Literature DB >> 12037229

Volume effect and exertional dyspnoea after bronchodilator in patients with COPD with and without expiratory flow limitation at rest.

E Boni1, L Corda, D Franchini, P Chiroli, G P Damiani, L Pini, V Grassi, C Tantucci.   

Abstract

BACKGROUND: A study was undertaken to investigate whether bronchodilators are associated with less breathlessness at rest and during light exercise in patients with moderate to severe chronic obstructive pulmonary disease (COPD) with resting tidal expiratory flow limitation (EFL; flow limited (FL)) compared with those without EFL (non-flow limited (NFL)).
METHODS: Twenty subjects (13 men) of mean (SD) age 65 (8) years (range 43-77) suffering from COPD with forced expiratory volume in 1 second (FEV(1)) 47 (18)% predicted were studied before and after inhalation of salbutamol (400 microg). Routine pulmonary function tests were performed in the seated position at rest. EFL was assessed by the negative expiratory pressure (NEP) method and changes in end expiratory lung volume (EELV) were inferred from variations in inspiratory capacity (IC). Dyspnoea was measured using the Borg scale at rest and at the end of a 6 minute steady state exercise test at 33% of the maximal predicted workload.
RESULTS: EFL occurred in 11 patients. Following salbutamol IC did not change in NFL patients but increased by 24% (95% CI 15 to 33) in FL patients (p<0.001). Maximal inspiratory pressure (PImax) improved at EELV from 45 (95% CI 26 to 63) to 55 (95% CI 31 to 79) cm H(2)O (p<0.05) in FL patients after salbutamol but remained unchanged in NFL patients. The workload performed during exercise amounted to 34 (95% CI 27 to 41) and 31 (95% CI 21 to 40) watts (NS) for patients without and with EFL, respectively. After salbutamol, dyspnoea did not change either at rest or during exercise in the NFL patients, but decreased from 0.3 (95% CI -0.1 to 0.8) to 0.1 (95% CI -0.1 to 0.4) at rest (NS) and from 3.7 (95% CI 1.7 to 5.7) to 2.6 (95% CI 1.1 to 4.0) at the end of exercise (p<0.01) in FL patients.
CONCLUSIONS: Patients with COPD with EFL may experience less breathlessness after a bronchodilator, at least during light exercise, than those without EFL. This beneficial effect, which is closely related to an increase in IC at rest, occurs even in the absence of a significant improvement in FEV(1) and is associated with a greater PImax.

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Year:  2002        PMID: 12037229      PMCID: PMC1746351          DOI: 10.1136/thorax.57.6.528

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  31 in total

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Review 3.  Lung volumes and forced ventilatory flows. Report Working Party Standardization of Lung Function Tests, European Community for Steel and Coal. Official Statement of the European Respiratory Society.

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4.  Detection of expiratory flow limitation during mechanical ventilation.

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5.  Effects and mechanism of fenoterol on fatigued canine diaphragm.

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7.  Acute bronchodilator trials in chronic obstructive pulmonary disease.

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8.  Exertional breathlessness in patients with chronic airflow limitation. The role of lung hyperinflation.

Authors:  D E O'Donnell; K A Webb
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9.  Inhaled bronchodilators reduce dynamic hyperinflation during exercise in patients with chronic obstructive pulmonary disease.

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10.  The effects of beta 2-agonists and caffeine on respiratory and limb muscle performance.

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2.  Effect of oxygen on recovery from maximal exercise in patients with chronic obstructive pulmonary disease.

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Journal:  Thorax       Date:  2004-08       Impact factor: 9.139

3.  Clinical dose-response relationship of fluticasone propionate in adults with asthma.

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4.  Inhaled corticosteroids reduce the progression of airflow limitation in chronic obstructive pulmonary disease: a meta-analysis.

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5.  Dynamic hyperinflation during the 6-min walk test in severely asthmatic subjects.

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6.  The clinical utility of forced oscillation technique during hospitalisation in patients with exacerbation of COPD.

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10.  A pilot study of inspiratory capacity and resting dyspnea correlations in exacerbations of COPD and asthma.

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