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      A randomised controlled trial to investigate the use of high-frequency airway oscillations as training to improve dyspnoea in COPD

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          Abstract

          Introduction

          Chronic obstructive pulmonary disease (COPD) is characterised by expiratory flow limitation resulting in symptomatic dyspnoea, sputum retention and ventilation heterogeneity. Changes in breathing mechanics affect the ability of respiratory muscles to respond to the ventilatory demands, increasing the sensation of dyspnoea. A high-frequency airway oscillating device has been developed to combine respiratory muscle training and oscillations to improve dyspnoea and sputum retention within COPD.

          Methods and analysis

          Patients with symptomatic COPD (Medical Research Council Breathlessness scale grade ≥2) will be recruited to a double-blind, randomised, sham-controlled trial. Both groups will follow an 8-week intervention phase using the device three times per day for 5 min at a time. This will be recorded in a self-reported diary. The device applies a flow resistive load and oscillations for combined training. Those receiving the sham device will follow the same protocol; however, the mechanism of action will be removed from the device. Improvements in the Chronic Respiratory Questionnaire-Dyspnoea domain will be the primary outcome measure. Secondary outcomes will explore respiratory muscle function, health-related quality of life, exercise capacity and physical activity. The Lung Clearance Index will be an exploratory outcome. Outcomes will be explored using the most appropriate statistical test, dependent on the sample distribution. Focus groups will be an exploratory outcome and analysed by thematic analysis.

          Ethics and dissemination

          Ethical approval has been obtained from the East Midlands-Leicester South Research Ethics Committee and the trial has been registered through the ISRCTN Registry. The study results will be disseminated to the appropriate stakeholders through presentations, conferences and peer-reviewed journals.

          Abstract

          A double-blind, placebo-controlled, randomised trial investigating the effects of high-frequency airway oscillations on dyspnoea, sputum, quality of life and exercise capacity in #COPD. http://bit.ly/2F8bQ6s

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          Most cited references19

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          Development of a shuttle walking test of disability in patients with chronic airways obstruction.

          The aim was to develop a standardised and externally paced field walking test, incorporating an incremental and progressive structure, to assess functional capacity in patients with chronic airways obstruction. The usefulness of two different shuttle walking test protocols was examined in two separate groups of patients. The initial 10 level protocol (group A, n = 10) and a subsequent, modified, 12 level protocol (group B, n = 10) differed in the number of increments and in the speeds of walking. Patients performed three shuttle walking tests one week apart. Then the performance of patients (group C, n = 15) in the six minute walking test was compared with that in the second (modified) shuttle walking test protocol. Heart rate was recorded during all the exercise tests with a short range telemetry device. The 12 level modified protocol provided a measure of functional capacity in patients with a wide range of disability and was reproducible after just one practice walk; the mean difference between trial 2 v 3 was -2.0 (95% CI -21.9 to 17.9) m. There was a significant relation between the distance walked in the six minute walking test and the shuttle walking test (rho = 0.68) but the six minute walking test appeared to overestimate the extent of disability in some patients. The shuttle test provoked a graded cardiovascular response not evident in the six minute test. Moreover, the maximal heart rates attained were significantly higher for the shuttle walking test than for the six minute test. The shuttle walking test constitutes a standardised incremental field walking test that provokes a symptom limited maximal performance. It provides an objective measurement of disability and allows direct comparison of patients' performance.
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            Impact of inspiratory muscle training in patients with COPD: what is the evidence?

            A meta-analysis including 32 randomised controlled trials on the effects of inspiratory muscle training (IMT) in chronic obstructive pulmonary disease (COPD) patients was performed. Overall and subgroup analyses with respect to training modality (strength or endurance training, added to general exercise training) and patient characteristics were performed. Significant improvements were found in maximal inspiratory muscle strength (P(I,max); +13 cmH₂O), endurance time (+261 s), 6- or 12-min walking distance (+32 and +85 m respectively) and quality of life (+3.8 units). Dyspnoea was significantly reduced (Borg score -0.9 point; Transitional Dyspnoea Index +2.8 units). Endurance exercise capacity tended to improve, while no effects on maximal exercise capacity were found. Respiratory muscle endurance training revealed no significant effect on P(I,max), functional exercise capacity and dyspnoea. IMT added to a general exercise programme improved P(I,max) significantly, while functional exercise capacity tended to increase in patients with inspiratory muscle weakness (P(I,max) <60 cmH₂O). IMT improves inspiratory muscle strength and endurance, functional exercise capacity, dyspnoea and quality of life. Inspiratory muscle endurance training was shown to be less effective than respiratory muscle strength training. In patients with inspiratory muscle weakness, the addition of IMT to a general exercise training program improved P(I,max) and tended to improve exercise performance.
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              The assessment of maximal respiratory mouth pressures in adults.

              Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) are simple, convenient, and noninvasive indices of respiratory muscle strength at the mouth, but standards are not clearly established. We review recent literature, update the 2002 American Thoracic Society/European Respiratory Society statement, and propose as the best choice using a flanged mouthpiece for reference values and lower limit of normal (LLN) values as a function of age for adults age up to about 70 years. Because male pressures are higher than female and MEP exceeds MIP, we present 4 linear regression reference equations as a function of age for adults age up to approximately 70 years: Male MIP=120-(0.41xage), and male MIP LLN=62-(0.15xage). Male MEP=174-(0.83xage), and male MEP LLN=117-(0.83xage). Female MIP=108-(0.61xage), and female MIP LLN=62-(0.50xage). Female MEP=131-(0.86xage), and female MEP LLN=95-(0.57xage). (Pressure in cm H2O and age in years.) We discuss normal values in older subjects, estimation of LLN values, and the relationship between vital capacity and respiratory muscle strength, and offer a guide to interpretation of maximal pressure measurements. The approach should allow direct implementation of MIP and MEP in a pulmonary function laboratory.
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                Author and article information

                Journal
                ERJ Open Res
                ERJ Open Res
                ERJOR
                erjor
                ERJ Open Research
                European Respiratory Society
                2312-0541
                July 2019
                29 July 2019
                : 5
                : 3
                : 00064-2019
                Affiliations
                [1 ]Centre of Exercise and Rehabilitation Sciences, Glenfield Hospital, Leicester, UK
                [2 ]NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Leicester, UK
                [3 ]University of Leicester, Leicester, UK
                Author notes
                Enya Daynes, Centre of Exercise and Rehabilitation Sciences, NIHR Leicester Biomedical Research Centre – Respiratory, Glenfield Hospital, Groby Road, Leicester, LE3 9QP, UK. E-mail: enya.daynes@ 123456uhl-tr.nhs.uk
                Author information
                https://orcid.org/0000-0003-0127-1649
                Article
                00064-2019
                10.1183/23120541.00064-2019
                6661317
                23479817-913b-4d4e-b0f3-5d3a06053c3f
                Copyright ©ERS 2019

                This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.

                History
                : 08 March 2019
                : 04 June 2019
                Funding
                Funded by: Actegy LTD
                Categories
                Study Protocol
                1

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