Community-Acquired Pneumonia (CAP)
Community-acquired pneumonia (CAP) is an acute infection of the lung parenchyma occurring in a non-hospitalized individual or developing ≤48 hours of hospital admission, not residing in long-term care and without recent healthcare exposure.
Category | Definition | Clinical relevance |
CAP | Outside hospital or ≤48 hr admission | Standard community pathogens |
HAP | ≥48 hr after admission | Higher MDR risk |
VAP | ≥48 hr after intubation | ICU-specific, highest MDR risk |
- Term Healthcare-associated pneumonia (HCAP) is obsolete → removed due to poor specificity for MDR pathogens.
Etiology
A. Typical Bacterial Pathogens
Organism | Notes |
Streptococcus pneumoniae | Most common worldwide |
Haemophilus influenzae | COPD, smokers |
Moraxella catarrhalis | Elderly, COPD |
Staphylococcus aureus | Post-influenza, necrotizing |
Gram-negative bacilli | Elderly, comorbidities |
B. Atypical Pathogens
Organism | Clinical Clues |
Mycoplasma pneumoniae | Young adults, dry cough |
Chlamydophila pneumoniae | Mild, prolonged |
Legionella pneumophila | Hyponatremia, diarrhea, confusion |
C. Viral Causes
- Influenza A/B
- RSV
- SARS-CoV-2
- Adenovirus
- Human metapneumovirus
Viral CAP often predisposes to secondary bacterial pneumonia
D. Risk-Based Pathogens
Risk Factor | Pathogen |
Alcoholism | Klebsiella pneumoniae |
Post-influenza | Staphylococcus aureus |
Aspiration | Anaerobes |
Structural lung disease | Pseudomonas aeruginosa |
Immunocompromised | Pneumocystis, fungi |
Pathogenesis
- Microaspiration of oropharyngeal flora (most common)
- Inhalation of aerosols
- Hematogenous spread (rare)
- Impaired host defenses:
- Smoking
- Alcohol
- COPD
- Diabetes
- Immunosuppression
Lung Response
- Alveolar macrophage activation
- Cytokine release (IL-1, TNF-α, IL-6)
- Neutrophil influx
- Consolidation and impaired gas exchange
Clinical Features
Typical Symptoms
- Fever
- Cough (productive or dry)
- Dyspnea
- Pleuritic chest pain
- Hemoptysis (occasionally)
Systemic Features
- Malaise
- Myalgia
- Confusion (elderly)
- GI symptoms (Legionella)
Physical Examination
- Tachypnea
- Tachycardia
- Fever or hypothermia
- Bronchial breath sounds
- Crackles
- Dullness to percussion
- Reduced air entry
Diagnosis
1. Clinical Diagnosis
- Compatible symptoms PLUS
- Radiographic evidence of pneumonia
2. Imaging
Chest X-ray (Mandatory)-No infiltrate = No pneumonia (except very early disease)
- Lobar consolidation
- Interstitial infiltrates
- Patchy bronchopneumonia
- Pleural effusion
- Cavitation (suggests necrotizing infection e.g., Staph, Klebsiella)
If CXR is inconclusive but suspicion high → CT chest (more sensitive)
CT Chest
- Reserved for:
- Complications
- Non-resolving pneumonia
- Immunocompromised
- Suspected malignancy
3. Laboratory Investigations
Routine Tests
- CBC (↑ WBC / leukopenia = severe)
- Neutrophilia with left shift
- CRP, Procalcitonin(bacterial > viral; helps in antibiotic stewardship)
- Renal function
- LFTs
- ABG (if hypoxemia)
4. Microbiological Work-up
Outpatients
- Not routinely required
Hospitalized / Severe CAP
- Sputum Gram stain & culture
- Blood cultures (before antibiotics)
- Urinary antigen:
- Streptococcus pneumoniae
- Legionella
- Viral PCR (influenza, SARS-CoV-2)
Severity Assessment
CURB-65 Score
Parameter | Point |
Confusion | 1 |
Urea >7 mmol/L | 1 |
RR ≥30/min | 1 |
BP <90 systolic or ≤60 diastolic | 1 |
Age ≥65 | 1 |
Interpretation
- 0–1: Outpatient
- 2: Hospital admission
- ≥3: Severe CAP → ICU(ICU admission based on ATS/IDSA criteria, not CURB-65 alone)
PSI (Pneumonia Severity Index)
- More accurate but complex
- Preferred for mortality prediction
ATS/IDSA Severe CAP Criteria (2019)
Major Criteria (Any 1 = ICU)
- Septic shock requiring vasopressors
- Respiratory failure requiring mechanical ventilation
Minor Criteria (≥3 = ICU)
- RR ≥30
- PaO₂/FiO₂ ≤250
- Multilobar infiltrates
- Confusion
- Uremia
- Leukopenia
- Thrombocytopenia
- Hypothermia
- Hypotension requiring fluids
Management
A. General Measures
- Oxygen therapy (target SpO₂ ≥92%)
- IV fluids (avoid overload)
- Antipyretics
- Early mobilization
- DVT prophylaxis (hospitalized)
B. Empiric Antibiotic Therapy (ATS/IDSA 2019)
1. Outpatient – No Comorbidities
- Amoxicillin
- OR Doxycycline
- OR Macrolide (only if pneumococcal resistance <25%)
2. Outpatient – With Comorbidities
(Chronic heart/lung/liver/kidney disease, diabetes, alcoholism)
- β-lactam (Amoxicillin-clavulanate or Cefuroxime)
PLUS macrolide or doxycycline
OR - Respiratory fluoroquinolone (Levofloxacin / Moxifloxacin)
3. Inpatient – Non-Severe CAP
- β-lactam + macrolide
- Ceftriaxone + Azithromycin
OR
- Ceftriaxone + Azithromycin
- Respiratory fluoroquinolone alone
4. Severe CAP (ICU)
- β-lactam + macrolide
OR - β-lactam + fluoroquinolone
5. MRSA Risk
(Add if prior MRSA, post-influenza, necrotizing pneumonia)
- Vancomycin
- Linezolid (preferred if necrotizing)
6. Pseudomonas Risk
(Add if structural lung disease, recent antibiotics)
- Piperacillin-tazobactam
- Cefepime
- Meropenem
Duration of Therapy
- Minimum 5 days
- Patient must be:
- Afebrile ≥48 hrs
- Clinically stable
Severe CAP: 7–10 days
MRSA / Pseudomonas: 10–14 days
Adjunctive Therapies
Corticosteroids
- NOT routine
- Consider if:
- Refractory septic shock
- Severe CAP with high inflammatory markers (selected cases)
Complications
Pulmonary
- Parapneumonic effusion
- Empyema
- Lung abscess
- ARDS
Systemic
- Sepsis
- Septic shock
- AKI
- Multiorgan failure
Non-Resolving Pneumonia
Defined as:
- No clinical improvement after 48–72 hrs
- Radiological non-resolution after 6–8 weeks
Causes:
- Wrong diagnosis
- Resistant organisms
- Tuberculosis
- Malignancy
- Pulmonary embolism
Prevention
Vaccination
- Pneumococcal vaccine
- PCV13 + PPSV23 (as per age/risk)
- Influenza vaccine (annual)
- COVID-19 vaccination
Risk Factor Control
- Smoking cessation
- Alcohol moderation
- Chronic disease control
