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Airway clearance techniques: overview and choice

Four papers asked a broad 7-mark question: "various airway clearance techniques with application, advantages and disadvantages" (S19, W24) and "mucus removal techniques in chronic respiratory disease" (W19), plus indications of bronchial hygiene therapy (W25). This card is the one-page answer; the detail of each technique is on its own card.

Syllabus
Ch 4(a) Bronchial hygiene therapy; 4(b) adjunct therapy
Priority
High yield. Asked as a 7-mark overview in 3 papers and as 3 marks in 1 (2016–2026).
Asked as
7m S19W19W24 3m W25
Usual split
7-mark overview table; 3-mark indications
Checked against
BTS/ACPRC physiotherapy guideline (2009); ERS bronchiectasis guideline (2025); Cystic Fibrosis Trust physiotherapy standards (2026). Full list under Sources.
Content checked
19 October 2026. Next review due October 2027.
My revision

1Why airway clearance is needed

Healthy airways clear mucus by the mucociliary escalator (cilia sweep a thin mucus layer upwards) and by coughing. Airway clearance techniques (ACTs) are needed when:

  • there is too much mucus, or it is too thick (bronchiectasis, cystic fibrosis, COPD with chronic bronchitis, chest infection);
  • the cilia work poorly (smoking, cystic fibrosis, ciliary dyskinesia, dry gas through a tracheal tube);
  • the cough is weak or painful (neuromuscular disease, after surgery, sedation).

Aims: remove mucus, reduce infections and the "vicious cycle" of infection and inflammation, improve ventilation and gas exchange, reduce cough and breathlessness, and improve quality of life.

2Classification

  • Breathing techniques: active cycle of breathing technique (ACBT), forced expiration technique and huffing, autogenic drainage, directed or assisted cough.
  • Gravity and manual techniques: postural drainage, percussion, vibration, shaking.
  • Positive expiratory pressure devices: PEP mask, oscillating PEP (Flutter, Acapella), bottle PEP.
  • Mechanical devices: chest wall oscillation vest, intrapulmonary percussive ventilation, cough assist (insufflation–exsufflation), IPPB.
  • Exercise (increases ventilation and loosens mucus).
  • Adjuncts: hydration and humidification, nebulised saline (normal or hypertonic), mucolytics, bronchodilator before treatment.
  • Suction when the patient cannot cough secretions out.

3Application, advantages and disadvantages (S19, W24)

TechniqueBest applied inAdvantagesDisadvantages
ACBTMost patients with sputum; post-op; exacerbations; asthma with mucusEasy to learn; no equipment; independent; adaptable to any positionNeeds co-operation; not for young children or confused patients
Autogenic drainageBronchiectasis, cystic fibrosis (older children and adults); unstable, wheezy airwaysGentle: little airway collapse, bronchospasm or desaturation; no equipmentHard to learn; slow (30–45 minutes); needs concentration
Postural drainage with percussion and vibrationLocalised disease in a known lobe; infants; dependent or ventilated patientsTargets a lobe; can be done by a carerTime-consuming; head-down tilt has many contraindications (reflux, breathlessness, raised ICP); usually needs a helper
PEP maskCystic fibrosis, bronchiectasis; post-op lung expansionIndependent, quick, portable; can combine with a nebuliserNeeds a device and training; not with untreated pneumothorax
Oscillating PEP (Flutter, Acapella)Bronchiectasis, cystic fibrosis, COPD with sputumAdds vibration; small; easy; motivatingCost; Flutter only works upright; must be cleaned well
Chest wall oscillation vestCystic fibrosis, neuromuscular diseaseHands-free; several areas at onceVery expensive; not portable
Cough assist and assisted coughWeak cough: neuromuscular disease, spinal cord injuryProduces an effective cough when muscles cannotEquipment and training; care with bullae and pneumothorax
ExerciseAll mobile patients, as part of the routineAlso improves fitness; enjoyableDoes not replace airway clearance for most people with daily sputum
SuctionIntubated, unconscious or very weak patientsRemoves central secretions directlyInvasive; hazards (hypoxaemia, bradycardia, trauma)

