Paeds - Resp Flashcards

1
Q

What is the mechanism of asthma?

A

Dendritic cells activate TH2 (T Helper Cells), and stimulate the release of cytokines,

which activates the humoral immune system,

which causes proliferation of mast cells, eosinophils and dendritic cells.

Cytokines also contribute to bronchoconstriction eg. Leukotriene C4 is toxic to epithelial cells.

Histamine released from mast cells contribute to production of exudate.

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2
Q

What is preschool wheeze?

A

Up to half of children will have atleast one significant episode of wheeze by their 5th bday.

Most preschoolers outgrow their wheeze, but up to 40% will have a wheeze that persists into older childhood.

2 patterns of preschool wheeze:

Episodic viral wheeze = wheezing only in response to viral infection and no interval symptoms

Multiple trigger wheeze = wheeze in response to viral infection but also to other triggers like exposure to aeroallergens and exercise

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3
Q

How does asthma present (+ on examination)

A
  • wheeze, cough, breathless, chest tightness
  • symptoms commonly episodic, worse at night or early morning
  • triggered/exacerbated by exercise/ viral infection/ exposure to cold air or allergens/ emotion or laughter in kids

Examination

  • expiratory polyphonic wheeze on auscultation
  • finger clubbing (more suggestive of CF or Bronchiectasis)
  • Chest shape = hyperinflated suggests poorly controlled asthma
  • wheeze
  • examine throat for tonsillar enlargement = infectious cause?
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4
Q

What kind of symptoms would point you towards asthma in particular?

A
  • episodic symptoms with intermittent exacerbations
  • Diurnal variability (worse at night and early morning)
  • dry cough + wheeze + SOB
  • typical triggers eg. dust, animals, cold air, exercise, smoke, food allergens
  • hx of other atopic conditions eg. eczema, hayfever, food allergies
  • fhx of asthma or atopy
  • bilateral widespread “polyphonic” wheeze heard on auscultation
  • symptoms improve with bronchodilators
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5
Q

How would you investigate asthma?

A
  • Spirometry if over 5 years old = obstructive pattern (FEV1:FVC <70%)
    • and improvement in FEV1 of >12% after bronchodilators
  • Exercise testing to assess where there is exercise induced symptoms
  • skin prick test, blood eosinophilia >4%, raised allergen specific IgE can indicate atopic status
  • Can consider Fractional Exhaled Nitric Oxide Testing to confirm eosinophilic airway inflammation
    • FENO of 35ppb or over is positive.

Rule out other diagnoses

  • Oesophgeal pH study to investigate GO Reflux
  • Bronchoscopy to exclude structural abnormality
  • Chloride sweat test to rule out CF
  • Nasal Brush Biopsy to exclude Primary Ciliary Dyskinesia
  • Serum IgG, IgA, IgM and response to vaccinations to exclude immunodeficiency
  • High Resolution CT to exclude bronchiectasis
  • Sputum Culture
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6
Q

How would you generally follow up asthma in children in the longterm?

A
  • Assess baseline asthma status using Asthma Control Questionnaire or lung function tests like Spirometry/ Peak Expiratory Flow
  • Up to date on vaccinations + annual influenza vaccine
  • Support Resources eg. Asthma UK
  • Advise parents on dangers of smoking and cessation
  • Monitor Peak Flows/ Spirometry at annual Asthma Reviews
  • Symptom score using Childhood Asthma Control Test
  • Monitor growth (height and weight centiles)
  • Demonstrate correct inhaler technique

*

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7
Q

What would you prescribe in an asthma patient under 5 years old?

