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Copyright ©ERS Journals Ltd 2004
Maintenance of inspiratory muscle training in COPD patients: one year follow-up
Dept of Medicine A, Hillel Yaffe Medical Center, Hadera, Israel
CORRESPONDENCE: P. Weiner, Dept of Medicine A, Hillel Yaffe Medical Center, Hadera, Israel 38100. Fax: 011 97246304522. E-mail: weiner@hillel-yaffe.health.gov.il
Keywords: inspiratory muscle training, sensation of dyspnoea, exercise performance
Received: May 29, 2003
Accepted September 1, 2003
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Abstract |
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 TOP Abstract Patients and methodsResultsDiscussionReferences |
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In most chronic obstructive pulmonary disease (COPD) patients, dyspnoea and functional exercise capacity may improve as a result of inspiratory muscle training (IMT). However, the long-term benefits of IMT have been investigated to a much lesser extent.
The present study investigated the short-term and long-term benefits of IMT on inspiratory muscle performance (strength and endurance), exercise capacity and the perception of dyspnoea.
Thirty-eight patients with significant COPD had 3 months of basic IMT and were then randomised into a group that received maintenance IMT for the next year, and a group that got training with very low load. Following the basic training there was a statistically significant increase in inspiratory muscle performance, 6-min walk test (6MWT), and a decrease in the dyspnoea. During the second stage of the study, the training group continued to maintain the improvement in all parameters, while there was already deterioration in the inspiratory muscle performance, exercise capacity and dyspnoea in the low intensity group during the 6–12 month period.
The present study concludes that, in patients with significant chronic obstructive pulmonary disease, inspiratory muscle training results in improvement in performance, exercise capacity and in the sensation of dyspnoea. The benefits of 12-weeks of inspiratory muscle training decline gradually over 1 yr of follow-up if maintenance training is not performed.
Patients with significant chronic obstructive pulmonary disease (COPD) have respiratory and peripheral muscle weakness 1. Respiratory muscle weakness may contribute to dyspnoea and to poor exercise performance 2, 3. Therefore, it was rational to try ventilatory muscle training in these patients, to enhance respiratory muscle function and potentially reduce the severity of breathlessness and improve exercise tolerance.
Inspiratory muscle training has been extensively investigated in patients with COPD. Although, in their meta-analysis, Smith et al. 4 concluded that inspiratory muscle training (IMT) in patients with COPD did not reveal significant treatment effect, it was later shown, in studies in which the training stimulus was adequate, that in most COPD patients, dyspnoea and functional exercise capacity may improve as a result of such training 5–7. The joint American College of Chest Physicians/American Association of Cardiovascular and Pulmonary Rehabilitation committee 8 declared that when the stimulus or load placed on the respiratory muscles during training is sufficient to augment inspiratory muscle strength, there is an associated increase in exercise capacity and decrease in dyspnoea. In a recent meta-analysis performed by Lötters et al. 9 it was concluded that IMT, alone or as an adjunct to general exercise reconditioning, decreases dyspnoea and improves functional exercise capacity in patients with COPD.
Despite the documented benefits of IMT in a rehabilitation program, longer-term effects are less clearly defined. While it is well documented that the benefits of multidisciplinary pulmonary rehabilitation gradually decline over 1 or 2 yrs 10–11, the long-term effects of IMT were investigated to a much lesser extent in COPD.
The present study was performed in order to investigate the short-term and the long-term effect of IMT on inspiratory muscle performance, exercise performance and the perception of dyspnoea, and the decline of these parameters following withdrawal from the maintenance training program in patients with significant COPD.
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Patients and methods |
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TOPAbstractPatients and methodsResultsDiscussionReferences |
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Subjects
Thirty-eight consecutive patients, 31 males and 7 females, with spirometric evidence of significant chronic air-flow limitation (forced expiratory volume in one second (FEV1) <50% predicted, FEV1/forced vital capacity (FVC) <70% pred) who were diagnosed as having COPD according to the criteria ofthe American Thoracic Society 12, were recruited from the community for the study. The eligibility rate was 65%. According to the statistician's power calculation a group size of 30 patients would allow the observation of significant differences between the groups.
