Inspiratory muscle training improves lung function and exercise capacity in adults with cystic fibrosis.

STUDY OBJECTIVES To investigate the effects of high-intensity inspiratory muscle training (IMT) on inspiratory muscle function (IMF), diaphragm thickness, lung function, physical work capacity (PWC), and psychosocial status in patients with cystic fibrosis (CF). DESIGN Twenty-nine adult patients with CF were randomly assigned to three groups. Two groups were required to complete an 8-week program of IMT in which the training intensity was set at either 80% of maximal effort (group 1; 9 patients) or 20% of maximal effort (group 2; 10 patients). A third group of patients did not participate in any form of training and acted as a control group (group 3; 10 patients). INTERVENTIONS In all patients, baseline and postintervention measures of IMF were determined by maximal inspiratory pressure (Pimax), and sustained Pimax (SPimax); pulmonary function, body composition, and physical activity status were also determined. In addition, diaphragm thickness was measured at functional residual capacity (FRC) and total lung capacity (TLC) [TDIcont], and the diaphragm thickening ratio (TR) was calculated (TR = thickness during Pimax at FRC/mean thickness at FRC). Subjects also completed an incremental cycle ergometer test to exhaustion and two symptom-related questionnaires, prior to and following training. RESULTS Following training, significant increases in Pimax and SPimax (p < 0.05), TDIcont (p < 0.05), TR (p < 0.05), vital capacity (p < 0.05), TLC (p < 0.05), and PWC (p < 0.05) were identified, and decreases in anxiety scores (p < 0.05) and depression scores (p < 0.01) were noted in group 1 patients compared to group 3 patients. Group 2 patients significantly improved Pimax and SPimax (both p < 0.05) only with respect to group 3 patients. No significant differences were observed in group 3 patients. CONCLUSION An 8-week program of high-intensity IMT resulted in significant benefits for CF patients, which included increased IMF and thickness of the diaphragm (during contraction), improved lung volumes, increased PWC, and improved psychosocial status.

[1]  John Everard Cotes,et al.  Handbook of Pulmonary Drug Therapy , 1993, Thorax.

[2]  T. Clanton,et al.  Improved pulmonary function and exercise tolerance with inspiratory muscle conditioning in children with cystic fibrosis. , 1993, Chest.

[3]  N. Høiby,et al.  Cystic fibrosis. 1. Pseudomonas aeruginosa infection in cystic fibrosis and its management. , 1990, Thorax.

[4]  G. Borg Psychophysical bases of perceived exertion. , 1982, Medicine and science in sports and exercise.

[5]  J Moxham,et al.  The respiratory muscles. , 1988, Praxis und Klinik der Pneumologie.

[6]  H. Folgering,et al.  Pulmonary rehabilitation in chronic obstructive pulmonary disease. , 1998, The European respiratory journal.

[7]  J. Benditt,et al.  Maximal inspiratory pressures and dimensions of the diaphragm. , 1997, American journal of respiratory and critical care medicine.

[8]  D. F. Rochester,et al.  Respiratory muscle strength and maximal voluntary ventilation in undernourished patients. , 2015, The American review of respiratory disease.

[9]  G. Guyatt,et al.  A measure of quality of life for clinical trials in chronic lung disease. , 1987, Thorax.

[10]  A. C. Bryan,et al.  Ventilatory muscle endurance training in normal subjects and patients with cystic fibrosis. , 2015, The American review of respiratory disease.

[11]  S. Godfrey,et al.  Pulmonary Function and Response to Exercise in Cystic Fibrosis , 1971, Archives of disease in childhood.

[12]  A. Ionescu,et al.  Inspiratory muscle function and body composition in cystic fibrosis. , 1998, American journal of respiratory and critical care medicine.

[13]  G H Guyatt,et al.  Respiratory muscle training in chronic airflow limitation: a meta-analysis. , 1992, The American review of respiratory disease.

[14]  L. Lands,et al.  Respiratory and peripheral muscle function in cystic fibrosis. , 1993, The American review of respiratory disease.

[15]  Rochester Df Tests of respiratory muscle function. , 1988 .

[16]  G. Kwakkel,et al.  Effects of controlled inspiratory muscle training in patients with COPD: a meta-analysis , 2002, European Respiratory Journal.

[17]  J N Morris,et al.  Assessment methods for physical activity and physical fitness in population studies: report of a NHLBI workshop. , 1986, American heart journal.

[18]  A. Grassino,et al.  Effect of pressure and timing of contraction on human diaphragm fatigue. , 1982, Journal of applied physiology: respiratory, environmental and exercise physiology.

[19]  A. Coates,et al.  The effects of inspiratory muscle training in patients with cystic fibrosis. , 2015, The American review of respiratory disease.

[20]  N. C. Sharp,et al.  Guidelines for Exercise Testing and Prescription , 1993 .

[21]  N. Pride,et al.  In vivo assessment of diaphragm contraction by ultrasound in normal subjects. , 1995, Thorax.

[22]  D. F. Rochester,et al.  Tests of respiratory muscle function. , 1988, Clinics in chest medicine.

[23]  N. Pride,et al.  Diaphragm thickness and inspiratory strength in patients with Duchenne muscular dystrophy. , 1997, Thorax.

[24]  S. Kelsey,et al.  The prognostic value of exercise testing in patients with cystic fibrosis. , 1992, The New England journal of medicine.

[25]  S.J.G. Semple,et al.  Lung function: Assessment and application in medicine , 1976 .

[26]  J. Benditt,et al.  Variability of diaphragm structure among healthy individuals. , 1997, American journal of respiratory and critical care medicine.

[27]  G. Huston The Hospital Anxiety and Depression Scale. , 1987, The Journal of rheumatology.

[28]  R. Goldstein Pulmonary rehabilitation in chronic respiratory insufficiency. 3. Ventilatory muscle training. , 1993, Thorax.

[29]  Guidelines for the measurement of respiratory function. Recommendations of the British Thoracic Society and the Association of Respiratory Technicians and Physiologists. , 1994, Respiratory medicine.

[30]  W. Yost,et al.  Diaphragmatic thickness-lung volume relationship in vivo. , 1989, Journal of applied physiology.

[31]  W. V. van Aalderen,et al.  Inspiratory muscle training in patients with cystic fibrosis. , 2001, Respiratory medicine.

[32]  Physiologists Guidelines for the measurement of respiratory function , 1994 .