A
  • SABA eg. salbutamol as required
  • Add low dose ICS or a leukotriene antagonist eg. oral montelukast
  • If uncontrolled, add a ICS/LA (triple therapy)
  • Refer to specialist
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8
Q

What would you prescribe in a 5-16 year old with asthma

A

Medication for 5-16 years old

  • 1st line = Short Acting B2 Agonist as reliever therapy PRN (salbutamol)
  • 2nd line = Inhaled regular low dose Corticosteroid as preventer therapy
    • If using SABA 3x or more a week, or asthma symptoms 3x or more a week, or woken up at night by asthma symptoms 1x or more weekly
  • 3rd line = additional therapy
    • add LABA (eg. salmeterol)
    • If improvement but not enough, increase ICS to medium dose
    • If LABA isn’t helping, swap to leukotriene receptor antagonist (montelukast)
  • If still uncontrolled, increase ICS dose to high dose
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9
Q

How would you classify asthma exacerbations?

A

Moderate

  • PEFR at least 50%
  • normal speech
  • no features of acute severe or life threatening

Acute Severe

  • PEFR 33-50%
  • RR atleast 25/min if >12 years old, 30/min from 5-12, 40/min in 2-5 year olds
  • HR atleast 110/min if >12 years old, 125/min from 5-12, 140/min in 2-5 year olds
  • Inability to complete sentences in one breath, accessory muscle use, inability to feed (infants)
  • O2 sats at least 92%

Life Threatening

  • PEFR less than 33%
  • O2 sats <92%
  • altered consciousness, exhaustion, cardiac arrhythmia, hypotension, cyanosis, poor resp effort, silent chest, confusion
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10
Q

How would you manage a mild acute exacerbation of asthma?

A
  • as an outpatient
  • regular salbutamol inhalers via a spacer
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11
Q

How would you manage a moderate-severe case of acute asthma?

A

Stepwise until control is acheived:

  1. salbutamol inhalers (SABA bronchodilator) via a spacer device. Start with 10 puffs every 2 hours.
  2. Nebulisers with salbutamol/ Ipratropium Bromide (antimuscarinic bronchodilator)
  3. IV Hydrocortisone (steroids to reduce airway inflammation). Oral prednisolone if they want oral.
  4. IV Magnesium sulphate (bronchodilators)
  5. IV aminophylline (bronchodilators)
  6. Call an anaesthetist and ICU for intubation/ ventilation!!!

Monitor serum K+ when high dose Salbutamol has been given.

Salbutamol SE = tachycardia and tremor

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12
Q

How would you discharge an asthma patient?

A
  • consider discharge when the child is well on 6 puffs at 4 hourly intervals of salbutamol
  • prescribe a reducing regime of salbutamol at home
  • SaO2> 94% in air
  • finish the course of steroids if they were started
  • provide safety net info about when to return to seek help
  • provide a written asthma action plan and explain to parents
  • assess/teach inhaler technique by asthma nurse
  • ask questions of compliance if symptoms were uncontrolled
  • GP to review the child 2 days after discharge
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13
Q

What is good inhaler technique?

A
  • remove cap
  • shake the inhaler
  • sit or stand up straight
  • lift chin slightly
  • fully exhale
  • make a tight seal around the inhaler with your lips
  • press canister while taking a steady breath
  • continue breathing for 3-4s after pressing canister
  • hold breath for 10 seconds
  • wait 30s before giving another dose
  • rinse mouth after using steroid inhaler to avoid oral thrush
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14
Q

What is bronchiolitis?

A

Viral infection of the bronchioles,

causes inflammation + mucus to obstruct small airways = wheeze and crackles,

generally affects children under 1 year,

commonly caused by respiratory syncytial virus (RSV)

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15
Q

pathophysiology of bronchiolitis

A

Starts with an Upper Resp Tract Infection with Coryzal symptoms.

Half get better, the other half develop chest symptoms within 1-2 days following onset of coryzal symptoms.

  • proliferation of goblet cells = excess mucus production
  • IgE mediated type 1 allergic reaction = inflammation
  • Bronchiolar constriction
  • Infiltration of lymphocytes = submucosal oedema
  • Infiltration of cytokines and chemokines

Mucus + Oedema + Infiltration of cells = Hyperinflation, increased airway resistance, atelectasis (lung collapse), ventilation perfusion mismatch

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16
Q

How would bronchiolitis present as symptoms?

