Community-Acquired Pneumonia
Pneumonia acquired outside of hospital or within 48 hours of admission. Most commonly caused by S. pneumoniae. Severity assessed using CURB-65 score.
Key Facts
S. pneumoniae causes 30-40% of CAP; followed by H. influenzae, M. pneumoniae, Legionella CURB-65 score determines management setting and antibiotic choice (NICE CG191) Amoxicillin 500mg TDS for 5 days is first-line for low-severity CAP Dual therapy (amoxicillin + clarithromycin) for moderate-severe CAP to cover atypical organisms Urinary antigens for pneumococcal and Legionella in moderate-severe cases Follow-up CXR at 6 weeks: essential to confirm resolution and exclude underlying malignancy Parapneumonic effusion occurs in ~40% of hospitalised CAP; empyema in ~5% 30-day mortality: score 0 (~0.7%), score 2 (~13%), score 5 (~57%)
Overview
Key Facts
Community-acquired pneumonia (CAP) is defined as an acute lower respiratory tract infection with radiological evidence of consolidation, acquired outside hospital or within 48 hours of admission. It is the most common infectious cause of death in developed countries.
Epidemiology
- Incidence: 5-11 per 1,000 adults per year in the UK
- Peak incidence in winter months
- Higher in extremes of age, immunosuppressed, chronic lung disease
- 22-42% require hospitalisation
- 5-10% of hospitalised CAP patients require ICU admission
Aetiology
- Streptococcus pneumoniae (~30-40%): most common; rusty sputum, lobar consolidation
- Haemophilus influenzae (~5-10%): COPD patients
- Mycoplasma pneumoniae (~5-15%): younger adults, 4-yearly epidemics, extrapulmonary features
- Legionella pneumophila (~2-5%): travel, cooling towers; hyponatraemia, deranged LFTs
- Staphylococcus aureus (~1-5%): post-influenza, IV drug users, cavitation
- Chlamydophila pneumoniae, psittaci: atypical pattern
- Viruses: influenza, SARS-CoV-2, RSV (~15-30% of cases)
- No organism identified in ~40-60% of cases
Pathophysiology
- Microaspiration of oropharyngeal organisms overwhelms local defences
- Alveolar macrophages and neutrophils initiate inflammatory response
- Exudate fills alveoli causing consolidation and impaired gas exchange
- Bacteraemia occurs in ~10-25% of pneumococcal pneumonia
- Parapneumonic effusion from pleural inflammation; empyema if infected
Clinical Presentation
Typical (Bacterial) Presentation
- Acute onset productive cough (purulent or rusty sputum)
- High fever with rigors
- Pleuritic chest pain
- Dyspnoea
- Tachycardia, tachypnoea
- Signs of consolidation: bronchial breathing, dull percussion, increased vocal resonance
Atypical Presentation
- Dry cough, gradual onset
- Headache, myalgia, malaise
- Extrapulmonary features (M. pneumoniae: erythema multiforme, cold agglutinins; Legionella: confusion, hyponatraemia, diarrhoea)
- Patchy rather than lobar infiltrates
Elderly Presentation
- Confusion or functional decline may be sole presentation
- Often afebrile
- Falls
Red Flags
- CURB-65 ≥3
- SpO₂ <92%
- Bilateral or multilobar disease
- Haemodynamic instability
- Failure to improve after 48 hours of appropriate antibiotics
- Cavitation on CXR (abscess, TB, Klebsiella, Staph aureus)
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Pulmonary embolism | Acute dyspnoea, pleuritic pain, VTE risk factors | CTPA, D-dimer |
| Acute exacerbation of COPD | Known COPD, no consolidation on CXR | CXR, spirometry |
| Tuberculosis | Chronic symptoms, upper lobe cavitation, weight loss | Sputum AFB, CXR, IGRA |
| Lung cancer | Non-resolving consolidation, weight loss, haemoptysis | CT, bronchoscopy |
| Heart failure (pulmonary oedema) | Bilateral effusions, cardiomegaly, oedema | BNP, echo, CXR |
| Organising pneumonia | Non-resolving consolidation, migratory infiltrates | HRCT, biopsy |
| Eosinophilic pneumonia | Eosinophilia, migratory infiltrates | FBC, BAL |
| Pulmonary haemorrhage | Haemoptysis, anaemia, renal impairment | CT, ANCA, anti-GBM |
Diagnosis / Investigation
Bedside
- Pulse oximetry: SpO₂ on air
