Article Text
PDF
Abstract
Introduction Non-invasive ventilation (NIV) is used in cystic fibrosis (CF) to support airway clearance techniques (ACTs) by augmenting tidal volumes and reducing patient effort. However, the evidence base for this is limited. We hypothesised that NIV, in addition to usual ACT, would increase sputum clearance. In addition, we investigated ease of sputum clearance (EoC), work of breathing (WoB) and NIV tolerability.
Methods Adults with CF (16+ years) at the end of hospitalisation for a pulmonary exacerbation were randomised to a cross-over trial of NIV-supported ACT or ACT alone in two consecutive days. No other changes to standard care were made. The primary outcome was the total 24-hour expectorated sputum wet weight after the intervention. Spirometry was completed pre-treatment and post-treatment. Oxygen saturations were measured pre-treatment, during treatment and post-treatment. EoC and WoB were assessed using Visual Analogue Scale.
Results 14 subjects completed the study (7 male, mean age 35 [SD 17] years, mean forced expiratory volume in 1 s [FEV1] 49 [20] % predicted). The difference between treatment regimens was −0.98 g sputum (95% CI −11.5 to 9.6, p=0.84) over 24 hours. During treatment oxygen saturations were significantly higher with NIV-supported ACT (mean difference 2.0, 95% CI 0.9 to 2.6, p=0.0004). No other significant differences were found in post-treatment FEV1, EoC, WoB, oxygen saturations or subject preference.
Conclusions There was no difference in treatment effect between NIV-supported ACT and ACT alone, although the study was underpowered. Oxygen saturations were significantly higher during NIV-supported ACT, but with no effect on post-treatment saturations. NIV was well tolerated.
Trial registration number NCT01885650.
- non-invasive ventilation
- airway clearance
- cystic fibrosis
- physiotherapy
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Statistics from Altmetric.com
Key messages
Does the addition of positive pressure support via the use of non-invasive ventilation (NIV) during chest physiotherapy improve sputum clearance for adults with cystic fibrosis (CF) compared with their usual airway clearance technique (ACT)?
This research concludes that while NIV has not been shown to be superior to the usual ACT, we cannot rule out that it has no clinical benefit especially for patients with lower lung function or who are acutely unwell, and so it is an important tool to be considered when assessing a person’s ACT needs.
This work discusses the outcomes of a randomised controlled cross-over trial investigating the use of NIV with ACT in adults with CF who were inpatients at our CF unit, and the difficulties of conducting research in this patient group, alongside the issues that investigators of ACT face due to the lack of accepted robust outcome measures available at present time.
Background
Cystic fibrosis (CF) is a genetic disorder affecting over 10 000 people in the UK.1 CF is characterised by the production of thickened bodily secretions, affecting the function of organs such as the pancreas and the lungs due to altered ion transport across cell membranes. Within the lungs, dehydration of the airway surface liquid alters normal mucociliary clearance mechanisms, resulting in airway obstruction, mucus plugging and infections.2 Recurrent infections and subsequent inflammation are thought to be the major mechanism towards lung tissue damage and the occurrence of fibrosis,3 4 which decreases lung function, lowers tissue oxygenation, and eventually leads to respiratory failure and death. Traditional CF management includes prevention of these complications by optimising removal of airway secretions. Combinations of mucolytic or hydrator therapy to make the secretions less viscous, and chest physiotherapy to mobilise secretions and improve airway clearance, are prescribed on an individual basis.5
There are a range of airway clearance techniques (ACTs) available for patients with CF, including breathing methods such as the active cycle of breathing techniques (ACBT) or autogenic drainage (AD), adjuncts such as positive expiratory pressure (PEP), and oscillatory devices such as the flutter or acapella. Selection of the optimal ACT is driven mostly by patient preference and thorough assessment and teaching by a trained physiotherapist,6 as current research indicates no differences in the effectiveness of techniques7 as long as they are performed correctly and regularly. During a pulmonary exacerbation or in end-stage severe disease, breathlessness, fatigue or excessive secretions can inhibit effective airway clearance. The addition of positive pressure via non-invasive ventilation (NIV) to ACTs has been shown to decrease patient fatigue8–11 and respiratory rate during clearance.8–10 Improvements in oxygenation,8 respiratory muscle strength,8 lung clearance index (LCI)12 and forced expiratory volume in 1 second (FEV1)11 have also been reported.
To date, no research has reported an increase in sputum expectorated with the addition of positive pressure; however, the ability to augment greater tidal volumes through positive pressure is thought to be a mechanism which could improve sputum clearance. We have previously reported the subjective viewpoints of patients using NIV to support ACT, in which they felt their sputum clearance had increased.13 The aim of the present study was to investigate this observation objectively by assessing sputum cleared in 24 hours in a randomised cross-over trial of usual ACT versus NIV-supported ACT.
