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DAILY THERAPY — AIRWAY CLEARANCE

Airway clearance therapy

A set of daily techniques and devices that loosen and move the thick mucus out of the lungs in cystic fibrosis, helping prevent infection and preserve lung function.
Treatments & procedures › Airway clearance therapy

What it is

In CF, thick sticky mucus clogs the airways and traps bacteria. Airway clearance therapy (ACT) physically loosens that mucus so it can be coughed out. Methods include chest physiotherapy (clapping/percussion and postural drainage), high-frequency chest wall oscillation using an inflatable “Vest,” positive expiratory pressure (PEP) and oscillating-PEP devices (like the Flutter or Acapella), and breathing techniques such as the active cycle of breathing and huff coughing. Most people with CF do some form of ACT every day, often paired with inhaled medicines.

How it’s done

Usually done once or more daily, typically for 20–30 minutes, and often combined with inhaled mucus-thinners and antibiotics (which are timed around clearance). The specific technique and device are chosen with the CF care team and respiratory therapist based on age, ability, and preference.

What to expect

ACT is an ongoing daily routine, not a one-time procedure. Consistency matters — regular clearance helps reduce infections and slow lung decline. Techniques are adjusted over time and during illness (“tune-ups”).

Considerations

  • Time-consuming — daily adherence can be a burden
  • Some positions or percussion aren’t suitable with reflux, certain surgeries, or bleeding
  • Devices need regular cleaning to avoid contamination
  • Best paired correctly with inhaled medicines (timing matters)

Alternatives

Inhaled mucus-thinners
Dornase alfa and hypertonic saline make mucus easier to clear
Exercise
Physical activity complements (but doesn’t fully replace) formal ACT
CFTR modulators
Reduce mucus burden for eligible patients but usually don’t eliminate ACT