Copyright ©ERS Journals Ltd 2002 Diaphragmatic function after intense exercise in congestive heart failure patientsDivision of Pulmonary and Critical Care Medicine, Veterans Administration Western New York Healthcare System, Dept of Medicine, State University of New York at Buffalo School of Medicine and Biomedical Sciences, Buffalo, NY, USA CORRESPONDENCE: T.J. Kufel, Division of Pulmonary and Critical Care Medicine (111S), VA Western New York Healthcare System, 3495 Bailey Avenue, Buffalo, New York, 14215, USA. Fax: 1 716 8628632. E-mail: thomas.kufel@med.va.gov Keywords: congestive heart failure, diaphragm, exercise, fatigue
Received: February 25, 2002
This study was supported by a Grant-in-Aid from the American Heart Association, New York State Affiliate, Inc., Syracuse, NY, USA.
Respiratory muscle strength and endurance is reduced in patients with congestive heart failure, making these patients susceptible to diaphragmatic fatigue during exercise. In order to determine whether or not contractile fatigue of the diaphragm occurs in patients with congestive heart failure following intense exercise, twitch transdiaphragmatic pressures (twitch Ptdi) were measured during unpotentiated and potentiated cervical magnetic stimulation (CMS) of the phrenic nerves before and at intervals after cycle endurance exercise.
Ten patients aged 65.7±6.0 yrs (mean±sd) with an ejection fraction of 31.2±9.8% performed a constant-load symptom-limited exercise test at 60% of their peak work capacity. Twitch Ptdi at baseline were 15.9±6.3 cmH2O (unpotentiated CMS) and 28.8±10.7 cmH2O (potentiated CMS) and at 10 min postexercise were 16.4±4.7 cmH2O (unpotentiated CMS) and 27.6±10.1 cmH2O (potentiated CMS). One patient demonstrated a sustained fall in twitch Ptdi of Contractile diaphragmatic fatigue is uncommon in untrained patients with congestive heart failure following high-intensity constant-workload cycle exercise. Therefore, diaphragmatic fatigue is an unlikely cause of exercise-limitation during activities of daily living in heart failure patients. Exercise intolerance due to dyspnoea and fatigue is a frequent and disabling symptom in patients with congestive heart failure (CHF). Some investigators believe that inspiratory muscle fatigue might be an important mediator of dyspnoea during exercise in CHF 1. Conclusive data showing that intense exercise causes diaphragmatic fatigue in patients with CHF are not available. The limb muscles of patients with heart failure undergo changes that predispose them to reduced endurance and contractile fatigue 2. Similar changes might occur in the inspiratory skeletal muscles. Studies have found respiratory muscle weakness 3 and reduced respiratory muscle endurance 4 in patients with CHF. In addition, patients with heart failure show an increased ventilatory response to exercise 5, further exacerbating the imbalance between inspiratory muscle capacity and load. Therefore, it is reasonable to hypothesise that diaphragmatic fatigue may occur in patients with CHF when stressed by exercise. The limited studies investigating respiratory muscle fatigue in patients with CHF after exercise are inconclusive. Mancini et al. 1 failed to demonstrate evidence of diaphragmatic fatigue after exercise using transcutaneous electrical stimulation of the phrenic nerves. However, the negative results may be explained partially by the fact that they failed to account for twitch potentiation, obtaining twitch measurements immediately after exercise 6. Furthermore, the work of Levine and Henson 7 suggests that an incremental exercise protocol, as used by Mancini et al. 1, is of insufficient intensity and duration to result in diaphragmatic fatigue. Recently, Hughes et al. 8 demonstrated a slowing of the inspiratory muscle relaxation rate (MRR) in CHF patients after exercise, implying that inspiratory muscle loading is excessive during exercise and the inspiratory muscles are in a potentially fatiguing pattern of contraction. However, this does not confirm that overt muscle fatigue is present since slowing of the MRR precedes overt muscle fatigue. Furthermore, Tikunov et al. 9 found an increased proportion of type I (slow-twitch fatigue-resistant) fibres and an increase in oxidative enzyme activity in the diaphragm of patients with CHF, suggesting that the diaphragm of heart failure patients may be more fatigue-resistant. These findings and the methodological problems described above prohibit definitive conclusions and warrant further investigation using new techniques and different methodology. Magnetic stimulation of the phrenic nerves is an accepted alternative to electrical stimulation and is a nonvolitional, simple and reproducible technique of assessing inspiratory muscle function that reduces the difficulties encountered with electrical stimulation 10. The purpose of the present study was to determine whether or not contractile fatigue of the diaphragm occurs in patients with moderately severe heart failure following intense exercise. Accordingly, transdiaphragmatic twitch pressure (twitch Ptdi) was measured during supramaximal cervical magnetic stimulation (CMS) before and after high-intensity endurance cycle exercise to the limits of tolerance in a group of patients with CHF.