We hypothesised that the inclusion of NIV in a patient’s normal ACT would objectively increase sputum clearance. In addition, we hypothesised that NIV would improve ease of sputum clearance (EoC) and work of breathing (WoB) and would be well tolerated.
Methods
Patient and public involvement
The research question stemmed from previously published research interviews completed with CF patient users of NIV for ACT,13 which on further discussion with these patients the authors felt was important to try and answer objectively. Patients with CF from the Royal Brompton Hospital were involved in designing the methodology to try and answer the question of whether sputum clearance changed with the addition of NIV. This same patient group made up the participants of this study, who were able to assess the burden of intervention themselves with the information provided prior to them giving written and informed consent. The results of the study were disseminated to participants via a letter.
Recruitment
Subjects were recruited from the adult CF centre at Royal Brompton Hospital, London. They were eligible to participate in the trial if they had a diagnosis of CF confirmed by standard criteria,14 were ≥16 years old, had been hospitalised for a pulmonary exacerbation which was resolving (by a clinician’s assessment), had been an inpatient for ≥7 days and had an established ACT regimen. Exclusion criteria included haemoptysis, pneumothorax, dependency on positive pressure support for ACT, history of spontaneous rib fracture, pregnancy, inability to give consent for participation, inclusion in another research study and requiring more than two supervised ACT sessions a day. Discontinuation criteria included voluntary withdrawal from the study, discharge from hospital prior to completion of the study or evidence of clinical deterioration during the study that required a change in medical treatment as determined by the CF medical team.
Written informed consent was gained prior to randomisation. Subjects were recruited between July 2013 and May 2017.
Treatment
The trial was a randomised cross-over design over 2 days, with subjects completing 1 day of their usual ACT regimen and 1 day of NIV-supported ACT using the Breas iSleep 25 (Breas Medical, Sweden). Randomisation was completed via a computerised program created by the trial statistician. Subjects were familiarised with NIV-supported ACT prior to randomisation. NIV settings were individually determined by a specialist physiotherapist based on the patient’s comfort and augmented thoracic expansion for each subject. NIV was administered via a mouthpiece with a Portex Thermovent heat and moisture exchange filter (Smiths Medical, UK) within the circuit. During the NIV session subjects completed 10 supported NIV breaths followed by up to four repetitions of the forced expiration technique and coughing as required. During the usual ACT subjects completed similar routines of forced expirations and coughs. Subjects received two 30 min sessions of supervised ACT a day from an adult CF specialist physiotherapist trained in NIV (GS). The same physiotherapist completed 93% of all trial treatment sessions and NIV familiarisation. No other changes to usual clinical care occurred during the trial period. No adverse events occurred during either treatment arm during the trial period.
Outcome measures
The primary outcome measure was the 24-hour total sputum wet weight expectorated timed from initiation of the first ACT session of a research day to the same time the following day. The secondary outcome measures were qualitative assessment of EoC, WoB during clearance and treatment satisfaction using a 10 cm Visual Analogue Scale (see online supplementary material 1), sputum expectorated during ACT sessions, FEV1, forced vital capacity (FVC), maximum expiratory flow at 25% of FVC (MEF25), maximum expiratory flow at 75% of FVC (MEF75), and oxygen saturations during ACT and post-ACT. Blinded independent observers completed all the outcome measurements pretreatment, immediately post-treatment and 30 min post-treatment, and weighed the 24-hour sputum. Oxygen saturations were recorded during the session and downloaded afterwards by the research team. At the end of the study, subjects completed a questionnaire asking their preferences on the different treatment regimens (see online supplementary material 2). Spirometry was completed according to the American Thoracic Society/European Respiratory Society guidelines15 using the MicroLoop hand-held spirometer (CareFusion UK 306, Basingstoke, UK; supplier: Williams Medical Supplies, Rhymney, UK). Oxygen saturations were recorded using a Pulsox-3i oximeter (Konica Minolta, Japan; supplier: Stowood Scientific Instruments, Stowood, UK).
Supplemental material
Supplemental material
Statistical analysis
A sample size calculation was completed (powered at 80% with 5% significance level) based on assuming an SD of 7.3 g for expectorated sputum, which required 28 participants to detect an absolute difference of 4 g of sputum. The sample size was calculated using the results from a previous randomised controlled trial on treatment effects.16 Data were described using mean (SD) or median (range) if non-parametric. Pretreatment and post-treatment effects were reported using mean difference (MD) and 95% CI, with paired t-tests completed to analyse significance levels. A p value of <0.05 was considered significant. An unplanned interim analysis was approved for completion by the London - Chelsea Research Ethics Committee and carried out at the halfway point of recruitment due to slow recruitment and to determine the feasibility of study completion.