Give some differentials

A

First present with URTI + Coryzal symptoms

  • typical viral URTI symptoms of runny nose, sneezing, mucus in throat, watery eyes

Increasing symptoms

  • Low grade fever <39C
  • poor feeding
  • dyspnoea
  • apneoa episodes
  • signs of resp distress
  • hyperinflated chest

Differential = pneumonia, croup, CF, HF, bronchitis

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17
Q

How would you recognise respiratory distress?

A
  • Abnormal airway noises eg. inspiratory crackles, expiratory wheeze
  • Raised RR
  • Accessory muscles when breathing eg. SCM, Abdo, Intercostal Muscles
  • Intercostal and Subcostal recessions
  • Nasal flaring
  • Grunting (exhaling with the glottis partially closed to increase +ve end-expiratory pressure)
  • Head bobbing
  • Tracheal tugging
  • Cyanosis
    *
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18
Q

How would you investigate bronchiolitis?

A
  • Nasopharyngeal aspirate or throat swab for RSV rapid testing and viral cultures
  • Blood and urine cultures if pyrexic
  • FBC
  • ABG if severely unwell
  • CXR if diagnostic uncertainty
    • Hyperinflation, Focal atelectasis, Air trapping, Flattened diaphragm, peribronchial cuffing
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19
Q

How would you manage bronchiolitis at home?

A

Initial

  • examine chest, record RR, HR, BP, O2 sats, Hydration status by measuring cap refill time/ skin turgor/ dryness of mucous membranes/ urine output

Home

  • paracetamol/ ibuprofen to treat child who is distressed due to fever
  • fluids and check on the child regularly especially at night
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20
Q

When would you admit a patient with bronchiolitis?

A
  • aged <3 months
  • pre-existing conditions like prematurity, Downs syndrome, CF
  • RR >70
  • O2 sats <92%
  • Mod-Severe Resp Distress eg. deep recessions, head bobbing
  • Apnoeas
  • 50-75% or less of their normal intake of milk
  • clinical dehydration (reduced skin turgour, cap refill >3s, dry mucous membranes, reduced urine output)
  • Parents need help
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21
Q

How would you manage a bronchiolitis patient in hospital?

A

Supportive management

  • ensuring adequate intake (oral, NG, IV)
    • do not overfeed as a full stomach can restrict breathing
  • Saline nasal drops and nasal suctioning prior to clear secretions
  • supplementary O2 if sats remain <92%
  • Ventilatory support if required
    • high flow humidified O2 via nasal cannula ie. Airvo
      • delivers air + o2 continuously and adds positive end-expiratory pressure to prevent airways from collapsing
    • OR CPAP (delivers higher and more controlled pressures than Airvo)
    • OR Intubation + ventilation
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22
Q

How woudl you try and protect high risk babies from RSV?

A
  • Palivizumab is a monoclonal antibody that targets Respiratory Syncytial Virus
  • Monthly injection given as prevention against bronchiolitis caused by RSV
  • Provides passive protection (need monthly top ups as the circulating antibody levels decrease over time.)
  • Give to high risk babies eg. ex-premature or congenital heart disease babies
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23
Q

How would a viral induced wheeze present as opposed to asthma?

A

Evidence of a viral illness (fever, cough, coryzal symptoms) for 1-2 days preceeding onset of..

  • SOB
  • signs of resp distress
  • Expiratory wheeze throughout the chest

Differentiates from asthma…

  • presents before 3 years of age
  • no atopic hx
  • only occurs during viral infections
    • asthma can also be triggered by infections, but also exercise/ cold weather/ dust/ strong emotions
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24
Q

What would you need to think when hearing a focal or widespread wheeze in the chest?

