The autogenic drainage breathing technique for helping people with cystic fibrosis to clear mucus from their airways


Cystic fibrosis affects the lungs by producing thick mucus lining the airways. This can lead to infection and inflammation causing lung damage. Physiotherapy can help to keep the airways clear of mucus and there are many methods used to do this including breathing techniques, manual techniques and mechanical devices. Autogenic drainage is a very controlled technique of breathing which uses different depths and speeds of exhaled breath to move mucus up the airways resulting in a spontaneous or voluntary cough. It can be used without help, but requires training, concentration and effort. We looked at the effect of using autogenic drainage on lung function measurements and quality of life in people with cystic fibrosis, to discover whether using autogenic drainage was better or worse than other existing physiotherapy techniques for clearing the lungs.

Search date

The evidence is current to: 06 July 2021.

Study characteristics

We searched the literature for studies comparing at least two sessions of autogenic drainage with other breathing techniques and devices which help to clear the lungs of mucus. We included eight studies in the review involving 212 people with cystic fibrosis, aged between seven and 63 years of age. People were randomly selected for one physiotherapy treatment or the other. The number of people in the studies ranged from 4 to 75, and had a wide range of disease severity. The studies lasted from four days to two years in total.

Key results

We did not find any clear evidence that autogenic drainage was better than the other techniques for lung function or quality of life in either the short-term or long-term studies. This was also true for our other outcome measures such as hospital admissions, additional antibiotic treatment, exercise tolerance and oxygen saturation, but people in one study autogenic drainage preferred autogenic drainage compared to postural drainage and percussion. The authors of this review wanted to compare exercise to autogenic drainage for airway clearance, but found no studies with this comparison, even though exercise is often used as an alternative by people with cystic fibrosis.

Certainty of the evidence

Overall, the certainty of the evidence from the studies was judged to be mainly low or very low. The main problems for this being the small numbers of participants in each study, the unclear reporting of results in the studies and the study design used. In one study, which was classed as having a high risk of bias due to incomplete results, those taking part had to change physiotherapy technique halfway through the study and there were many who dropped out and did not comply with the postural drainage and percussion treatment arm.  Six of the eight studies used research staff to assess results who did not know which technique each person was using and this improved the quality of the evidence and reduced any bias in this respect.

Authors' conclusions: 

Autogenic drainage is a challenging technique that requires commitment from the individual. As such, this intervention merits systematic review to ensure its effectiveness for people with cystic fibrosis, particularly in an era where treatment options are changing rapidly. From the studies assessed, autogenic drainage was not found to be superior to any other form of airway clearance technique. Larger studies are required to better evaluate autogenic drainage in comparison to other airway clearance techniques in view of the relatively small number of participants in this review and the complex study designs. The studies recruited a range of participants and were not powered to assess non-inferiority. The varied length and design of the studies made the analysis of pooled data challenging.

Read the full abstract...

Autogenic drainage is an airway clearance technique that was developed by Jean Chevaillier in 1967. The technique is characterised by breathing control using expiratory airflow to mobilise secretions from smaller to larger airways. Secretions are cleared independently by adjusting the depth and speed of respiration in a sequence of controlled breathing techniques during exhalation. The technique requires training, concentration and effort from the individual but it has previously been shown to be an effective treatment option for those who are seeking techniques to support and promote independence.  However, at a time where the trajectory and demographics of the disease are changing, it is important to systematically review the evidence demonstrating that autogenic drainage is an effective intervention for people with cystic fibrosis.


To compare the clinical effectiveness of autogenic drainage in people with cystic fibrosis with other physiotherapy airway clearance techniques.

Search strategy: 

We searched the Cochrane Cystic Fibrosis Trials Register, compiled from electronic database searches and handsearching of journals and conference abstract books. We also searched the reference lists of relevant articles and reviews, as well as two ongoing trials registers (02 February 2021).

Date of most recent search of the Cochrane Cystic Fibrosis Trials Register: 06 July 2021.

Selection criteria: 

We identified randomised and quasi-randomised controlled studies comparing autogenic drainage to another airway clearance technique or no therapy in people with cystic fibrosis for at least two treatment sessions.

Data collection and analysis: 

Data extraction and assessments of risk of bias were independently performed by three authors. The authors assessed the quality of the evidence using the GRADE system. The authors contacted seven teams of investigators for further information pertinent to their published studies.

Main results: 

Searches retrieved 64 references to 37 individual studies, of which eight (n = 212) were eligible for inclusion. One study was of parallel design with the remaining seven being cross-over in design; participant numbers ranged from 4 to 75. The total study duration varied between four days and two years. The age of participants ranged between seven and 63 years with a wide range of disease severity reported. Six studies enrolled participants who were clinically stable, whilst participants in two studies received treatment whilst hospitalised with an infective exacerbation. All studies compared autogenic drainage to one (or more) other recognised airway clearance technique. Exercise is commonly used as an alternative therapy by people with cystic fibrosis; however, there were no studies identified comparing exercise with autogenic drainage.

The certainty of the evidence was generally low or very low. The main reasons for downgrading the level of evidence were the frequent use of a cross-over design, outcome reporting bias and the inability to blind participants.

The review's primary outcome, forced expiratory volume in one second, was the most common outcome measured and was reported by all eight studies; only three studies reported on quality of life (also a primary outcome of the review). One study reported on adverse events and described a decrease in oxygen saturation levels whilst performing active cycle of breathing techniques, but not with autogenic drainage. Seven of the eight included studies measured forced vital capacity and three of the studies used mid peak expiratory flow (per cent predicted) as an outcome. Six studies reported sputum weight. Less commonly used outcomes included oxygen saturation levels, personal preference, hospital admissions, intravenous antibiotics and pseudomonas gene expression. There were no statistically significant differences found between any of the techniques used with respect to the outcomes measured except when autogenic drainage was described as being the preferred technique of the participants in one study over postural drainage and percussion.