JC14 (Medicine) - Lower respiratory tract infections Flashcards

(58 cards)

1
Q

Define pneumonia

A

inflammation of lung parenchyma, commonly due to infective agents

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2
Q

Typical clinical picture of acute pneuomia

A

Symptoms:
Systemic: fever, rigors, shivering, malaise, headache, ↓appetite, ± delirium

Pulmonary:
→ Cough: short, painful, dry (initial) → productive with mucopurulent sputum ± haemoptysis (later)
→ Pleuritic chest pain when visceral pleura is involved
→ Dyspnoea

Others:
→ Upper abdominal tenderness if lower lobe pneumonia or associated hepatitis

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3
Q

Explain how pneumonia leads to dyspnea and pleurisy

A

Pathological: form of acute respiratory infection that alveoli are filled with pus and fluid, making breathing painful and limits O2 intake

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4
Q

Classify pneumonia by anatomical regions involved

A

Anatomical:
→ Lobar pneumonia: homogeneous consolidation of ≥1 lobes

→ Bronchopneumonia: more patchy alveolar consolidation a/w bronchial and bronchiolar inflammation

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5
Q

Classify pneumonia by aetiological organisms (3)

A

Aetiological: bacterial, viral, fungal

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6
Q

Types of pneumonia (5)

A

→ Community-acquired pneumonia (CAP)
→ Hospital-acquired pneumonia (HAP)
→ Ventilator-associated pneumonia
→ Aspiration pneumonia
→ Pneumonia in immunocompromised patients

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7
Q

List causative bacteria of Community acquired pneumonia

A

Gram +

  • Streptococus pneumoniae*
  • Haemophilus influenzae non-typeable*

Atypical
- Mycoplasma pneumoniae, Chlaymdophila pneumoniae, Legionelaa pneumophila

(Gram -)
Klebsiella pneumoniae
Pseudomonas aeruginosa

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8
Q

List causative bacteria of hospital acquired pneumonia

A

Gram +

  • Streptococus pneumoniae*
  • Haemophilus influenzae non-typeable*
  • Methicillin-resistance staphylococcus aureus (MRSA)

Gram -

  • Klebsiella pneumoniae ***
  • Pseudomonas aeruginosa ***

Anaerobes
- Bacteroides species

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9
Q

List causative bacteria of aspiration pneumonia

A

Gram -

  • Klebsiella pneumoniae *
  • Pseudomonas aeruginosa *
  • Other nosocomial gram - bacteria

Anaerobes
- Bacteroides species **

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10
Q

Typical PE signs of lobar pneumonia

A

□ Vitals: fever, ↓BP, ↑HR, ↑RR, ± ↓SpO2

□ Chest
→ Decrease air entry
→ Coarse crackles
→ Consolidation signs: percussion dullness, bronchial breath sounds, ↑vocal resonance

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11
Q

Baseline investigations for suspected pneumonia **

A
  1. CXR
    - gold-standard for CAP diagnosis
    - clinical suspicious with negative CXR > CT/MRI
  2. Blood (severity)
    - CBC with WBC differential
    - RFT
    - LFT
    - ESR/CRP
    - Arterial blood gas
  3. Microbiology
    - Sputum: gram stain, C/ST
    - Blood: culture and serology
    - Nasopharyngeal aspirate: RAT for influenze, PCR for virus, M. pneumoniae
    - Urine: RAT for Legionella, S. pneumoniae
    - BAL/ Transbronchial biopsy, thoracoscopic biopsy
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12
Q

Describe atypical pneumonia syndrome

A

□ Cause: usually refers to M. pneumoniae, C. pneumoniae and L. pneumophila

□ Characterized by:
→ Symptomatology: less severe, prominent systemic complaints
→ Ix: relatively normal WBC counts (vs neutrophilia in typical bacterial pneumonia

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13
Q

Clinical approach to pneumonia

A
  • Diagnosis of CAP
  • Assessment of severity
  • Empirical treatment based on:
     Likely causative pathogens
     Clinical severity
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14
Q

Ddx of pneumonia

A
  • Pulmonary oedema
  • Pulmonary/pleural TB
  • Eosinophilic pneumonia
  • Bronchoalveolar carcinoma
  • Cryptogenic organizing pneumonia (rare)
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15
Q