4Choosing a technique

  • No single technique is best for everyone (BTS/ACPRC 2009); short-term studies show they all help clear sputum. Choose by the patient's age, condition, ability, preference and what they will actually keep doing.
  • Children: infants need modified postural drainage, gentle percussion and active play; older children PEP, bubble PEP and ACBT.
  • Unstable airways or wheeze with forced breaths: autogenic drainage, PEP.
  • Weak cough: assisted cough, cough assist, suction.
  • Order with medicines: bronchodilator → mucoactive drug (for example hypertonic saline) → airway clearance → inhaled antibiotic or steroid.
  • Review the technique regularly; adjust frequency during exacerbations.

5Mucus removal in chronic respiratory disease (7 marks in W19)

  1. Assess: daily sputum amount and colour, how easily it comes up, X-ray or CT (which lobes), breathlessness, previous techniques.
  2. Prepare the mucus: enough fluids; humidified or nebulised saline if sputum is thick; bronchodilator first in reactive airways.
  3. Daily routine: one main technique (ACBT, autogenic drainage or oscillating PEP), in a gravity-assisted position for the worst lobe if tolerated; 10–30 minutes, once or twice a day.
  4. Exacerbation plan: increase to 2–3 times a day; early medical review for antibiotics.
  5. Exercise: regular aerobic exercise as part of pulmonary rehabilitation.
  6. Pelvic floor: ask about urine leakage with coughing (common in women) and teach pelvic floor contraction before huffs and coughs.
  7. Review: outcome measures such as sputum weight, cough or bronchiectasis quality-of-life scores, exacerbation count.

6Indications of bronchial hygiene therapy (3 marks in W25)

  • Large amounts of sputum (classically more than about 25–30 mL a day) or difficulty clearing it.
  • Mucus plugging with lobar or segmental collapse.
  • Weak or painful cough: neuromuscular disease, after surgery, sedated or ventilated patients.
  • Chronic suppurative lung disease (bronchiectasis, cystic fibrosis) as a daily routine.

7Exam corner

Past questions (MUHS, 2016–2026)

  • 7-mark questionsVarious airway clearance techniques: application, advantages and disadvantages of each (S19). Mucus removal techniques in chronic respiratory disease (W19). Various airway clearance techniques (W24).
  • 3-mark questionThree indications of bronchial hygiene therapy (W25).

Answer skeleton: "various airway clearance techniques", 7 marks

  1. [1] Why: mucociliary clearance and cough fail; aims of ACTs.
  2. [1] Classification list.
  3. [4] The comparison table for 5–6 techniques.
  4. [1] Choosing: no single best technique; patient factors; order with medicines.

Test yourself

3 mClassify airway clearance techniques with one example of each.

Breathing techniques (ACBT); gravity and manual (postural drainage with percussion); PEP devices (Acapella); mechanical devices (cough assist); exercise; adjuncts (nebulised hypertonic saline); suction.

MCQWhich technique is most suitable for a 3-month-old with cystic fibrosis?A. Autogenic drainage done by the infantB. Modified postural drainage with gentle percussion and active playC. FlutterD. Incentive spirometry

B. Infants cannot do active techniques; drainage without head-down tilt, gentle percussion and play are used.

 Sources

  1. MUHS BPTh syllabus (2012) and MUHS IV BPTh question papers 2016–2026 (muhsonline.com, unofficial archive; Dhole Patil College of Physiotherapy past-paper page).
  2. Bott J, et al. Guidelines for the physiotherapy management of the adult, medical, spontaneously breathing patient (BTS/ACPRC). Thorax 2009;64 Suppl 1:i1–51.
  3. European Respiratory Society guideline for the management of adult bronchiectasis (2025 update).
  4. Cystic Fibrosis Trust. Standards of care and good clinical practice for the physiotherapy management of cystic fibrosis, 5th edition (2026).
  5. Structure and classical content: Pryor & Prasad (2008); Main & Denehy (2016); Frownfelter & Dean (2022).

Educational notes for exam preparation. Not medical advice.

Version 1. Content checked 19 October 2026. Next review October 2027.