Pneumonia
Acute infection of the lung parenchyma causing consolidation and impaired gas exchange. Classified by setting of acquisition: community-acquired (CAP), hospital-acquired (HAP), or aspiration.
Key Facts
Commonest cause of infection-related death in the UK; ~5-10% mortality for hospitalised CAP Most common organism: Streptococcus pneumoniae (~30-40% of CAP) CURB-65 score guides severity assessment and management setting: 0-1 (community), 2 (consider hospital), 3-5 (severe, consider ICU) NICE CG191: amoxicillin 500mg TDS for 5 days is first-line for low-severity CAP; add clarithromycin 500mg BD if moderate-severe CXR within 4 hours of hospital admission for suspected CAP Blood cultures and sputum MC&S before antibiotics in moderate-severe pneumonia Follow-up CXR at 6 weeks to confirm resolution and exclude underlying malignancy Annual influenza vaccination and pneumococcal vaccination reduce risk in at-risk groups
Overview
Key Facts
Pneumonia is an acute lower respiratory tract infection causing inflammation and consolidation of the lung parenchyma. It remains a major cause of morbidity and mortality, particularly in the elderly, immunocompromised, and those with chronic diseases.
Epidemiology
- Incidence: 5-11 per 1,000 adults per year in the UK
- ~300,000 adults diagnosed annually in the UK
- ~29,000 deaths per year in England and Wales from pneumonia
- 6th leading cause of death in the UK
- 5-10% mortality for hospitalised CAP; <1% for community-managed CAP
Aetiology
Community-acquired pneumonia (CAP):
- Streptococcus pneumoniae (30-40%) — most common
- Haemophilus influenzae (5-10%)
- Mycoplasma pneumoniae (5-15%, epidemic every 4 years)
- Staphylococcus aureus (1-5%, post-influenza)
- Legionella pneumophila (2-5%)
- Chlamydophila pneumoniae, Moraxella catarrhalis, respiratory viruses
Hospital-acquired pneumonia (HAP):
- Gram-negative bacilli (E. coli, Klebsiella, Pseudomonas)
- Staphylococcus aureus (including MRSA)
- Anaerobes
Pathophysiology
- Pathogen reaches alveoli via inhalation, aspiration, or haematogenous spread
- Alveolar macrophages and neutrophils mount inflammatory response
- Exudate fills alveoli → consolidation → impaired gas exchange
- Four pathological stages: congestion → red hepatisation → grey hepatisation → resolution
- Complications: parapneumonic effusion, empyema, lung abscess, ARDS, sepsis
Clinical Presentation
Typical Presentation
- Cough (productive with purulent or rusty sputum)
- Fever and rigors
- Pleuritic chest pain
- Breathlessness
- Malaise and myalgia
Clinical Signs
- Pyrexia (>38°C)
- Tachypnoea, tachycardia
- Reduced chest expansion on affected side
- Dull percussion note
- Bronchial breathing over consolidation
- Increased tactile vocal fremitus
- Coarse crackles
Atypical Presentations
- Elderly: confusion, falls, functional decline without fever
- Immunocompromised: indolent course, atypical organisms
- Atypical pneumonia: dry cough, headache, myalgia, extrapulmonary features
Red Flags
- CURB-65 score ≥3 (severe pneumonia)
- SpO₂ <92% or PaO₂ <8 kPa
- Bilateral or multilobar involvement
- Systolic BP <90 mmHg
- Confusion (new onset)
- Age >65 years
- Significant comorbidities
- Failure to respond to initial antibiotics within 48-72 hours
Differential Diagnosis
| Diagnosis | Key Features | Investigation |
|---|---|---|
| Pulmonary embolism | Pleuritic pain, haemoptysis, risk factors, tachycardia | CTPA, D-dimer |
| Lung cancer | Haemoptysis, weight loss, finger clubbing, non-resolving consolidation | CXR, CT, bronchoscopy |
| Tuberculosis | Chronic cough, weight loss, night sweats, upper lobe cavitation | CXR, sputum AFB, IGRA |
| Heart failure | Bilateral crackles, orthopnoea, oedema, raised JVP | BNP, CXR, echo |
| Pleural effusion | Stony dull percussion, reduced breath sounds | CXR, USS, diagnostic tap |
| Pulmonary vasculitis | Haemoptysis, systemic features, renal involvement | ANCA, urinalysis, CT |
| Cryptogenic organising pneumonia | Non-resolving consolidation despite antibiotics | HRCT, biopsy |