Typical RFT and LFT results for community-acquired pneumonia

A

□ RFT: ↑urea*, hypoNa*, renal dosing of Abx
□ LFT: liver involvement (in basal pneumonia), ↓Alb*

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16
Q

List all samples needed for microbiological diagnosis of pneumonia

A
  • Sputum: gram stain, C/ST
  • Blood: culture and serology
  • Nasopharyngeal aspirate: RAT for influenze, PCR for virus, M. pneumoniae
  • Urine: RAT for Legionella, S. pneumoniae
  • BAL/ Transbronchial biopsy, thoracoscopic biopsy
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17
Q

Most common pathogen causing acute CAP in elderly

A

Strep. pneumoniae (most common)

Haemophilus pneumoniae

Klebsiella pneumoniae (esp. DM, alcoholic)

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18
Q

Most common pathogen causing acute CAP in the young

A

Mycoplasma pneumoniae

Streptococcus pneumoniae

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19
Q

Complications of mycoplasma pneumoniae infection

A

haemolysis (60%), cold agglutinin disease, erythema multiforme, encephalitis

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20
Q

Complications of Klebsiella pneumoniae infection

A

UTI and renal abscess, liver abscess, endophthalmitis

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21
Q

Typical route of spread for Legionella pneumophila

A

from aqueous environment (water tanks, cooling towers, spas…)

Route of infection: breathe in contaminated droplets and mists from artificial water systems (eg. hot water baths) or handle garden soils, compost, potting mixes

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22
Q

Typical presentation of Legionella pneumophila infection

A

S/S: classically prodromal flu-like S/S with CNS (confusion) and GI (diarrhea) involvement

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23
Q

Specific investigations and diagnostic tests for Legionella pneumophila infection

A

→ Bloods: classically lymphopenia w/o marked leukocytosis, T1RF, SIADH, dLFT

→ CXR: lobar or multilobar consolidation

→ Microbiology: G- bacillus not well-visualized on Gram stain (WBC++ no organisms), culture require special selective media and takes 1-3w → usually diagnosed by urine antigen test (for serotype 1)