- ABG: if SpO₂ <92% or severe features
- CURB-65 score: calculate on admission
- Urinary antigens: pneumococcal + Legionella (moderate-severe)
Bloods
- FBC: leucocytosis, or leucopenia (poor prognosis)
- CRP: elevated; monitor for treatment response
- U&Es: urea >7 (CURB-65), renal function
- LFTs: deranged in Legionella
- Blood cultures x2: before antibiotics in moderate-severe
- Procalcitonin: may guide antibiotic duration
- Lactate: if sepsis suspected
Imaging
- CXR PA: lobar consolidation, air bronchograms, parapneumonic effusion
- Repeat CXR at 6 weeks: essential in all patients to confirm resolution (NICE CG191)
- CT chest: non-resolving, complicated, or alternative diagnosis
- Pleural USS: guide aspiration of effusion
Special Tests
- Sputum MC&S: before antibiotics where possible
- Pleural fluid analysis: if significant effusion (pH, protein, LDH, glucose, MC&S, cytology)
- Mycoplasma serology: IgM (acute), complement fixation titre
- Legionella PCR: on respiratory samples
- Viral PCR: influenza, SARS-CoV-2, RSV (nasal/throat swab)
- Bronchoscopy with BAL: immunocompromised or non-resolving
Management
Non-pharmacological
- Supplemental oxygen (target SpO₂ 94-98% or 88-92% if COPD risk)
- IV fluid resuscitation if septic or dehydrated
- Adequate analgesia for pleuritic pain (paracetamol, NSAIDs if no contraindication)
- VTE prophylaxis (enoxaparin 40mg SC OD)
- Nutritional support
Pharmacological
NICE CG191 empirical antibiotics:
Low severity (CURB-65 0-1):
- Amoxicillin 500mg TDS PO for 5 days
- Penicillin allergy: doxycycline 200mg then 100mg OD or clarithromycin 500mg BD
Moderate severity (CURB-65 2):
- Amoxicillin 500mg TDS PO + clarithromycin 500mg BD PO for 5 days
- Penicillin allergy: doxycycline 200mg then 100mg OD
High severity (CURB-65 3-5):
- Co-amoxiclav 1.2g IV TDS + clarithromycin 500mg IV BD
- Switch to oral at 48-72 hours when improving
- Total course: 7-10 days for severe (may be shorter for uncomplicated)
Specific pathogens:
- Legionella: fluoroquinolone or clarithromycin ± rifampicin; notifiable disease
- Influenza-associated: oseltamivir 75mg BD + anti-staphylococcal cover
- PVL-producing Staph aureus: linezolid + clindamycin (suppress toxin) + rifampicin
Surgical/Interventional
- Chest drain insertion for empyema (pH <7.2) or large complicated effusion
- Intrapleural fibrinolytics (alteplase 10mg + DNase 5mg BD) for loculated empyema
- CT-guided drainage for lung abscess not responding to antibiotics
Referral Criteria
- ICU if CURB-65 ≥3 or clinical deterioration
- Non-resolving pneumonia at 6 weeks: respiratory/radiology review
- Recurrent pneumonia same lobe: bronchoscopy to exclude obstruction
- Immunocompromised patients: early infectious diseases/respiratory input
Prognosis
- Outpatient CAP mortality: <1%
- Hospitalised CAP mortality: 5-10%
- ICU-admitted CAP: 25-50% mortality
- CURB-65 score 0: ~0.7% mortality; score 5: ~57% mortality
- Pneumococcal bacteraemia mortality: ~20%
- Most improve within 48-72 hours of appropriate antibiotics
- CXR resolution: 50% at 2 weeks, 75% at 6 weeks, 95% at 12 weeks
- Post-pneumonia cardiovascular events increased for 1-2 years
- Pneumococcal vaccination reduces invasive disease by ~50-80% in elderly
Other Relevant Information
CURB-65 Score Interpretation
| Score | 30-day Mortality | Action |
|---|---|---|
| 0 | 0.7% | Home treatment |
| 1 | 3.2% | Home or short admission |
| 2 | 13% | Hospital admission |
| 3 | 17% | Hospital; assess for ICU |
| 4 | 41.5% | ICU admission |
| 5 | 57% | ICU admission |
Common Organisms and Clues
| Organism | Clinical Clue |
|---|---|
| S. pneumoniae | Rusty sputum, lobar consolidation, acute onset |
| H. influenzae | COPD, purulent sputum |
| M. pneumoniae | Young adult, dry cough, erythema multiforme, cold agglutinins |
| Legionella | Travel, hyponatraemia, LFT derangement, confusion, diarrhoea |
| S. aureus | Post-influenza, IV drug use, cavitating |
| Klebsiella | Alcoholism, red-currant jelly sputum, upper lobe, cavitating |