SUPPLEMENTAL OXYGEN AND EXERCISE PERFORMANCE IN PATIENTS WITH CYSTIC-FIBROSIS WITH SEVERE PULMONARY-DISEASE

被引:40
作者
MARCUS, CL
BADER, D
STABILE, MW
WANG, CI
OSHER, AB
KEENS, TG
机构
[1] CHILDRENS HOSP,DIV NEONATOL & PEDIAT PULM,4650 SUNSET BLVD,LOS ANGELES,CA 90077
[2] UNIV SO CALIF,SCH MED,LOS ANGELES,CA 90033
关键词
D O I
10.1378/chest.101.1.52
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Patients with cystic fibrosis (CF) and advanced pulmonary disease have pulmonary limitation of exercise, often associated with arterial oxygen desaturation. Improving oxygenation during exercise by providing supplemental oxygen may improve exercise performance in these patients. To test this, we performed graded exercise stress tests in 22 CF patients with severe pulmonary disease (mean PaO2, 64 +/- 2 mm Hg [+/- SE]; PaCO2 46 +/- 2 mm Hg; RV/TLC, 57 +/- 4 percent; FEV1, 38 +/- 4 percent of predicted; FEF25-75%, 13 +/- 2 percent of predicted; median age, 26 years) and compared them to 21 controls (RV/TLC, 27 +/- 4 percent; FEV1, 112 +/- 2 percent of predicted; FEF25-75%, 80 +/- 4 percent of predicted; median age, 29 years). Each subject performed graded exercise stress tests while breathing FIo2 of 0.21 and FIo2 of 0.30. Subjects were blinded to the composition of the inspired gas, and the order of testing was randomized. We found that CF subjects exercised longer, had a higher maximal Vo2, higher O2 pulse, and less arterial oxygen desaturation when receiving supplemental O2. Control subjects exercised longer when breathing supplemental O2 but had no significant change in maximal Vo2, O2 pulse, or SaO2. Both CF and control subjects had increased end-tidal Pco2 when exercising while breathing supplemental O2. We conclude that CF patients with advanced pulmonary disease have increased exercise tolerance and aerobic capacity when exercising while breathing supplemental O2.
引用
收藏
页码:52 / 57
页数:6
相关论文
共 36 条
[1]   LONG-TERM EFFECTS OF PHYSICAL EXERCISE ON WORKING CAPACITY AND PULMONARY-FUNCTION IN CYSTIC-FIBROSIS [J].
ANDREASSON, B ;
JONSON, B ;
KORNFALT, R ;
NORDMARK, E ;
SANDSTROM, S .
ACTA PAEDIATRICA SCANDINAVICA, 1987, 76 (01) :70-75
[2]  
ASTIN TW, 1970, AM REV RESPIR DIS, V102, P382
[3]  
BENSON LN, 1984, AM REV RESPIR DIS, V130, P987
[4]  
BRADLEY BL, 1978, AM REV RESPIR DIS, V118, P239
[5]   EXERCISE PERFORMANCE IN CHRONIC OBSTRUCTIVE PULMONARY-DISEASES [J].
BROWN, HV ;
WASSERMAN, K .
MEDICAL CLINICS OF NORTH AMERICA, 1981, 65 (03) :525-547
[6]  
BYE PTP, 1985, AM REV RESPIR DIS, V132, P236
[7]   HOSPITAL THERAPY IMPROVES EXERCISE TOLERANCE AND LUNG-FUNCTION IN CYSTIC-FIBROSIS [J].
CERNY, FJ ;
CROPP, GJA ;
BYE, MR .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1984, 138 (03) :261-265
[8]  
CERNY FJ, 1982, AM REV RESPIR DIS, V126, P217
[9]  
CHERNIACK RM, 1972, AM REV RESPIR DIS, V106, P38, DOI 10.1164/arrd.1972.106.1.38
[10]   THE ROLE OF NUTRITIONAL-STATUS, AIRWAY-OBSTRUCTION, HYPOXIA, AND ABNORMALITIES IN SERUM-LIPID COMPOSITION IN LIMITING EXERCISE TOLERANCE IN CHILDREN WITH CYSTIC-FIBROSIS [J].
COATES, AL ;
BOYCE, P ;
MULLER, D ;
MEARNS, M ;
GODFREY, S .
ACTA PAEDIATRICA SCANDINAVICA, 1980, 69 (03) :353-358