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24
Q

Typical viruses that cause acute CAP

A

influenza, parainfluenza, RSV, measles*

More common in children than adults

25
Specific pathogen that cause opportunistic infection and pneumonia in HIV patients
Pneumocystis jirovecii patients with HIV or severe immunocompromised state (eg. post-chemo)
26
Criteria for assessment of clinical severity of CAP
CURB-65 Confusion Urea \> 7mmol/L Respiratory rate \> 30/min Blood pressure: SBP \< 90 or DBP \<60 Age \> 65 0 or 1 = home treatment 2 or more factors = immediate hospital admission 3 or more = ICU
27
Outline management of CAP
1. Oxygen therapy - all patients with resp. failure - Target SaO2 \> 92% - High concentration oxygen/ CPAP/ Mechanical ventilation 2. Fluid rehydration 3. Antibiotics coverage 4. Analgesia for pleuritic pain - simple analgesics 5. Manage complications
28
Antibiotics coverage for CAP - Timing - Coverage - Choice of antibiotics
- Admin within 6-8 hours, duration 7-10d - All CAP needs Strep. pneumoniae coverage; All severe CAP needs Legionella pneumophila coverage Typical pathogen: □ Penicillin + β-lactamase inhibitor → Eg. augmentin Atypical pathogens: □ ± macrolide or tetracycline → Eg. clarithromycin (klacid), azithromycin, doxycycline
29
Risk factors for multi-drug resistant pathogens causing CAP
□ Recent or frequent Abx use □ Recent or frequent hospitalization □ Nursing home resident □ Immunocompromised state
30
Choice of antibiotics for: - Outpatient CAP - Moderate inpatient CAP - Severe inpatient CAP
- Outpatient CAP PO amoxicillin-clavulanate (Augmentin) ± macrolide or doxycycline - Moderate inpatient CAP PO/IV amoxicillin-clavulanate (Augmentin) ± macrolide or doxycycline Alternatives: IV ceftriaxone or cefotaxime ± macrolide or doxycycline - Severe inpatient CAP IV piperacillin-tazobactam (Tazocin) or ceftriaxone or cefepime ± macrolide or doxycycline
31
Follow-up for CAP
Chest physiotherapy: helps expectoration clinical review 6 weeks later CXR if persistent S/S or suspect underlying malignancy
32
Possible ddx for delayed recovery from CAP
→ Complications, eg. abscess, parapneumonic effusion → Alternative dx, eg. ILD, TB → Underlying cause, eg. obstruction, recurrent aspiration
33
Complications of CAP
□ Respiratory failure □ Lung abscess □ Pathogen Spread: → Septicaemia with multi-organ failure → Parapneumonic effusion → Empyema thoracis □ Systemic effects: → Electrolyte abnormalities, eg. hypoNa due to SIADH → Cardiac complications: acute MI, cardiac arrhythmia (esp AF)
34
Causes of recurrent CAP
→ Underlying structural disease, eg. bronchial obstruction, bronchiectasis → Host factors, eg. recurrent aspiration, immunocompromised state
35
# Define Hospital-Acquired Pneumonia (HAP) Typical route of infection?
pneumonia occurring ≥48h after hospitalization + excluding incubating infection at admission aspiration of oropharyngeal secretions colonized by hospital-acquired organisms
36
Predisposing factors of HAP
□ General debility and old age □ Smoking and COPD □ ↑risk of aspiration: post-GA, nasogastric tube □ ↓gastric aciditiy: antacids, H2 blockers (↑GI colonization) □ Mechanical ventilation (ventilator-associated pneumonia (VAP))
37
Typical bacteria causing HAP
□ Early onset (\<4-5d of admission): similar to CAP □ Late-onset: → Gram - bacilli, eg. Escherichia, Klebsiella spp → Non-fermenters, eg. Pseudomonas, Acinetobacter baumanii → Multi-resistant bacteria, eg. MRSA → Anaerobes, eg. Bacteroides
38
Empirical treatment for HAP
Early onset: 3rd generation cephalosporin OR β-lactam/β-lactamase inhibitor (Augmentin, Unasyn) Late onset: Anti-pseudomonal β-lactam/β-lactamase inhibitor (Tazocin) OR Anti-pseudomonal cephalosporin (Cefepime [4G]) OR Anti-pseudomonal carbapenem (imipenem, meropenem) ± aminoglycoside OR fluoroquinolone ± vancomycin after careful assessment of indications
39
Define aspiration pneumonia
pneumonia due to aspiration of a relatively large amount of material
40
Predisposing factors of aspiration pneumonia
□ Impaired gag reflex: ↓GCS, alcoholism, bulbar palsy, vocal cord palsy, terminal illness □ Regurgitation/vomiting: dysphagia and oesophageal diseases, vomiting, drowning □ Others: severe dental infection or URTI, tracheo-esophageal fistula
41
Causative agents of aspiration pneumonia
□ Chemical pneumonitis due to aspiration of acidic materials □ Infection by oropharyngeal flora → Anaerobes, eg. Bacteroides, Porphyromonas, Prevotella, Fusobacterium → Others: Streptcoccus, S. aureus, G- bacilli
42
Investigations for aspiration pneumonia
□ CXR: consolidations, usually in dependent parts of lungs → Lower lobes (classically recurrent RLL pneumonia) → Posterior segments of upper lobe (if recumbent) □ VFSS for swallowing problems → Follow-up CXR shows contrast medium in lung fields
43
Management of aspiration pneumonia
