Respiratory Flashcards

1
Q

Pneumonia

A

Infection of the lower respiratory tract and lung parenchyma which leads to consolidation.

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2
Q

Highest incidence of Pneumonia is in who?

A

in infants

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3
Q

What is the more common cause of Pneumonia in young infants- viral or bacterial ?

A

Viral

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4
Q

What is the more common cause of Pneumonia in older children?

A

Bacterial

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5
Q

Viral disease for Pneumonia is more common in ____

A

Winter

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6
Q

Causes of Pneumonia in Neonates

A

Group B Strep, E coli, Klebsiella, Staph Aureus

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7
Q

Causes of Pneumonia in Infants

A

Strep pneumoniae, Chlamydia

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8
Q

Causes of Pneumonia in School Age children

A

Strep pneumoniae
Staph Aureus
Group A Step
Mycoplasma pneumoniae

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9
Q

Pneumonia is usually preceded by ____

A

an upper respiratory tract infection

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10
Q

Symptoms of Pneumonia

A

Fever - SOB - Lethargy

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11
Q

Signs of Pneumonia

A

Signs of respiratory distress
Auscultation signs: dullness to percuss, crackles, decreased breath sounds, bronchial breathing
Wheeze and hyperinflation more typical of viral infection

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12
Q

Ix for Pneumonia

A

Mainly clinical
CXR - fluid in the lungs (associated with Staph)
Perinasal swab

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13
Q

Tx for Pneumonia

A

Management at home with analgesia
If admitted: Oxygen therapy and IV fluids
Abx

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14
Q

Abx for Pneumonia - Neonates

A

Broad spec IV Abx (meropenem, piperacillin, tazobactam, cefepime)

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15
Q

Abx for Pneumonia - Infants

A

Amoxicillin/Co-Amoxiclav

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16
Q

Abx for Pneumonia in children> 5 y/o

A

Amoxicillin/Erythromycin

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17
Q

Complications of Pneumonia

A

Risk of parapneumonic collapse and empyema if so follow up at 4-6 weeks with a fluid sample

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18
Q

Croup

A

Acute laryngotracheobronchitis (Mucosal inflammation anywhere between the nose and the trachea). Mucosal Inflammation of upper airways.

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19
Q

Croup is common in children between :

A

6 months - 3 years old

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20
Q

Peak incidence of croup is at

A

2 years old

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21
Q

Which seasons is Croup common in

A

Autumn and Spring

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22
Q

Is Croup more common in boys or girls

A

boys

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23
Q

Causative organims for Croup

A

Parainfluenza virus mainly
Adenovirus
Rhinovirus
Enterovirus

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24
Q

Clinical features of mild croup

A

Occasional barking cough with no audible stridor, no recession, child happy to eat and drink as normal

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25
Q

Clinical features of moderate croup

A

Frequent barking cough with audible stridor at rest, suprasternal recession, child not agitated

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26
Q

Clincal features of severe croup

A

Frequent barking cough, prominent stridor (high pitched breathing indicating an upper airway obstruction), marked sternal recession, agitated and distressed child potentially with tachycardia

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27
Q

Symptoms of Croup

A

1-4 days history of non-specific rhinorrhea (thin, nasal discharge), fever and barking cough
Worse at night
Harsh Inspiratory Stridor

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28
Q

Signs of Croup

A

Decreased bilateral air entry
Tachypnoea
Costal recession

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29
Q

Respiratory failure red flags

A

Drowsiness
Lethargy
Cyanosis
Tachycardia
Laboured breathing

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30
Q

Ix for croup

A

Bloods: FBC, CRP U+E
CXR to exclude foreign body

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31
Q

Tx for croup

A

Paracetamol/Ibuprofen for fever/sore throat
Admission if moderate/severe and consider if dehydrated
Single dose dexamethasone 0.15mg/kg or prednisolone
Nebulised adrenaline for relief of severe symptoms
Oxygen if required
Monitor for needed ENT intervention if suspected airway blockage

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32
Q

First Line Tx for Croup

A

Single dose Oral Dexamethasone (0.15 mg/kg)

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33
Q

Complications of Croup

A

Otitis Media
Dehydration due to reduced fluid intake
Superinfection: pneumonia

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34
Q

How long do symptoms from Croup last.

