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Article

Effects of Non-Invasive Ventilation Combined with Oxygen Supplementation on Exercise Performance in COPD Patients with Static Lung Hyperinflation and Exercise-Induced Oxygen Desaturation: A Single Blind, Randomized Cross-Over Trial

by
Maud Koopman
1,*,
Martijn A. Spruit
1,2,3,4,
Frits M.E. Franssen
1,2,3,
Jeannet Delbressine
1,
Emiel F.M. Wouters
1,3,
Denny Mathew
5,
Anton Vink
5 and
Lowie E.G.W. Vanfleteren
1,6
1
Department of Research & Development, CIRO, Center of Expertise for Chronic Organ Failure, 6085 NM Horn, The Netherlands
2
NUTRIM, School of Nutrition and Translational Research in Metabolism, 6200 MD Maastricht, The Netherlands
3
Department of Respiratory Medicine, Maastricht University Medical Center (MUMC), 6202 AZ Maastricht, The Netherlands
4
REVAL—Rehabilitation Research Center, BIOMED—Biomedical Research Institute, Faculty of Rehabilitation Sciences, Hasselt University, 3590 Diepenbeek, Belgium
5
Philips Research, 5656 AE Eindhoven, The Netherlands
6
COPD Center, Sahlgrenska University Hospital, Institute of Medicine, University of Gothenburg, SE-413 45 Gothenburg, Sweden
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2019, 8(11), 2012; https://doi.org/10.3390/jcm8112012
Submission received: 9 October 2019 / Revised: 8 November 2019 / Accepted: 12 November 2019 / Published: 18 November 2019
(This article belongs to the Special Issue Pulmonary Rehabilitation, Exercise Training and Physical Activity Coaching for Chronic Lung Disorders)
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Versions Notes

Abstract

:
The effects of non-invasive ventilation (NIV) in addition to supplemental oxygen on exercise performance in patients with chronic obstructive pulmonary disease (COPD) with hyperinflation and exercise-induced desaturation (EID) remain unclear. We hypothesized that these patients would benefit from NIV and that this effect would be an add-on to oxygen therapy. Thirteen COPD patients with a residual volume >150% of predicted, normal resting arterial oxygen pressure (PaO2) and carbon-dioxide pressure (PaCO2) and EID during a six-minute walk test were included. Patients performed four constant work-rate treadmill tests, each consisting of two exercise bouts with a recovery period in between, wearing an oronasal mask connected to a ventilator and oxygen supply. The ventilator was set to the following settings in fixed order with clockwise rotation: Sham (continuous positive airway pressure (CPAP) 2 cm H2O, FiO2 21%), oxygen (CPAP 2 cm H2O, FiO2 35%), NIV and oxygen (inspiratory positive airway pressure (IPAP) 14 cm H2O/expiratory positive airway pressure (EPAP) 6 cm H2O, inspired oxygen fraction (FiO2) 35%), intermittent (walking: Sham setting, recovery: NIV and oxygen setting). During the first exercise, bout patients walked further with the oxygen setting compared to the sham setting (225 ± 107 vs 120 ± 50 meters, p < 0.05), but even further with the oxygen/NIV setting (283 ± 128 meters; p < 0.05). Recovery time between two exercise bouts was shortest with NIV and oxygen. COPD patients with severe static hyperinflation and EID benefit significantly from NIV in addition to oxygen during exercise and recovery.

1. Introduction

Ventilatory inefficiency and exercise-induced oxygen desaturation (EID) are key determinants of exercise intolerance in patients with severe COPD [1,2]. Ventilatory inefficiency represents an abnormal increase in the ratio of minute ventilation to carbon dioxide production [3], and combined with expiratory flow limitation causes dynamic hyperinflation [4,5]. Ventilatory inefficiency is related to greater mechanical constraints, worsening pulmonary gas exchange, higher dyspnea scores and poorer exercise capacity [6]. Excess breathing at higher lung volumes has negative hemodynamic consequences resulting in impaired oxygen delivery and/or utilization by the skeletal muscles [7].
EID can also be a result of a ventilation/perfusion mismatch during exercise, caused by diffusion impairment and loss of elastic recoil of the lungs, which is associated with emphysema [8]. The combination of these pathophysiologic features, which occurs in about 25% of the COPD patients [9], results in exertional dyspnea and early exercise termination [10].
Particularly COPD patients with chronic hypercapnic respiratory failure respond well to non-invasive ventilation (NIV) during exercise. Glöckl et al. recently showed that high inspiratory pressure NIV improved cycle endurance time, reduced exercise-induced hypercapnia and reduced exertional dyspnea [11]. In addition, NIV during exercise training in patients with chronic hypercapnic respiratory failure and long term NIV and long-term oxygen supplementation resulted in improvement of cycling endurance time after training [12].
To date, the effects of NIV in addition to supplemental oxygen during exercise and recovery from exercise in non-hypercapnic COPD patients with lung hyperinflation and EID are less studied. NIV can reduce the load of overburdened inspiratory muscles and reduce the work of breathing. The use of inspiratory pressure support during exercise increases endurance time and reduces dyspnea in patients with COPD [13,14]. Unloading respiratory muscles by proportional assisted ventilation in COPD patients improves leg muscle oxygenation, dyspnea and leg fatigue symptoms and prevents exercise-induced diaphragmatic fatigue [15,16]. Moreover, a preliminary study suggested that bi-level positive airway pressure (BiPAP) during recovery after treadmill walking can reduce recovery time [17]. Oxygen supplementation during exercise can improve endurance time, stabilize oxygen saturation and reduce dyspnea in COPD patients [18,19], mainly in those with resting hypoxemia or EID [20]. Improved exercise-capacity with oxygen has shown to be, at least partly, explained by a reduction in DH related to a decreased breathing frequency for a given exercise [21]. The combination of NIV and oxygen during ramp-incremental cycle ergometry in COPD patients with EID and hyperinflation can improve central hemodynamics during exercise; however, this study did not show an improvement of peak work rate when using NIV and oxygen [22].
We hypothesized that non-hypercapnic patients with COPD with lung hyperinflation and EID would benefit from NIV and that this effect would be an add-on to oxygen therapy. Consequently, we aimed to study the effects of NIV in addition to oxygen therapy, compared to oxygen alone, or no support on exercise duration, perceived dyspnea and time to recovery from exercise in this disease phenotype.

2. Methods

2.1. Patients

Clinically stable COPD patients confirmed by post-bronchodilator spirometry [23], aged 40–80 years, with a residual volume >150% of predicted, resting arterial oxygen pressure (PaO2) > 7.3 kPa, resting arterial carbon-dioxide pressure (PaCO2) < 6.5 kPa, and transcutaneous oxygen saturation (SpO2) during a 6-minute walking test (6MWT) < 88% were included. Patients were excluded if they had an active malignancy, previous pulmonary surgery, unstable cardiovascular disease, orthopedic problems that could impair the walking tests, and/or if they had to use a walking aid or wheelchair. Lastly, patients were not included when they had a contraindication for the use of BiPAP (i.e., acute sinusitis, otitis media, low blood pressure, inability to adequately clear secretions) as determined by the chest physician. Patients were recruited during a baseline assessment for an inpatient comprehensive pulmonary rehabilitation (PR) program at CIRO (Horn, the Netherlands) between January and December 2016. The study-related tests were performed during the first two weeks of PR.
The study protocol was approved by the medical ethical committee of Maastricht University Medical Center, the Netherlands, filed under NL54204.100.15 R15.077/VOS COPD. Informed consent was signed by all patients.