The interim analysis showed that the difference between the two treatment arms was −0.98 g sputum (95% CI −11.5 to 9.6, p=0.84) over 24 hours, with NIV-supported ACT clearing less than the usual ACT. Analysis by the trial statistician indicated that based on the true difference in the mean response of the matched pairs of the data collected, the trial would require over 6000 pairs of subjects to be able to reject the null hypothesis that the response difference was zero with probability (power) of 0.8. There was a high (0.05) probability of a type I error associated with this test of the null hypothesis. Due to these results the decision was made to terminate the study early.
Results
Participant demographics
Fourteen subjects completed the study, 7 were men, with a mean (SD) age of 35.3 (17.1) years and a mean FEV1 of 48.9 (20) % predicted. Figure 1 illustrates the flow of recruitment, and table 1 shows the details of subjects’ baseline characteristics.
Participant baseline characteristics
CONSORT diagram of the study. ACT, airway clearance technique; CONSORT, Consolidated Standards of Reporting Trials; 1; NIV, non-invasive ventilation.
Treatment details
The median NIV settings were an inspiratory positive airway pressure of 25 cmH2O (IQR 25–75, 24.6–25) and an expiratory positive airway pressure of 5.8 cmH2O (IQR 25–75, 5–6).
A variety of usual ACTs were included, with AD completed by five subjects (36%), PEP by six subjects (43%), an oscillatory device by two subjects (14%) and ACBT by one subject (7%).
Before and after treatment results
No significant differences in sputum (table 2), spirometry, or pre-treatment to post-treatment oxygen saturations were found (see online supplementary material 3).
Supplemental material
Sputum pre-treatment, post-treatment and 30 min post-treatment
Comparisons between regimens
The MD between treatment regimens indicated that NIV-supported ACT cleared 1 g less sputum over 24 hours (95% CI −11.5 to 9.6) than the usual ACT (p=0.84) (table 2). During treatment the mean oxygen saturations were significantly higher during NIV-supported ACT (95.7%, SD 2.3) compared with the usual ACT (94%, SD 2.5) (MD 2.0, 95% CI 0.9 to 2.6, p=0.004) (figure 2). Post-treatment values for FEV1 (p=0.16), FVC (p=0.97), MEF 25 (p=0.70) and MEF 75 (p=0.19) did not differ significantly between the two regimens (see online supplementary materials 1–3). No significant differences in patient-reported outcome measures, which included EoC and WoB, were found (table 3).
Participant ease of clearance questionnaire
Oxygen saturation during treatment. ACT, airway clearance technique; NIV, non-invasive ventilation.
The results of the questionnaire asking subjects’ opinions of the two techniques were analysed for themes. Eight (57%) subjects had a preference for the usual ACT and six (47%) for NIV-supported ACT. The main reasons for preferring usual ACT were that the person was used to it (n=4) and that the techniques were more portable (n=3); the reasons for preferring NIV-supported ACT included feeling that it would be easier when feeling unwell (n=4), feeling like they got deeper breath (n=5) and that deeper deposits of sputum were cleared (n=3).
Discussion
Airway clearance, especially in severe CF, is a complex process, and physiotherapists and patients strive to find techniques which are effective, while easy to perform and low in effort. In this study we tested the hypothesis that the addition of NIV to the usual ACT would be more effective in clearing sputum than the usual ACT alone.
This study found no significant difference in the primary outcome measure (the amount of sputum cleared in 24 hours) between the usual ACT and NIV-supported ACT, which is comparable with the results of other studies investigating NIV and ACT,8 9 and agrees with findings of the recent Cochrane review on NIV for CF.17 However, the study was significantly underpowered. Additional explanations for concluding no treatment difference include the short-term duration of the intervention and possibly due to NIV-supported ACT being comparable in effect with usual ACTs.
Significant differences were determined in oxygen saturations of the participants during the ACT session, with subjects having higher saturations when using NIV, although it can be argued that a 2% difference in oxygen level is not a clinically relevant difference. We also did not demonstrate a carryover of these improvements after the session, unlike Holland et al.8 During ACT sessions oxygen saturations are an important clinical consideration when completing ACT, especially with more acutely unwell patients or those with advanced lung disease, and it may be that this is an area where NIV-supported ACT has a role.
Airway clearance research has been debated within the physiotherapy, CF and wider research community as lacking in a robust outcome measure which appropriately measures the effect of ACT. Sputum weight has been criticised as being a subjective measure, based on the will of the subject to expectorate and at risk of contamination with saliva, which could alter the results.6 18 FEV1 is thought to be difficult to use as a short-term outcome due to its effort dependency and lack of sensitivity to small changes.6 7 18 19 This may explain why we found no significant differences in FEV1 and other spirometric measures during this study. There was a slight trend for an increase in FVC after NIV-supported ACT, especially in the morning session, and although this did not reach statistical significance it may make NIV support a viable consideration in patients with loss of lung volume.