Subjects Ten male patients with CHF aged 65.7±6.0 yrs (mean±sd), of height 1.77±0.09 m and weight 89.7±15.7 kg, volunteered for the present study. The diagnosis of CHF was based on a history of dyspnoea on exertion, fluid retention, fatigue and a left ventricular ejection fraction of 35%. All patients were clinically stable at the time of the study and free from overt pulmonary, musculoskeletal or neurological disease that could affect exercise performance. Patients with peripheral vascular disease, a pacemaker, uncontrolled hypertension, or abnormal electrolyte or haemoglobin levels were excluded. The aetiology of the CHF was ischaemic in nine of the patients and idiopathic in the remaining patient. The medications taken included digoxin (n=2), diuretics (n=9), angiotensin-converting enzyme inhibitor (n=10), nitrates (n=6) and ß-blockers (n=2). Four patients were in New York Heart Association functional Class II and six in Class III. The appropriate institutional review boards approved the study and informed consent was obtained from all subjects.
Study design
A maximal symptom-limited incremental cycle exercise test was performed to determine the peak work capacity (Wpeak) of each subject as previously described 12. Several days after the incremental exercise test, subjects performed constant-workload exercise at 60% of Wpeak until they were no longer able to maintain a pedalling frequency of >50 revolutions per minute despite verbal encouragement. All exercise tests, calculations of peak and mean inspiratory pressure swings, and measurement of arterialised lactate levels were performed as described previously 12. Immediately after exercise was discontinued, patients were asked to choose the symptom that they felt was most responsible for stopping exercise. CMS of the phrenic nerve was achieved using a commercial magnetic stimulator (Magstim 200; Magstim Co. Ltd., Whitland, UK) and a 90-mm coil (n=10) 9. The technical details of this procedure have been described previously 12. Recent work suggests that the potentiated twitch may be a more sensitive index of fatigue 17, 18. Therefore, Ptdi twitch force (twitch Ptdi) was measured using CMS 5 s after a 5-s maximal Mueller manoeuvre against an occluded airway in eight patients. Diaphragmatic compound muscle action potentials (M-wave) were recorded with surface electrodes. The technical details of this procedure have been described previously 12. Magnetic stimulation often results in a large shock artefact that obscures the initial portion of the M-wave. However, with repositioning of the surface electrodes and ground before initial measurements, satisfactory M-waves were obtained before and after exercise in five subjects. Twitch Ptdi was defined as the peak amplitude above the immediately preceding Ptdi baseline. Approximately eight twitches by CMS and five potentiated twitches were obtained before and 10, 30 and 60 min after exercise. In order to prevent twitch potentiation, the unpotentiated twitches were obtained prior to measuring the potentiated twitch. Individual twitches were rejected from analysis using previously defined criteria 19.
Statistical analysis
Cardiopulmonary parameters during exercise The peak oxygen consumption (V'O2) measured during incremental exercise was 1.29±0.31 L·min1 or 14.4±2.3 mL·kg1·min1, which was 59±18% of the predicted maximum. The Wpeak was 95±17 W (64±19% of the predicted maximum). During incremental exercise, peak ventilation was 53±14 L·min1, which represented 49±15% of the 12-s maximum voluntary ventilation (MVV) and the peak cardiac frequency was 134±22 beats·min1 (87±1% of the predicted maximum).
Cardiopulmonary parameters measured during the constant-load endurance test are shown in table 2
The patients exercised for a mean of 10.1±3.4 min during the constant-load test at a workload of 57±11 W (60±2% of Wpeak). The peak V'O2 during constant-load exercise was 1.39±0.21 L·min1, which was 111±16% of the peak V'O2 obtained during the incremental exercise test. The peak ventilation attained during constant-load exercise was 51±9 L·min1, representing 48±14% of the 12-s MVV. Peak cardiac frequency was 131±16 beats·min1 (85±11% of the predicted maximum). At the end of exercise, four patients cited "shortness of breath" as the cause of exercise termination and six stopped exercise because of "leg fatigue".
Diaphragm twitch force
A diaphragmatic electromyogram was recorded for all subjects. Diaphragmatic M-wave amplitude was not significantly different from baseline at any time after exercise in the five subjects in whom it could be accurately measured at all times points. In the five subjects for whom M-waves could be obtained, there was no significant change in twitch Ptdi at any time after exercise compared with baseline. PI,max was 94±21 cmH2O at baseline and 93±25 cmH2O immediately after exercise (p=ns).
Breathing pattern during exercise
Lactate measurements Lactate concentration increased from 1.6±0.6 mEq·L1 at baseline to 5.1±1.4 mEq·L1 immediately after exercise (p=0.001) and had recovered to 2.9±0.7 mEq·L1 at 30 min after exercise (p=ns).
The major conclusion of the present study is that contractile fatigue of the diaphragm is uncommon in untrained patients with moderately severe CHF.
