LRTI I Flashcards

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1
Q

Bronchitis epidemiology

A

Characterised by emporary (self-limited) inflammation of the large and mid-sized bronchial tubes.

There is season variation with the peak incidence in winter, and where influenza (outbreak?) is present in the community.

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2
Q

Risk factors for bronchitis

A
  • Age (children <5 years of age; and the elderly)
  • Underlying disease (ie. chronic obstructive pulmonary disease [COPD], asthma(
  • Exposure to second hand smoke
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3
Q

Bronchitis microbiology

A

Viral

  • Influenza virus
  • Rhinovirus
  • Adenovirus
  • Respiratory synctial virus (RSV)
  • Parainfluenza virus
  • Human metapneumovirus

Bacterial (10% of cases)

  • Mycoplasma pneumoniae
  • Chlamydophila pneumoniae
  • *Bordatella pertussis *(rare cases)
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4
Q

Pathophysiology of bronchitis

A

A virus(es) replicating in the epithelial cells of the upper respiratory tract can spread to the lower airways resulting in:

  • Inflammation of the bronchial/bronchiolar epithelia (ie. infiltartion of mononuclear cells)

Necrotic epithelia sloughed off into the lumina of the airways, together with inflammation and increase mucus production and oedema, can cause obstruction characterised by ‘wheezing’

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5
Q

Clinical manifestations of bronchitis

A

Symptoms usually begin with common cold syndrome:

  • Nasal congestion, rhinitis, sore throat and general malaise
  • Low grade fever (37.5-38)
  • Cough (dry at first/becomes productive [white; green; yellow sputum])
  • Wheezing
  • Symptoms and signs usually resolve over 7-10 days for otherwise healthy person
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6
Q

Bronchitis diagnosis

A

Made on clinical presentation; suspected in any person with acute respiratory illness where cough is the dominant symptom.

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7
Q

Bronchitis differential diagnosis

A

Pertussis (whooping cough)

Pneumonia (ie CXR with signs of infiltrates/consolidation)

Chronic obstructive pulmonary disease (COPD); asthma

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8
Q

Bronchitis treatment

A

Supportive therapy: adequate hydration; cough suppressants; decongestants; antihistamines

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9
Q

Bronchiolitis epidemiology

A

Described inflammation of the smaller air passages, bronchioles of the lung.

Season occurence: peak incidence is during winter to early spring; usually correlates with the prevalence of RSV in the community.

More common during the first year of life

  • Each year 1-3% of infants <12 months are hospitalised with bronchiolitis, in 80% of these cases the infants are <6 months of age
  • More common in boys
  • Children with chronic underlying conditions (i.e. cardiopulmonary function decline)
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10
Q

Bronchiolitis risk factors

A
  • Young maternal age
  • Lower cord blood antibody titres to RSV
  • Lower socioeconomic status
  • Crowded living conditions
  • Bottle feeding
  • Tobacco-smoke exposure
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11
Q

Bronchiolitis microbiology

A

Virus

  1. RSV
  2. Rhinovirus
  3. Influenza
  4. Parainfluenza
  5. Adenovirus
  6. Bocavirus
  7. Non-SARS coronaviruses
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12
Q

Bronchiolitis clinical manifestations

A

Prodrome (range 2-7 days) of signs of URTI

  • Coryza
  • Cough
  • Fever (usually mild)

Followed by:

  • Wheezing
  • Dyspnoea
  • Dehydration (due to coughing spasm associated vomiting/poor oral intake)
  • Recovery usually over a period of 1-2 weeks
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13
Q

Diagnosis of bronchiolitis

A

Based on child’s history and physical examination

Usually suspected in children <2 years of age with:

  • Cough
  • Wheezing
  • Increased respiratory effort
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14
Q

Differential dianosis of bronchiolitis

A

Usually broad and includes:

  • obstruction of airways by foreign bodies
  • Retropharyngeal abscess
  • Cystic fibrosis
  • Congestive heart failure
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15
Q

Treatment of bronchiolitis

A
  • Supportive care for outpatient and inpatient
  • Maintain comfort and hydration
  • Treat for fever where necessary
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16
Q

Fatcors which increase risk fo community-acquired pneumonia

A
  • Age over 50 years
  • Alcoholism
  • Asthma
  • COPD
  • Dementia
  • Heart failure
  • Diabetes
  • Immunosuppression
  • Indigenous background
  • Institutionalisation
  • Seizure disorders
  • Smoking
  • Stroke
17
Q

Factors that might perturb airway defence systems, pridisposing to pneumonia

A
  • Cigarette smoke: disrupts muociliary function and macrophage activity.
  • Alteration in consciousness: stroke, seizures, anaesthesia, alcohol abuse, normal sleep
  • Iatrogenic manipulations: endotracheal tubes, nasogastric tubes, other respiatory therapy machinery.
  • Congenital defects in ciliary activity: immotile cilia syndrome
  • Underlying respiratory tract disorders: chronic obstructive pulmonary disease [COPD], bronchiectasis, cystic fibrosis
18
Q

