Paediatrics Flashcards

1
Q

Management of viral induced wheeze

A

Episodic viral wheeze:
- 1st line = short acting beta 2 agonists (e.g. salbutamol) or anticholinergic via a spacer

  • 2nd line = intermittent leukotriene receptor antagonist (montelukast) or intermittent inhaled corticosteroids, or both

Multiple trigger wheeze
- trial of either inhaled corticosteroids or a leukotriene receptor antagonist (montelukast), typically for 4-8 weeks

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2
Q

Most common cause of bronchiolitis

A

RSV

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3
Q

Features of bronchiolitis

A

coryzal symptoms (including mild fever) precede:

  • dry cough
  • increasing breathlessness
  • wheezing
  • fine inspiratory crackles
  • feeding difficulties associated with increasing dyspnoea are often the reason for hospital admission
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4
Q

When would you refer immediately (999), for bronchiolitis?

A
  1. apnoea (observed or reported)
  2. child looks seriously unwell to a healthcare professional
  3. severe respiratory distress, for example grunting, marked chest recession, or a respiratory rate of over 70 breaths/minute
  4. central cyanosis
  5. persistent oxygen saturation of less than 92% when breathing air.
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5
Q

Ix for bronchiolitis

A

immunofluorescence of nasopharyngeal secretions

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6
Q

Management of bronchiolitis

A

Management is largely supportive:
1. humidified oxygen is given via a head box (if O2 sats < 92%)

  1. nasogastric feeding may be needed if children cannot take enough fluid/feed by mouth
  2. suction is sometimes used for excessive upper airway secretions
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7
Q

What is laryngomalacia?

A

Congenital abnormality of the larynx.

Infants typical present at 4 weeks of age with:
stridor

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8
Q

What is haemolytic uraemic syndrome?

A

Tirad of:

  1. acute kidney injury
  2. microangiopathic haemolytic anaemia
  3. thrombocytopenia
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9
Q

Ix for HUS

A
  1. full blood count: anaemia, thrombocytopaenia, fragmented blood film
  2. U&E: acute kidney injury
  3. stool culture
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10
Q

Management of HUS

A
  1. treatment is supportive e.g. Fluids, blood transfusion and dialysis if required
  2. No Abx, despite the preceding diarrhoeal illness in many patients
  3. plasma exchange is reserved for severe cases of HUS not associated with diarrhoea
  4. eculizumab (in adults)
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11
Q

What is cradle cap?

A

Early sign of seborrhoeic dermatitis

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12
Q

How does cradle cap present?

A

Erythematous rash with coarse yellow scales

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13
Q

Management of cradle cap

A

mild-moderate: baby shampoo and baby oils

severe: mild topical steroids e.g. 1% hydrocortisone

Usually resolves spontaneously by 8 months

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14
Q

What is urticaria?

A

local or generalised superficial swelling of the skin ( hives)

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15
Q

Features of urticaria

A
  1. pale, pink raised skin. Variously described as ‘hives’, ‘wheals’, ‘nettle rash’
  2. pruritic
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16
Q

Management of urticaria

A

1st line = non-sedating antihistamines

Severe or resistent = prednisolone

17
Q

What is kawasaki disease?

A

type of vasculitis which is predominately seen in children

18
Q

Features of kawasaki disease

A
  1. high-grade fever which lasts for > 5 days.
    - Fever is characteristically resistant to antipyretics
  2. conjunctival injection
  3. bright red, cracked lips
  4. strawberry tongue
  5. cervical lymphadenopathy
  6. red palms of the hands and the soles of the feet which later peel
19
Q

Ix for kawasaki disease

A

clinical diagnosis

20
Q

Management of kawasaki disease

A
  1. high-dose aspirin
  2. intravenous immunoglobulin
  3. echocardiogram is used as the initial screening test for coronary artery aneurysms
21
Q

What is syndrome of inappropriate ADH secretion (SIADH) ?

A

hyponatraemia secondary to the dilutional effects of excessive water retention.

22
Q

Management of SIADH

A
  1. correction must be done slowly
  2. fluid restriction
  3. demeclocycline: reduces the responsiveness of the collecting tubule cells to ADH
  4. ADH (vasopressin) receptor antagonists have been developed
23
Q

Typical presentation of flat feet

A

All ages

Absent medial arch on standing

Typically resolves between the ages of 4-8 years

24
Q

Bow legs

A

1st-2nd year

Typically resolves by the age of 4-5 years

25
Q

Screening for developmental dysplasia of the hip

A

all infants are screened at both the newborn check and also the six-week baby check using the Barlow and Ortolani tests

26
Q

Ix for DDH

A

USS confirms diagnosis

27
Q

Management of DDH

A
  1. most unstable hips will spontaneously stabilise by 3-6 weeks of age
  2. Pavlik harness (dynamic flexion-abduction orthosis) in children younger than 4-5 months
  3. older children may require surgery
28
Q

What is Perthes?

A

Degenerative condition affecting the hip joints of children, typically between the ages of 4-8 years

Due to avascular necrosis of the femoral head, specifically the femoral epiphysis

29
Q

Features of perthes’

A
  1. hip pain: develops progressively over a few weeks
  2. limp
  3. stiffness and reduced range of hip movement
30
Q

Diagnosis of perthes’

A

plain x-ray

  • early changes include widening of joint space
  • later changes include decreased femoral head size/flattening
31
Q

Management of perthes’

A
  1. To keep the femoral head within the acetabulum: cast, braces
  2. If less than 6 years: observation
  3. Older: surgical management with moderate results
  4. Operate on severe deformities