They were all new to a rehabilitation program, and none had any additional regular exercise or dietary supplements. All were on regular long-acting bronchodilators, and 28 were on regular inhaled corticosteroid therapy.
They were all observed during a 4-week run-in period, when their regular treatment was maintained, to verify stability in their clinical and functional status. Their characteristics are summarised in table 1
. Patients with cardiac disease, poor compliance, a requirement of supplemental oxygen, or carbon dioxide retention (carbon dioxide arterial tension >6.65 kPa (>50 mmHg)) were excluded from the study.
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Study design
All tests were performed before and 3, 6, 9, 12, and 15 months after starting the training period.
After completion of 3 months of IMT the patients were randomised, using a random numbers table, into two groups: a group of patients assigned to receive IMT for the next year, and a group of patients assigned as a control group, who got training with very low load.
In all the patients several practice tests were performed before the baseline value in order to correct possible training and learning effect. All the data was collected by the same collector, who was blinded to the training group, as well as by the patients themselves, who were also blinded to the mode of treatment.
The study protocol was approved by the institutional ethics committee and informed consent was obtained from all the subjects.
Tests
Spirometry
The FVC and the FEV1 were measured 3 times on a computerised spirometer (Compact, Vitalograph, Buckingham, England) and the best trial is reported.
6-minute walk test
The distance the patient was able to walk in 6 min was determined in a measured corridor as described for the 12-min walk test by McGavin et al. 13. The patients were instructed to walk at their fastest pace and cover the longest possible distance over 6 min under the supervision of a physiotherapist. The test was performed twice and the best result is reported.
Inspiratory muscle strength
Inspiratory muscle strength was assessed by measuring the maximal inspiratory mouth pressure (PI,max) at residual volume, as previously described by Black and Hyatt 14. Mouth pressures were measured with a vacuumed 1002 mouthpiece (Vista, Ventura, CA, USA), that has a small air leak to prevent pressure generation by glottis closure, connected to a pressure transducer (1050 BP transducer; Biopac Systems Inc, Santa Barbara, CA, USA) and recorded on a strip chart recorder. The value obtained from the best of at least three efforts was used.
Inspiratory muscle endurance
To determine inspiratory muscle endurance a device similar to that proposed by Nickerson and Keens 15 was used. Subjects inspired through a two-way Hans-Rudolph valve (Hans-Rudolph, Kansas City, MO, USA) whose inspiratory port was connected to a chamber and plunger to which weights could be added externally. Inspiratory elastic work was then increased by the progressive addition of 25–100 g weights (to get 5–7 measurements during the test), at 2-min intervals, as previously described by Martyn et al. 16, until thesubjects were exhausted and could no longer inspire. The pressure achieved with the heaviest load (tolerated for at least 60 s) was defined as the peak inspiratory pressure (PIP).
Dyspnoea
Dyspnoea was assessed using two techniques: 1) dyspnoea in daily activities was assessed with Mahler's baseline dyspnoea index (BDI) 17, and by the transition dyspnoea index (TDI), following training. 2) the perception of dyspnoea (POD) was also measured while the subject breathed through the same device proposed by Nickerson and Keens 15. The subjects breathed against progressive resistance, at 1 min intervals, in order to achieve mouth pressure of 0 (no resistance), 5, 10, 20 and 30 cmH2O. After breathing for 1 min in each inspiratory load, in a protocol similar to the one previously described by the current authors' group 18, the subjects rated the sensation of difficulty in breathing (dyspnoea) using a modified Borg scale 19. This is a linear scale of numbers ranking the magnitude of difficulty in breathing, ranging from 0 (none) to 10 (maximal).