□ Treatment of underlying conditions □ Abx to cover oropharyngeal flora: augmentin ± metronidazole □ Non-oral feeding (eg. PEG tube, NG tube) → prevent further aspiration
44
Diagnostic tests of influenza
Rapid antigen test on nasopharyngeal aspirate RT-PCR Viral Culture Serology
45
Influenza - Incubation period - S/S
Incubation period: 1-4 days □ Systemic: fever (37.8-40oC), myalgia, arthralgia, malaise □ URTI: running nose, sore throat, cough, sputum
46
List major influenza types in humans, avians and swines
Notable influenza types: Human: H1N1 (Spanish), H2N2 (Asian), H3N2 (Hong Kong) Avian: H5N1, H7N7, H7N9 Swine: H1N1
47
Extra-respiratory manifestations of influenza infection
Pneumonia: primary viral or superimposed bacterial (S. pneumoniae, S. aureus, esp \>65y) GI involvement: vomiting, diarrhea CNS involvement: encephalitis, transverse myelitis, aseptic meningitis, GBS Others: myositis, myocarditis, pericarditis, Reye’s syndrome
48
Management of influenza infection
□ General: personal hygiene, symptomatic Tx, droplet precaution □ Neuraminidase inhibitors: effective in both flu A/B Examples: oseltamivir (Tamiflu, PO 75mg BD x5d), zanamivir (Relenza, 10mg BD inhaler puff x5d) MoA: inhibit neuraminidase → cannot cleave sialic acid on cell surface → interfere with release of progeny → decrease viral propagation
49
Define bronchiectasis
pathological dilatation of bronchi
50
Causes of bronchiectasis
□ Congenital: → Cystic fibrosis (rare in Chinese) → Ciliary dysfunction: eg. ciliary dyskinesia, Kartagener syndrome → Predisposition to infections (eg. 1o hypoγglobulinemia) □ Acquired: → Previous infections, eg. TB, suppurative pneumonia, childhood measles or pertussis → Obstruction, eg. foreign body, tumours → Rhuematic disorders, eg. RA, Sjogren’s syndrome → Gastro-esophageal reflux (leading to chronic aspiration) → Lung fibrosis (leading to traction bronchiectasis)
51
Typical symptoms of bronchiectasis
Chronic course (years) with acute infective exacerbations - Cough (98%): chronic, persistent - Daily sputum production (78%): copious, tenacious, purulent, foul-smelling - Haemoptysis (27%): only streaks of blood - Exertional dyspnoea ± wheezes - Pleuritic pain - Systemic symptoms: weight loss, fatigue, anorexia
52
Signs of bronchiectasis on PE
□ General: cachexia, clubbing, halitosis □ Varies with severity: - Coarse crackles that disappear/change in quality after coughing - Obstructive pattern → ↓breath sounds, ↓chest wall movement - Chronic localized fibrosis → bronchial breath sounds - Cor pulmonale (↑JVP, peripheral oedema, hepatic congestion, parasternal heave, loud P2) - Respiratory failure (central cyanosis)
53
Ddx bronchiectasis
COPD: also with recurrent bouts of dyspnoea, productive cough, wheezes, coarse crackles Asthma: also with recurrent exacerbation of dyspnoea, productive cough and wheezes Lung fibrosis: also with dyspnoea, cough, crackles and finger clubbing
54
Typical radiological features of bronchiectasis on CXR
CXR: only abnormal in 50% → Ring shadows: dilated bronchi seen from front → Tramline shadows: dilated bronchi seen from side (usually in lower lobes) → Tubular shadows: dilated bronchi filled with secretions → Cystic dilatation ± fluid levels in severe cases
55
Typical radiological features of bronchiectasis on HRCT
1) Thickened, dilated airways (ring shadows) - Wider than accompanying arterioles (signet ring sign) - No peripheral tapering with visible peripheral airway ≤1cm of pleural lining 2) Mucus plugging (darker than airway wall): - Air-fluid levels visible within cystic dilatation of airway - Tree-in-bud appearance when peripheral airways are involved 3) Atelactasis, consolidation, abscesses
56
5 specific diagnostic tests for underlying cause of bronchiectasis
→ Immunoglobulins and neutrophil function test for immunodeficiency → Auto-Ab (eg. RF) for autoimmune diseases → Ba studies or 24h oesophageal pH monitoring for aspiration causes → Ciliary and sperm analysis for primary ciliary dyskinesia → Sweat test for cystic fibrosis
57
Causes of acute exacerbation of bronchiectasis Treatment
Potential organisms: H. influenzae, S. aureus, P. aeruginosa (if long-standing) □ Choice of Abx: → Anti-pseudomonal penicillins (first-line), eg. piperacillin-tazobactam (tazocin) → 3rd and 4th generation cephalosporin, eg. ceftazidime → Carbapenems, eg. meropenem, imipenem → Aminoglycosides, eg. amikacin → Fluoroquinolones, eg. levofloxacin □ Duration: recommend 14 days
58
Long-term management of bronchiectasis
□ Treatment of underlying aetiology, eg. GERD, immunodeficiency □ Long-term (≥3mo) antibiotics for immunomodulatory effect to decrease exacerbations - Oral Macrolides □ Airway clearance: - Chest physiotherapy - Expectorant or mucolytic □ Adjuncts: - Bronchodilators (esp β-agonist): for SOB and obstructive pattern, bronchospasm - Inhaled corticosteroids (not routine) □ Surgery (rare) → Excision of bronchiectactic areas (eg. lobectomy) → Percutaneous embolization of bronchial vessels