A

Widespread wheeze = viral induced wheeze or asthma

Focal wheeze = urgent senior review, investigate for focal air obstruction like an inhaled foreign body or tumour

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25
Q

What is whooping cough?

A

An upper resp tract infection caused by Bordetella pertussis (G-ve bacteria)

  • child is unable to take in air between severe coughing fits, so after coughing is finished they forcefully suck in air with a “whooping” sound
  • presents with midl coryzal symptoms + low grade fever + mild dry cough
  • Paroxysmal cough = coughing fits with cough free periods in between
  • coughing fits generally build up and get more severe until the patient is completely out of breath
  • coughing can be so hard patients can faint, vomit or develop pneumothorax
  • then patient produces a loud inspiratory “whoop” when coughing ends
  • some infants with pertussis can present with apnoeas instead of a cough
26
Q

How would you diagnose whooping cough?

A
  • nasopharyngeal or nasal swab with PCR testing or bacterial culture
    • can confirm diagnosis within 2-3 weeks of onset of symptoms
  • if coughing has been present for >2 weeks, test patients for anti-pertussis toxin immunoglobulin G
    • tested for in oral fluid of kids 5-16
    • tested for in blood of kids >17
27
Q

How would you manage whooping cough?

A
  • Pertussis is a notifiable disease! notify Public Health
  • Admit if…
    • <6 months old
    • vulnerable or acutely unwell
    • apnoeas, cyanosis, severe coughing fits
  • Macrolide antibiotics within first 21 days (azithromycin, erythromycin, clarithromycin)
    • co-trimoxazole as alternative
  • Prophylactic antibiotics for close contacts if vulnerable
  • Prevent spread via avoiding vulnerable people, careful hand hygiene, etc

Symptoms typically resolve within 8 weeks but can last months.

28
Q

What is croup?

/ Acute Viral Laryngotracheobronchitis

A

an acute upper resp tract infection typically affecting kids from 6 months to 2 years old.

  • causes oedema in the larynx
  • clasically caused by parainfluenza virus
    • other causes are influenza, adenovirus, RSV
    • Croup caused by diptheria can lead to epiglottitis (vaccination has made this rare)
29
Q

How does croup present?

A
  • increased work of breathing
  • “Barking” cough occuring in clusters of coughing episodes
  • hoarse voice
  • stridor
  • low grade fever
  • usually improves in less than 48 hours and responds well to treatment

posterior-anterior view Xray = subglottic narrowing (steeple sign)

30
Q

How would you manage croup?

A

Most cases:

  • can manage at home with supportive treatment (fluids, rest)
  • sit child up and comfort them during attacks
  • prevent spread of infection = hand washing, stay off school
  • Medication = oral dexamethasone (single dose 150mcg/kg repeated in 12 hours if needed)

Severe croup (step up to get control of symptoms):

  • oral dexamethasone
  • Oxygen
  • Neb budesonide
  • Neb adrenaline
  • Intubation and ventilation
31
Q

What is epiglottitis?

A

Inflammation and swelling of the epiglottis casued by infection (classically Haemophilus Influenza Type B)

  • epiglottis can swell to completely obscrue airway within hours of symptoms onset (life threatening!!!)
  • now rare due to vaccination against haemophilus
32
Q

What presentation would make you suspect epiglottitis?

A
  • quick onset over hours (croup = days)
  • sore throat and soft whispering stridor
    • (croup = harsh rasping stridor and barking cough)
  • Drooling
  • Tripod position (sat foward with a hand on each knee)
  • High fever >38.5C
  • difficulty or painful swallowing
  • muffled voice, reluctant to speak
  • scared and quiet child
  • septic and unwell appearance
  • unable to eat or drink
33
Q

How would you investigate suspected epiglottitis?

A
  • Lateral Xray of the neck = “thumb sign” or “thumbprint sign”
    • soft tissue shadow that looks like thumb pressed into trachea
    • caused by oedematous and swollen epiglottis
    • Neck Xray also used to exclude foreign body
34
Q

How would you manage epiglottitis?

