Abstract
We have recently shown that patients with chronic obstructive pulmonary disease (COPD) develop contractile fatigue of their quadriceps muscle following endurance exercise. Pulmonary rehabilitation can produce physiological adaptations in patients with COPD. We hypothesized that if pulmonary rehabilitation induces physiological adaptations in the exercising muscle, it should become more fatigue resistant. Twenty one patients with COPD, mean age 69.9 ± 1.9 yr, FEV1 45 ± 4% predicted, participated in an 8-wk outpatient, supervised pulmonary rehabilitation exercise program. Quadriceps contractile fatigue was detected by a fall in quadriceps twitch force postexercise. Twitch force was measured during magnetic stimulation of the femoral nerve. Because potentiated twitches may be more sensitive at detecting fatigue, both unpotentiated (TwQu) and potentiated (TwQp) twitches were obtained before and 10, 30, and 60 min after constant load cycle exercise. Prerehabilitation, during constant load exercise, patients exercised at 37 ± 4 W for 11.2 ± 1.8 min. Prerehabilitation, TwQu fell significantly postexercise down to a minimum value of 82.5 ± 3.1% of the baseline preexercise value (p < 0.001). Similarly, prerehabilitation, TwQp fell significantly postexercise down to a minimum value of 73.9 ± 3.9% of baseline (p < 0.001). Postrehabilitation, for the same intensity and duration of exercise, TwQu was not significantly different from baseline at any time postexercise. Postrehabilitation, TwQp fell significantly postexercise but the fall in TwQp with exercise was significantly less postrehabilitation compared with prerehabilitation (p < 0.001). In conclusion, pulmonary rehabilitation resulted in increased fatigue resistance of the quadriceps muscle in patients with COPD.
Pulmonary rehabilitation of patients with chronic obstructive pulmonary disease (COPD) decreases exertional dyspnea and improves exercise endurance (1-3). The mechanistic basis for these improvements remains unclear. Psychological factors believed to be potentially important include increased patient motivation, phobic desensitization to unpleasant sensations induced by exertion (dyspnea, leg discomfort), and a decrease in the degree of dyspnea and leg discomfort at any given exercise workload. In healthy subjects, a vigorous endurance exercise program leads to physiological adaptations in the cardiovascular system and exercising muscle. It was initially believed that patients with COPD could not exercise at sufficient intensities to induce a physiological training effect (4). However, patients with COPD are often severely deconditioned. Following an intense pulmonary rehabilitation program, increases in the oxidative capacity of the exercised muscle has been demonstrated indicative of physiological adaptations within the exercising muscle (5).
We have recently shown that patients with COPD develop fatigue of the quadriceps muscle following endurance exercise to the limits of tolerance (6). Fatigue was assessed by measuring quadriceps twitch force during magnetic stimulation of the femoral nerve before and after exercise (7). We hypothesized that if pulmonary rehabilitation induces physiological adaptations in the exercising muscle, it should become more fatigue resistant after pulmonary rehabilitation. Accordingly, we compared the degree of quadriceps contractile fatigue elicited by the same intensity and duration of exercise before and after pulmonary rehabilitation. We hypothesized that exercise would induce less contractile fatigue following pulmonary rehabilitation.
Twenty-nine consecutive patients with COPD who entered our pulmonary rehabilitation program agreed to participate in the study. Five patients did not complete the program and were excluded. Maximal or near maximal stimulation of the femoral nerve could not be achieved in three patients. Thus, 21 patients were included in the study. There were 20 males and 1 female, aged 69.9 ± 1.9 yr. Their height and weight were 1.75 ± 0.02 m and 83.5 ± 3.4 kg, respectively. The study was approved by the appropriate institutional review boards and written informed consent was obtained from all subjects.
Pulmonary function was measured using standard techniques according to ATS recommendations (8). Pulmonary function measurements are shown in Table 1. Maximal incremental and constant workload cycle exercise was performed as previously described (6). Lactate levels were obtained before and after constant load exercise (6). After pulmonary rehabilitation was complete, three exercise tests were performed on separate days. On the first day, the maximal exercise test was repeated. On the second day the endurance test was repeated and the test was stopped by the investigator when the prerehabilitation endurance time was reached (for quadriceps and lactate measurements). On the final day, the endurance test was repeated but the patient was allowed to continue exercising to the limits of tolerance (to evaluate any potential improvement in exercise endurance).