Pneumonia common bacterial causes

A

Common bacterial causes

  • Strepcoccus pneumoniae
  • Staphylococcus aureus
  • Haemophilus influenzae
  • Anaerobes (*Bacteroides *species; *Fusobacterium *species; Prevotella species)
  • Escherichia coli
  • Klebsiella pneumoniae
  • *Enterbacter *species
  • *Serratia *species
  • Pseudomonas aeruginosa

19
Q

Pneumonia intracellular/atypical bacterial causes

A
  • Legionella pneumophila
  • Mycoplasma pnumoniae
  • Chlamydophila psittaci
  • Chlamydophila pneumoniae
  • Chlamydia trachomatis
  • Mycobacterium tuberculosis
  • Coxiella burnetti
20
Q

Pneumonia common viral causes

A

Children

  • Respiratory synctial virus (RSV)
  • Parainfluenza virus types 1-3
  • Influenza A virus

Adults

  • Influenza A virus
  • Influenza B virus
  • RSV
  • Human metapneumovirus
  • Adenovirus types 4 and 7 (ie. military staff)
21
Q

Fungal causes of pneumonia

A
  • Histoplasma capsulatum
  • Coccidiodes immitis
  • *Rhizopus *species
  • *Absidia *species
  • *Mucor *species
  • *Aspergillus *species
  • *Candida *species
22
Q

Important features of a history in pneumonia

A

History should define

  • Clinical setting (community-acquired/hospital-acquired)
  • Predisposing/underlying disorders in patients (diabetes; and see earlier slides)
  • Possible exposures to specific pathogens (travel to tropical areas [Burkholderia pseudomallei; Acinetobacter baumanii]; occupation; pets)
23
Q

Clinical findings in pneumonia

A
  • Fever (elderly patients may present only with confusion)
  • Rigors
  • New onset cough
  • Sputum production (with changes in colour)
  • Chest discomfort/pain
  • Dyspnoea
  • Non-respiratory symptoms (fatigue; sweats; headache; nausea; myalgia)
24
Q

Physical examination in pneumonia

A
  • Body temperature (taken rectally to reduce error caused by rapid breathing)
  • Tachypnoea
  • Tachycardia
  • BP
  • State of consciousness
  • Dentition
  • Cyanosis
  • Signs of sepsis
  • Splinting (inspiratory lag on affected side)

Chest examination

  • Crackles
  • Consolidation: dullness on percussion

CXR (required for diagnosis): need to differentiate if new lung ingiltrate is caused by atelectasis; non-infective pneumonitis; haemorrhage; or cardiac failure.

25
Q

Diagnostic investigations pneumonia

A

1. Microcopy and culture of respiratory samples

  • Sputum
  • Induced sputum (40-60% of patients cannot expectorate)
  • Bronchial washing
  • Bronchoalveolar lavage
  • Endotracheal aspirates
  • Lung biopsy (usually reserved for cases of pneumonia in impaired hosts/paediatric populations)

2. Examination of sputum: observation of colour, amount, consistency and odour.

3. Sputum gram stain and culture

4. Additional tests

  • *PCR: *on respirtaory samples; nose and throat swabs for viruses like Influenza A.
  • Antigen testing: ie urinary antigen tests
  • *Blood chemistry/full cell count; blood cultures; and serology *(required acute and convalescent serum samples; acute serum helpful for the serodiagnosis of *M. pneumoniae *and other ‘atypical’ bacteria).
26
Q

Characteristic types of sputum in pneumonia

A
  • Mucopurulent: bacterial pneumonia
  • Scant/watery: viral, mycoplasma/atypical pneumonias
  • Rusty: alveolar involvement with pneumococci
  • Dark red mucoid: currant jelly-like; Klebsiella pneumoniae
  • Foul-smelling: ie mixed anaerobic infections
27
Q

Sputum gram stain and culture

A
  • Before abx are administered; can aid in identifying the causative agent and guide choide of abx therapy.
  • Samples might be inappropriate because of prior abx use and oropharygeal flora contamination
  • Diagnostic value high when number of neutrophils >25, and epithelial cells <10 (under 100x magnification)
  • Gram stain and culture of sputum sample should usually show a dominant organism.
28
Q

Management and treatment on pneumonia

A

The most appropriate empiric abx, and duration of therapy dependent upon:

  • Child/adult patient
  • Community acquired or hospital-acquired
  • Complications (ie. lung abscess)
  • Severity score
  • Geographical region (tropical vs non-tropical)

It is important to note that clinical judgement should be used regarding:

  • hypoxia
  • stability of home situation
  • ability to take oral medications
  • reliability in taking medications
  • emotional and psycholoicla instability
  • likelihood to return for follow-up testing
29
Q

CORB assessment

A

CORB provides a relatively simple and quick assessment because it can be done in the absence of investigation results:

  • Confusion (acute)
  • Oxygen saturation 90% or less
  • Respiratory rate 30 breaths or more per minute
  • BP (systolic) less than 90mmHg or diastolic BP 60mmHg or less

Severe community acquired pneumonia is diagnosed as having at least two of the above four features.

30
Q

SMART-COP assessment

A
  • 0-2 points: low risk of needing IRVS
  • 3-4 points: moderate (1 in 8) risk of needing IRVS
  • 5-6 points: high (1 in 3) risk of needing IRVS
  • 7 or more points: very high (2 in 3) risk of needing IRVS