Training protocol
Stage I
All subjects trained daily, six times a week, each session consisting of 30 min, for 3 months. The training was performed using a threshold inspiratory muscle trainer (ThresholdTM Inspiratory Muscle Trainer, Healthscan, New Jersey, NJ, USA). They started breathing at a resistance that required generation of 15% of their PI,max for 1 week. The load was then increased incrementally, 5–10% each session, to reach generation of 60% of their PI,max at the end of the first month. Specific IMT (SIMT) was then continued at 60% of their PI,max adjusted weekly to the new PI,max achieved.
The training was performed in the current authors' rehabilitation centre for 1 month under the supervision of a respiratory therapist followed by home training, verified by a respiratory therapist, daily by phone, and once weekly by apersonal visit, for the next 2 months.
Stage II
At the end of 3 months IMT, the patients were randomised into an IMT group and a control group that got training with very low load.
The IMT group continued to train three times a week, each session consisting of 30 min, for the next 12 months at 60% of their PI,max, adjusted monthly to the new PI,max achieved.
The control group trained for the same sessions with a fixed load that required generation of mouth pressure of 7 cmH2O.
The training was performed at home, verified by the respiratory therapist, daily by phone, and once weekly by a personal visit, for the next year.
Data analysis
The results are expressed as mean±sem. Comparisons of lung function, respiratory muscle strength and endurance, the 6-min walk test (6MWT), and rating of dyspnoea, within and between the two groups were carried out using the two-way repeated measures analysis of variance.
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Results |
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TOPAbstractPatients and methodsResultsDiscussionReferences |
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There were no significant differences between the two groups in age, height, weight, mean baseline FEV1 and FVC, PI,max, or PIP, and the 6MWT, at the beginning of the study. Six patients dropped out of the study during the basic training period (one of whom died and three had exacerbations) so the results reported at the end of the first stage are on the 32 remaining patients. The attendance rate in the first stage was 83%±7%. During the next year four patients from the training group dropped out of the study (two of whom died) and seven patients from the control group (four of whom died). The attendance rate in the second stage of the study was 72%±7% in the training group and 69%±8% in the control group.
Spirometry
Following the basic training period, there was no significant change in the FEV1 or in the FVC either in the training groups or in the control group. Following the second stage of the study there was a statistically insignificant trend for decrease in FEV1 and FVC in the control group but not in the study group (fig. 1). There was a statistically significant difference between the groups at the ninth months stage.
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: control group.Inspiratory muscle strength and endurance
Following the basic training period there was a similar statistically significant increase in PI,max in the training and the control groups (from 66±4.7 cmH2O to 87±5.3 cmH2O and from 63±4.0 cmH2O to 84±4.9 cmH2O, respectively p<0.005) with no difference between the groups. During the second stage of the study the training group continued to show a small increase in the PI,max, while already at the 6month period there was a significant decrease in the PI,max inthe control group (p<0.01) with a significant difference between the groups (p<0.01). This difference was maintained until the end of the fifteenth month (fig. 2
).
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The inspiratory muscle endurance, as assessed by the PIP showed the same pattern. While following the basic training period there was a similar statistically significant increase in PIP in the training and the control groups, during the second stage of the study the training group continued to show a small increase in the PIP, while the control group showed a continuous decrease in the PIP (fig. 3
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6-minute walk test
There was statistically significant improvement in the 6MWT following the basic training period, in both groups.
During the second stage of the study there was a gradual decrease in the 6MWT in the control group but not in the training group. The difference between the groups became statistically significant at the end of the twelfth month (fig. 4).
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Dyspnoea
Mahler's baseline dyspnoea index
There was no statistically significant difference between the two groups in the different components of the BDI.
Following the basic training period there was a similar statistically significant increase in the TDI in the training and the control groups. During the second stage of the study the training group continued to show the same degree of TDI, while the control group returned to the baseline values (table 2).
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Perception of dyspnoea
There was no difference in the POD between the two groups before training. A statistically significant decrease in the mean Borg score during breathing against resistance was associated with the increase in the inspiratory muscle strength, following the basic training.