| Actual | % Predicted* | |||
|---|---|---|---|---|
| FEV1, L | 1.48 ± 0.12 | 45 ± 4 | ||
| FVC, L | 2.95 ± 0.16 | 68 ± 4 | ||
| FEV1/FVC, % | 48 ± 2 | |||
| RV, L | 4.55 ± 0.33 | 183 ± 13 | ||
| TLC, L | 7.60 ± 0.28 | 109 ± 4 | ||
| Dl CO, ml/min/mm Hg | 14.2 ± 1.2 | 55 ± 5 | ||
| MIP, cm H2O | 64.7 ± 8.0 | 62 ± 7 | ||
| MVV, L/min | 56.3 ± 4.4 | 46 ± 4 |
Six-minute walking tests were administered before (the best of three tests) and after completion of the rehabilitation program (one walk) as an additional test of functional capacity. Subjects were given standardized instructions to cover the greatest distance possible in 6 min. Standardized verbal encouragement was given each minute.
Quadriceps twitch force was measured as previously described (6). In many of the patients, magnetic stimulation of the femoral nerve elicited a large shock artifact that obscured the compound motor action potential (M-wave). However, with careful positioning of the surface electrodes and ground, M-waves were obtained before rehabilitation in 10 patients and after rehabilitation in 8 patients. Following a vigorous voluntary contraction, the subsequent twitch is significantly increased in size (twitch potentiation) (14). Recent studies have suggested that the potentiated twitch is more sensitive at detecting fatigue than the unpotentiated twitch, particularly when the amount of fatigue is small (15, 16). Accordingly, we measured both the unpotentiated and potentiated twitch before and 10, 30, and 60 min after exercise. Unpotentiated and potentiated twitches were measured as previously described (6, 18). To determine the degree to which our subjects could voluntarily activate their quadriceps muscle, twitch interpolation was employed during maximum voluntary contraction maneuvers as previously described (6, 17). An example is shown in Figure 1. To determine if exercise could elicit both high- and low-frequency fatigue, paired stimuli were obtained in 20 subjects as previously described (18). The paired stimuli were given at interstimulus intervals of 100 ms, 50 ms, and 10 ms corresponding to stimulation frequencies of 10, 20, and 100 Hz. The unpotentiated twitch was ensemble averaged and then digitally subtracted from the ensemble- averaged paired stimuli to obtain the amplitude of the second twitch, T2. A significant decrease in T2 postexercise would be indicative of fatigue at that particular stimulation frequency (19). A representative example is shown in Figure 2.
Fig. 1. Representative example of a superimposed twitch during a maximum voluntary contraction (MVC) maneuver. The patient did not make a perfect square wave and the superimposed twitch was not always obtained at the time of peak force development during the MVC maneuver. Thus, the degree of activation during the MVC maneuver will be slightly underestimated.
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Fig. 2. Representative example to demonstrate how the T2 amplitude is calculated. Ensemble average of the unpotentiated twitch (–) and paired twitch at 10 Hz (– – –), 20 Hz (– –), and 100 Hz (– ·· – ·· –). The ensemble average was obtained by lining up all acceptable twitches at the same zero point and then obtaining the digital average. T2 is obtained by digital subtraction of the ensemble averaged unpotentiated twitch from the ensemble averaged paired twitch at each stimulation frequency. T2 is shown at 10 Hz (— — —), 20 Hz (– · –), and 100 Hz (· · ·).
[More] [Minimize]Patients underwent supervised exercise sessions three times a week for 8 wk. Patients exercised on the cycle ergometer and treadmill, performed calisthetics/stretching exercises (20) and received weekly educational sessions.
Changes in variables over time were analyzed by repeated measures analysis of variance and paired t test with Bonferroni correction. Data are expressed as the mean ± SE. Changes in measurements before and after pulmonary rehabilitation were compared by analysis of variance and paired t test. Correlations between continuous variables were made using simple linear regression. An online data supplement to the Methods section providing further details on subject characteristics, exercise, and quadriceps measurements and the pulmonary rehabilitation program is available online at www.atsjournals.org.
Patients had moderately severe airflow obstruction with an FEV1 of 1.48 ± 0.12 l, 48 ± 2% of the predicted value, air trapping (residual volume of 183 ± 13% of predicted value) and a moderately decreased diffusing capacity, 55 ± 5% of predicted value (Table 1).