Critique of methods
Patients were exercised at 60% of their peak workload based on prior studies performed in the authors' laboratory. Normal subjects demonstrated evidence of diaphragmatic fatigue after voluntary hyperpnoea at a V'E of 60% MVV sustained for
Twitch potentiation 6 and lung volume changes 25 are important variables that can influence twitch Ptdi. A vigorous voluntary contraction can increase twitch Ptdi amplitude (twitch potentiation). It has previously been shown that diaphragmatic twitch potentiation decays exponentially with the greatest change occurring within the first 2 min and was minimal (<4% above baseline) 8 min after a vigorous muscle contraction 6. Therefore, the first set of post-exercise twitch measurements were obtained 10 min after exercise and subsequent sets of unpotentiated twitches were obtained
Some may argue that significant recovery could occur during the 10-min period after stopping exercise that was allowed in the present study for the effects of twitch potentiation to resolve. However, reductions in twitch force after a fatiguing task reflect low-frequency fatigue that is known to recover very slowly. Laghi et al. 17 demonstrated a reduction in twitch Ptdi after resistive loading that did not return to baseline levels when measured
Diaphragmatic fatigue and exercise
Recently, data on 10 healthy elderly subjects aged 68.3 yrs were reported 20. These subjects exercised at The present authors and others have observed diaphragmatic fatigue after endurance exercise in young healthy adults 22, 24. Why might healthy young people develop diaphragmatic fatigue after exercise while older patients with CHF do not? It is felt that exercise-induced diaphragmatic fatigue requires a high level of sustained diaphragmatic work and an unspecified exercise-dependent factor 29. The present subjects sustained exercise for a sufficient duration to result in fatigue. However, was the diaphragmatic work of high enough intensity to result in diaphragmatic fatigue? The pressure/time product and tension/time index were measured as estimates of inspiratory muscle work during exercise. In the present authors' laboratory, the peak pressure/time product of the oesophagus for young sedentary subjects who demonstrated diaphragmatic fatigue after exercise was significantly greater than that achieved by the patients with CHF (585±52 cmH2O·s1·min1 (mean±sem), p<0.001) 22. However, maximal inspiratory muscle strength was lower in the elderly CHF patients than in subjects of the previous study of younger healthy subjects 22. Thus, the tension/time index of the oesophagus in the heart failure patients was not significantly different from that observed in the young sedentary subjects (0.066±0.01 versus 0.083±0.009, p=ns). This suggests that the heart failure patients performed similar amounts of inspiratory muscle work relative to their capacity, and, despite exercising intensely for sufficient duration, the majority of patients did not display evidence of diaphragmatic fatigue after exercise. Could the present subjects have attained higher levels of inspiratory muscle work? The heart failure patients were highly motivated and exercise data indicate that they terminated exercise at their physiological limits. At the end of endurance exercise, peak V'O2 was 111±16% of the peak V'O2 obtained during the incremental maximal exercise test, and peak cardiac frequency was 85±11% of the predicted maximum. The peak lactate levels generated by the heart failure patients were significantly lower than those observed in the healthy elderly (mean±sd 5.1±1.4 versus mean±sem 6.8±0.6 mEq·L1; p=0.03) 20, but was not significantly different from that observed in a group of patients with COPD (mean±sem 4.8±0.5 mEq·L1; p=ns) 30. Thus, the present subjects appear to have exercised maximally. The rationale for getting patients to exercise at 60% of their incremental Wpeak is reviewed above. A greater workload could have resulted in greater inspiratory muscle work, although peak exercise ventilation was similar during the endurance and maximal incremental exercise tests, but it is unlikely that patients with heart failure would be capable of sustaining higher workloads for very long. It is possible that the present subjects could not attain higher levels of inspiratory muscle work because they were forced to stop exercise because of peripheral leg muscle fatigue. It has previously been shown that quadriceps muscle fatigue occurs following endurance exercise in elderly patients 20 and in patients with COPD 30. This possibility deserves further investigation in heart failure patients. The present data are consistent with the increased proportion of type I (slow-twitch fatigue-resistant) fibres and increase in oxidative enzyme activity in the diaphragm of patients with CHF demonstrated by Tikunov et al. 9. Perhaps the increased work of breathing observed in patients with CHF trains the respiratory muscles as postulated for patients with COPD. These adaptations make the diaphragm more fatigue-resistant and offer an attractive explanation for the present findings. It is well known that ageing and chronic disease result in a reduction in physical activity, deconditioning and a reduction in maximal work capacity. Exercise training in patients with CHF is increasing in popularity and has been shown to increase exercise capacity, reduce mortality and improve quality of life 31. Whether a trained heart failure patient can perform enough work during exercise to develop diaphragmatic fatigue remains to be determined.
Contractile diaphragmatic fatigue is uncommon in untrained patients with moderately severe heart failure after a bout of constant workload exercise of greater intensity than is commonly expected during the activities of daily living for such patients. Thus, diaphragmatic fatigue is unlikely to be an important cause of exertional symptoms and exercise limitation in the majority of untrained patients with heart failure.
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