A
  • do not distress the patient! can result in closure of the airway
    • don’t do examinations, etc.
  • alert senior paediatrician and anaesthetist
  • Secure the airway
    • Intubation or tracheostomy if necessary and airway completely closes
    • if intubated, transfer to ICU
  • Once airway is secure…
    • IV antibiotics eg. ceftriaxone
    • Steroids eg. dexmethasone
35
Q

What is bronchiectasis?

A

Abnormal dilation of the airways + associated destruction of bronchial tissue.

36
Q

What are some common infectious causes of bronchiectasis?

A

Post-infection =

  • inflammatory response leads to structural damage within bronchial walls which causes dilation
  • scarring as a result of the immune response will result in reduced cilia within the bronchi
  • this predisposes the individual to further infections

Common organisms..

  • Strep pneumonia
  • Staphylococcus aureus
  • Adenovirus
  • Measles
  • Influenza virus
  • Bordetella pertussis
  • Mycobacterium tuberculosis
37
Q

What are 5 other non-infective causes of Bronchiectasis?

A
  • commonly CF
  • Immunodeficiency
  • Primary Ciliary Dyskinesia
  • Post obstructive causes eg. foreign body aspiration
  • Congenital syndromes
38
Q

What are the congenital syndromes associated with bronchiectasis?

A

Young’s syndrome = associated with bronchiectasis, reduced fertility and rhinosinusitis

Yellow-nail syndrome = associated with pleural effusions, lymphoedema and dystrophic nails

39
Q

What immunodeficiencies are associated with bronchiectasis?

A
  • Antibody defects
    eg. agammaglobulinaemia, IgA/IgG deficiency
  • HIV infection
  • Ataxia telangiectasia
40
Q

How would bronchiectasis present? (hx and exam)

A

Hx

  • key feature = chronic productive cough
  • bringing up purulent sputum
  • chest pain
  • wheeze
  • breathless on exertion
  • haemoptysis
  • recurrent or persistent infections of the Lower Resp Tract

Exam

  • finger clubbing
  • inspiratory crackles
  • wheezing sometimes
41
Q

How would you investigate bronchiectasis?

A
  • Diagnosis = High resolution CT
    • bronchial wall thickening, diameter of bronchus larger than that of accompanying bronchial artery (signet ring sign), visible peripheral bronchi
    • Bilateral upper lobe bronchiectasis = CF
    • Unilateral upper lobe bronchiectasis = post-TB infection
    • Focal bronchiectasis (lower lobe) = post foreign body inhalation
  • CXR can show bronchial wall thickening or airway dilation
  • Bronchoscopy + ciliary brush biopsy if there was focal bronchiectasis on HRCT, or evidence of abnormal airway
  • Spirometry = obstructive or mixed obstructive/restrictive as scarring begins to compromise lung compliance

Rule out other differentials…

  • Chloride sweat test and CFTR gene mutation analysis to rule out CF
  • FBC for lymphocyte and neutrophil counts
  • Immunoglobulin panel for immunoglobulin deficiency
  • Specific antibody levels to vaccinations eg. pneumococcal or Haemophilus influenzae B vaccine
  • HIV test
42
Q

How would you manage bronchiectasis?

A
  • Chest physiotherapy for mucus clearance
  • Antibiotics or pseudomonas eradication if there are infective exacerbations
  • Bronchodilators in those who have a wheeze
  • Follow up
43
Q

What is pneumonia and some common organisms?

A

Infection of lung tissue causing inflammation and sputum to fill the airways and alveoli (seen as consolidation on CXR).