Maximal incremental exercise test results are shown in Table 2. Exercise capacity was severely decreased, 59 ± 6 W, 41 ± 4% predicted. Peak oxygen consumption (V˙o 2) averaged 47 ± 3% predicted. End exercise heart rate reached 87 ± 2% of the predicted maximum. Peak exercise minute ventilation (V˙e) averaged 81 ± 4% of the 12 s maximal voluntary ventilation (MVV). Endurance exercise results are shown in Table 3. At baseline, patients exercised at 37 ± 4 W for 11.2 ± 1.8 min. Lactate levels 5 min postexercise were 4.1 ± 0.4 meq/L.
| Prerehabilitation | Postrehabilitation End Exercise | Postrehabilitation Isowork | ||||
|---|---|---|---|---|---|---|
| Workload, W | 59 ± 6* | 79 ± 7† | 58 ± 6 | |||
| V˙ o 2, L/min | 0.96 ± 0.06 | 1.17 ± 0.07† | 0.94 ± 0.07 | |||
| HR, beats/min | 131 ± 3 | 135 ± 5 | 115 ± 4† | |||
| V˙ e, L/min | 45.0 ± 3.1 | 48.4 ± 4.1† | 38.7 ± 3.7 | |||
| F, breath/min | 35 ± 8 | 35 ± 1 | 28 ± 1† | |||
| Vt, L | 1.33 ± 0.09 | 1.48 ± 0.10 | 1.36 ± 0.10 |
| Prehabilitation | Postrehabilitation End Exercise | Postrehabilitation Exercise Isotime | ||||
|---|---|---|---|---|---|---|
| Endurance time, min | 11.2 ± 1.8* | 23.7 ± 3.0† | 11.2 ± 1.8 | |||
| V˙ o 2, L/min | 0.92 ± 0.08 | 1.05 ± 0.06† | 0.98 ± 0.07 | |||
| HR, beats/min | 134 ± 4 | 136 ± 3 | 123 ± 4† | |||
| V˙ e, L/min | 42.5 ± 3.3 | 42.5 ± 3.0 | 39.7 ± 2.2† | |||
| F, breaths/min | 34 ± 2 | 35 ± 1 | 32 ± 1 | |||
| Vt, L | 1.35 ± 0.09 | 1.28 ± 0.08 | 1.32 ± 0.07 | |||
| Peak lactate, meq/L | 4.1 ± 0.4 | 3.7 ± 0.3 |
Peak exercise responses during incremental exercise before and after pulmonary rehabilitation are shown in Table 2. Maximum exercise capacity increased from 59± 6 at baseline to 79 ± 7 W (34% improvement) (p < 0.0001) (Table 2) postrehabilitation. Similarly, peak V˙o 2 increased from 0.96 ± 0.06 to 1.17 ± 0.07 L/min (22% improvement) (p = 0.0003) postrehabilitation (Table 2). Peak ventilation also increased postrehabilitation.
Responses to identical levels of exercise (isowork) are also shown in Table 2. The highest workload reached by the patient during both the pre- and postrehabilitation exercise test was used for comparison. At the same workload, heart rate was significantly lower postrehabilitation (Table 2) (p < 0.005). Exercise Ve also tended to be lower postrehabilitation (p = 0.05). The reduction in Ve postrehabilitation was entirely due to a reduction in respiratory rate (p = 0.001) whereas tidal volume (Vt) was unchanged (Table 2). Because V˙o 2 and carbon dioxide production (Vco 2) were unchanged postrehabilitation, significant reductions in V˙e/Vco 2 (p < 0.025) and V˙e/V˙o 2 (p < 0.005) were observed after rehabilitation.
Endurance exercise responses (constant workload) before and after pulmonary rehabilitation are shown in Table 3. Endurance time increased from 11.2 ± 1.8 at baseline to 23.7 ± 3.0 min after pulmonary rehabilitation (p < 0.0001). Despite the large increase in endurance exercise time, there were no significant changes in peak Ve, breathing pattern (f, Vt), or heart rate. Prerehabilitation, 11 patients stopped exercise because of shortness of breath, 9 patients stopped exercise because of leg fatigue, and 1 patient stopped exercise because of nasal irritation. Postrehabilitation, 8 patients stopped exercise because of shortness of breath, 11 patients stopped exercise because of leg fatigue, and 1 patient stopped exercise because of knee pain and nasal irritation, respectively. Exercise responses at equivalent exercise duration (isotime) are also shown in Table 3. The longest duration reached by the patient during both the pre- and postrehabilitation exercise test was used for comparison. At exercise isotime, both heart rate (p = 0.002) and V˙e (p < 0.02) were significantly lower postrehabilitation. Respiratory rate also tended to be lower postrehabilitation (p = 0.068). Arterialized venous lactate levels obtained 5 min after exercise were not significantly different after rehabilitation for the group as a whole. A significant reduction (p < 0.02) in lactate levels was seen postrehabilitation in patients with milder disease (FEV1 > 40%) but not in patients with severe disease (FEV1 < 40%).
