Ja. Alison et al., THE EFFECT OF A COMPREHENSIVE, INTENSIVE INPATIENT TREATMENT PROGRAM ON LUNG-FUNCTION AND EXERCISE CAPACITY IN PATIENTS WITH CYSTIC-FIBROSIS, Physical therapy, 74(6), 1994, pp. 583-593
Background and Purpose. The purpose of this investigation was to measu
re the effects of a 10- to 14-day comprehensive, intensive hospital tr
eatment program on peak exercise capacity, endurance capacity, respira
tory function, weight change, and maximum inspiratory and expiratory m
outh pressures in patients with cystic fibrosis with a pulmonary exace
rbation. Subjects. Fourteen young adults with cystic fibrosis admitted
to a hospital for an exacerbation of their pulmonary disease were stu
died. Methods. Subjects performed pulmonary function tests, inspirator
y and expiratory mouth pressure tests, and stationary bicycle exercise
tests at admission and discharge. Comprehensive therapy provided duri
ng the hospital admission consisted of intravenous antibiotics, physic
al therapy, high-calorie diet, and daily medical review. Results. The
patients showed improvements in forced expiratory volume in 1 second (
46%-55% of predicted values) and forced vital capacity (62%-68% of pre
dicted values). Maximum inspiratory and expiratory mouth pressures als
o improved (118%-131% and 78%-92% of predicted values, respectively).
There was a mean weight gain of 2 kg Maximum work capacity on a bicycl
e ergometer improved from a mean of 45% to 52% of predicted values The
most impressive result was the marked increase in exercise endurance
time from a mean of 9.5 minutes on admission to 16.6 minutes at discha
rge. Conclusion and Discussion. This study indicates that young adults
with cystic fibrosis and an exacerbation of their pulmonary disease o
btain measurable benefits from a comprehensive, intensive treatment pr
ogram, particularly improvement in their capacity for endurance exerci
se [Alison JA, Donnelly PM, Lennon M, et al. The effect of a comprehen
sive, intensive inpatient treatment program on lung function and exerc
ise capacity in patients with cystic fibrosis.