Paeds chronic airway disease (CED/HDU) Flashcards

1
Q

What problems come under long-term upper airway disease?

A

Snoring
Mouth breathing
Recurrent ear infections
Recurrent croup

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

What problems come under long-term lower airway disease?

A

Recurrent wheeze
Asthma
Cystic fibrosis
Non-CF bronchiectasis

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

What are the common presentations of long-term respiratory disease in children?

A
  • Cough
  • Wheeze
  • Nasal obstruction (snoring, nasal blockage, mouth breathing)
  • Reduced ability to participate in active sports
  • Difficulty in breathing
  • Chronic production of sputum – white, green, blood-stained
  • Chest wall deformity
  • Clubbing
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How does Cystic fibrosis affect different parts of the body?

A
  • Sinusitis
  • Lungs: thick, sticky mucus build up, bacterial infections, and widened airways
  • Skin: sweat glands produce salty sweat
  • Blocked pancreatic duct
  • Cannot fully absorb nutrients
  • Complications to reproductive organs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the screening programme for cystic fibrosis?

A

In the heal prick test

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

What is meconium ileus?

A

A bowel obstruction that occurs when the meconium in the child’s intestine is even thicker and stickier than normal meconium

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

What are some history findings in children for cystic fibrosis?

A

Cough, wheeze, shortness of breath, fatty stools, poor weight gain, sputum production, haemoptysis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How is the sweat test used to diagnose cystic fibrosis?

A

It measures the amount of chloride in sweat

Kids with cystic fibrosis can have 2-5 times the normal amount of chloride in their sweat

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

What are the childhood problems caused by cystic fibrosis?

A
  • Infancy
    Meconium ileus, prolonged neonatal jaundice, hypoproteinaemia
  • Childhood
    Recurrent lower respiratory infections, failure to thrive, rectal prolapse, nasal polyps and sinusitis
  • Adolescence
    Diabetes mellitus, cirrhosis, distal intestinal obstruction, pneumothorax, haemoptysis, allergic bronchopulmonary aspergillosis, arthropathy, male infertility, psychological issues
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is included in management of CF?

A

GI: managing bowel obstructions

Pulmonary: physiotherapy, anti-microbial therapy, nebulised DNAse, hypertonic saline, inhaled bronchodilators, fluv accination, oral azithromycin

Nutritional management – pancreatic supplements, high calorie diet, salt supplements, fat-soluble vitamin supplements

Psychology / social work / family support through difficult times

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

What is chronic lung disease of prematurity?

A

Causes breathing difficulty, cough, mucus (sputum) production and wheezing

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

What is congenital cystic adenomatoid malformation?

A

When lobes of the lung form as a fluid-filled sac (cyst) and doesn’t function as normal lung tissue

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

What is Congenital pulmonary sequestration?

A

When a segment or lobe of dysplastic lung tissue exists with no communication with the rest of the tracheobronchial tree and receives an anomalous systemic vascular supply, separate from the rest of the lung

It is, therefore, a non-functional tissue

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

What is Congenital lobar emphysema?

A

When the air can enter the lungs but cannot escape, causing hyperinflation of the lobes of the lung

Sometimes it doesn’t become apparent till adulthood

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

What is Pierre-Robin sequence?

A

A birth defect causing an underdeveloped jaw, backward displacement of the tongue and upper airway obstruction

Cleft palate is also commonly present beside it

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

What is non-CF bronchiectasis?

A

A chronic, progressive respiratory disorder characterised by irreversibly and abnormally dilated airways, persistent cough, excessive sputum production and recurrent pulmonary infections

Flare ups treated with antibiotics

17
Q

What are some causes of non-CF bronchiectasis?

A

Idiopathic
Immunoglobulin deficiency
Connective tissue disease
COPD or asthma
Foreign body inhalation
Post infective
Ciliary dysfunction
Inflammatory bowel disease related

18
Q

How can aminophylline used in asthma?

A

Used in life-threatening situations when no others medications have worked

19
Q

Why are tetracycline antibiotics no prescribed to children under 12?

A

Because they cause staining and dental hypoplasia

20
Q

Which medications are given to children for oral cadidiasis?

A

Miconazole oral gel for age 4 months + or nystatin

21
Q

What type of murmur does a ventricular septal defect cause?

A

Pan systolic