A randomized controlled trial of a 3-year home exercise program in cystic fibrosis

医学 有氧运动 囊性纤维化 养生 物理疗法 随机对照试验 肺功能测试 最大VO2 肺活量 内科学 心率 肺功能 血压 扩散能力
作者
Jane Schneiderman‐Walker,S.L. Pollock,Mary Corey,Donna D. Wilkes,Gerard J. Canny,Linda Pedder,Joseph Reisman
出处
期刊:The Journal of Pediatrics [Elsevier BV]
卷期号:136 (3): 304-310 被引量:263
标识
DOI:10.1067/mpd.2000.103408
摘要

To evaluate the effects of a 3-year home exercise program on pulmonary function and exercise tolerance in mildly to moderately impaired patients with cystic fibrosis (CF) and to assess whether regular aerobic exercise is a realistic treatment option.Seventy-two patients with CF (7-19 years) were randomly assigned to an exercise group (a minimum of 20 minutes of aerobic exercise, at a heart rate of approximately 150 beats/min, 3 times weekly) or a control group (usual physical activity participation). Pulmonary function, exercise tolerance, clinical status, hospitalizations, and compliance with therapy were monitored during scheduled visits to the hospital's CF clinic.Sixty-five patients were included in the analyses. The control group demonstrated a greater annual decline in percent of predicted forced vital capacity compared with the exercise group (mean slope +/- SD, -2.42 +/- 4.15 vs -0.25 +/- 2.81; P =.02), with a similar trend for forced expiratory volume in 1 second (-3.47 +/- 4.93 vs -1.46 +/- 3. 55; P =.07). Patients remained compliant with the exercise program over the study period. An improved sense of well-being was reported with exercise.Pulmonary function declined more slowly in the exercise group than in the control group, suggesting a benefit for patients with CF participating in regular aerobic exercise. Consistent compliance with the home exercise program and a self-reported positive attitude toward exercise provide further evidence of the feasibility and value of including an aerobic exercise program in the conventional treatment regimen of patients with CF.
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