During the second stage of the study the training group continued to show a similar degree of Borg score during breathing against resistance increase while at the 9 month period there was already a significant increase in the POD in the control group (p<0.01) with a significant difference between the groups (p<0.01). This difference was maintained until the end of the fifteenth month (fig. 5).
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Discussion |
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TOPAbstractPatients and methodsResultsDiscussionReferences |
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This study shows that in patients with significant COPD, inspiratory muscles can be trained with improvement of both muscle strength and endurance. The improvement in the inspiratory muscle performance is associated with improved exercise performance and in the sensation of dyspnoea in daily activities with no improvement in pulmonary function. The benefits of a 12-week inspiratory muscle training decline gradually over 1 year of follow-up when maintenance training is not performed.
All of the patients had at least some degree of inspiratory muscle weakness. Inspiratory muscle weakness is found in the majority of patients with significant COPD 2. Patients with COPD must breathe at high lung volumes to maintain patency of their narrowed airways. The major abnormality of respiratory muscle function in these patients is thought to be the mechanical disadvantage caused by this hyperinflation. Hyperinflation depresses the dome of the diaphragm, shortens its fibres, and forces it to work on an ineffective portion of its length/tension curve.
The results of the basic training program parallel other studies in which significantly increased inspiratory muscle performance was associated with improved exercise tolerance and decreased dyspnoea 9. The improvements observed in the present study are mainly physiological and the translation of those benefits to daily activities are yet to be investigated.
Most of the benefits of training in the present study did not persist 12 months after the basic training if maintenance training was not applied. PI,max, PIP, 6MWT and the POD decreased gradually and this decrease became statistically significant 9 months, 12 months, 12 months and 6 months following the completion of the basic training, respectively.
The outcomes of the current study could have been influenced by learning effects due to the type of training. However, in all the patients several practice tests were performed before the baseline value in order to correct possible training and learning effect. Also, it can be expected that if a learning effect plays a role in the outcomes it would be the same in the various groups of patients.
Several studies have evaluated longer-term general rehabilitation interventions, with mixed results. However, IMT was included in only some of them. In the study of Guell et al. 20 the benefits of pulmonary rehabilitation were present but diminished over the second year of follow-up. Troosters etal. 10 have shown that 6 months of general training was associated with improved exercise tolerance and quality of life that persisted over the next year. Two other studies 21, 22 were unable to show long-term benefits of general pulmonary rehabilitation.
Failure to obtain long-term benefits from short-term intervention is not limited to pulmonary or exercise training. Long-term maintenance of behavioural changes have also been difficult to demonstrate in research on smoking cessation 23, weight loss 24, or exercise adherence 25.
In the current study, the improvement in the dyspnoea indexes and in functional exercise capacity, following the basic training, was not only statistically significant but also exceeded the minimal clinically-important difference for improvement (>20%) 10, 26. In the current study, after the basic SIMT had been completed the average minimal clinically-important improvement for functional exercise capacity and for the dyspnoea score only persisted for 6 months.
The present study contributes additional information to the knowledge regarding the benefits of IMT on exercise capacity and dyspnoea. It supports previous data that an outpatient program can provide benefits to patients with COPD.
A second important finding of the current study is that maintenance training should be applied. Otherwise, the useful benefit of the intensive basic training is not maintained beyond 6 months. Whether the maintenance training should be performed on a regular basis or by pulse training once in a while, is still to be determined.
The third important outcome of the current study, although comparison to an inpatient program was not made, is that IMT in patients with significant COPD may be performed at home, under some supervision, with relatively good compliance and with low monetary cost.
The current study was not designed to determine whether domiciliary inspiratory muscle training reduces exacerbations and hospital admissions in chronic obstructive pulmonary disease patients. Further studies should be performed in order to resolve these questions.
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Footnotes |
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For editorial comments see page 5.
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