A

48 hours - 1 week

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35
Q

Asthma

A

Reversible paroxysmal constriction of the airways with inflammatory exudate and followed by airway remodelling

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36
Q

What is the most chronic condition of children?

A

Asthma

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37
Q

Aetiology of Asthma

A

Genetic
Prematurity
Low birth weight
Parental smoking
Viral bronchiolitis in early life
Cold air
Allergen exposure e.g. dust

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38
Q

Symptoms of Asthma

A

Episodic wheeze which is infrequent/frequent and persistent most days and nights
Dry cough often worse at night
SOB
Wheeze

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39
Q

Ix of Asthma

A
  • Reduced peak flow - FEV1 significantly reduced
  • FVC normal
  • FEV1:FVC may be <70% if poorly controlled
  • Reversible spirometry is highly suggestive of asthma
  • ENO levels of nitric oxide correlate to inflammation
  • Baseline chest x ray
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40
Q

Management of Asthma includes how many steps?

A

7

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41
Q

Step 1 of Asthma Management

A

SABA PRN - Salbutamol

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42
Q

Step 2 of Asthma Management

A

ICS Preventer therapy - Beclomethasone

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43
Q

Step 3 of Asthma Management

A

LTRA Montelukast

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44
Q

Step 4 of Asthma Management

A

Strop LTRA if hasn’t helped and add LABA - Salmeterol

45
Q

Step 5 of Asthma Management

A

Switch ICS/LABA for ICS MART: Formoterol and ICS

46
Q

Step 6 of Asthma Management

A

Add a separate LABA

47
Q

Step 7 of Asthma Management

A

High dose ICS (>400mcg), referral

48
Q

Management of Asthma in children < 5 y/o involves how many steps?

49
Q

Step 1 of Asthma Managment in <5 y/o

A

SABA PRN - Salbutamol

50
Q

Step 2 of Asthma Managment in <5 y/o

A

SABA + 8 week trial of ICS if symptoms reoccur within 4 weeks, restart ICS

51
Q

Step 3 of Asthma Managment in <5 y/o

A

Refer to specialist

52
Q

Viral Induced Wheeze : Episodic Wheeze

A
  • a symptom of viral URTI and symptom free in between events
53
Q

Viral Induced Wheeze : Multiple trigger Wheeze

A
  • URTI and other factors trigger wheeze
54
Q

Viral Induced Wheeze - Symtomatic Tx

A

SABA inhaler via spacer maximum of 4 hourly up to 10 puffs
LTRA and ICS via spacer
Multiple trigger wheeze: trial ICS or LTRA for 4-8 weeks

55
Q

Causes of Viral Induced Wheeze

A

RSV or Rhinovirus

56
Q

Symptoms of Viral Induced Wheeze

A

-Under 3 years old
-Viral illness 1 to 2 days preceding
-SOB
-Signs of respiratory distress
-Expiratory wheeze throughout the chest

57
Q

Management of Viral Induced Wheeze

A

-SABA inhaler -± LTRA and ICS via spacer

58
Q

Bronchiolitis

A

Viral infection of the bronchioles

59
Q

Bronchiolitis commonly affects children under the age of ___

A

2 (commonly infants (rare after 1 y/o))

60
Q

Which seasons is Bronchiolitis common in

A

winter and spring months

61
Q

Bronchiolitis is commonly caused by…

A

RSV (Respiratory Syncytial Virus)

62
Q

Risk factors for Bronchiolits

A

Breastfeeding for < 2 months
Smoke exposure
Older siblings who attend nursery/school
Chronic lung disease of prematurity

63
Q

Pathophysiology of Bronchiolitis

A

RSV invades nasopharyngeal epithelium –> increased mucus production –> bronchial obstruction

