Colony Morphology & ID

Community-acquired pneumonia (CAP), healthcare-associated pneumonia (HCAP), and infections in cystic fibrosis (CF) patients are distinct clinical entities with unique diagnostic and therapeutic considerations. Understanding these differences is crucial for effective patient management

Community-Acquired Pneumonia (CAP)

  • Definition: Pneumonia acquired outside of a healthcare setting
  • Common Pathogens
    • Streptococcus pneumoniae: Most common cause
    • Haemophilus influenzae
    • Moraxella catarrhalis
    • Legionella pneumophila: Less common but important
    • Staphylococcus aureus: Less common
  • Diagnostic Approach
    • Sputum: Sputum collection
    • Gram Stain: Quality is assessed. Provides initial diagnostic information
    • Culture: On BAP and CHOC. Culture allows the identification of the organisms
    • Special Tests: Legionella
    • Other Tests: Blood cultures
  • Key Considerations
    • Patient age, underlying medical conditions
    • Severity of illness
    • Presence of complications

Healthcare-Associated Pneumonia (HCAP)

  • Definition: Pneumonia that develops in a patient with specific healthcare exposures, or with certain risk factors
  • Pathogens
    • High Risk of MDROs: Multidrug-resistant organisms (MDROs) are more common
    • Acinetobacter baumannii complex
    • Enterobacteriaceae (e.g., Klebsiella pneumoniae)
    • Pseudomonas aeruginosa
    • Stenotrophomonas maltophilia
    • Staphylococcus aureus
  • Diagnostic Approach
    • Specimen Sources: Sputum, ETA, BAL
    • Quantitative cultures may be used
    • Culture and Gram stain on different types of media: including BAP, CHOC, and selective media
    • Antimicrobial Susceptibility Testing: Essential to guide treatment
  • Key Considerations
    • Risk factors
    • Presence of MDROs
    • Prompt antibiotic therapy

Cystic Fibrosis (CF)

  • Chronic, Polymicrobial Infections: Chronic infections
  • Pathogens
    • Pseudomonas aeruginosa: The most common, chronic
    • Staphylococcus aureus: Early colonizer
    • Haemophilus influenzae
    • Burkholderia cepacia complex (Bcc): Serious, transmissible
  • Diagnostic Approach
    • Specimen Sources: Sputum, BAL
    • Sputum Quality: This should be assessed
    • Culture
      • BAP and CHOC
      • Selective media for Bcc
      • Incubation times
      • Antimicrobial Susceptibility Testing
    • Identification: Species identification for Bcc
  • Key Considerations
    • Chronic infections
    • Polymicrobial
    • Antibiotic resistance
    • Airway clearance

Key Differentiators

Feature CAP HCAP Cystic Fibrosis (CF)
Setting Community Healthcare Chronic disease with respiratory involvement
Common Pathogens S. pneumoniae, H. influenzae MDROs: Acinetobacter, Enterobacteriaceae, Pseudomonas, S. aureus Pseudomonas aeruginosa, S. aureus, Haemophilus influenzae, Burkholderia cepacia complex
Antibiotic Resistance Less common More common Common, especially Pseudomonas
Specimen Source Sputum Sputum, ETA, BAL Sputum, BAL
Reporting Gram stain, culture, ID Gram stain, culture, quantitative/semi-quantitative, ID, AST Gram stain, culture, ID, AST
Additional factors Patient’s health and clinical status Healthcare risk, patient history CF-specific issues and patient history

Role of the Laboratory

  • Provide Accurate and Timely Results: The lab plays a crucial role in the diagnosis and management
  • Employ Appropriate Methods: Labs must use the right methods
  • Communicate Effectively: All lab results must be communicated