| Eosinophilic pneumonia | Blood/BAL eosinophilia, migratory infiltrates | FBC, BAL, CT |
Diagnosis / Investigation
Bedside
- Pulse oximetry: SpO₂ on air
- ABG: if SpO₂ <92% or severe pneumonia
- Urinary antigens: pneumococcal and Legionella (moderate-severe CAP)
- Sputum sample: MC&S before antibiotics if possible
Bloods
- FBC: leucocytosis (or leucopenia in severe sepsis)
- CRP: elevated; useful for monitoring response
- U&Es: urea (CURB-65 component), renal function
- LFTs: baseline; abnormal in Legionella, Mycoplasma
- Blood cultures: x2 before antibiotics in moderate-severe
- Procalcitonin: may guide antibiotic duration
- HIV test: consider in all pneumonia patients aged 15-59 (NICE)
Imaging
- Chest X-ray: within 4 hours of admission — lobar consolidation, air bronchograms, parapneumonic effusion
- Follow-up CXR at 6 weeks: confirm resolution, exclude underlying malignancy (especially smokers >50 years)
- CT chest: if non-resolving, complicated, or alternative diagnosis suspected
Special Tests
- Pleural fluid aspiration and analysis: if significant effusion (pH, glucose, protein, LDH, MC&S, cytology)
- Bronchoscopy with BAL: if immunocompromised, non-resolving, or unusual organism suspected
- Atypical serology: Mycoplasma IgM, Chlamydophila, Legionella if clinical suspicion
Management
Non-pharmacological
- Oxygen therapy (target SpO₂ 94-98%, or 88-92% if at risk of hypercapnia)
- IV fluids if dehydrated or unable to take oral
- Chest physiotherapy for sputum clearance
- VTE prophylaxis for inpatients (enoxaparin 40mg SC OD)
Pharmacological
NICE CG191 — empirical antibiotics for CAP:
Low severity (CURB-65 0-1, treat in community):
- Amoxicillin 500mg TDS for 5 days
- If penicillin allergic: doxycycline 200mg loading then 100mg OD, or clarithromycin 500mg BD
Moderate severity (CURB-65 2, consider hospital):
- Amoxicillin 500mg TDS PO + clarithromycin 500mg BD PO for 5 days
- If penicillin allergic: doxycycline 200mg then 100mg OD
High severity (CURB-65 3-5, hospital/ICU):
- Co-amoxiclav 1.2g IV TDS + clarithromycin 500mg IV BD
- Or piperacillin-tazobactam 4.5g IV TDS + clarithromycin 500mg IV BD if very severe
- Step down to oral when improving (typically 48-72 hours)
Specific organisms:
- Legionella: clarithromycin/azithromycin ± rifampicin (notify PHE)
- MRSA: vancomycin or linezolid
- Pseudomonas: piperacillin-tazobactam or meropenem
Surgical/Interventional
- Chest drain: for empyema or large complicated parapneumonic effusion
- CT-guided drainage: for lung abscess not responding to antibiotics
Referral Criteria
- CURB-65 ≥2: hospital admission
- CURB-65 ≥3: ICU assessment
- Non-resolving pneumonia at 6 weeks: urgent CXR, consider CT and respiratory referral
- Recurrent pneumonia in same lobe: bronchoscopy to exclude obstruction
Prognosis
- Community-managed CAP: mortality <1%
- Hospitalised CAP: mortality 5-10%
- ICU-admitted CAP: mortality 25-50%
- 30-day mortality by CURB-65: score 0 (~0.7%), 1 (~3.2%), 2 (~13%), 3 (~17%), 4 (~41.5%), 5 (~57%)
- Pneumococcal bacteraemia increases mortality 2-3 fold
- Most patients show clinical improvement within 48-72 hours of appropriate antibiotics
- CXR changes may take 6-8 weeks to resolve completely
- Long-term: pneumonia survivors have increased cardiovascular risk for 1-2 years post-event
Other Relevant Information
CURB-65 Score
| Factor | Points |
|---|---|
| Confusion (AMT ≤8 or new disorientation) | 1 |
| Urea >7 mmol/L | 1 |
| Respiratory rate ≥30/min | 1 |
| Blood pressure (SBP <90 or DBP ≤60 mmHg) | 1 |
| Age ≥65 years | 1 |
Management by CURB-65 Score
| Score | Mortality Risk | Management |
|---|---|---|
| 0-1 | Low (<3%) | Community treatment |
| 2 | Intermediate (~13%) | Hospital admission |
| 3-5 | High (>17%) | ICU assessment |
Light's Criteria (Exudative Effusion)
| Criterion | Value |
|---|---|
| Pleural protein/serum protein | >0.5 |
| Pleural LDH/serum LDH | >0.6 |
| Pleural LDH | >2/3 upper limit of normal |