2.2. Sample Size

We performed a sample size calculation using GPower 3.1.9 (Heinrich Heine Universität Düsseldorf, Germany), based on the hypothesis that NIV during recovery will result in a clinically relevant improvement of recovery time of at least 40 seconds, according to a study with 19 patients who used NIV during recovery after treadmill walking compared to a baseline control test [17]. For the sample size calculation, we used a mean of 126 seconds, standard deviation 13 seconds, significance level α = 0.05 and power 1-β = 0.80. We used an effect size of 0.40 and an estimated moderate correlation between the repeated measurements of 0.5, which provided a sample size of 12. Considering a 10% drop-out rate, we estimated an allocation sample size of 13 patients.

2.3. Baseline Assessment

Patients underwent a series of tests and questionnaires as part of a routine three-day pre-rehabilitation assessment [24]. The chest physician performed a physical examination and reviewed the patient’s medical history. Post-bronchodilator forced expiratory volume in the first second (FEV1) and forced vital capacity (FVC) were collected using standardized spirometry (MasterScreen® Body, Carefusion, Germany). Additionally, whole-body plethysmography was performed to assess residual volume (RV) and carbon monoxide transfer factor (DLCO, by single breath-hold method) was determined (MasterScreen® Body, Carefusion, Germany). Prior to lung function measurement, 200 μg of salbutamol was provided via an autohaler device. All measurements, executed by a trained lung function technician, were repeated at least three times to ensure repeatability [25]. Reference values for spirometry and lung volume measurements were in accordance with the official statement of the European Respiratory Society [26,27]. Among other tests, patients also performed two 6MWTs. The test with the longest 6-minute walk distance (6MWD) was used for further analysis and to define the treadmill walking speed [28].

2.4. Interventions

An overview and description of the different exercise settings are presented in Figure 1. Each test consisted of two bouts of exercise with a timed recovery period in between. The following tests were performed on two consecutive days, with one set of tests in the morning, and one set in the afternoon on both days:
(1)
Setting 1 (‘Sham’): Continuous positive airway pressure (CPAP) 2 cm H2O with an inspired oxygen fraction (FiO2) of 21%.
(2)
Setting 2 (‘Oxygen’): CPAP 2 cm H2O with FiO2 35%.
(3)
Setting 3 (‘NIV and oxygen’): BiPAP with inspiratory positive airway pressure of 14 cm H2O and expiratory positive airway pressure of 6 cm H2O, with FiO2 35%.
(4)
Setting 4 (‘Intermittent’): Setting 1 during walking (2 cm H2O), when the patient had an unintended stop the setting was switched to setting 3 (IPAP 14, EPAP 6 cm H2O). When the patient started walking again, the setting was switched back to setting 1.
The CPAP pressures were chosen to overcome the pressure gradients of the tube and mask, and were the lowest available pressures on the device. The BiPAP pressures were based on the pressures used when NIV is introduced in the acute clinical setting. The intermittent setting was included to specifically identify whether the use of NIV and oxygen helps shorten recovery time following a bout of exercise.
Randomization of tests was done with a fixed order of tests, but the clockwise rotation of the starting test for each consecutive patient. All patients were blinded for the settings.
To measure recovery time, i.e., the time they needed to recover enough to restart exercise, patients were asked to perform two consecutive constant work rate treadmill walking tests with a timed recovery period in between. Before the start of the first exercise bout, patients were instructed to walk as long as possible, with a maximum duration of six minutes. With the completion of the first exercise bout patients stayed on the treadmill and were instructed to start with the second exercise bout the moment they recovered to a Borg dyspnea score ≤2. Patients were then again instructed to walk as long as possible, with a maximum duration of six minutes. The start of their second bout of exercise was marked as the end of the recovery period. The walking speed at the treadmill was set at 125% of the mean walking speed during the 6MWT. This speed was chosen to increase the likelihood that the patient will stop walking within six minutes.
The sham and NIV support and oxygen supply during the treadmill tests were provided by the Philips Respironics V60 ventilator connected to a wall oxygen supply, using an oronasal mask connected by a tube to the ventilator.
All tests were supervised by a physician who watched over the settings of the non-invasive ventilator and the oxygen supplementation. A biomedical engineer instructed the patients and guided all exercise tests. During testing days, patients did not perform any endurance training. They were allowed to perform resistance training if they felt able to do so.
Treadmill walking time and distance, Borg dyspnea (D) and fatigue (F) score, transcutaneous PaCO2 (tcPaCO2) and SpO2, heart rate (HR), breathing frequency (BF) and tidal volume (Vt) were collected throughout the tests. The V-Sign System from Sentec was used to measure tcPaCO2, SpO2 and HR, with a sensor connected to the earlobe. In two patients, measurements of tcPaCO2, SpO2 and HR with the Sentec device gave an unreliable signal, and SpO2 and HR were measured with a Nonin WristOx2 wrist pulse-oximeter. BF and Vt were continuously measured by the V60. All parameters were noted before and after each treadmill test. Because the parameters on the Sentec and the V60 changed every five seconds, all parameters were also noted 10 seconds before and after the start and stop, the mean of these three numbers was finally taken into the calculations. To get continuous data of the parameters, a GoPro HERO action camera was set to film the monitors of the Sentec and V60. The vital data were compared within the four test settings at 20/40/60/80/100% of isotime, in which the shortest walking time was set at 100% isotime. Minute ventilation was calculated by multiplying BF and Vt.
All tests were performed in the same training room, air-conditioned in temperature and humidity, on the same treadmill, and the same ventilator was used in all patients.

2.5. Statistical Analysis

Statistics were performed using SPSS version 23.0. Data were analysed for outliers and normality. Results were expressed as mean ± SD when normally distributed, otherwise as median and interquartile range, or count (%). Differences in exercise duration, recovery, Borg D and F, PaCO2, SpO2, HR, BF and Vt were compared using a one-way repeated measures ANOVA. Participants with missing data were excluded from the ANOVA analyses. A generalized estimated equation (GEE) analyses were used with all available data. Statistical significance was assumed if a two-tailed p-value was <0.05.

3. Results

Five hundred fifty-two subjects took part in a regular rehabilitation program after an initial assessment. Of the screened patients, 530 did not meet the inclusion criteria, and 22 declined to participate (Figure 2). Sixteen patients volunteered to participate. Thirteen patients completed the four exercise settings. Three patients withdrew informed consent as the mask made them feel anxious and unable to complete the first bout of exercise. Baseline characteristics of the 13 patients (nine women) who completed all four tests are outlined in Table 1. Patients generally had severe airflow obstruction, severe static hyperinflation, and EID during the 6MWD (lowest SpO2 during 6MWT: 82.5 ± 5.1%).

