What is the recommended nebulisation protocol for acute respiratory symptoms?

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Nebulisation Protocol for Acute Respiratory Symptoms

For acute severe asthma, administer nebulised salbutamol 5 mg (or terbutaline 10 mg) driven by oxygen at 6-8 L/min, repeated every 20-30 minutes for the first hour, then 4-6 hourly; add ipratropium bromide 500 µg if poor initial response. 1

Equipment Setup

Driving Gas Selection

  • Use oxygen as the driving gas only in acute severe asthma because these patients are hypoxic and require simultaneous treatment of both bronchospasm and hypoxemia 1, 2
  • Use compressed air (not oxygen) for COPD exacerbations to prevent worsening carbon dioxide retention and acidosis 1, 3
  • If supplemental oxygen is needed during air-driven nebulisation, administer low-flow oxygen (4 L/min) via nasal cannulae simultaneously 1, 2

Flow Rate and Equipment

  • Set gas flow rate at 6-8 L/min to generate particles of 2-5 µm diameter for optimal small airway deposition 1, 2
  • Use jet nebulisers with electrical compressors (more accurate and cost-effective than cylinder flow meters) 1, 2
  • Fill nebuliser chamber with 2.0-4.5 ml total volume; if residual volume >1.0 ml, make up drug volume to minimum 4.0 ml with 0.9% sodium chloride (never water, which causes bronchoconstriction) 1

Drug Dosing by Condition

Acute Severe Asthma (Adults)

Severity criteria: Cannot complete sentences, respiratory rate ≥25/min, heart rate ≥110/min, peak flow ≤50% predicted 1

Initial treatment:

  • Salbutamol 5 mg OR terbutaline 10 mg via oxygen-driven nebuliser 1, 3
  • Repeat every 20-30 minutes for first hour if improving 1
  • Add ipratropium bromide 500 µg if poor response after first dose 1, 3
  • Combined therapy (salbutamol + ipratropium) provides 16-32% greater peak flow improvement than salbutamol alone 4, 5

Ongoing treatment:

  • Continue 4-6 hourly until peak flow >75% predicted and diurnal variability <25% 1
  • For severe cases, frequent dosing of 0.3 mg/kg salbutamol hourly (maximum 10 mg/hour) or 1-3 mg/hour terbutaline may be used 1

Acute Severe Asthma (Children)

Severity criteria: Cannot talk or feed, respiratory rate >50/min, heart rate >140/min, peak flow <50% predicted 1

  • Salbutamol 5 mg (or 0.15 mg/kg) OR terbutaline 10 mg (or 0.3 mg/kg) 1
  • Repeat 1-4 hourly if improving 1
  • If no improvement at 30 minutes, add ipratropium bromide 250 µg and continue hourly 1

COPD Exacerbations

Mild exacerbations:

  • Use hand-held inhaler with salbutamol 200-400 µg or terbutaline 500-1000 µg 1

Moderate-to-severe exacerbations:

  • Salbutamol 2.5-5 mg OR terbutaline 5-10 mg OR ipratropium bromide 500 µg 1, 3
  • Give 4-6 hourly for 24-48 hours or until clinical improvement 1
  • Use combined therapy (β-agonist 2.5-10 mg + ipratropium 250-500 µg) in severe cases or poor response to monotherapy 1
  • Critical: Drive nebuliser with air if patient has carbon dioxide retention/acidosis or if blood gases cannot be measured 1, 3

Administration Technique

Interface Selection

Use masks for:

  • Acutely ill patients (too breathless to hold mouthpiece) 1
  • Babies and young children with poor coordination 1

Use mouthpieces for:

  • Nebulised steroids (prevents facial deposition) 1
  • Nebulised antibiotics (allows filter attachment) 1
  • Anticholinergics in patients at risk for glaucoma 1, 3
  • When using ipratropium, ensure tight-fitting mask or mouthpiece to prevent eye contact causing pupil dilation or glaucoma precipitation 3, 6

Treatment Duration

  • Bronchodilators: 10 minutes should be sufficient 1
  • Continue until approximately 1 minute after "spluttering" occurs (5-15 minutes typical) 1, 6
  • Tap nebuliser cup toward end of treatment to mobilize remaining solution 1
  • Do not use "dryness" as endpoint; specify upper time limit 1

Drug Compatibility and Mixing

  • Ipratropium bromide can be mixed with salbutamol or terbutaline in the nebuliser if used within 1 hour 6
  • Do not mix with other drugs; stability and safety not established 6
  • Never use water as diluent—only 0.9% sodium chloride 1, 2

Critical Safety Considerations

Common Pitfalls to Avoid

  • Never use oxygen-driven nebulisers routinely in COPD due to carbon dioxide retention risk 1, 2
  • Measure arterial blood gases in hospitalized patients; if CO₂ retention present, use air-driven nebulisation 1
  • Continuous nebulisation shows no advantage over intermittent dosing in acute severe asthma 7
  • MDI with spacer may be equally effective as nebulisation but is not yet widely adopted in acute settings 1, 8

Monitoring Response

  • Reassess at 15,30,60,120,180, and 240 minutes 4
  • Failure to respond or shortened duration of effect is a warning sign requiring urgent medical attention 1
  • Switch to hand-held inhaler 24-48 hours before hospital discharge 1

Equipment Maintenance

  • Wash mouthpiece/mask and nebuliser chamber after every use (minimum once daily) with warm water and detergent, rinse thoroughly, and dry completely 1
  • Change disposable components (tubing, nebuliser cup, mask/mouthpiece) every 3 months 1, 3
  • Service compressors annually 1
  • For antibiotics, use separate equipment and change every 3 months; use filters to prevent environmental contamination 1, 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Compressed Air for Nebulization in Respiratory Conditions

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Medication Delivery via Nebulizers

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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