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Pneumonias
Dr O. B. Ozoh
 Infection of lung parenchyma…
 …distal to terminal bronchi
 Associated with clinical
& radiological evidence
of consolidation
Epidemiology
• High economic burden
• 4.7-11.6/1000 increasing with age
• 22% -51% hospital admission rate
• 7% mortality in those admitted to the hospital
• 21% mortality in severe pneumonia
Pathogenesis
• Overwhelmed respiratory defence
mechanisms
• Increased virulence of infecting agent
• Large size of inoculum
• Impaired host defence mechanisms eg
immunosuppression, diabetes, HIV etc
• Risk of infection vs risk of severity
Risk factors 1
• Age; 22-45 per 1000 vs 4.7-11.6 in those over 65
years.
– Increases mortality due to increased co-morbidities 9
vs 219/100,000
• Institutionalization
– Organisms somewhat different from CAP
• Malnutrition
• Aspiration, increases to 70% when unconscious
or intubated, anaerobes implicated in gross
aspiration
• Associated conditions or comorbidities
Risk factors 2
• Alcoholism
• Cigarette smoking
• Miscellaneous factors
– Soldiers
– South African gold miners
– Previous hospitalization within one year
 Microaspiration ~ oropharyngeal secretions
 Most common route
 Gross aspiration
 Anaerobes
 Haematogenous spread (embolic)
 Staph
 Aerosolization
 MTB
Classification 1
• Based on setting (where and how)
– Community acquired pneumonia (CAP)
– Nosocomial pneumonia
– Health care associated pneumonia
– Ventilator associated pneumonia
– Aspiration pneumonia
• Based on infecting agent
– Bacterial eg S. pneumonia, staph, H. influenza, gram –ves,
mycoplasma, chlamydia, legionella, anaerobes, norcadia,
brucella, coxiella etc
– Viral eg influenza, adeno viruses, RSV
– Fungal eg aspergillus,
– Parasitic eg malaria,
Classification 2
• Based on pathology
– Lobar pneumonia
– Bronchopneumonia
– Interstitial pneumonia
– Miliary pneumonia
 Vital capacity, FRC and TLC
 Lung compliance
 V:Q mismatch
 Shunting

Hypoxaemia
Clinical features
Typical pnuemonia (CAP)
• Abrupt onset
• Fever, chills, productive cough
and pleuritic chest pain
• Focal clinical signs
• Lobar or segmental
radiographic findings
• Leucocytosis and positive
sputum gram stain
• Due to extracellular organisms
Atypical pneumonia
• Progressive onset
• Fever without chills, dry
cough, headache, myalgia
• Diffuse crackles
• Interstitial infiltrates more
dramatic than findings
• Modest leucocytosis
• Negative gram stain
• Due to intracellular organisms
eg legionella, chlamydia,
mycoplasma, coxiella, viruses
etc
 Streptococcus pneumoniae +++
 Haemophilis influenzae ++
 Mycoplasma pneumoniae ++
 Chlamydophila pneumoniae ++
 Aerobic gram – negative bacilli +
E.g.: Klebsiella pneumoniae
 S aureus, S pyogenes, M catarrhalis
 Respiratory viruses
E.g.: RSV, influenza, adeno
 CXR (Gold standard!)