Treadmill Test Outcomes

Compared to sham, patients were able to walk further during a bout of exercise when oxygen was continuously provided (mean 120 ± 50 meters versus 225 ± 107 meters, respectively; p = 0.03, Table 2), but recovery time did not significantly change. Total endurance time of exercise bout one and two was longest in the setting with NIV and supplemental oxygen (mean 414 ± 208 seconds, Figure 3), with the shortest recovery time in between two exercise bouts (mean 117 ± 51 seconds, Table 2, Figure 3). Recovery time was comparable when NIV and oxygen were only provided during recovery (setting 4; mean 119 seconds, Table 2, Figure 3). Despite the shortened recovery, patients were not able to walk further after recovery compared to the sham setting. Individual results on the four tests before recovery are shown in Figure 4, individual results after recovery are not shown but were comparable.
Although patients walked furthest with setting 3, no increase in Borg D or F was noted. Alternatively, Borg D was lower after the first test in the oxygen/NIV setting compared to the oxygen setting. Interestingly, leg fatigue was lowest after recovery during the test in which patients walked with sham settings and recovered with NIV and oxygen (Table 2).
No desaturation was seen when walking with oxygen or oxygen/NIV, compared to marked desaturation when walking with setting 1 and 4. Saturation normalized in all test settings during recovery (Table 2).
tcPaCO2 levels were comparable before starting the first exercise bout (mean tcPaCO2 5.1-5.5 kPa, Table 2), but increased at a significantly faster rate when providing oxygen without NIV during the first exercise bout. tcPaCO2 levels continued to increase during recovery, but stayed levelled during the second round of tests (mean tcPaCO2 6.0-6.6 kPa, Table 2). There were no significant differences in tcPaCO2 levels at the end of the four sets between the four settings.
No significant results between the treadmill tests were found when looking at differences in BF, Vt and ventilation after exercise and recovery (Table 2).
Figure 5 shows the results of the isotime values on tcPaCO2, SpO2, HR, BF and Vt of the first round of treadmill tests. SpO2 declined with a significantly steeper slope with sham or intermittent settings compared to oxygen with or without NIV, but SpO2 values between the oxygen and oxygen/NIV setting were comparable. The trends of tcPaCO2, HR and BF seemed to be lowest, and Vt seemed to be highest during exercise with NIV and oxygen compared to the other settings, but these differences were not significant.

4. Discussion

This study showed that normoxemic COPD patients with severe hyperinflation and EID significantly improved exercise endurance time with oxygen supplementation during exercise, which further improved when NIV was added to oxygen. Endurance time increased with the same level of dyspnea and faster post-exercise recovery. The combination of NIV and oxygen supplementation provided only during recovery after exercise shortened recovery time with less leg fatigue, but did not improve subsequent exercise endurance time after recovery.
Oxygen supplementation in COPD patients has previously shown to decrease the respiratory rate and thereby reduce DH in hyperinflated patients [18,19]. We observed no differences in the ventilatory response to exercise and DH was not measured. Correction of desaturation on itself has been shown to improve exercise capacity [18,19], which might be one of the explanatory factors for improved exercise in our patients.
This study shows that NIV, in addition to oxygen therapy, significantly further improves the exercise capacity in non-hypercapnic, severely hyperinflated patients with EID. The physiological mechanism behind this improvement is clearly beyond the correction of EID. A physiological study in COPD patients with EID, using non-invasive open ventilation utilizing a volume-regulation ventilation system, showed that although this type of ventilation does decrease the inspiratory effort as measured by decreasing accessory inspiratory muscle EMG, exercise endurance was not significantly affected by non-invasive ventilation alone if oxygen was not administered [29]. Moreover, use of the non-invasive open ventilation system was associated with a slower breathing rate and a higher oxygen saturation than generally achieved using oxygen, without a change in pulmonary gas exchange efficiency.
It has been described that by providing BiPAP, the inspiratory threshold load to initiate inspiration is lowered, expiration is eased by preventing small airways closure, and DH might be decreased [30]. Acute-on-chronic hyperinflation in COPD patients may result in a reduction in peripheral muscle blood flow, due to the central hemodynamic consequences or cardiac output redistribution towards the overloaded respiratory muscles [31,32]. In addition, decreased ventilatory efficiency and desaturation can contribute to this process.
A previous study explored the effects of additional NIV to oxygen in a comparable patient cohort [22]. Thirteen normoxemic COPD patients with hyperinflation (mean RV 187% pred.) and EID performed ramp-incremental cycle ergometry with supplemental oxygen and NIV (16 cm H2O inspiratory pressure support (IPS) and 5 cm H2O positive end-expiratory pressure (PEEP)) or sham NIV (7 cm H2O IPS and 5 cm H2O PEEP). Improvements in central hemodynamics were reported, but no significant differences in peak work rate and ventilation were seen. Although speculative, the different ‘’sham’’ NIV, with fairly higher pressures than we used, possibly preventing small airways closure by counterbalancing the PEEPi might be one of the reasons for the difference in results [33]. Next to different settings, we also used walking on a treadmill at a constant work rate to test exercise capacity, which can be considered as endurance exercise rather than incremental exercise.
In patients with resting lung hyperinflation, the low inspiratory reserve capacity limits the possibility of Vt expansion during exercise, and thus, the maximal achievable ventilation [34,35]. Theoretically, by increasing the inspiratory capacity during exercise by providing BiPAP, the moment that patients reach their plateau in tidal volume/peak ventilation relation will be postponed. The lack of difference in isotime and end of exercise Vt and ventilation in the current study suggests all patients walked until they reached maximum ventilation, but when NIV was added to oxygen, they were able to walk longer with the same level of ventilation. These findings might imply that in our population, NIV in addition to oxygen had a more beneficial effect on dyspnea sensation and redistribution of blood flow from respiratory muscles to limb muscles rather than on respiratory mechanics. This blood flow redistribution might explain why patients experienced less leg fatigue after they received NIV and oxygen during recovery but had walked with sham settings.
Another explanation for the beneficial effect of NIV in addition to oxygen might be the improvement of the ventilation/perfusion ratio. Imaging analysis techniques have shown improvement of ventilation/perfusion and gas exchange related to long-term NIV treatment in patients with COPD [36]. However, no differences in SpO2 after exercise were noted when NIV was added to oxygen. In summary, the mechanisms by which NIV in addition to oxygen supplementation improved exercise endurance time in this study remain unclear.
Although overall, there are clinical significant differences in distance and recovery time, we noted heterogeneity in response among individual subjects (Figure 4), similar to other studies [14]. We used fixed ventilator settings in all patients. Individualized settings for NIV would possibly have resulted in more comparable effects for all patients. On the contrary, it seems that some patients respond better to oxygen; others respond better to NIV. This variability in responses is probably related to the differential pathological mechanisms causing patients to terminate their exercise; in some patients, this can be due to ventilatory mechanics, and in other patients, diffusion might be the dominating problem, but also variable beneficial effects on hemodynamics might play a role in individual variance. The current sample size, however, does not allow to investigate these differences further.
Recovery time is shorter with NIV and oxygen support but does not result in a longer walking distance after recovery without continuous NIV and oxygen support. It might indicate that the recovery time was sufficient to recover from the given exercise, but we did not assess muscle recovery. Indeed, prolonged skeletal muscle recovery after exercise has been observed in hypoxemic COPD patients [37]. The efficacy of postexercise O2 supplementation, however, is still debated [38]. Interestingly, leg fatigue was lower when subjects walked with sham conditions, but recovered with NIV and oxygen. This might be partly related to the fact that patients stopped because of dyspnea before the legs got tired. The degree of leg fatigue was indeed lower after the two settings in which patients walked with sham (i.e., ‘’sham’’ and ‘’intermittent’’ setting), although not significantly different. Conversely, leg fatigue improved more pronounced if NIV and oxygen was applied during recovery, suggesting a beneficial effect on lower limb skeletal muscle.
The isotime data did not convincingly explain the beneficial effect of NIV and supplemental oxygen compared to the other settings. However, these curves only provide data of part of the tests with oxygen with or without NIV, as the shortest (sham or intermittent) test is used to define isotime. A recently published study investigated the differences in exercise duration in 20 severely hyperinflated patients with chronic hypercapnic respiratory failure when using oxygen with or without high-pressure NIV [11]. Similar to our study, cycle endurance time was significantly longer when NIV was added to oxygen. Contrary to our study, isotime evaluation during exercise showed lower PaCO2 and higher SpO2 during NIV use, which may be related to different characteristics of study populations.
The current results provide evidence for individualizing pulmonary rehabilitation programs. In selected patients with high dyspnea sensation related to (dynamic) hyperinflation who are unable to perform exercise training, NIV is a viable option. It, however, remains to be studied whether and to what extent training with NIV and oxygen in this subgroup extents functional outcomes.
Strengths of this study are the standardized and highly controlled laboratory conditions, the inclusion of a sham setting and blinding of the patient for the setting used. The study also has limitations. Although, theoretically, CPAP is not a real ventilation mode, it might reduce dyspnea and increase exercise tolerance in COPD patients by reducing the DH-associated increased inspiratory threshold load on the inspiratory muscles through counterbalancing PEEPi [39,40]. The use of CPAP might also improve ventilation/perfusion in patients with COPD and hyperinflation Nevertheless, this ‘’sham’’ setting was provided to assure that patients remained blinded to the intervention being applied, and the pressure of 2 cm H2O should be enough to overcome the pressure gradients in the tube and mask. Second, three patients (19%) dropped out because of NIV-intolerance. This rate is comparable to other NIV studies [12,15]. Third, although the different tests were done in a consecutive clockwise rotation scheme with a different starting test setting, no real randomization was done. Because this study was not randomized, we used GEE for all available data to correct for this (data not presented), which did not influence the results. Fourth, we limited the exercise time with a maximum of six minutes for the treadmill tests, which potentially could influence exercise time interpretation. Of the 104 exercise bouts performed in total, only four of them reached the six minutes limit. Hence, we believe this effect is negligible. Given that one of these bouts was in the oxygen setting and three in the NIV/oxygen setting, the influence would be towards an underestimation of the intervention effect. Fifth, we did not study the effects of NIV without oxygen supplementation in our cohort, and therefore, we cannot draw conclusions related to an NIV only effect. Sixth, a resting Vt of 800 ml is relatively high, especially in COPD patients (Table 2). The Vt we documented is measured by the ventilator. However, non-invasive ventilators do not measure tidal volume directly but give an estimation through a built-in software [41]. We mainly used the Vt to evaluate the different test settings. Lastly, we studied a small sample size, and larger studies regarding this topic are needed to establish the effects of NIV in addition to oxygen in this population.