Bacterial =

strep pneumonia, Group A strep (strep pyogenes), Group B strep (in pre-vaccinated infants, often contracted during birth as it colonises the vag), Staph aureus, Haem influenza (in pre-vaccinated or unvaccinated kids), Mycoplasma pneumonia (atypical bacteria with extra-pulmonary manifestations like erythema multiforme)

Viral =

Respiraotry syncytial virus, Parainfluenza virus, Influenza virus

44
Q

How would pneumonia present? + on exam

A
  • wet productive cough
  • high fever >38.5C
  • Tachypnoea
  • Tachycardia
  • Increased work of breathing
  • Lethargy
  • Delirium
  • Sepsis secondary to pneumonia (tachypnoea, tachycardia, hypoxia, hypotension, fever, confusion)

Exam =

  • bronchial breath sounds (harsh breath sounds on inspiration and expiration)
  • focal coarse crackles
  • dullness to percussion
45
Q

How would you investigate pneumonia?

A
  • CXR for diagnosis (consolidation)
  • sputum cultures and throat swabs for bacterial cultures and viral PCR
  • Sepsis = blood cultures
  • capillary blood gas analysis to assess for resp or metabolic acidosis and lactate levels
46
Q

How would you manage pneumonia?

A

Treat according to local guidelines

  • 1st line = amoxicillin
  • add macrolide (eg. erythromycin, clarithromycin, azithromycin) to cover atypical pneumonia
    • macrolides are also used as monotherapy in patients allergic to penicillin
  • IV antibiotics if sepsis or a problem with intestinal absorption
  • O2 to maintain sats above 92%
47
Q

What is primary ciliary dyskinesia?

A

An autosomal recessive condition known as Kartagner’s syndrome, affecting the cilia of various cells in the body

  • more common in populations with consanguinity (parents are related)
  • most commonly affects motile cilia in the resp tract, resulting in the buildup of mucus in the lungs and predisposing to infection
    • similar resp presentation to CF = frequent and chronic chest infections, poor growth, bronchiectasis
  • Also affects cilia in the fallopian tubes and the tails (flagella) of sperm = reduced or absent fertility
  • There is a strong link between PCD and Situs Inversus (organs in chest and abdo are in a mirror image to normal anatomy)
48
Q

What is the Kartagner’s triad

A

Paranasal Sinusitis

  • inflammation of the mucous membranes in the paranasal sinuses

Bronchiectasis

Situs Inversus

  • all internal visceral organs are mirrored inside the body (heart on right, liver on left, etc)
49
Q

How would you diagnose Primary Ciliary Dyskinesia?

A
  • hx of recurrent resp tract infections
  • fhx of consanguinity in parents
  • Imaging to diagnose situs inversus
  • Semen analysis to investigate for male infertility
  • Diagnostic = take a sample of ciliated epithelium of the upper airway via Bronchoscopy or Nasal Brushing and examine the action of the cilia
50
Q

How would you manage PCD?

A

similarly to CF and bronchiectasis

  • daily physiotherapy
  • high calorie diet
  • antibiotics
51
Q

What is Cystic Fibrosis?

A
  • An autosomal recessive condition.
  • genetic mutation of the Cystic Fibrosis Transmembrane Conductance Regulatory Gene on Chromosome 7
    • this gene codes for chloride channels
  • Results in thick pancreatic and biliary secretions = blockage of ducts = lack of digestive enzymes like pancreatic lipase in the digestive tract
  • Low vol thick airway secretions that reduce airway clearance = bacterial colonisation and susceptibility to infections
  • Congenital bilateral abscence of the vas deferens in males = male infertility (with healthy sperm)
52
Q

How would CF first present soon after birth?

A
  • if not picked up in newborn bloodspot test
  • Meconium ileus is the 1st sign of CF
    • in CF babies, meconium is thick and sticky and gets stuck and obstructs bowel
    • meconium is not passed within 24 hours, results in abdo distension and vomiting
  • Presents later in childhood as recurrent resp tract infections, failure to thrive, pancreatitis
53
Q

What are some symptoms and signs of CF?