 Confirms diagnosis ~ consolidation
 Opacity (with no change in volume)
 Air-bronchograms
 Silhouette-sign
 Delineate extent ~ number of lobes
 Denotes complications
 Complications ~ empyema, abscess
 Some idea aetiology
 CXR
Air-bronchograms
 CXR
Silhouette-sign
 CXR
Pleural effusion
 Aetiological Diagnosis (Hospitalised patient)
 Blood cultures
 Sputum
 Gram stain
 Culture (& sensitivity)
 AFBs +/- PCJ
 Pleural aspiration (Effusion)
 pH
 Stain, culture & sensitivity (incl TB)
 Chemistry, incl ADA
 Aetiological Diagnosis (Hospitalised patient)
 Serology
 Not routine
 Atypical infections
ELISA or CIE ~ S Pneumoniae
Sputum / Urine / Serum
 Bronchoscopy (if intubated)
 Washings
 Severity (Hospitalised patient)
 Blood gasses
 Full blood count ~ ? White cell count
 C-Reactive Protein (CRP)
 Procalcitonin (PCT)
 Renal function tests (U&e-)
 Liver function tests (LFTs)
> 3 ng/ml ~ Pneumonia (vs PTB)
 Conditions mimicking pulmonary infections:
 Drug-induced pneumonitis
 Hypersensitivity pneumonitis, radiation
 Eosinophylic pneumonia
 Neoplasms
 Sarcoidosis
 Pulmonary infarction, edema, hemorrhage
 Lung collapse
 Clinical Indicators of Severe Pneumonia:
 Confusion / decreased consciousness
 Low BP
 BP < 90/60 mmHg
 Need for vasopressors > 4 hrs
 Respiratory rate > 30 / minute
 Multilobar consolidation
 Extra-thoracic septic complications
 Presence
 Laboratory Indicators of Severe Pneumonia:
 Hypoxaemia (pO2 < 8kPa)
 White cell count
 < 4 x 109/l
 > 30 x 109/l
 Abnormal renal or liver function tests
 CXR
 Rapidly expanding / multi-lobar
 Cavitations
 Decision to Hospitalise:
 Age > 60 years
 Co-morbid illnesses
 Diabetes mellitus
 Renal or liver disease
 Chronic cardiorespiratory disease
 Severe pneumonia (previous slides)
 Complications of infection
 CURB – 65 Score (Easy to remember)
 Confusion
 Urea > 7 mmol/l
 Respiratory rate > 30/min
 Blood pressure low
 Age > 65 years
Score ≥ 2 Hospitalise!
Hospitalise ?
No Yes
Treatment
High dose amoxycillin
+/- Macrolide
(Alt: Co-amoxiclav or 2nd Gen Cephalosporin)
E.g. Erythromycin
Or Newer Fluoroquinolones:
E.g.: Moxiflofloxacin or Gatifloxacin
Pneumococci: High
prevalence of
resistance to
Macrolides
Exception:
Telitromycin
Hospitalise ?
No Yes
Severe ?
Yes No
Treatment
Co-amoxiclav
+ Macrolide (Or Fluoroquinolones)
Aminoglycoside
(Alt: 2nd /3rd Gen Cephalosporin)
Combination
lowers mortality
(Bacteraemic
Pnemocococcal)
Hospitalise ?
No Yes
Severe ?
Yes No
Age > 60 or
Comorbidity?
Support
Analgesics
Hydration (IV)
Physiotherapy
Rest
Hospitalise ?
No Yes
Severe ?
Yes No
Age > 60 or
Comorbidity?
Treat Complications
Supplementary O2
Chest drain (empyema)
ICU admission
Mechanical ventilation
Hospitalise ?
No Yes
Severe ?
Yes No
Age > 60 or
Comorbidity?
Duration of Antibiotics
5 – 10 days
14 days for atypical
2-3 weeks if severely ill ?
Little evidence
 CXR 4 - 6 weeks after discharge
 50% should resolve within 2 weeks
 66% should resolve within 4 weeks
 75% should resolve within 6 weeks
 Indications for further investigations:
 CXR at 4 weeks ~ no improvement
 CXR at 12 weeks ~ not completely resolved
 Local
 Pleural effusions / empyema
 Abscess
 Respiratory failure (type 1)
 ARDS
 Broncho-pleural fistula (pneumothorax)
 Systemic
 Septicaemia
 Metastatic Abscesses
 Multi-organ dysfunction
 Immune compromised patient
 HIV
 Other – age, comorbidity
 Underlying pulmonary abnormality
 Bronchiectasis
 Bronchial obstruction (carcinoma)
 Organism
 Resistant or virulent strain
 Atypical bacteria
 TB
 Complication has developed
 Parapneumonic effusion
 Abscess
 Septicaemia
 Metastatic abscesses
 Drug fever
 Incorrect diagnosis
 Non – infective (see differential diagn)
 Practical approach
 “Careful” History & Examination
 Repeat basis investigations
 Second line investigations
CT Chest
Bronchoscopy +/- BAL, TBB
Open lung biopsy
 CXR
 Serology
 Antibody titre
 Organisms not amenable to culture
 Baseline serum taken on admission
 Follow-up specimen 2 weeks later
 Need 4x increase in antibody-titre
or high single titre
 Lab findings may point towards aetiology
 Cold haemagglutinins ~ Mycoplasma
 Hyponatraemia, abn LFTs ~ Leigonella
 Raised LDH ~ Pneumocystis
 General Management & Follow Up
 As for Typical CAP
 Infection of lung parenchyma
 > 48 hours after admission
 Not incubating at time of admission
 Synonym: “Hospital acquired”
 Different aetiology (than CAP)
 Often gram negative organisms
 Requires broad spectrum empiric antibiotics
 Advanced age, smoking, alcohol abuse
 Immunosuppressive state
 Prior care facility
 Intubation and mechanical ventilation
 Head trauma, coma
 Aspiration
 Emergency surgery
 Severe underlying disease
 Aerobic gram – negative bacilli +++
E.g.: Klebsiella
Pseudomonas spp
E. Coli, Enterobacter
Acinotobacter
 Staphylococcus aureus ++
 Anaerobes +
 Streptococcus pneumoniae
 Other
 New / progressive pulmonary infiltrate
 At least two of the following:
 Fever
 Leucocytosis
 Purulent sputum
 New pulmonary infiltrate
 Mortality: 20 – 40 %
 General / supportive measures
 As for CAP
 Antibiotics ~ Broad spectrum!