An alternative outcome measure which has been suggested is the LCI, which is derived from multiple breath washout. One recent study comparing NIV-supported ACT with PEP used the LCI as an outcome measure, and reported a significant reduction (improvement) in LCI when subjects used NIV compared with PEP.12 Their study provides support for this outcome measure, although other published research investigating ACTs with LCI as an outcome have reported variable LCI results.20
A key aspect of ACT is the patient’s own perspective, as fundamentally it is the patient who will be required to complete the technique daily. Using our self-designed questionnaires, subjects reported that NIV-supported ACT did not differ significantly from their usual ACT in terms of EoC, breathlessness, comfort or fatigue. There were trends for lower reported levels of breathlessness and fatigue with the use of NIV, but these did not reach significance. This differs from our previously reported results where subjects did subjectively rate NIV-supported ACT significantly higher for EoC and reduced effort13; however, those results were from a more severe patient group (median FEV1 26%) over a 1-year period. Several of the participants of the current study commented that they felt NIV would be useful for them if they were more unwell, breathless or unable to expectorate, as they felt it would be more supportive at that time, which may then provide more comparable data. This suggestion has been supported by Moran et al17 in their recent Cochrane review and may be where NIV-supported ACT has a role. A consideration for future ACT studies is the timing of the intervention for maximal effect, as our subjects were nearing the end of admission, with many of them feeling very well, which may have reduced the effect of ACT. However, it is noted that studying more unwell patients would have its own difficulties in terms of the need for treatment changes and ethical considerations.
This study has several limitations. First is the low number of participants, which resulted in early termination of the study. Recruitment, even on a busy CF unit, was difficult due to tight inclusion criteria, especially the need to be stable and being at the end of a hospital admission. Clinical practice and patient preference for early discharge meant that often these patients were sent home to complete their intravenous antibiotics, rendering them unable to complete the study. These difficulties led to a long recruitment time for the study, which was not ideal. Recently O’Neill et al21 reported similar difficulties with recruitment and participant inclusion in their work looking at the timing of hypertonic saline and ACT, again resulting in early termination of the study. In our clinical practice, NIV is considered to support ACT in patients with CF with advanced lung disease who are struggling with their usual ACT. In order to replicate this practice in this study, we would have needed to only include patients with a low FEV1; however, due to recruitment, we included all FEV1 ranges, which may explain why differences with NIV were not identified, as patients with good lung function probably do not require NIV assistance to aid them in taking deep breaths. Another limitation, particularly in subjects with higher lung function, was the limited positive pressure support that the Breas iSleep 25 could offer; often these participants were asking for more pressure for a deeper breath which the NIV was unable to provide. We included all ACT techniques to compare against NIV-supported ACT—this decision was taken to ensure familiarity of technique to the patient, but in doing so we accept this introduced more variability in the control arm. It may be that NIV-supported ACT is more effective than some usual ACTs, for example PEP as described by Rodriguez Hortal et al,12 but due to the low number of participants it was not possible to analyse the techniques separately.
Although the study was underpowered, we believe it provides important insights into the role of NIV-supported ACT. A recent review of the UK’s national data registry has shown that NIV use is increasing with beneficial effects on lung function decline,22 and so research investigating the optimal use of NIV for our patients remains essential. From this study we cannot provide definitive conclusions about efficacy, but NIV was well tolerated and improved oxygenation during the intervention. NIV—for select patients—is likely to be where it fits, but further studies are required. With careful clinical consideration, we suggest it should be included in the specialist CF physiotherapist’s airway clearance ‘toolbox’, as concluded by Moran et al.17 Low participant numbers and insensitive outcome measures are well-recognised problems of ACT trials.7 18 19 21 23 Our work provides important context for future ACT trial design as more robust outcome measures need to be developed. Further work needs to be done with these more robust outcome measures to optimise power so that we can better understand who will benefit from this intervention and when it should be introduced.
Acknowledgments
Our thanks to Professor Stuart Elborn for his helpful discussions of this work and the physiotherapy team of the Royal Brompton Hospital for their help with this research. Finally we would like to thank the patients who participated in the design and completion of this study.
References
Footnotes
Contributors GS, HP, PA and DB conceived and designed this research. GS recruited the patients, performed treatment, collected clinical data and performed the treatments. HP led the team who completed the independent observer role. GS, WB and NS analysed the data. GS and NS wrote the paper.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests NS has consulted for Vertex Pharmaceuticals, Chiesi, Roche, Pulmocide, PTC Therapeutics and Gilead.
Patient consent for publication Not required.
Ethics approval Ethical approval was granted by the London - Chelsea Research Ethics Committee (reference number 13/LO/0565).
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.