囊性纤维化
医学
汗水
物理疗法
肺功能测试
体位引流
重症监护医学
内科学
作者
David M. Orenstein,Kathe G. Henke,Frank J. Cerny
标识
DOI:10.1080/00913847.1983.11708434
摘要
In brief: Cystic fibrosis (CF) patients are likely to be less fit than their normal peers, but most can exercise safely. Recent studies show that exercise programs can increase fitness and exercise tolerance. They can also increase the endurance of the respiratory muscles, although pulmonary function will not change. Exercise may be as beneficial as traditional chest physical therapy and postural drainage for getting mucus up from the lungs, but the authors recommend that patients continue therapy until this is confirmed. Because CF patients lose significantly more salt in their sweat than normal people, the authors recommend ample water intake and free access to the salt shaker.
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