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

DiagnosisKey FeaturesInvestigation
Pulmonary embolismPleuritic pain, haemoptysis, risk factors, tachycardiaCTPA, D-dimer
Lung cancerHaemoptysis, weight loss, finger clubbing, non-resolving consolidationCXR, CT, bronchoscopy
TuberculosisChronic cough, weight loss, night sweats, upper lobe cavitationCXR, sputum AFB, IGRA
Heart failureBilateral crackles, orthopnoea, oedema, raised JVPBNP, CXR, echo
Pleural effusionStony dull percussion, reduced breath soundsCXR, USS, diagnostic tap
Pulmonary vasculitisHaemoptysis, systemic features, renal involvementANCA, urinalysis, CT
Cryptogenic organising pneumoniaNon-resolving consolidation despite antibioticsHRCT, biopsy
Eosinophilic pneumoniaBlood/BAL eosinophilia, migratory infiltratesFBC, 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

FactorPoints
Confusion (AMT ≤8 or new disorientation)1
Urea >7 mmol/L1
Respiratory rate ≥30/min1
Blood pressure (SBP <90 or DBP ≤60 mmHg)1
Age ≥65 years1

Management by CURB-65 Score

ScoreMortality RiskManagement
0-1Low (<3%)Community treatment
2Intermediate (~13%)Hospital admission
3-5High (>17%)ICU assessment

Light's Criteria (Exudative Effusion)

CriterionValue
Pleural protein/serum protein>0.5
Pleural LDH/serum LDH>0.6
Pleural LDH>2/3 upper limit of normal