5. Conclusions

COPD patients with severe hyperinflation and exercise-induced desaturation benefit NIV in addition to oxygen during exercise; they walk further with the same level of dyspnea and recover faster. These results may contribute to individualized treatment during exercise training.

Author Contributions

Conceptualization: L.E.G.W.V., M.A.S., A.V., D.M.; Methodology: M.K., L.E.G.W.V., M.A.S., D.M., A.V.; Validation: M.K., L.E.G.W.V.; Formal Analysis: M.K., J.D.; Investigation: M.K., J.D., L.E.G.W.V.; Resources: D.M., A.V., E.F.M.W.; Data Curation: M.K., J.D., L.E.G.W.V.; Writing—Original Draft Preparation: M.K., L.E.G.W.V., M.A.S.; Writing—Review and Editing: L.E.G.W.V., M.A.S., F.M.E.F., E.F.M.W., D.M., A.V., J.D.; Visualization: M.K., L.E.G.W.V., M.A.S.; Supervision: L.E.G.W.V., F.M.E.F., M.A.S., E.F.M.W.; Project Administration: M.K., L.E.G.W.V.; Funding acquisition: L.E.G.W.V., M.A.S. All co-authors critically revised the article and gave final approval of this version to be published.

Funding

This research was funded by Philips Research, Eindhoven, the Netherlands by providing the ventilator, tubes, masks and GoPro used in this study, and CIRO, center of expertise for chronic organ failure, Horn, the Netherlands.

Conflicts of Interest

M.K., M.A.S., F.M.E.F., J.D., E.F.M.W., D.M., A.V. and L.E.G.W.V. declare that they have no real or perceived conflict of interest with regard to the topic of this manuscript. The study was partly funded by Philips Research. This manuscript has not been submitted to another journal, and has not been published in whole or in part elsewhere previously.

