Cardiology Flashcards

(32 cards)

1
Q

What are TORCH infections?

A

Toxoplasma
Rubella
CMV
Herpes

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2
Q

What is the most common cardiac problem in trisomy 21?

A

ASD most common

VSD

AVSD less common

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3
Q

What is most common cardiac problem in turner syndrome?

A

Co-arctation of aorta

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4
Q

What is most common cardiac problem in noonan syndrome?

A

pulmonary stenosis

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5
Q

What is most common cardiac problem in williams syndrome?

A

Supravalvular aortic stenosis

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6
Q

What would central cyanosis indicate (cardiac)?

A

Right to left shunt

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7
Q

What would feeding problems indicate (cardiac)?

A

Heart failure

Restless during feeding, sweating during feeds

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8
Q

What symptoms could indicate a paediatric heart problem?

A

Feeding, weight and development

Cyanosis

Tachypnoea, dyspnoea

Exercise tolerance

Chest pain

Syncope

Palpitation

joint problems

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9
Q

What examination features could indicate a heart problem in children?

A

Weight and height

Dysmorphic features

Cyanosis

Clubbing

Tachy/dyspnoea

Pulses/apex (remember femoral)

Heart sounds

Murmurs

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10
Q

How can murmurs be characterised?

A

Cardiac timing
- systole/diastole/continuous

Duration

  • early/mid/late
  • ejection/holo- or pansystolic

Pitch/quality

  • harsh or mixed frequency
  • soft or indeterminate
  • vibratory/pure frequency
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11
Q

What does radio-femoral delay indicate?

A

Coarctation of aorta (late stage)

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12
Q

What investigations can be used to assess cardiac problems?

A
BP
O2 sats
ECG
CXR
Echo
Angiography
MRI
Exercise testing

ABG rarely bc painful

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13
Q

Describe innocent murmurs

A

70-80%

NOT a diagnosis of exclusion

Specific features

4 types

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14
Q

What are features of innocent murmurs?

A

Systolic murmur (continuous in venous hum)
No other signs cardiac disease
Soft murmur, grade 1/6 or 2/6
Vibratory, muscial
Localised
Varies with position, respiration, exercise

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15
Q

Describe Still’s murmur

A

LV outflow murmur

Age 2-7

Soft systolic; vibratory, musical, “twangy”

Apex, left sternal border

increases in supine position and with exercise

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16
Q

Describe pulmonary outflow murmur

A

Age 8-10

Soft systolic; vibratory

Upper left sternal border, well localised, not radiating to back

Increases in supine position, with exercise

Often children with narrow chest

17
Q

Describe carotid/brachiocephal IC arterial bruits

A

Age 2-10

1/6 or 2/6 systolic; harsh

Supraclavicular, radiates to neck

Increases with exercise, decreases on turning head or extending neck

18
Q

Describe venous hum

A

Age 3-8

Soft, indistinct

Continuous murmur, sometimes with diastolic accentuation

Supraclavicular

Only in upright position, disappears on lying down or turning head

19
Q

What are the types of VSD?

A
  • subaortic
  • perimembranous
  • muscular
20
Q

What type of shunt is present in VSD?

A

left to right shunt

not cyanotic

21
Q

How does VSD present?

A

Pansystolic murmur lower left sternal edge, sometimes with thrill

In small; early systolic murmur

Very large; diastolic rumble

Signs of cardiac failure in large VSDs leasing to biventricular hypertrophy and pulmonary hypertension

22
Q

What is eisenmenger syndrome?

A

Any untreated cardiac defect which leads to pulmonary hypertension, reversal of flow and cyanosis

23
Q

How is a VSD closed?

A

Amplatzer or other occlusion device, trans-catheter

patch closure, open heart surgery

24
Q

Describe atrial septal defects

A

few clinical signs in early childhood, good chance spontaneous closure

Sometimes detected in adulthood with AF, heart failure or pulmonary hypertension

Wide fixed splitting of 2nd heart sound, pulmonary flow murmur

25
Describe AVSD
Associated with trisomy 21
26
Describe pulmonary stenosis
Asymptomatic in mild in moder and severe; exertional dyspnoea and fatigue Ejection systolic murmur upper left sternal border with radiation to back
27
Describe aortic stenosis
Mostly asymptomatic If severe; reduced exercise tolerance, exertional chest pain, syncope Ejection systolic murmur upper right sternal border, radiation into carotids
28
What are changes in foetal circulation at birth?
``` Pulmonary vascular resistance falls Pulmonary blood flow rises Systemic vascular resistance is increased Ductus arteriosus closes Foramen ovale closes Ductus venosus closes ```
29
How is pulmonary stenosis managed?
Balloon valvoplasty *replacement of valve not considered until stopped growing as child will outgrow valve
30
How can aortic stenosis be treated?
Balloon aortic valvuloplasty
31
Describe patent ductus arteriosus
Very common pre-term infants Treat with fluid-restriction/diuretics, prostaglandin inhibitors Can use surgical ligation In term babies; good chance spontaneous closure, not prostaglandin sensitive
32
How is co-arctation of aorta managed?
Re-open DA with prostaglandin E1 or E2 (stabilisation) Resection with end-to-end anastomosis Subclavian patch repair Balloon aortoplasty