Six minute walk distance increased from 1069 ± 71 at baseline to 1245 ± 63 ft postrehabilitation (p < 0.0001). The mean difference 176 ft (53.7 m) 95% confidence intervals 110–243 ft (33.5–74 m) is at the threshold (54 m, 95% confidence intervals 37–71 m) suggested as the minimal improvement in walking distance that can be reliably detected by patients as a significant improvement in functional status (21).
TwQu before and after exercise, pre- and postrehabilitation is shown in Figure 3. At baseline, TwQu averaged 6.9 ± 0.3 kg prerehabilitation and increased to 7.6 ± 0.4 kg (p = 0.049, 9.7% increase) postrehabilitation. Prerehabilitation, TwQu fell significantly postexercise to a minimum of 82.5 ± 3.1% of the baseline value at 30 min postexercise (p < 0.0001) and remained significantly decreased at 1 h postexercise. In contrast, postrehabilitation for the same duration and intensity of exercise, TwQu was unchanged from baseline at all times postexercise.
Fig. 3. Unpotentiated quadriceps twitch force (TwQu) expressed as a percentage of baseline before and 10, 30, and 60 min postexercise prerehabilitation (open circles) and postrehabilitation (closed circles). *Significant difference from baseline. †Significant difference from the postrehabilitation value. TwQu fell significantly pre- but not postrehabilitation.
[More] [Minimize]TwQp before and after exercise, pre- and postrehabilitation is shown in Figure 4. TwQp at baseline averaged 12.7 ± 0.7 kg prerehabilitation and increased to 13.8 ± 0.7 kg (p = 0.05, 8.8% increase) postrehabilitation. Prerehabilitation, TwQp fell significantly postexercise to a minimum of 73.9 ± 3.9% of the baseline value at 10 min postexercise (p < 0.0001) and remained significantly decreased at 1 h postexercise. Postrehabilitation, TwQp also fell significantly postexercise reaching a minimum of 85 ± 4% at 10 min postexercise (p < 0.005) and remained significantly decreased at 1 h postexercise. However, the fall in TwQp postexercise was significantly larger pre- than postrehabilitation (p < 0.001, ANOVA).
Fig. 4. Potentiated quadriceps twitch force (TwQp) expressed as a percentage of baseline before and 10, 30, and 60 min postexercise prerehabilitation (open circles) and postrehabilitation (closed circles). *Significant difference from baseline. †Significant difference from the postrehabilitation value. The fall in TwQp postexercise was significantly less post- than prerehabilitation.
[More] [Minimize]Paired twitch data showed similar results (Figure 5). Prerehabilitation, T2 was significantly decreased postexercise at 10 and 20 Hz down to minimum values of 76.4 ± 4.9% and 77.5 ± 3.6% of baseline, respectively. Prerehabilitation T2 also fell significantly postexercise at 100 Hz but to a much smaller extent down to a minimum value of 86.8 ± 5.0%. In contrast, postrehabilitation T2 was not significantly different from baseline at any time postexercise at any stimulation frequency.
Fig. 5. Twitch force elicited by the second of a paired stimuli ( T2 response) at 10, 20, and 100 Hz before (closed circles) and 10 (closed squares), 30 (open triangles), and 60 (open circles) min postexercise. Prerehabilitation results are shown in A. Postrehabilitation results are shown in B. *Significant difference from baseline. T2 fell significantly postexercise pre- but not postrehabilitation. Prerehabilitation, the fall in T2 postexercise was greater at 10 and 20 Hz than at 100 Hz consistent with low-frequency fatigue.