References

  1. O’Donnell, D.E.; Webb, K.A. The major limitation to exercise performance in COPD is dynamic hyperinflation. J. Appl. Physiol. (1985) 2008, 105, 753–755, discussion 755–757. [Google Scholar] [CrossRef]
  2. Spruit, M.A.; Singh, S.J.; Garvey, C.; ZuWallack, R.; Nici, L.; Rochester, C.; Hill, K.; Holland, A.E.; Lareau, S.C.; Man, W.D.; et al. An official American Thoracic Society/European Respiratory Society statement: Key concepts and advances in pulmonary rehabilitation. Am. J. Respir. Crit. Care Med. 2013, 188, e1364. [Google Scholar] [CrossRef]
  3. Rocha, A.; Arbex, F.F.; Sperandio, P.A.; Mancuso, F.; Marillier, M.; Bernard, A.C.; Alencar, M.C.N.; O’Donnell, D.E.; Neder, J.A. Exercise intolerance in comorbid COPD and heart failure: The role of impaired aerobic function. Eur. Respir. J. 2019, 53, 2018. [Google Scholar] [CrossRef]
  4. American Thoracic, S.; American College of Chest, P. ATS/ACCP Statement on cardiopulmonary exercise testing. Am. J. Respir. Crit. Care Med. 2003, 167, 211–277. [Google Scholar] [CrossRef]
  5. Force, E.R.S.T.; Palange, P.; Ward, S.A.; Carlsen, K.H.; Casaburi, R.; Gallagher, C.G.; Gosselink, R.; O’Donnell, D.E.; Puente-Maestu, L.; Schols, A.M.; et al. Recommendations on the use of exercise testing in clinical practice. Eur. Respir. J. 2007, 29, 185–209. [Google Scholar] [CrossRef]
  6. Caviedes, I.R.; Delgado, I.; Soto, R. Ventilatory inefficiency as a limiting factor for exercise in patients with COPD. Respir. Care 2012, 57, 583–589. [Google Scholar] [CrossRef] [PubMed]
  7. Whipp, B.J. The bioenergetic and gas exchange basis of exercise testing. Clin. Chest Med. 1994, 15, 173–192. [Google Scholar] [PubMed]
  8. Andrianopoulos, V.; Celli, B.R.; Franssen, F.M.; Pinto-Plata, V.M.; Calverley, P.M.; Vanfleteren, L.E.; Vogiatzis, I.; Vestbo, J.; Agusti, A.; Bakke, P.S.; et al. Determinants of exercise-induced oxygen desaturation including pulmonary emphysema in COPD: Results from the ECLIPSE study. Respir. Med. 2016, 119, 87–95. [Google Scholar] [CrossRef] [PubMed]
  9. Augustin, I.M.L.; Spruit, M.A.; Houben-Wilke, S.; Franssen, F.M.E.; Vanfleteren, L.; Gaffron, S.; Janssen, D.J.A.; Wouters, E.F.M. The respiratory physiome: Clustering based on a comprehensive lung function assessment in patients with COPD. PLoS ONE 2018, 13, e0201593. [Google Scholar] [CrossRef] [PubMed]
  10. Marin, J.M.; Carrizo, S.J.; Gascon, M.; Sanchez, A.; Gallego, B.; Celli, B.R. Inspiratory capacity, dynamic hyperinflation, breathlessness, and exercise performance during the 6-minute-walk test in chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 2001, 163, 1395–1399. [Google Scholar] [CrossRef]
  11. Gloeckl, R.; Andrianopoulos, V.; Stegemann, A.; Oversohl, J.; Schneeberger, T.; Schoenheit-Kenn, U.; Hitzl, W.; Dreher, M.; Rembert Koczulla, A.; Kenn, K. High-pressure non-invasive ventilation during exercise in COPD patients with chronic hypercapnic respiratory failure: A randomized, controlled, cross-over trial. Respirology 2018. [Google Scholar] [CrossRef] [PubMed]
  12. Vitacca, M.; Kaymaz, D.; Lanini, B.; Vagheggini, G.; Ergun, P.; Gigliotti, F.; Ambrosino, N.; Paneroni, M. Non-invasive ventilation during cycle exercise training in patients with chronic respiratory failure on long-term ventilatory support: A randomized controlled trial. Respirology 2017. [Google Scholar] [CrossRef] [PubMed]
  13. Van’t Hul, A.; Kwakkel, G.; Gosselink, R. The acute effects of noninvasive ventilatory support during exercise on exercise endurance and dyspnea in patients with chronic obstructive pulmonary disease: A systematic review. J. Cardiopulm. Rehabil. 2002, 22, 290–297. [Google Scholar] [CrossRef] [PubMed]
  14. Van’t Hul, A.; Gosselink, R.; Hollander, P.; Postmus, P.; Kwakkel, G. Acute effects of inspiratory pressure support during exercise in patients with COPD. Eur. Respir. J. 2004, 23, 34–40. [Google Scholar] [CrossRef]
  15. Borghi-Silva, A.; Carrascosa, C.; Oliveira, C.C.; Barroco, A.C.; Berton, D.C.; Vilaca, D.; Lira-Filho, E.B.; Ribeiro, D.; Nery, L.E.; Neder, J.A. Effects of respiratory muscle unloading on leg muscle oxygenation and blood volume during high-intensity exercise in chronic heart failure. Am. J. Physiol. Heart Circ. Physiol. 2008, 294, 2465–2472. [Google Scholar] [CrossRef]
  16. Babcock, M.A.; Pegelow, D.F.; Harms, C.A.; Dempsey, J.A. Effects of respiratory muscle unloading on exercise-induced diaphragm fatigue. J. Appl. Physiol. (1985) 2002, 93, 201–206. [Google Scholar] [CrossRef]
  17. Mahadevan, A.; Brouqueyre, L.; Cain, C.; Cropp, A.; ZuWallack, R. Philips Respironics. Impact of Positive Airway Pressure in Post-Exercise Recovery from Dyspnea in COPD Patients. In Proceedings of the ATS, San Diego, CA, USA; Available online: https://www.atsjournals.org/doi/abs/10.1164/ajrccm-conference.2014.189.1_MeetingAbstracts.A2648 (accessed on 2 May 2015).
  18. Emtner, M.; Porszasz, J.; Burns, M.; Somfay, A.; Casaburi, R. Benefits of supplemental oxygen in exercise training in nonhypoxemic chronic obstructive pulmonary disease patients. Am. J. Respir. Crit. Care Med. 2003, 168, 1034–1042. [Google Scholar] [CrossRef]
  19. Garrod, R.; Paul, E.A.; Wedzicha, J.A. Supplemental oxygen during pulmonary rehabilitation in patients with COPD with exercise hypoxaemia. Thorax 2000, 55, 539–543. [Google Scholar] [CrossRef]
  20. Jarosch, I.; Gloeckl, R.; Damm, E.; Schwedhelm, A.L.; Buhrow, D.; Jerrentrup, A.; Spruit, M.A.; Kenn, K. Short-term Effects of Supplemental Oxygen on 6-Min Walk Test Outcomes in Patients With COPD: A Randomized, Placebo-Controlled, Single-blind, Crossover Trial. Chest 2017, 151, 795–803. [Google Scholar] [CrossRef]
  21. O’Donnell, D.E.; Bain, D.J.; Webb, K.A. Factors contributing to relief of exertional breathlessness during hyperoxia in chronic airflow limitation. Am. J. Respir. Crit. Care Med. 1997, 155, 530–535. [Google Scholar] [CrossRef]
  22. Rodrigues, M.K.; Oliveira, M.F.; Soares, A.; Treptow, E.; Neder, J.A. Additive effects of non-invasive ventilation to hyperoxia on cerebral oxygenation in COPD patients with exercise-related O2 desaturation. Clin. Physiol. Funct. Imaging 2013, 33, 274–281. [Google Scholar] [CrossRef] [PubMed]
  23. Vogelmeier, C.F.; Criner, G.J.; Martinez, F.J.; Anzueto, A.; Barnes, P.J.; Bourbeau, J.; Celli, B.R.; Chen, R.; Decramer, M.; Fabbri, L.M.; et al. Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Lung Disease 2017 Report: GOLD Executive Summary. Arch. Bronconeumol. 2017, 53, 128–149. [Google Scholar] [CrossRef] [PubMed]
  24. Spruit, M.A.; Vanderhoven-Augustin, I.; Janssen, P.P.; Wouters, E.F. Integration of pulmonary rehabilitation in COPD. Lancet 2008, 371, 12–13. [Google Scholar] [CrossRef]