 4th Gen Cef (e.g. Cefepime)
 Aminoglycosides Combination
 Vancomycin
 Carbapenems (e.g. Imipenem)
 Pip – Taz
 Discuss with Microbiology!
 Aspiration & pulmonary sequelae
 Acid Chemical pneumonitis
 Bacteria Aspiration pneumonia
 Inert fluids Mechanical obstruction
(reflex airway closure)
 Particles Mechanical obstruction
 Aspiration of oropharyngeal bacteria
 Patients predisposed to aspiration
 Alcohol abuse
 Decreased consciousness
 Epileptics
 Bronchial occlusion
 Tumours
 Foreign objects
 Poor periodontal hygiene
 Anaerobes (aspiration, poor oral hygiene)
 Peptostreptococci
 Bacteroides
 Fusobacterium
 Other
 Aerobes (less frequent)
 Staphylococcus aureus
 Streptococcus pyogenes
 Klebsiella
 Nocardia
 Predisposition to aspiration
 Longer duration before presentation
 Great variation:
 Anaerobic infections
 Indolent, mimics pulmonary TB
 Cough ~ initially dry, later productive
 Foul smelling sputum
 Shortness of breath, fever, weight loss
 Pleuritic chest pain
 General Measures as for CAP
 Antibiotics
 Clindamycin (best response)
 Cefuroxime & Metronidazole
 Augmentin
 High dose Pen G
 CXR
 Sputum
 Bronchoscopy
 Lavage
 Brush
 Biopsies
 Other
 Varies according to setting
 May need a varying combination of
 Antibiotics
 Antifungal therapy
 Antiviral therapy
 General support
Pneumonias.pptx

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Pneumonias.pptx

  • 2.  Infection of lung parenchyma…  …distal to terminal bronchi  Associated with clinical & radiological evidence of consolidation
  • 3. Epidemiology • High economic burden • 4.7-11.6/1000 increasing with age • 22% -51% hospital admission rate • 7% mortality in those admitted to the hospital • 21% mortality in severe pneumonia
  • 4. Pathogenesis • Overwhelmed respiratory defence mechanisms • Increased virulence of infecting agent • Large size of inoculum • Impaired host defence mechanisms eg immunosuppression, diabetes, HIV etc • Risk of infection vs risk of severity
  • 5. Risk factors 1 • Age; 22-45 per 1000 vs 4.7-11.6 in those over 65 years. – Increases mortality due to increased co-morbidities 9 vs 219/100,000 • Institutionalization – Organisms somewhat different from CAP • Malnutrition • Aspiration, increases to 70% when unconscious or intubated, anaerobes implicated in gross aspiration • Associated conditions or comorbidities
  • 6. Risk factors 2 • Alcoholism • Cigarette smoking • Miscellaneous factors – Soldiers – South African gold miners – Previous hospitalization within one year
  • 7.  Microaspiration ~ oropharyngeal secretions  Most common route  Gross aspiration  Anaerobes  Haematogenous spread (embolic)  Staph  Aerosolization  MTB
  • 8. Classification 1 • Based on setting (where and how) – Community acquired pneumonia (CAP) – Nosocomial pneumonia – Health care associated pneumonia – Ventilator associated pneumonia – Aspiration pneumonia • Based on infecting agent – Bacterial eg S. pneumonia, staph, H. influenza, gram –ves, mycoplasma, chlamydia, legionella, anaerobes, norcadia, brucella, coxiella etc – Viral eg influenza, adeno viruses, RSV – Fungal eg aspergillus, – Parasitic eg malaria,