64
Q

Symptoms of Bronchiolitis

A

Symptom onset in 2-5 days
Low grade fever
Rhinorrhea and nasal congestion
Cough
Reduced feeding

65
Q

Signs of Bronchiolitis

A

Signs of Respiratory distress: nasal flaring, tracheal tug, head bobbing, grunting, sub/intercostal recessions
Inspiratory crackles

66
Q

Ix for Bronchiolitis

A

Nasopharyngeal aspirate for RSV culture
FBC
Urine
Blood gas if severely unwell
CXR - not used usually

67
Q

What might be seen on CXR for Bronchiolitis

A

hyperinflation, air trapping and flattened diaphragm

68
Q

Management of Bronchiolitis

A

Supportive management from home + Palvizumab vaccine against bronchiolitis

69
Q

Palvizumab vaccine against bronchiolitis should be considered in who?

A
  1. Infants and young children with certain underlying health conditions:
    • Premature infants (especially those born before 29 weeks of gestation).
    • Infants with chronic lung disease of prematurity or bronchopulmonary dysplasia (BPD).
    • Infants with congenital heart disease, particularly those with hemodynamically significant heart disease.
    1. Infants under 12 months of age who are at high risk of RSV infection during the RSV season (typically fall through spring in many regions).
    2. Children younger than 2 years old who have severe immunocompromising conditions, such as those undergoing stem cell transplantation or receiving chemotherapy.
70
Q

Urgent Hospital Admission for Bronchiolitis

A

Apnoea
Resp Rate > 70
Central cyanosis
SpO2 < 92%

71
Q

Non-Urgent Hospital Admission for Bronchiolitis

A

Resp Rate > 60 - Clinical dehydration

72
Q

Inpatient Managment for Bronchiolitis

A

Oxygen to bring SpO2 up
Fluids
CPAP if in respiratory failure
Suctioning of secretions
Ribavirin for severe cases
- No evidence for bronchodilatory, antibiotics or steroids in bronchiolitis

73
Q

Prophylaxis for Bronchiolitis

A

-IM Palivizumab -Monthly injections for high risk babies (autumn to winter months)

74
Q

What is cystic fibrosis?

A

Cystic fibrosis is a genetic condition caused by mutations in the CFTR gene, leading to defective chloride ion transport and resulting in thick, sticky secretions in various organs, especially the lungs and pancreas.

75
Q

Cystic fibrosis is caused by mutations in the ________ gene, affecting chloride ion transport.

76
Q

What is the inheritance pattern of cystic fibrosis?

A

Cystic fibrosis is inherited in an autosomal recessive manner.

77
Q

The inheritance pattern of cystic fibrosis is ________.

A

Autosomal recessive

78
Q

What is the most common mutation causing cystic fibrosis?

A

The most common mutation is ΔF508, a deletion of phenylalanine at position 508 in the CFTR protein.

79
Q

The most common CFTR mutation in cystic fibrosis is ________.

80
Q

What are the respiratory features of cystic fibrosis?

A

Chronic cough with sputum production.
Recurrent respiratory infections.
Bronchiectasis.
Nasal polyps.
Sinusitis.

81
Q

Respiratory features of cystic fibrosis include chronic ________, bronchiectasis, and recurrent ________ infections.

A

Cough; respiratory

82
Q

What gastrointestinal complications are associated with cystic fibrosis?

A

Meconium ileus in neonates.
Pancreatic insufficiency leading to malabsorption and steatorrhea.
Failure to thrive.
Rectal prolapse.
CF-related liver disease (e.g., biliary cirrhosis).

83
Q

Meconium ________ is a neonatal gastrointestinal complication of cystic fibrosis.

84
Q

How does cystic fibrosis affect the pancreas?

A

CF causes pancreatic insufficiency due to blockage of pancreatic ducts by thick secretions, leading to malabsorption of fats and fat-soluble vitamins (A, D, E, and K).

85
Q

Pancreatic insufficiency in cystic fibrosis leads to malabsorption of ________ and fat-soluble ________.