  25. Miller, M.R.; Crapo, R.; Hankinson, J.; Brusasco, V.; Burgos, F.; Casaburi, R.; Coates, A.; Enright, P.; van der Grinten, C.P.; Gustafsson, P.; et al. General considerations for lung function testing. Eur. Respir. J. 2005, 26, 153–161. [Google Scholar] [CrossRef]
  26. Quanjer, P.H.; Stanojevic, S.; Cole, T.J.; Baur, X.; Hall, G.L.; Culver, B.H.; Enright, P.L.; Hankinson, J.L.; Ip, M.S.; Zheng, J.; et al. Multi-ethnic reference values for spirometry for the 3–95-yr age range: The global lung function 2012 equations. Eur. Respir. J. 2012, 40, 1324–1343. [Google Scholar] [CrossRef]
  27. Stocks, J.; Quanjer, P.H. Reference values for residual volume, functional residual capacity and total lung capacity. ATS Workshop on Lung Volume Measurements. Official Statement of The European Respiratory Society. Eur. Respir. J. 1995, 8, 492–506. [Google Scholar] [CrossRef]
  28. Singh, S.J.; Puhan, M.A.; Andrianopoulos, V.; Hernandes, N.A.; Mitchell, K.E.; Hill, C.J.; Lee, A.L.; Camillo, C.A.; Troosters, T.; Spruit, M.A.; et al. An official systematic review of the European Respiratory Society/American Thoracic Society: Measurement properties of field walking tests in chronic respiratory disease. Eur. Respir. J. 2014, 44, 1447–1478. [Google Scholar] [CrossRef]
  29. Porszasz, J.; Cao, R.; Morishige, R.; van Eykern, L.A.; Stenzler, A.; Casaburi, R. Physiologic effects of an ambulatory ventilation system in chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 2013, 188, 334–342. [Google Scholar] [CrossRef]
  30. Brochard, L. Intrinsic (or auto-) positive end-expiratory pressure during spontaneous or assisted ventilation. Intensive Care Med. 2002, 28, 1552–1554. [Google Scholar] [CrossRef]
  31. Aliverti, A.; Dellaca, R.L.; Lotti, P.; Bertini, S.; Duranti, R.; Scano, G.; Heyman, J.; Lo Mauro, A.; Pedotti, A.; Macklem, P.T. Influence of expiratory flow-limitation during exercise on systemic oxygen delivery in humans. Eur. J. Appl. Physiol. 2005, 95, 229–242. [Google Scholar] [CrossRef]
  32. Aliverti, A.; Macklem, P.T. The major limitation to exercise performance in COPD is inadequate energy supply to the respiratory and locomotor muscles. J. Appl. Physiol. (1985) 2008, 105, 749–751, discussion 755-747. [Google Scholar] [CrossRef] [PubMed]
  33. Keilty, S.E.; Ponte, J.; Fleming, T.A.; Moxham, J. Effect of inspiratory pressure support on exercise tolerance and breathlessness in patients with severe stable chronic obstructive pulmonary disease. Thorax 1994, 49, 990–994. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. O’Donnell, D.E.; Guenette, J.A.; Maltais, F.; Webb, K.A. Decline of resting inspiratory capacity in COPD: The impact on breathing pattern, dyspnea, and ventilatory capacity during exercise. Chest 2012, 141, 753–762. [Google Scholar] [CrossRef] [Green Version]
  35. Guenette, J.A.; Webb, K.A.; O’Donnell, D.E. Does dynamic hyperinflation contribute to dyspnoea during exercise in patients with COPD? Eur. Respir. J. 2012, 40, 322–329. [Google Scholar] [CrossRef]
  36. Hajian, B.; De Backer, J.; Sneyers, C.; Ferreira, F.; Barboza, K.C.; Leemans, G.; Vos, W.; De Backer, W. Pathophysiological mechanism of long-term noninvasive ventilation in stable hypercapnic patients with COPD using functional respiratory imaging. Int. J. Chronic Obstr. Pulm. Dis. 2017, 12, 2197–2205. [Google Scholar] [CrossRef] [Green Version]
  37. Wuyam, B.; Payen, J.F.; Levy, P.; Bensaidane, H.; Reutenauer, H.; Le Bas, J.F.; Benabid, A.L. Metabolism and aerobic capacity of skeletal muscle in chronic respiratory failure related to chronic obstructive pulmonary disease. Eur. Respir. J. 1992, 5, 157–162. [Google Scholar]
  38. Layec, G.; Hart, C.R.; Trinity, J.D.; Kwon, O.S.; Rossman, M.J.; Broxterman, R.M.; Le Fur, Y.; Jeong, E.K.; Richardson, R.S. Oxygen delivery and the restoration of the muscle energetic balance following exercise: Implications for delayed muscle recovery in patients with COPD. Am. J. Physiol. Endocrinol. Metab. 2017, 313, E94–E104. [Google Scholar] [CrossRef] [Green Version]
  39. O’Donnell, D.E.; Sanii, R.; Younes, M. Improvement in exercise endurance in patients with chronic airflow limitation using continuous positive airway pressure. Am. Rev. Respir. Dis. 1988, 138, 1510–1514. [Google Scholar] [CrossRef]
  40. Petrof, B.J.; Calderini, E.; Gottfried, S.B. Effect of CPAP on respiratory effort and dyspnea during exercise in severe COPD. J. Appl. Physiol. (1985) 1990, 69, 179–188. [Google Scholar] [CrossRef]
  41. Contal, O.; Vignaux, L.; Combescure, C.; Pepin, J.L.; Jolliet, P.; Janssens, J.P. Monitoring of noninvasive ventilation by built-in software of home bilevel ventilators: A bench study. Chest 2012, 141, 469–476. [Google Scholar] [CrossRef] [Green Version]
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Figure 1. Interventions. Abbreviations: 6MWD = six-minute walking distance, NIV = non-invasive ventilation, BORG D = Borg dyspnea, CPAP = continuous positive airway pressure, BiPAP = bilevel positive airway pressure, FiO2 = inspired oxygen fraction.
Figure 1. Interventions. Abbreviations: 6MWD = six-minute walking distance, NIV = non-invasive ventilation, BORG D = Borg dyspnea, CPAP = continuous positive airway pressure, BiPAP = bilevel positive airway pressure, FiO2 = inspired oxygen fraction.
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Figure 2. Study flow chart. Abbreviations: COPD = chronic obstructive pulmonary disease, 6MWD = six minute walking distance, NIV = non-invasive ventilation.
Figure 2. Study flow chart. Abbreviations: COPD = chronic obstructive pulmonary disease, 6MWD = six minute walking distance, NIV = non-invasive ventilation.
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Figure 3. Results of walking time bout 1 and 2 and time till recovery in four tests with different ventilator settings. Statistical significant differences (p < 0,05); * = sham vs. oxygen, ˟ = sham vs. NIV and O2, ° = sham vs. intermittent, ± = oxygen vs. NIV and O2, • = oxygen vs. intermittent, ÷ = NIV and O2 vs. intermittent; Abbreviations: NIV = non-invasive ventilation, O2 = oxygen, s = seconds.
Figure 3. Results of walking time bout 1 and 2 and time till recovery in four tests with different ventilator settings. Statistical significant differences (p < 0,05); * = sham vs. oxygen, ˟ = sham vs. NIV and O2, ° = sham vs. intermittent, ± = oxygen vs. NIV and O2, • = oxygen vs. intermittent, ÷ = NIV and O2 vs. intermittent; Abbreviations: NIV = non-invasive ventilation, O2 = oxygen, s = seconds.
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Figure 4. Individual results with different settings on the first bout of exercise. Abbreviations: s = seconds, NIV = non-invasive ventilation.
