How Many Maneuvers Should We Do for Maximal Inspiratory and Expiratory Muscle Pressure Testing in Children: A Retrospective Review in Children with Cystic Fibrosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pulmonary and Respiratory Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00408-021-00422-0.pdf
Reference39 articles.
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2. Verma R, Chiang J, Qian H, Amin R (2019) Maximal static respiratory and sniff pressures in healthy children. A systematic review and meta-analysis. Ann Am Thorac Soc 16(4):478–487. https://doi.org/10.1513/AnnalsATS.201808-506OC
3. Heinzmann-Filho JP, Marostica PJC, Donadio M (2012) Ventilatory muscle strength in cystic fibrosis patients: a literature review. Monaldi Arch Chest Dis 77:134–138. https://doi.org/10.4081/monaldi.2012.147
4. Szeinberg A, England S, Mindorff C, Fraser IM, Levison H (1985) Maximal inspiratory and expiratory pressures are reduced in hyperinflated, malnourished, young adult male patients with cystic fibrosis. Am Rev Respir Dis 132(4):766–769. https://doi.org/10.1164/arrd.1985.132.4.766
5. Dekerlegand RL, Hadjiliadis D, Swisher AK, Parrott JS, Heuer AJ, Myslinski MJ (2015) Inspiratory muscle strength relative to disease severity in adults with stable cystic fibrosis. J Cyst Fibros 14(5):639–645. https://doi.org/10.1016/j.jcf.2015.05.003
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