A

Fats; vitamins

86
Q

What is the gold standard test for diagnosing cystic fibrosis?

A

The sweat chloride test, which measures elevated chloride levels in sweat (>60 mmol/L in CF).

87
Q

The gold standard test for diagnosing cystic fibrosis is the ________ chloride test.

88
Q

What newborn screening test is used for cystic fibrosis?

A

Immunoreactive trypsinogen (IRT) is used as a part of newborn screening for CF.

89
Q

Newborn screening for cystic fibrosis measures elevated levels of ________.

A

Immunoreactive trypsinogen (IRT)

90
Q

What are the common pathogens causing respiratory infections in cystic fibrosis patients?

A

Staphylococcus aureus (early in life).
Pseudomonas aeruginosa (later stages).
Haemophilus influenzae.
Burkholderia cepacia complex.

91
Q

The most common pathogen causing respiratory infections in early cystic fibrosis is ________, while ________ is more common in later stages.

A

Staphylococcus aureus; Pseudomonas aeruginosa

92
Q

What treatments are used to manage respiratory symptoms in cystic fibrosis?

A

Airway clearance techniques (e.g., chest physiotherapy).
Mucolytics (e.g., dornase alfa, hypertonic saline).
Inhaled antibiotics for Pseudomonas (e.g., tobramycin).
Bronchodilators.
Vaccination (e.g., influenza, pneumococcal).

93
Q

Airway clearance in cystic fibrosis is achieved through ________ physiotherapy and mucolytics like ________ alfa.

A

Chest; dornase

94
Q

What is the role of CFTR modulators in cystic fibrosis treatment?

A

CFTR modulators, such as ivacaftor and lumacaftor, improve the function of the defective CFTR protein and are specific to certain mutations.

95
Q

CFTR modulators, like ________, improve the function of the defective ________ protein in cystic fibrosis.

A

Ivacaftor; CFTR

96
Q

What nutritional support is recommended for children with cystic fibrosis?

A

High-calorie, high-fat diet.
Pancreatic enzyme replacement therapy (PERT) ; CREON tablets
Fat-soluble vitamin supplementation (A, D, E, K).
Salt supplementation in hot weather.

97
Q

Nutritional support in cystic fibrosis includes a high-________ diet and pancreatic ________ replacement therapy.

A

Calorie; enzyme

98
Q

What are some complications of cystic fibrosis?

A

Chronic respiratory failure.
CF-related diabetes (CFRD).
Osteoporosis.
Liver disease (e.g., biliary cirrhosis).
Infertility (especially in males due to absence of vas deferens).

99
Q

A common endocrine complication of cystic fibrosis is CF-related ________.

A

Diabetes (CFRD)

100
Q

What is Epiglottits?

A

Life threatening emergency. Severe swelling of the epiglottis and surrounding tissues

101
Q

Who does Epiglottis affect?

A

Common in ages 4-6, but can affect all ages

102
Q

Epiglottitis is caused by ____

A

Caused by Haemophilus Influenzae Type B

103
Q

Symptoms of Epiglottitis

A

Rapid onset - High fever - Stridor - Drooling and saliva
- Patient finds it easier to breathe leaning forward and extending neck (tripoding position)

104
Q

Dx of Epiglottitis

A

Clinical
CXR (do not let the child lie down).
- Lateral XR of neck
- thumb print sign and exclude foreign body

105
Q

What might CXR show for Epiglottitis ?

A

Thumb sign and acute epiglottis swelling

106
Q

Should you examine the throat for someone with suspected Epiglottitis ?

A

Do not examine throat as there is a risk of acute airway obstruction

107
Q

Management of Epiglottitis

A

O2
Nebulised adrenaline
IV Abx ; 3rd gen cephalosporins e.g. Ceftriaxone (7-10days)

108
Q

Complications of Epiglottis

A

Epiglottic abscess,
bacteraemia
meningitis
airway obstruction
death

109
Q

How does Epiglottis compare to Croup?

A

Fever, No cough, salvia drooling