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

被引:121
作者
Enright, S [1 ]
Chatham, K
Ionescu, AA
Unnithan, VB
Shale, DJ
机构
[1] Univ Salford, Sch Hlth Care Profess, Manchester M6 6PU, Lancs, England
[2] Llandough Hosp, NHS Trust, Cardiff, S Glam, Wales
[3] Syracuse Univ, Dept Exercise Sci, Syracuse, NY USA
关键词
diaphragm thickness; exercise tolerance; lung volumes; respiratory muscle training;
D O I
10.1378/chest.126.2.405
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
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.
引用
收藏
页码:405 / 411
页数:7
相关论文
共 31 条
[1]  
*AM COLL SPORTS ME, 1995, GUID EX TEST PRESCR
[2]  
[Anonymous], 1994, RESP MED, V88, P165
[3]  
ARORA NS, 1982, AM REV RESPIR DIS, V126, P5
[4]  
ASHER MI, 1982, AM REV RESPIR DIS, V126, P855
[5]   EFFECT OF PRESSURE AND TIMING OF CONTRACTION ON HUMAN DIAPHRAGM FATIGUE [J].
BELLEMARE, F ;
GRASSINO, A .
JOURNAL OF APPLIED PHYSIOLOGY, 1982, 53 (05) :1190-1195
[6]   PSYCHOPHYSICAL BASES OF PERCEIVED EXERTION [J].
BORG, GAV .
MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 1982, 14 (05) :377-381
[7]  
COTES JE, 1993, LUNG FUNCTION ASSESS, P445
[8]   Cystic fibrosis [J].
Davis, PB ;
Drumm, M ;
Konstan, MW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (05) :1229-1256
[9]   Inspiratory muscle training in patients with cystic fibrosis [J].
De Jong, W ;
Van Aalderen, WMC ;
Kraan, J ;
Koëter, GH ;
Van der Schans, CP .
RESPIRATORY MEDICINE, 2001, 95 (01) :31-36
[10]   Diaphragm thickness and inspiratory strength in patients with Duchenne muscular dystrophy [J].
DeBruin, PF ;
Ueki, J ;
Bush, A ;
Khan, Y ;
Watson, A ;
Pride, NB .
THORAX, 1997, 52 (05) :472-475