A

Symptoms

  • Chronic cough
  • thick sputum production
  • recurrent resp tract infections
  • loose greasy stools (steatorrhoea) due to lack of fat digesting lipase enzymes
  • abdo pain and bloating
  • parents may report the child tastes salty when they kiss them (conc salt in their sweat)
  • poor weight and heigh gain (failure to thrive)

Signs

  • low weight or height on growth charts
  • nasal polyps
  • finger clubbing
  • crackles and wheezes on auscultation
  • abdo distension
54
Q

What are some common causes of clubbing in kids?

A
  • hereditary clubbing
  • cyanotic heart disease
  • infective endocarditis
  • cystic fibrosis
  • TB
  • inflammatory bowel disease
  • Liver cirrhosis
55
Q

How would you diagnose CF?

A
  • Newborn blood spot testing at birth
  • Genetic Testing for CFTR Gene during pregnancy by amniocentesis or chorionic villous sampling, or as blood test after birth
  • Gold standard diagnosis is the sweat test
    • pilocarpine is applied to a patch of skin
    • electrodes are placed either side of teh patch and a current passed between them
    • this causes the skin to sweat
    • sweat is absorbed with filter paper and sent to the lab for testing for Chloride Conc
    • Diagnostic CF chloride conc is >60mmol/L
56
Q

What are some common organisms that affect CF?

A
  • Staphylococcus aureus
  • Haemophilus influenza
  • Klebsiella pneumoniae
  • Escherichia coli
  • Burkhodheria cepacia
  • Pseudomonas aeruginosa
57
Q

How would you manage CF?

A
  • Chest physiotherapy multiple times a day to clear mucus
  • Exercise helps clear sputum
  • High calorie diet to compensate for malabsorption, increased resp effort, coughing, physiotherapy
  • CREON tablets to digest fats in patients with pancreatic insufficiency
  • Prophylactic flucloxacillin tablets to reduce risk of Staph aureus infection
  • Bronchodilators like salbutamol inhalers to treat bronchoconstriction
  • Nebulised DNase (dornase alfa) is an enzyme that can help break down resp secretions and make them easier to clear
  • Nebulised hypertonic saline
  • Vaccinations eg. pneumococcal, influenza, varicella
  • Treat chest infections:
    • Pseudomonas = long term neb antibiotics like tobramycin or oral ciprofloxacin
  • Lung transplant in end stage resp failure
  • Liver transplant in liver failure
  • Fertility treatment eg. testicular sperm extraction for infertile males
  • Genetic counselling
58
Q

How would you monitor CF patients?

A
  • follow up every 6 months in specialist clinics
  • regular monitoring of their sputum for colonisation of bacteria like pseudomonas
  • screen for diabetes, osteoporosis, vit D deficiency, liver failure
59
Q

What is chronic lung disease of prematurity?

A

Also known as bronchopulmonary dysplasia.

Occurs in premature babies (typically those born before 28 weeks gestation).

These babies suffer from respiratory distress syndrome and require oxygen therapy or intubation and ventilation at birth.

Diagnosis is made based on CXR changes and when the infant requires O2 therapy after they reach 36 weeks gestational age.

60
Q

What are some features of Chronic Lung Disease of Prematurity?

A
  • Low O2 sats
  • Increased work of breathing
  • Poor feeding and weight gain
  • Crackles and wheezes on chest auscultation
  • Increased susceptibility to infection
61
Q

How would you prevent and manage CLDP?

A

Prevention

  • give corticosteroids eg. betamethasone to mothers that show signs of premature labour
    • can help speed up development of foetal lungs before birth
  • Use CPAP rather than intubation+ventilation
  • Use Caffeine to stimulate respiratory effort
  • Do not over-oxygenate with supplementary oxygen

Management

  • sleep study to assess O2 sats during sleep
  • babies can be discharged from NNU with low dose O2 to continue at home via nasal cannula
    • wean them off throughout the first year of life
  • Monthly injections of palivizumab to protect against RSV and bronchiolitis