Paediatric Respiratory Flashcards

1
Q

What are some causes of stridor?

A
Croup
Epiglottitis
Laryngomalacia
Adenotonsillar hypertrophy
Subglottal stenosis
Vocal cord palsy
Quinsy
Anaphylaxis -> laryngeal oedema
Foreign body
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2
Q

What are some signs of respiratory distress?

A
Recession (subcostal and intercostal)
Tracheal tug
Tachypnoea/ raised RR
Tachycardia
Grunting
Nasal flaring
Cyanosis
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3
Q

What would spirometry show in a child with asthma?

A

Obstructive pattern
FEV1 reduced less than 80% predicted
FEV1:FVC ratio <0.7
Reversibility with use of bronchodilators

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4
Q

Exhaled nitric oxide test is used for patients with which condition?

A

Asthma

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5
Q

What conservative management measures can be implemented for a child with asthma?

A

Check their inhaler technique and that they are using a space
Written asthma management plan
Annual review

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6
Q

How is monteleukast administered?

A

Orally

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7
Q

For a 4 year old child whose asthma is not adequately controlled with SABA and regular ICS, what is the next step in their management?

A

Add a LTRA e.g. monteleukast

If they were over 5 years old, we would add a LABA instead

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8
Q

How is cystic fibrosis inherited?

A

Autosomal recessively

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9
Q

How may children with cystic fibrosis present?

A

Neonate: meconium ileus, prolonged jaundice
Infants/ Children: rectal prolapse, recurrent chest infections, diabetes, failure to thrive and vitamin deficiency, nasal polyps, hyperinflated chest, steatorrhea, clubbing

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10
Q

How is CF managed?

A
Physio twice a day
Mucolytics
Pancreatic enzymes
Vitamin A, D, E supplements 
High calorie diet
Psychological support
Prophylactic abx for presumed viral infections
Twice yearly follow ups
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11
Q

Abnormally raised immunoreactive trypsinogen is suggestive of which condition?

A
Cystic fibrosis 
(This is measured in newborns on day 5/6 as part of the Guthrie screen, samples with high IRT will then undo CFTR mutation screening)
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12
Q

What is bronchiectasis?

A

Permanent dilation and thickening of the bronchi
Due to chronic inflammation of the airways, associated with CF, immunodeficiency, or may develop after lung infections, or aspiration

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13
Q

How could a child with bronchiectasis present?

A
Cough
Dyspnoea
Haemoptysis
Coarse crackles 
Wheeze in one third of patients 
Respiratory failure
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14
Q

What is the gold standard investigation for bronchiectasis?

A

HRCT
Will show bronchial wall thickening and signet ring sign where the diameter of the bronchus is wider than the bronchial artery

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15
Q

How is bronchiectasis managed in children?

A
  • physio for airway clearance
  • longer course or prophylactic abx
  • encourage healthy diet and exercise
  • influenza vaccine
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16
Q

What triad of symptoms are characteristic of croup?

A

Barking cough
Hoarse voice
Stridor

17
Q

Outline your management plan for a child presenting with croup.

A

Steroids
Nebulised adrenaline
Rest

18
Q

What is the typical presentation of Petussis?

A

Prolonged severe bouts of coughing often associated with vomiting

19
Q

What presentation would warrant hospital admission for an infant with bronchiolitis?

A

Apnoeic episodes
Feeding less than 50 to 75%
Raised RR
Low sats

20
Q

What is the investigation of choice for suspected bronchiolitis?

A

Nasal pharyngeal aspirate

21
Q

What causes epiglottitis?

A

Haemophilus influenza type B

22
Q

How would you manage a child with epiglottitis?

A

Don’t examine!

Send child for intubation and IV Abx

23
Q

What investigation would you want to perform in a child with suspected bronchiolitis?

A

Nasopharyngeal aspirate for rapid RSV testing

24
Q

What are some causes of acute wheezes, and of chronic wheezes?

A

Acute and chronic: asthma, viral episodic wheeze
Acute: FB, anaphylaxis, atypical pneumoniae
Chronic: bronchiectasis, FB, CF, recurrent aspiration, tracheobronchomalacia, tracheal web, cystic tumour

25
Q

What are some causes of cyanosis in a child?

A

Airway: choanal atresia, micrognathia, larnygeal web/ stenosis, hemangioma, laryngomalacia, vascular rings, Pierre Robin sequence

Breathing: hypoventilation, pulmonary hypoplasia, diaphragmatic hernia, pneumonia, phrenic nerve palsy

Circulation: anaemia, polycythaemia, pulmonary stenosis/ atresia, tetralogy, tricuspid atresia, transposition great arteries, persistent pulmonary hypertension of newborn

26
Q

When is stridor exacerbated for an infant with laryngomalacia?

A

When feeding, crying, lay on their back

27
Q

How would you treat an infant with suspected whooping cough?

A

If presenting within 21days, offer macrolide antibiotic e.g. azithromycin
Abx prophylaxis for household members
Notify public health England

28
Q

How do severe asthma attacks present compared to life threatening asthma attacks?

A

Severe:
PEF 33-50%, sats <92%, too breathless to talk, use of accessory muscles, raised HR and RR

Life threatening:
PEF<33%, sats <92%, silent chest, cyanosis, altered consciousness