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Physical training: vital for survival and quality of life in cystic fibrosis

Louise Lannefors
Breathe 2012 8: 308-313; DOI: 10.1183/20734735.022111
Louise Lannefors
Respiratory Medicine and Allergology, Lund University Hospital, Lund, Sweden
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  • For correspondence: louise.lannefors@med.lu.se
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    Figure 1

    Mean±sd annual mortality rate and median age at death in the Swedish cystic fibrosis population [5].

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    Figure 2

    Current and estimated survival rates of four different cohorts of Swedish cystic fibrosis patients [5]. Vertical ticks indicate estimates and years indicate patient birth date.

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    Figure 3

    Airway clearance therapy based on physical exercise combined with assisted autogenic drainage, performed in an infant.

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    Figure 4

    The physiological airway clearance treatment strategy illustrated schematically. The four numbered steps are included in a cycle that is repeated over and over again. TLC: total lung capacity; VT: tidal volume; FRC: functional residual capacity; RV: residual volume.

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    Figure 5

    A severely ill patient (forced expiratory volume in 1 s ∼25% predicted) performing physical exercise with supplementary oxygen, while on the list for lung transplantation.

Tables

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  • Table 1 Mean lung function in all Swedish cystic fibrosis patients ≥7 years of age in two age groups
    Age
    7–17 years≥18 years
    Subjects %4852
    FEV1 % pred9073
    VC % pred9691
    • FEV1: forced expiratory volume in 1 s; % pred: % predicted; VC: vital capacity. Data from [14].

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Physical training: vital for survival and quality of life in cystic fibrosis
Louise Lannefors
Breathe Jun 2012, 8 (4) 308-313; DOI: 10.1183/20734735.022111

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Physical training: vital for survival and quality of life in cystic fibrosis
Louise Lannefors
Breathe Jun 2012, 8 (4) 308-313; DOI: 10.1183/20734735.022111
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