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      Mechanical correlates of dyspnea in bronchial asthma

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          Abstract

          We hypothesized that dyspnea and its descriptors, that is, chest tightness, inspiratory effort, unrewarded inspiration, and expiratory difficulty in asthma reflect different mechanisms of airflow obstruction and their perception varies with the severity of bronchoconstriction. Eighty‐three asthmatics were studied before and after inhalation of methacholine doses decreasing the 1‐sec forced expiratory volume by ~15% (mild bronchoconstriction) and ~25% (moderate bronchoconstriction). Symptoms were examined as a function of changes in lung mechanics. Dyspnea increased with the severity of obstruction, mostly because of inspiratory effort and chest tightness. At mild bronchoconstriction, multivariate analysis showed that dyspnea was related to the increase in inspiratory resistance at 5 Hz ( R 5) ( r 2 = 0.10, P = 0.004), chest tightness to the decrease in maximal flow at 40% of control forced vital capacity, and the increase in R 5 at full lung inflation ( r 2 = 0.15, P = 0.006), inspiratory effort to the temporal variability in R 5‐19 ( r 2 = 0.13, P = 0.003), and unrewarded inspiration to the recovery of R 5 after deep breath ( r 2 = 0.07, P = 0.01). At moderate bronchoconstriction, multivariate analysis showed that dyspnea and inspiratory effort were related to the increase in temporal variability in inspiratory reactance at 5 Hz ( X 5) ( r 2 = 0.12, P = 0.04 and r 2 = 0.18, P < 0.001, respectively), and unrewarded inspiration to the decrease in X 5 at maximum lung inflation ( r 2 = 0.07, P = 0.04). We conclude that symptom perception is partly explained by indexes of airway narrowing and loss of bronchodilatation with deep breath at low levels of bronchoconstriction, but by markers of ventilation heterogeneity and lung volume recruitment when bronchoconstriction becomes more severe.

          Abstract

          In asthma, respiratory symptom perception is qualitatively different depending on the level of bronchoconstriction. During the early phases of an attack dyspnea and its descriptors appear to be related to the severity of airway narrowing and loss of bronchodilatation with deep breath, whereas when narrowing worsens they depend on more profound changes in lung periphery as suggested by increased ventilation heterogeneity and reduced lung volume recruitment with breathing.

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          Most cited references39

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          The forced oscillation technique in clinical practice: methodology, recommendations and future developments.

          The forced oscillation technique (FOT) is a noninvasive method with which to measure respiratory mechanics. FOT employs small-amplitude pressure oscillations superimposed on the normal breathing and therefore has the advantage over conventional lung function techniques that it does not require the performance of respiratory manoeuvres. The present European Respiratory Society Task Force Report describes the basic principle of the technique and gives guidelines for the application and interpretation of FOT as a routine lung function test in the clinical setting, for both adult and paediatric populations. FOT data, especially those measured at the lower frequencies, are sensitive to airway obstruction, but do not discriminate between obstructive and restrictive lung disorders. There is no consensus regarding the sensitivity of FOT for bronchodilation testing in adults. Values of respiratory resistance have proved sensitive to bronchodilation in children, although the reported cutoff levels remain to be confirmed in future studies. Forced oscillation technique is a reliable method in the assessment of bronchial hyperresponsiveness in adults and children. Moreover, in contrast with spirometry where a deep inspiration is needed, forced oscillation technique does not modify the airway smooth muscle tone. Forced oscillation technique has been shown to be as sensitive as spirometry in detecting impairments of lung function due to smoking or exposure to occupational hazards. Together with the minimal requirement for the subject's cooperation, this makes forced oscillation technique an ideal lung function test for epidemiological and field studies. Novel applications of forced oscillation technique in the clinical setting include the monitoring of respiratory mechanics during mechanical ventilation and sleep.
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            Self-organized patchiness in asthma as a prelude to catastrophic shifts.

            Asthma is a common disease affecting an increasing number of children throughout the world. In asthma, pulmonary airways narrow in response to contraction of surrounding smooth muscle. The precise nature of functional changes during an acute asthma attack is unclear. The tree structure of the pulmonary airways has been linked to complex behaviour in sudden airway narrowing and avalanche-like reopening. Here we present experimental evidence that bronchoconstriction leads to patchiness in lung ventilation, as well as a computational model that provides interpretation of the experimental data. Using positron emission tomography, we observe that bronchoconstricted asthmatics develop regions of poorly ventilated lung. Using the computational model we show that, even for uniform smooth muscle activation of a symmetric bronchial tree, the presence of minimal heterogeneity breaks the symmetry and leads to large clusters of poorly ventilated lung units. These clusters are generated by interaction of short- and long-range feedback mechanisms, which lead to catastrophic shifts similar to those linked to self-organized patchiness in nature. This work might have implications for the treatment of asthma, and might provide a model for studying diseases of other distributed organs.
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              Oscillation mechanics of lungs and chest in man.

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                Author and article information

                Journal
                Physiol Rep
                Physiol Rep
                physreports
                phy2
                Physiological Reports
                Wiley Periodicals, Inc.
                2051-817X
                1 December 2013
                8 December 2013
                : 1
                : 7
                : e00166
                Affiliations
                [1 ]Allergologia e Fisiopatologia Respiratoria, ASO S. Croce e Carle, Cuneo, Italy
                [2 ]Fisiopatologia Respiratoria, Dipartimento di Medicina Interna, Università di Genova, Genova, Italy
                [3 ]TBM Lab, Dipartimento di Elettronica, Informazione e Bioingegneria, Politecnico di Milano, Milano, Italy
                [4 ]Pneumologia‐Fisiopatologia Respiratoria, AOU S. Luigi Gonzaga, Orbassano (Torino), Italy
                [5 ]Dipartimento di Medicina Interna, Sezione di Immunologia Clinica, Allergologia e Malattie Respiratorie, Università di Firenze, Firenze, Italy
                Author notes
                CorrespondenceRiccardo Pellegrino, Allergologia e Fisiopatologia Respiratoria, ASO S. Croce e Carle, Cuneo, 12100 Italy.Tel. +39 0171616755Fax: +39 0171616798E‐mail: pellegrino.r@ 123456ospedale.cuneo.it
                Article
                phy2166
                10.1002/phy2.166
                3970739
                722b4f5d-561c-42c5-af75-ba2e6b4d6788
                © 2013 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 23 October 2013
                : 29 October 2013
                Categories
                Original Research

                airway mechanics,dyspnea descriptors,forced oscillation technique,lung hyperinflation,methacholine

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