Figure 4. Individual results with different settings on the first bout of exercise. Abbreviations: s = seconds, NIV = non-invasive ventilation.
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Figure 5. Isotime results on PaCO2, SpO2, heart rate, breathing frequency and tidal volume of different settings during bout 1 of all patients. (a) PaCO2 test 1, (b) SpO2 test 1, (c) Heart rate test 1, (d) Breathing frequency test 1, (e) Tidal volume test 1.
Figure 5. Isotime results on PaCO2, SpO2, heart rate, breathing frequency and tidal volume of different settings during bout 1 of all patients. (a) PaCO2 test 1, (b) SpO2 test 1, (c) Heart rate test 1, (d) Breathing frequency test 1, (e) Tidal volume test 1.
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Table
Table 1. Baseline characteristics n = 13.
Table 1. Baseline characteristics n = 13.
Baseline CharacteristicsMean
Age, years61.5 ± 6.8
Female, n (%) 9 (69)
BMI, kg/m225.4 ± 5.0
mMRC score, median (IQR)3.0 (2.0)
Ex-smoker, n (%)13 (100%)
Packyears40.8 ± 15.2
FEV1, % predicted34.0 ± 10.2
FEV1/FVC, %27.9 ± 4.2
FRC, % predicted171.9 ± 18.3
RV, % predicted193.4 ± 32.0
TLC, % predicted128.4 ± 13.5
RV/TLC ratio0.59 ± 0.08
DLCO, % predicted (n = 12)46.7 ± 12.8
PaO2, kPa9.2 ± 1.5
PaCO2, kPa5.6 ± 0.6
6MWD, m403.2 ± 73.6
6MWD, % predicted 66.1 ± 13.2
6MWD SpO2 start, %92.2 ± 3.2
6MWD SpO2 stop, %82.5 ± 5.1
6MWD HR start, b/min83.0 ± 13.6
6MWD HR stop, b/min108.2 ± 13.1
6MWD Borg D start2.3 ± 1.3
6MWD Borg D stop5.4 ± 1.8
6MWD Borg F start2.2 ± 1.4
6MWD Borg F stop4.5 ± 1.1
Abbreviations: FEV1 = forced expiratory volume in 1 second, FVC = forced vital capacity, FRC = functional residual capacity, RV = residual volume, TLC = total lung capacity, DLCO = diffusion capacity of the lung for carbon monoxide, BMI = body mass index, mMRC = modified medical research council, PaO2/PaCO2 = partial arterial pressure of oxygen/carbon dioxide, 6MWD = 6 minute walking distance, SpO2 = saturation of peripheral oxygen, HR = heart rate, Borg D = Borg dyspnea, Borg F = Borg fatigue.
Table
Table 2. Results of 13 COPD patients with hyperinflation and exertional oxygen desaturation completing four sets of treadmill tests with different settings of the ventilator.
Table 2. Results of 13 COPD patients with hyperinflation and exertional oxygen desaturation completing four sets of treadmill tests with different settings of the ventilator.
Exercise Bout OneExercise Bout Two
1 Sham2 Oxygen3 NIV and Oxygen4 Intermittent1 Sham2 Oxygen3 NIV and Oxygen4 Intermittent
Total distance walked, m120 (50)225 (107) *283 (128) ˟ ±123 (38) • ÷107 (69)188 (109) *261 (136) ˟ ±119 (45) • ÷
Endurance time, seconds91 (36)171 (88) *216 (105) ˟ ±91 (27) • ÷80 (47)145 (92) *198 (103) ˟ ±89 (34) • ÷
Recovery time, seconds170 (49)150 (48)117 (51) ˟119 (37) º •
Pre-test HR, bpm84 (12.2)84 (14.4)83 (14.8)84 (13.2)91 (15.4)91 (14.3)92 (16.1)89 (13.0)
Post- test HR, bpm100 (19.9)105 (16.7)105 (19)104 (15.5)106 (13.8)107 (17.6)110 (17.5)102 (13.6)
Recovery HR, bpm91 (15.4)91 (14.3)92 (16.1)89 (13.0)92 (10.6)92 (16.0)94 (16.9)93 (15.1)
Pre-test BF, bpm21 (5.0)21 (6.5)18 (4.1)20 (4.7) ÷21 (8.0)24 (5.6)24 (4.3)23 (4.5)
Post-test BF, bpm31 (10)28 (7.8)27 (6.7)32 (5.4) ÷30 (7.7)29 (8.1)28 (5.8)32 (8.7)
Recovery BF, bpm21 (8.0)24 (5.6)24 (4.3)23 (4.5)22 (5.2)23 (5.7)22 (5.5)24 (4.5)
Pre-test SpO2, %94 (3.0)96 (2.5)98 (2.6)95 (2.1)93 (4.4)98 (2.7) *99 (1.0) ˟99 (1.0) º
Post-test SPO2, %84 (6.6)96 (5.2) *98 (1.2) ˟85 (4.6) •84 (7.0)97 (3.2) *99 (1.5) º85 (4.6) • ÷
Recovery SpO2, %93 (4.4)98 (2.7) *99 (1.0) ˟99 (1.0) º90 (5.0)98 (2.6) *99 (0.8) ˟90 (5.9) • ÷
Pre-test tcPaCO2, kPa (n = 1)5.3 (0.7)5.4 (0.7)5.1 (0.9)5.2 (0.7)6.1 (0.9)6.7 (0.9) *6.3 (1.2)5.9 (0.7) •
Post-test tcPaCO2, kPa (n = 11)5.6 (0.8)6.3 (1.1) *5.9 (1.1)5.5 (0.7) •6.1 (0.9)6.6 (1.4)6.5 (1.3)6.0 (0.9)
Δ tcPaCO2, kPa (n = 11)0.3 (0.2)1.0 (0.9) *0.9 (0.6) ˟0.3 (0.3) ÷6.4 (0.9)7.1 (1.2) *6.6 (1.2)6.4 (0.9) •
Recovery tcPaCO2, kPa (n = 11)6.1 (0.9)6.7 (0.9) *6.3 (1.2)5.9 (0.7) •0.02 (0.1)-0.06 (0.8)0.1 (0.3)0.1 (0.2)
Pre-test tidal volume, mL (Median (IQR))808 (354) (696 (398))822 (383) (699 (479))954 (214) (919 (242))800 (298) (709 (255))1059 (276) (1031 (405))921 (290) * (849 (463))1130 (284) ± (1075 (424))1020 (245) (954 (252))
Post-test tidal volume, mL (Median (IQR))1075 (296) (1034 (336))1145(338) (1051 (519))1166 (257) (1263 (441))1119 (249) (1066 (407))1128 (291) (1018 (381))1122 (304) (1083 (440))1141 (410) (1161 (463))1039 (289) (977 (412))
Δ tidal volume, mL (Median (IQR))267 (241) (360 (448))323 (336) (306 (530))212 (256) (166 (321))318 (228) (313 (260))68 (170) (117 (257))201 (234) (166 (302))11 (287) (29 (207))19 (165) (−18 (229))
Recovery tidal volume, mL (Median (IQR))1059 (276) (1031 (405))921 (290) * (849 (463))1130 (284) ± (1075 (424))1020 (245) (954 (252))1208 (421) (1143 (588))1124 (437) (981 (862))1285 (348) (1223 (357))1202 (334) (1169 (515))
Pre-test ventilation, L/min15.9 (3.2)15.4 (3.1)16.8 (4.0)15.3 (2.6)22.0 (8.7)20.7 (4.7)26.5 (5.7) ±22.6 (5.5) ÷
Post-test ventilation, L/min31.1 (9.8)30.6 (8.4)30.9 (9.3)35.9 (10.3)32.1 (8.0)30.9 (8.2)32.3 (12.2)31.7 (8.2)
Pre-test Borg-D, points (Median (IQR))0.7 (1.0) (0.5 (1.5))0.8 (0.9) (0.5 (2.0))0.5 (0.6) (0.5 (1.0))0.8 (1.2) (0.0 (1.5))1.8 (0.6) (2.0 (0.0))1.9 (0.4) (2.0 (0.0))1.8 (0.4) (2.0 (0.0))1.7 (0.7) (2.0 (0.0))
Post-test Borg-D, points (Median (IQR))4.1 (2.1) (5.0 (2.0))5.2 (2.1) (4.0 (3.0))4.3 (1.4) ± (4.0 (1.0))5.2 (1.4) (5.0 (3.0))4.9 (2.4) (4.0 (3.0))4.8 (2.2) (4.0 (3.5))4.7 (1.8) (4.0 (2.5))5.1 (1.7) (5.0 (2.0))
Recovery Borg-D, points (Median (IQR))1.8 (0.6) (2.0 (0.0))1.9 (0.4) (2.0 (0.0))1.8 (0.4) (2.0 (0.0))1.7 (0.7) (2.0 (0.0))1.9 (0.6) (3.0 (0.5))1.8 (0.5) (2.0 (0.0))1.8 (0.6) (2.0 (0.5))2.0 (0.4) (2.0 (0.5))
Pre-test Borg-F, points (Median (IQR))1.0 (1.1) (0.5 (2.0))1.0 (1.1) (0.25 (2.0))0.6 (0.6) (0.75 (1.0))0.6 (0.8) (0.25 (1.0))1.7 (0.9) (2.0 (1.0))1.8 (1.0) (2.0 (2.0))1.7 (1.2) (1.0 (2.0))0.6 (0.8) º • ÷ (0.0 (1.0))
Post-test Borg-F, points (Median (IQR))2.8 (1.9) (2.0 (2.5))3.3 (1.6) (3.0 (1.0))3.1 (1.5) (3.0 (2.0))2.6 (2.0) (3.0 (2.8))2.4 (1.4) (2.0 (2.5))2.8 (1.3) (3.0 (1.0))3.2 (1.9) (3.0 (2.5))2.3 (1.6) (2.0 (2.3))
Recovery Borg-F, points (Median (IQR))1.7 (0.9) (2.0 (1.0))1.8 (1.0)(2.0 (2.0))1.7 (1.2) (1.0 (2.0))0.6 (0.8) º • ÷ (0.0 (1.0))1.9 (0.8) (2.0 (1.0))1.7 (1.1) (2.0 (2.0))1.8 (1.0) (1.0 (0.5))1.6 (0.8) (1.0 (1.0))
Statistical significant differences per bout of exercise (p < 0,05); * = 1 vs. 2, ˟ = 1 vs. 3, º = 1 vs. 4, ± = 2 vs. 3, • = 2 vs. 4, ÷ = 3 vs. 4; Abbreviations: Δ = delta, Borg D = Borg dyspnea, Borg F = Borg fatigue, SpO2 = saturation of peripheral oxygen, HR = heart rate, BF = breathing frequency, tcPaCO2 = transcutaneous partial pressure of carbon dioxide, VT = tidal volume, IQR = interquartile range.