  • 9. Classification 2 • Based on pathology – Lobar pneumonia – Bronchopneumonia – Interstitial pneumonia – Miliary pneumonia
  • 10.  Vital capacity, FRC and TLC  Lung compliance  V:Q mismatch  Shunting  Hypoxaemia
  • 11. Clinical features Typical pnuemonia (CAP) • Abrupt onset • Fever, chills, productive cough and pleuritic chest pain • Focal clinical signs • Lobar or segmental radiographic findings • Leucocytosis and positive sputum gram stain • Due to extracellular organisms Atypical pneumonia • Progressive onset • Fever without chills, dry cough, headache, myalgia • Diffuse crackles • Interstitial infiltrates more dramatic than findings • Modest leucocytosis • Negative gram stain • Due to intracellular organisms eg legionella, chlamydia, mycoplasma, coxiella, viruses etc
  • 12.  Streptococcus pneumoniae +++  Haemophilis influenzae ++  Mycoplasma pneumoniae ++  Chlamydophila pneumoniae ++  Aerobic gram – negative bacilli + E.g.: Klebsiella pneumoniae  S aureus, S pyogenes, M catarrhalis  Respiratory viruses E.g.: RSV, influenza, adeno
  • 13.  CXR (Gold standard!)  Confirms diagnosis ~ consolidation  Opacity (with no change in volume)  Air-bronchograms  Silhouette-sign  Delineate extent ~ number of lobes  Denotes complications  Complications ~ empyema, abscess  Some idea aetiology
  • 17.  Aetiological Diagnosis (Hospitalised patient)  Blood cultures  Sputum  Gram stain  Culture (& sensitivity)  AFBs +/- PCJ  Pleural aspiration (Effusion)  pH  Stain, culture & sensitivity (incl TB)  Chemistry, incl ADA
  • 18.  Aetiological Diagnosis (Hospitalised patient)  Serology  Not routine  Atypical infections ELISA or CIE ~ S Pneumoniae Sputum / Urine / Serum  Bronchoscopy (if intubated)  Washings
  • 19.  Severity (Hospitalised patient)  Blood gasses  Full blood count ~ ? White cell count  C-Reactive Protein (CRP)  Procalcitonin (PCT)  Renal function tests (U&e-)  Liver function tests (LFTs) > 3 ng/ml ~ Pneumonia (vs PTB)
  • 20.  Conditions mimicking pulmonary infections:  Drug-induced pneumonitis  Hypersensitivity pneumonitis, radiation  Eosinophylic pneumonia  Neoplasms  Sarcoidosis  Pulmonary infarction, edema, hemorrhage  Lung collapse
  • 21.  Clinical Indicators of Severe Pneumonia:  Confusion / decreased consciousness  Low BP  BP < 90/60 mmHg  Need for vasopressors > 4 hrs  Respiratory rate > 30 / minute  Multilobar consolidation  Extra-thoracic septic complications  Presence
  • 22.  Laboratory Indicators of Severe Pneumonia:  Hypoxaemia (pO2 < 8kPa)  White cell count  < 4 x 109/l  > 30 x 109/l  Abnormal renal or liver function tests  CXR  Rapidly expanding / multi-lobar  Cavitations
  • 23.  Decision to Hospitalise:  Age > 60 years  Co-morbid illnesses  Diabetes mellitus  Renal or liver disease  Chronic cardiorespiratory disease  Severe pneumonia (previous slides)  Complications of infection
  • 24.  CURB – 65 Score (Easy to remember)  Confusion  Urea > 7 mmol/l  Respiratory rate > 30/min  Blood pressure low  Age > 65 years Score ≥ 2 Hospitalise!
