Literature DB >> 3674055

Flow-volume loop changes reflecting respiratory muscle weakness in chronic neuromuscular disorders.

W G Vincken1, M G Elleker, M G Cosio.   

Abstract

In order to identify the changes in pulmonary function and in the flow-volume loop due to respiratory muscle weakness, two groups of 10 nonsmokers with stable, chronic neuromuscular disease but without respiratory symptoms were studied: one without (Group 1) and one with (Group 2) respiratory muscle weakness as assessed by measurement of maximal static inspiratory and expiratory pressures. In Group 1, pulmonary function was normal except for increased ratio of one-second forced expiratory volume to forced vital capacity and forced expiratory flow at 25 to 75 percent forced vital capacity, which may reflect increased elastic lung recoil. Group 2 had mild volume restriction, appropriate for the degree of respiratory muscle weakness, and reduced inspiratory and expiratory flow rates. Pulmonary function was significantly more disturbed in Group 2 than in Group 1, and correlated well with maximal static inspiratory and expiratory pressures. Analysis of the flow-volume loop configuration revealed that four parameters describing effort-dependent portions were significantly related to maximal static inspiratory pressure and maximal static expiratory pressure. These parameters were peak expiratory flow, the slope of the ascending limb of the maximal expiratory curve, a drop of forced expiratory flow near residual volume, and forced inspiratory flow at 50 percent of vital capacity. A flow-volume loop score obtained from these four parameters was significantly higher in Group 2 than in Group 1 (2.8 +/- 1.03 versus 1.1 +/- 1.37; p less than 0.01). A flow-volume loop score of 2 or more had 80 percent specificity and 90 percent sensitivity in predicting respiratory muscle weakness in these patients with chronic neuromuscular disease. These data suggest that sensitive assessment of the flow-volume loop configuration as part of routine pulmonary function testing may help to suspect and identify respiratory muscle weakness.

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Year:  1987        PMID: 3674055     DOI: 10.1016/0002-9343(87)90897-7

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  3 in total

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Journal:  PLoS One       Date:  2019-04-24       Impact factor: 3.240

2.  Effects of yoga breathing exercises on pulmonary function in patients with Duchenne muscular dystrophy: an exploratory analysis.

Authors:  Marcos Rojo Rodrigues; Celso Ricardo Fernandes Carvalho; Danilo Forghieri Santaella; Geraldo Lorenzi-Filho; Suely Kazue Nagahashi Marie
Journal:  J Bras Pneumol       Date:  2014 Mar-Apr       Impact factor: 2.624

3.  Treatment effect of idebenone on inspiratory function in patients with Duchenne muscular dystrophy.

Authors:  Gunnar M Buyse; Thomas Voit; Ulrike Schara; Chiara S M Straathof; Maria Grazia D'Angelo; Günther Bernert; Jean-Marie Cuisset; Richard S Finkel; Nathalie Goemans; Christian Rummey; Mika Leinonen; Oscar H Mayer; Paolo Spagnolo; Thomas Meier; Craig M McDonald
Journal:  Pediatr Pulmonol       Date:  2016-08-29
  3 in total

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