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Koopman, M.; Spruit, M.A.; Franssen, F.M.E.; Delbressine, J.; Wouters, E.F.M.; Mathew, D.; Vink, A.; Vanfleteren, L.E.G.W. Effects of Non-Invasive Ventilation Combined with Oxygen Supplementation on Exercise Performance in COPD Patients with Static Lung Hyperinflation and Exercise-Induced Oxygen Desaturation: A Single Blind, Randomized Cross-Over Trial. J. Clin. Med. 2019, 8, 2012. https://doi.org/10.3390/jcm8112012

AMA Style

Koopman M, Spruit MA, Franssen FME, Delbressine J, Wouters EFM, Mathew D, Vink A, Vanfleteren LEGW. Effects of Non-Invasive Ventilation Combined with Oxygen Supplementation on Exercise Performance in COPD Patients with Static Lung Hyperinflation and Exercise-Induced Oxygen Desaturation: A Single Blind, Randomized Cross-Over Trial. Journal of Clinical Medicine. 2019; 8(11):2012. https://doi.org/10.3390/jcm8112012

Chicago/Turabian Style

Koopman, Maud, Martijn A. Spruit, Frits M.E. Franssen, Jeannet Delbressine, Emiel F.M. Wouters, Denny Mathew, Anton Vink, and Lowie E.G.W. Vanfleteren. 2019. "Effects of Non-Invasive Ventilation Combined with Oxygen Supplementation on Exercise Performance in COPD Patients with Static Lung Hyperinflation and Exercise-Induced Oxygen Desaturation: A Single Blind, Randomized Cross-Over Trial" Journal of Clinical Medicine 8, no. 11: 2012. https://doi.org/10.3390/jcm8112012

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