  • 25. Hospitalise ? No Yes Treatment High dose amoxycillin +/- Macrolide (Alt: Co-amoxiclav or 2nd Gen Cephalosporin) E.g. Erythromycin Or Newer Fluoroquinolones: E.g.: Moxiflofloxacin or Gatifloxacin Pneumococci: High prevalence of resistance to Macrolides Exception: Telitromycin
  • 26. Hospitalise ? No Yes Severe ? Yes No Treatment Co-amoxiclav + Macrolide (Or Fluoroquinolones) Aminoglycoside (Alt: 2nd /3rd Gen Cephalosporin) Combination lowers mortality (Bacteraemic Pnemocococcal)
  • 27. Hospitalise ? No Yes Severe ? Yes No Age > 60 or Comorbidity? Support Analgesics Hydration (IV) Physiotherapy Rest
  • 28. Hospitalise ? No Yes Severe ? Yes No Age > 60 or Comorbidity? Treat Complications Supplementary O2 Chest drain (empyema) ICU admission Mechanical ventilation
  • 29. Hospitalise ? No Yes Severe ? Yes No Age > 60 or Comorbidity? Duration of Antibiotics 5 – 10 days 14 days for atypical 2-3 weeks if severely ill ? Little evidence
  • 30.  CXR 4 - 6 weeks after discharge  50% should resolve within 2 weeks  66% should resolve within 4 weeks  75% should resolve within 6 weeks  Indications for further investigations:  CXR at 4 weeks ~ no improvement  CXR at 12 weeks ~ not completely resolved
  • 31.  Local  Pleural effusions / empyema  Abscess  Respiratory failure (type 1)  ARDS  Broncho-pleural fistula (pneumothorax)  Systemic  Septicaemia  Metastatic Abscesses  Multi-organ dysfunction
  • 32.  Immune compromised patient  HIV  Other – age, comorbidity  Underlying pulmonary abnormality  Bronchiectasis  Bronchial obstruction (carcinoma)  Organism  Resistant or virulent strain  Atypical bacteria  TB
  • 33.  Complication has developed  Parapneumonic effusion  Abscess  Septicaemia  Metastatic abscesses  Drug fever  Incorrect diagnosis  Non – infective (see differential diagn)
  • 34.  Practical approach  “Careful” History & Examination  Repeat basis investigations  Second line investigations CT Chest Bronchoscopy +/- BAL, TBB Open lung biopsy
  • 36.  Serology  Antibody titre  Organisms not amenable to culture  Baseline serum taken on admission  Follow-up specimen 2 weeks later  Need 4x increase in antibody-titre or high single titre
  • 37.  Lab findings may point towards aetiology  Cold haemagglutinins ~ Mycoplasma  Hyponatraemia, abn LFTs ~ Leigonella  Raised LDH ~ Pneumocystis
  • 38.  General Management & Follow Up  As for Typical CAP
  • 39.  Infection of lung parenchyma  > 48 hours after admission  Not incubating at time of admission  Synonym: “Hospital acquired”
  • 40.  Different aetiology (than CAP)  Often gram negative organisms  Requires broad spectrum empiric antibiotics
  • 41.  Advanced age, smoking, alcohol abuse  Immunosuppressive state  Prior care facility  Intubation and mechanical ventilation  Head trauma, coma  Aspiration  Emergency surgery  Severe underlying disease
  • 42.  Aerobic gram – negative bacilli +++ E.g.: Klebsiella Pseudomonas spp E. Coli, Enterobacter Acinotobacter  Staphylococcus aureus ++  Anaerobes +  Streptococcus pneumoniae  Other
  • 43.  New / progressive pulmonary infiltrate  At least two of the following:  Fever  Leucocytosis  Purulent sputum  New pulmonary infiltrate  Mortality: 20 – 40 %
  • 44.  General / supportive measures  As for CAP
  • 45.  Antibiotics ~ Broad spectrum!  4th Gen Cef (e.g. Cefepime)  Aminoglycosides Combination  Vancomycin  Carbapenems (e.g. Imipenem)  Pip – Taz  Discuss with Microbiology!
  • 46.  Aspiration & pulmonary sequelae  Acid Chemical pneumonitis  Bacteria Aspiration pneumonia  Inert fluids Mechanical obstruction (reflex airway closure)  Particles Mechanical obstruction
  • 47.  Aspiration of oropharyngeal bacteria  Patients predisposed to aspiration  Alcohol abuse  Decreased consciousness  Epileptics  Bronchial occlusion  Tumours  Foreign objects  Poor periodontal hygiene
  • 48.  Anaerobes (aspiration, poor oral hygiene)  Peptostreptococci  Bacteroides  Fusobacterium  Other  Aerobes (less frequent)  Staphylococcus aureus  Streptococcus pyogenes  Klebsiella  Nocardia
  • 49.  Predisposition to aspiration  Longer duration before presentation  Great variation:  Anaerobic infections  Indolent, mimics pulmonary TB  Cough ~ initially dry, later productive  Foul smelling sputum  Shortness of breath, fever, weight loss  Pleuritic chest pain
  • 50.  General Measures as for CAP  Antibiotics  Clindamycin (best response)  Cefuroxime & Metronidazole  Augmentin  High dose Pen G
  • 51.  CXR  Sputum  Bronchoscopy  Lavage  Brush  Biopsies  Other
  • 52.  Varies according to setting  May need a varying combination of  Antibiotics  Antifungal therapy  Antiviral therapy  General support