TextbookRespiratory MedicineAspiration Pneumonia

Aspiration Pneumonia

Pulmonary infection resulting from inhalation of oropharyngeal or gastric contents into the lower airways. Commonly affects the right lower lobe due to anatomy of the right main bronchus.

Key Facts

Risk factors: reduced consciousness (stroke, anaesthesia, alcohol), dysphagia (neurological disease), GORD, NG tube, poor dentition, oesophageal pathology Right lower lobe most commonly affected (right main bronchus is wider, shorter, and more vertical) Organisms: mixed oropharyngeal flora including anaerobes (Bacteroides, Fusobacterium, Peptostreptococcus) + aerobes (S. pneumoniae, S. aureus, Gram-negatives) Distinguish from aspiration pneumonitis (chemical inflammation without initial infection — Mendelson syndrome) Antibiotic: co-amoxiclav 1.2g IV TDS provides aerobic + anaerobic cover; metronidazole 400mg TDS if penicillin allergic (with another agent) Lung abscess is a recognised complication; may require prolonged antibiotics (4-6 weeks) or percutaneous drainage SALT (speech and language therapy) assessment is essential for swallowing assessment and aspiration prevention Mortality: ~20-30% in hospitalised patients

Overview

Key Facts

Aspiration pneumonia is a lung infection caused by the inhalation of colonised oropharyngeal or gastric contents into the lower respiratory tract. It should be distinguished from aspiration pneumonitis, which is a chemical inflammatory response to aspirated gastric acid without initial bacterial infection.

Epidemiology

  • Accounts for ~5-15% of community-acquired pneumonia cases
  • Up to 50% of pneumonias in nursing home residents
  • Incidence increases markedly with age (>75 years) and institutional care
  • Stroke patients: 30-50% aspirate; ~15-25% of these develop pneumonia

Aetiology

  • Mixed oropharyngeal flora: anaerobes (Bacteroides, Fusobacterium, Peptostreptococcus, Prevotella) + aerobes
  • Community-acquired: S. pneumoniae, H. influenzae + anaerobes
  • Hospital-acquired: Gram-negative bacilli, S. aureus, Pseudomonas + anaerobes
  • Poor oral hygiene significantly increases anaerobic load

Pathophysiology

  • Aspiration of oropharyngeal secretions colonised with pathogenic bacteria
  • Normal protective mechanisms impaired: cough reflex, mucociliary clearance, epiglottic closure
  • Gravity-dependent segments affected: right lower lobe (upright), posterior segments of upper lobes (supine)
  • Aspiration → chemical pneumonitis (hours) → bacterial superinfection (24-72 hours)
  • Necrotising pneumonia may develop with anaerobes → lung abscess → empyema

Clinical Presentation

Typical Presentation

  • Cough with foul-smelling purulent sputum (anaerobic infection)
  • Fever (may be low-grade initially)
  • Breathlessness
  • Witnessed aspiration event in some cases
  • Usually in context of known risk factor (stroke, altered consciousness, dysphagia)

Clinical Signs

  • Signs of consolidation, typically right lower lobe
  • Pyrexia
  • Tachypnoea, tachycardia
  • Reduced SpO₂
  • Poor dentition (significant risk factor)

Aspiration Pneumonitis vs Pneumonia

  • Pneumonitis (Mendelson syndrome): acute chemical lung injury from gastric acid; rapid onset (hours), diffuse bilateral crackles, self-limiting in ~48-72 hours without antibiotics
  • Pneumonia: bacterial infection; slower onset (24-72 hours post-aspiration), localised consolidation, purulent sputum

Red Flags

  • Lung abscess (non-resolving consolidation, air-fluid level on CXR)
  • Empyema
  • Rapidly progressive necrotising pneumonia
  • Recurrent aspiration events
  • Inability to protect airway

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Aspiration pneumonitisAcute onset post-aspiration, bilateral infiltrates, no infection initiallyClinical, CXR
Community-acquired pneumoniaNo aspiration risk factor, typical organismsCURB-65, CXR, cultures
Lung abscessCavitation, air-fluid level, prolonged symptomsCXR, CT
Pulmonary embolismPleuritic pain, risk factors, no consolidationCTPA
TuberculosisChronic, upper lobe cavitation, weight lossSputum AFB
Bronchial obstruction (tumour)Recurrent same-lobe pneumonia, non-resolvingBronchoscopy, CT

