The Value of Measuring Inspiratory Capacity in Subjects With Cystic Fibrosis.

BACKGROUND: Inspiratory capacity (IC) is often overlooked as an important measured index of spirometry in patients with cystic fibrosis (CF). Abnormally low IC may indicate the onset of static/dynamic hyperinflation, which may be accompanied by dyspnea and an increase in the work of breathing. This...

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Publicado en:Respiratory Care Vol. 63; no. 8; pp. 981 - 988
Autores principales: Vilozni, Daphna, Dagan, Adi, Lavie, Moran, Sarouk, Ifat, Bar-Aluma, Bat-El, Ashkenazi, Moshe, Mendelovich, Sarina Levy, Betzalel, Yael, Efrati, Ori
Formato: CEU research tables/charts Journal Article
Publicado: Mary Ann Liebert, Inc. Aug2018
Acceso en línea:Ver este registro en EBSCOhost