[More] [Minimize]Prerehabilitation maximum voluntary contraction (MVC) was 39.2 ± 2.4 kg at baseline. Prerehabilitation, MVC decreased significantly postexercise reaching a minimum value of 88.1 ± 2.7% of baseline at 30 min postexercise (p < 0.005). In contrast, postrehabilitation MVC was not significantly different from baseline at any time postexercise. Prerehabilitation, twitches superimposed upon the MVC maneuver at baseline averaged 16.6 ± 2.3% of the resting potentiated twitch indicating that patients did not fully activate their quadriceps muscle during the MVC maneuver (83.4 ± 2.3% of full activation). The degree of activation of the quadriceps muscle was not significantly different from baseline at any time postexercise. Postrehabilitation, the superimposed twitch averaged 13.3 ± 2.5% of the resting potentiated twitch (patients achieved 86.7 ± 2.5% of full activation). The degree of activation of the quadriceps muscle was not significantly different post- compared with prerehabilitation. Similar to prerehabilitation, the degree of activation of the quadriceps muscle was not significantly different from baseline at any time postexercise. Postrehabilitation, the MVC was 14.9 ± 5.0% (p < 0.01) larger than prerehabilitation, indicating that rehabilitation elicited a significant improvement in quadriceps strength.
Quadriceps M-waves were not significantly different from baseline at any time postexercise either pre- or postrehabilitation.
The major finding of this study was that pulmonary rehabilitation resulted in a significant improvement in quadriceps fatigability in patients with COPD. Quadriceps fatigability was measured with an effort-independent method (fall in TwQ postexercise). Thus, pulmonary rehabilitation must have resulted in changes within the exercising limb muscles that increased their fatigue resistance.
In a previous study, we found that patients with COPD develop contractile fatigue of the quadriceps muscle following endurance exercise to the limits of tolerance (6). In that study, examination of individual responses revealed that 11 of 19 (58%) subjects had a > 15% reduction in TwQu, indicative of significant contractile fatigue. In the present study, we measured both the unpotentiated and potentiated twitch. Recent evidence has suggested that the potentiated twitch is a more sensitive index of contractile fatigue (15, 16). In the present study 10 of 21 (48%) patients had a > 15% reduction in TwQu postexercise. In contrast 17 of 21 (81%) patients had a > 15% reduction in TwQp postexercise, supporting the view that TwQp is a more sensitive index of contractile fatigue. Furthermore, our TwQp results show that most patients with COPD develop contractile fatigue of the exercising limb muscles following exercise to the limits of tolerance.
M-waves were unchanged postexercise in all patients in whom they could be measured (not obscured by stimulation artifact) indicating that transmission fatigue did not occur. The fatigue was long lasting (still present at 1 h). T2 was significantly decreased from baseline postexercise at all stimulation frequencies but the amount by which T2 fell was larger at the lower stimulation frequencies (10 and 20 Hz). Similarly, the MVC fell postexercise but to a lesser extent than the twitch. These results show that as expected, the fatigue induced by endurance exercise was predominantly low-frequency fatigue.
Following pulmonary rehabilitation, the fall in measures of quadriceps contractility postexercise that occurred prerehabilitation was either abolished (TwQu, MVC, T2 at all stimulation frequencies) or significantly ameliorated (TwQp). Thus, for the some exercise duration and intensity, the degree of exercise-induced quadriceps fatigue was clearly less postrehabilitation. What are the potential mechanisms for this increased fatigue resistance?
We were somewhat surprised to find that the quadriceps MVC increased by 15 ± 5% postrehabilitation indicating an increase in quadriceps strength. Our rehabilitation program focused on endurance exercise (bicycle and treadmill) and specific strength exercises were not performed. Thus, the endurance leg training performed in our rehabilitation program must have been sufficient to induce an increase in quadriceps strength as has also been observed in another study (22). An increase in quadriceps strength could be responsible for the increase in fatigue resistance. However, in the eight patients who did not have an increase in quadriceps MVC postrehabilitation, a significant reduction in exercise-induced quadriceps fatigue was still observed (22.3 ± 7.3%, p < 0.02 versus 23.3 ± 8.4%). Similarly, there was no correlation (r = +0.28) between the increase in quadriceps strength and the reduction in exercise-induced quadriceps fatigue. Thus, increased quadriceps strength does not appear to be responsible for the increased fatigue resistance observed postrehabilitation. Following an endurance training program above a critical minimum intensity, healthy subjects display a number of changes within the exercising muscle. These include proliferation of muscle capillaries (which increases oxygen delivery to the exercising muscle), transformation of type 2b fibers to type 2a (which have a higher oxidative capacity), increase in the size and number of mitochondria within the muscle fiber, and an increase in enzymes responsible for oxidative phosphorylation. All of these changes could increase the muscle's fatigue resistance. An increase in enzyme oxidative capacity has been demonstrated following pulmonary rehabilitation in patients with COPD, indicating that such changes are possible in this patient population (5). It would be interesting to determine whether increases in muscle oxidative capacity would correlate with improvements in fatigue resistance.
