Paediatric Respiratory Disease Flashcards
(119 cards)
What respiratory conditions MUST I know about?
- Asthma
- LRTI
- URTI
What else would be good to know about?
- Pleural effusions
- Inhaled forgein body
- TB
- Whooping cough
A newborn presents with a harsh expiratory sound on breathing.
Form a list of differentials for stridor in this age group.
- Pharyngeal collapse
- Laryngeal atresia/webbing
- Vocal cord paralysis
- Micrognathia (small jaw e.g. in DiGeorge syndrome)
- Subglottic stenosis
An infant presents with a harsh expiratory sound on breathing.
Form a list of differentials for stridor in this age group.
- Viral croup
- Rhinitis
- Laryngomalacia
- Subglottic stenosis
- Laryngeal web/cyst
How can upper airway obstruction be subdivided?
- Supraglottic
- Glottic
- Subglottic
A small child presents with a harsh expiratory sound on breathing.
Form a list of differentials for stridor in this age group.
- Viral croup
- Bacterial tracheitis
- Forgein body
- Retropharyngeal abscess
- Tonsilar/adenoid hypertrophy
An older child presents with a harsh expiratory sound on breathing.
Form a list of differentials for stridor in this age group.
- Inhalation injury
- Foreign body
- Angioedema
- Anaphylaxis
- Trauma
- Peritonsilar abscess
- Mononucleosis
What is the most common cause of chronic upper airway obstruction in children?
Adenoid or tonsillar hypertrophy
Tell me about adenoid or tonsillar hypertrophy.
- Often due to recurrent infection/allergy/inhaled irritants
- Predisposes to recurrent/persistent otitis media
- Assess with lateral radiography
- Rx with removal
Define croup.
Viral infection of the middle respiratory tract in infants causing airway inflammation.
What are the common pathogens that cause croup?
- Respiratory syncytial virus (RSV)
- Parainfluenza virus 1, 2, 3, & 4.
A child a year old is brought in by his father because he has stridor and difficulty breathing. Croup is suspected.
What might we see on examination of the child?
- Inspiratory stridor, although may be biphasic
- Laboured breathing
- Recession (suprasternal/intercostal/subcostal)
- Wheeze, if lower airway involved
What is the most common life limiting autosommal recessive condition in caucasians?
Cystic fibrosis
What is the pathophysiology of CF?
AR defect in the CF transmembrane protein leading to defective ion transport in exocrine glands.
When and how do most people with CF present?
As a newborn via the blood spot testing done at 5-8 days
If the blood spot test doesn’t pick up CF in a newborn, how else might they present?
- Prolonged jaundice (14 days +)
- Meconium ileus
How many CF mutations can the Guthrie card pick up?
29 CFTR gene mutations
How do most children present with CF? (Not Guthrie test)
With:
- Malabsorption
- Failure to thrive
- Recurrent chest infections
How can we investigate suspected CF?
- Sweat test
- CXR
- Lung function
- Genetic testing for known CF mutations
- IRT levels
What is the positive sweat teast for CF?
Chloride levels above 60mmol/L
Part of the screening programme for CF is measuring IRT.
A parent wants to know what this means. What should you tell them.
One of the organs affected by CF is the pancreas.
This produces enzymes which normally empties into the small intestine.
In CF, the ducts from pancreas to gut get blocked, so the enzymes back up and build up.
Immunoreactive trypsin is the built up enzyme which is present in the gut.
A neonate is diagnosed with CF.
What complications should you tell the parents they might have to deal with in infancy?
- Meconium ileus
- Neonatal jaundice
- Hypoproteinaemia and oedema
A child is diagnosed with CF.
What complications should the child and parents look out for?
- Recurrent LRTIs
- Poor appetite
- Rectal prolapse
- Bronchiectasis
A child is diagnosed with CF.
What problems might they develop in their adolescence?
- Bronchiectasis
- Diabetes mellitus
- Cirrhosis and portal HTN
- Pneumothorax
- Haemoptysis
- Psychological problems