Determinants of dyspnea and alveolar hypoventilation during exercise in cystic fibrosis: Impact of inspiratory muscle endurance Sylvie Leroy, Thierry.

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Determinants of dyspnea and alveolar hypoventilation during exercise in cystic fibrosis: Impact of inspiratory muscle endurance Sylvie Leroy, Thierry Perez, Rémy Neviere, Bernard Aguilaniu, Benoît Wallaert Journal of Cystic Fibrosis Volume 10, Issue 3, Pages 159-165 (May 2011) DOI: 10.1016/j.jcf.2010.12.006 Copyright © 2010 European Cystic Fibrosis Society. Terms and Conditions

Fig. 1 Borg dyspnea at the end of the incremental exercise testing on a cycloergometer as a function of the inspiratory muscle endurance (IME) expressed as a percentage of maximal inspiratory pressure (Plim2/PImax%) (r=−0.72). Triangles represent patients from Group LwD and squares represent patients from Group SvD. Journal of Cystic Fibrosis 2011 10, 159-165DOI: (10.1016/j.jcf.2010.12.006) Copyright © 2010 European Cystic Fibrosis Society. Terms and Conditions

Fig. 2 PaCO2 at rest and at peak exercise are represented for both groups. Group A is represented by white rectangles. Group B is represented by grey rectangles. Journal of Cystic Fibrosis 2011 10, 159-165DOI: (10.1016/j.jcf.2010.12.006) Copyright © 2010 European Cystic Fibrosis Society. Terms and Conditions