It should be noted that our patients had a very favorable response to pulmonary rehabilitation with a significant increase in peak V˙o 2 during maximal incremental exercise, a functionally significant increase in 6 min walking distance, and a marked increase in submaximal exercise endurance time. The response to pulmonary rehabilitation is not always this favorable, probably reflecting differences in the exercise program and the patient population. It is probable that lesser improvement in overall performance might also be associated with less improvement in quadriceps fatigue resistance.
In our prior study, we found that patients with severe COPD (FEV1 < 40% predicted) had just as much exercise-induced quadriceps fatigue as those with milder disease despite exercising at lower intensities (6). Patients in this study behaved similarly. We interpreted this finding as suggesting that patients with more severe disease had greater muscle deconditioning and increased susceptibility to fatigue. The degree of improvement in exercise-induced quadriceps fatigue postrehabilitation, however, was similar in patients with severe COPD (21.0 ± 10.5%, n = 9) compared with those with milder disease (24.4 ± 6.7%, n = 12) demonstrating that the exercising muscle can be conditioned in patients with severe COPD as well as it can in patients with less severe disease.
In our previous study, some patients (4 of 12) stopped exercise because of leg discomfort but did not demonstrate a significant reduction (> 15%) in TwQu postexercise. In the present study, we also measured TwQp, a more sensitive index of contractile fatigue. In the present study, only four patients did not show a significant reduction in TwQp postexercise prerehabilitation. All of these patients stopped exercise because of shortness of breath. However, there were seven patients who stopped exercise because of shortness of breath who displayed a significant reduction in TwQp postexercise, demonstrating that contractile fatigue of the quadriceps muscles commonly occurs postexercise in patients who stop exercise because of shortness of breath.
As mentioned above, increased quadriceps fatigue resistance is a sign that the patient underwent changes within the exercising muscle following pulmonary rehabilitation. In healthy subjects, the purpose of an exercise training program is to induce physiological adaptations that lead to improved exercise performance. In patients with COPD, there is the concern that patients will stop exercise because of shortness of breath before they can stress their exercising muscles and heart sufficiently to induce physiological adaptations, that is, exercise will be below a critical minimum intensity. In our study, we have shown that the quadriceps muscle will undergo adaptations secondary to an exercise program in the majority of patients, even those with severe COPD. Others have also provided evidence that physiological adaptations can be produced in patients with severe COPD (5, 23, 24).
Conversely, however, when physiological adaptations probably did not occur (4), performance during endurance exercise still improved postrehabilitation. In our study, in the four patients who stopped exercise prerehabilitation because of shortness of breath prior to developing fatigue of the quadriceps muscle and therefore might have been the hardest to effectively train, improvements in exercise endurance time similar to the group as a whole were observed (11.1 ± 4.0 min). In these patients, the improvement in exercise endurance might be due to other factors such as desensitization to dyspnea, improved efficiency, and increased motivation.
In our study, we were unable to demonstrate a correlation between the improvement in quadriceps fatigue resistance and the improvement in exercise performance (r = 0.13). The lack of correlation may be because we have compared changes over time in two relatively variable measurements (fall in TwQ postexercise, exercise endurance time), that is, the noise in the measurements may have obscured a relationship between the two variables. Improved quadriceps function may indirectly influence endurance time by reducing ventilatory demands for a given exercise workload. However, the reduction in Ve at exercise isotime postrehabilitation also did not significantly correlate with improvements in exercise endurance time (r = 0.34). Finally, the lack of correlation between the two variables may be because other factors are more important determinants of exercise endurance time in patients with COPD. Similar to our findings, O'Donnell and colleagues found that improvements in quadriceps strength and a simple effort-dependent measure of quadriceps endurance did not correlate with improvements in exercise endurance (22).
In conclusion, an exercise training regimen (at 50% of Wmax) is capable of increasing the fatigue resistance of the exercising muscle (quadriceps) in patients with COPD including those with severe disease.
The authors thank Raymond Carter, LPN, and Sandra Brucato, RN, for helping to supervise the exercise training program.
Supported by the American Heart Association Western New York Affiliate.
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This article has an online data supplement, which is accessible from this issue's table of contents online at www.atsjournals.org
