Longitudinal pulmonary function testing outcome measures in Duchenne muscular dystrophy: long-term natural history with and without glucocorticoids

2017 ◽  
Vol 27 ◽  
pp. S115-S116 ◽  
Author(s):  
C. McDonald ◽  
H. Gordish-Dressman ◽  
E. Henricson ◽  
T. Duong ◽  
N. Joyce ◽  
...  
2018 ◽  
Vol 28 (11) ◽  
pp. 897-909 ◽  
Author(s):  
Craig M. McDonald ◽  
Heather Gordish-Dressman ◽  
Erik K. Henricson ◽  
Tina Duong ◽  
Nanette C. Joyce ◽  
...  

2018 ◽  
Vol 5 (1) ◽  
pp. 47-58 ◽  
Author(s):  
T. Bernard Kinane ◽  
Oscar H. Mayer ◽  
Petra W. Duda ◽  
Linda P. Lowes ◽  
Stephanie L. Moody ◽  
...  

2018 ◽  
Vol 143 (08) ◽  
pp. 593-596 ◽  
Author(s):  
Wolfram Windisch ◽  
Carl Criée

AbstractPulmonary function testing is essential for diagnosis and treatment-guidance of chronic obstructive pulmonary disease (COPD). Airway obstruction as assessed by spirometry should follow the reference-values provided by the Global Lung Initiative (GLI) of the European Respiratory Society (ERS). In addition, lung function testing should also include the assessment of lung hyperinflation and pulmonary emphysema by full-body plethysmography and determination of diffusion capacity. This is important since both, lung hyperinflation and pulmonary emphysema, can present without existing airway obstruction. Even though this formally excludes the diagnosis of COPD, these entities still belong to this disease complex. However, strictly speaking, pharmaceutical treatment is valid only for those patients with co-existing airway obstruction according to Global Lung Initiative for Chronic Obstructive Lung Disease (GOLD) criteria – since the absence of airway obstruction serves as exclusion criterion in nearly all randomized controlled trials. Nevertheless, progressive symptoms still require detailed pulmonary function testing for the guidance of non-pharmaceutical treatment – such as endoscopic or surgical lung volume reduction, long-term oxygen therapy, long-term non-invasive ventilation, and lung transplantation.


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