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is coarctation of the aorta?

A

Narrowing of the descending aorta –> LV pressure overload, CHF, HTN and hypo perfusion of lower body

17
Q

What are the clinical features of coarctation of the aorta?

A

Raised BP
Radio-femoral delay +/- weak femoral pulse
Systolic murmur in left intraclavicular area + below left scapula
Early heart failure if severe

18
Q

What might be seen on CXR in coarctation of the aorta?

A

CHF

Rib notching

19
Q

How is coarctation of the aorta diagnosed?

A

Echo

If unclear –> CT or MRI

20
Q

How is coarctation of the aorta managed?

A

Surgery:

  • indications: CHF or severe HTN
  • -> open angioplasty or balloon angioplasty with stenting
21
Q

What are the features of a PDA?

A
Asymptomatic or SOB + poor feeding in infancy
Continuous machine like murmur
Left subclavicular systolic thrill
Displaced, heavy apex beat
Collapsing pulse and wide pulse pressure
22
Q

How is PDA diagnosed?

23
Q

How is PDA managed in a preterm infant?

A

Treat if symptomatic:

  • IV NSAIDs (first line)
  • surgical ligation (second line)
24
Q

What is the most common congenital heart defect?

25
What are the risk factors for VSD?
``` Maternal diabetes Maternal rubella Foetal alcohol syndrome Uncontrolled maternal PKU Family history of VSD Trisomy 21, 13 and 18 ```
26
What are the complications of VSD?
Endocarditis
27
What are the four features of Tetralogy of Fallot?
VSD Pulmonary stenosis Right ventricular hypertrophy Overriding aorta
28
What are the risk factors for TOF?
``` Males Family history of CHD Teratogens: - alcohol - warfarin - trimethadione (anti epileptic) Genetics: - CHARGE syndrome - Di George syndrome - VACTERL association ```
29
What are the features of CHARGE syndrome?
``` Coloboma Heart defects Atresia choanae Retardation of growth/development Genitourinary anomalies Ear anomalies ```
30
What are the features of VACTERL?
``` Vertebral anomalies Anorectal malformation Cardiac defects Tracheo-oesophageal fistula Renal anomalies Limb malformations ```
31
What are the clinical features of TOF?
``` Poor growth SOB including acute hypoxic episodes Cyanosis + clubbing Ejection systolic murmur Toddlers may squat to increase peripheral resistance and hence reduce right --> left shunt ```
32
How is TOF diagnosed?
Echo
33
What might be seen on CXR in TOF?
Boot shaped heart
34
How is TOF managed?
``` Surgery by 1 year (earlier if severe) Medical therapy until then if symptomatic: - oxygen - morphine - beta blockers - prostaglandins to keep ducts open ```
35
What is transposition of the great arteries?
Aorta + pulmonary artery the wrong way round
36
What are the features of transposition of the great arteries?
Cyanosis in first 24 hours of life Prominent right ventricular heave Systolic murmur if VSD present No signs of respiratory distress
37
How is transposition of the great arteries diagnosed?
Echo
38
What does transposition of the great arteries look like on CXR?
'Egg on a string'
39
How is transposition of the great arteries managed?
Initial: - emergency prostaglandin to keep ductus arteriosus open - correct metabolic acidosis - atrial balloon septostomy to allow mixing Definitive: - surgical correction, usually before 4 weeks