Wiesemann H G
Monatsschr Kinderheilkd. 1985 Oct;133(10):726-9.
Lung function tests as tools in the lifelong care of patients with cystic fibrosis can help to assess results of different therapeutic regimes and the prognosis, as there is a typical sequence of alterations of lung function parameters. They allow to assess the degree of disablement more precisely and more adequately than do clinical data; this is of special concern in questions related to social rehabilitation and the finding of an adequate job. Appropriate parameters are forced vital capacity, maximal mid-exspiratory flow, residual volume and partial pressure of oxygen and carbon dioxide in arterial blood.
肺功能测试作为囊性纤维化患者终身护理的工具，有助于评估不同治疗方案的效果和预后，因为肺功能参数存在典型的变化顺序。与临床数据相比，它们能够更精确、更充分地评估残疾程度；这在与社会康复和找到合适工作相关的问题中尤为重要。合适的参数包括用力肺活量、最大呼气中期流速、残气量以及动脉血中氧气和二氧化碳的分压。