Diagnosis / Investigation

Bedside

  • Pulse oximetry: assess oxygenation
  • ABG: if SpO₂ <92%
  • SALT assessment: swallowing evaluation to prevent recurrence

Bloods

  • FBC: leucocytosis
  • CRP: elevated
  • U&Es: renal function, hydration status
  • Blood cultures: before antibiotics in moderate-severe
  • Procalcitonin: distinguish pneumonitis from pneumonia

Imaging

  • Chest X-ray: consolidation (typically right lower lobe), air-fluid level (abscess)
  • CT chest: if abscess suspected, non-resolving, or to guide drainage

Special Tests

  • Sputum MC&S: anaerobic and aerobic cultures
  • Bronchoscopy: if foreign body suspected or non-resolving
  • Video fluoroscopy/FEES: formal swallowing assessment
  • Barium swallow: if oesophageal pathology or fistula suspected

Management

Non-pharmacological

  • Nil by mouth until SALT assessment
  • Positioning: sit upright (30-45° head-of-bed elevation)
  • Oral hygiene: regular mouth care, dental assessment
  • Oxygen therapy (target SpO₂ 94-98%)
  • IV fluids if nil by mouth or dehydrated
  • NG tube feeding only after SALT assessment (NG tubes themselves increase aspiration risk)

Pharmacological

Antibiotics (must cover anaerobes):

  • Co-amoxiclav 1.2g IV TDS (covers aerobes + anaerobes) — first-line
  • Or amoxicillin 1g IV TDS + metronidazole 500mg IV TDS
  • Penicillin allergy: clindamycin 600mg IV QDS or moxifloxacin 400mg OD
  • Hospital-acquired aspiration: piperacillin-tazobactam 4.5g IV TDS
  • Duration: 7-14 days (longer for abscess/empyema — up to 4-6 weeks)

Lung abscess:

  • Prolonged antibiotics (4-6 weeks minimum)
  • Co-amoxiclav or piperacillin-tazobactam
  • CT-guided percutaneous drainage if >6cm or failed medical therapy

Surgical/Interventional

  • Chest drain for empyema
  • CT-guided drainage for lung abscess
  • Tracheostomy for patients with recurrent aspiration and inability to protect airway
  • PEG feeding: consider for chronic dysphagia (though does not eliminate aspiration risk)

Referral Criteria

  • SALT assessment for all patients with aspiration pneumonia
  • Respiratory referral for recurrent aspiration or lung abscess
  • ENT/gastroenterology for structural causes of aspiration
  • Palliative care if aspiration due to end-stage neurological disease

Prognosis

  • Mortality: ~20-30% for hospitalised aspiration pneumonia
  • Higher mortality in elderly, nursing home residents, and mechanically ventilated patients
  • Lung abscess mortality: ~5-10% with appropriate treatment
  • Recurrence rate is high (~30%) without addressing underlying cause
  • Chronic aspiration leads to progressive lung damage and bronchiectasis
  • Outcomes improve with early SALT assessment and dysphagia management

Other Relevant Information

Risk Factors for Aspiration

FactorMechanism
StrokeImpaired swallowing reflex
Reduced consciousness (alcohol, drugs, anaesthesia)Loss of airway protection
Parkinson diseaseOropharyngeal dysphagia
Motor neurone diseaseBulbar weakness
Oesophageal disorders (achalasia, stricture)Regurgitation
GORDAcid reflux and microaspiration
NG/PEG tubeAltered oesophageal sphincter function
Poor dentitionHigh oral bacterial load
Mechanical ventilationBypasses upper airway defences

Aspiration Pneumonitis vs Pneumonia

FeaturePneumonitisPneumonia
CauseChemical (gastric acid)Bacterial infection
OnsetHours24-72 hours
CXRBilateral, diffuseLocalised consolidation
SputumNon-purulentPurulent, foul-smelling
TreatmentSupportive (no initial antibiotics)Antibiotics essential