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    A randomized, placebo-controlled trial of bronchodilators for bronchoscopy in patients with COPD

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    Authors
    Stolz, Daiana
    Pollak, Vincent
    Chhajed, Prashant N.
    Gysin, Christian
    Pflimlin, Eric
    Tamm, Michael
    UMass Chan Affiliations
    Department of Pulmonary, Allergy and Critical Care Medicine
    Document Type
    Journal Article
    Publication Date
    2007-03-16
    Keywords
    Administration, Inhalation
    Adult
    Aged
    Aged, 80 and over
    Albuterol
    Bronchodilator Agents
    *Bronchoscopy
    Double-Blind Method
    Female
    Forced Expiratory Volume
    Humans
    Male
    Middle Aged
    Premedication
    Pulmonary Disease, Chronic Obstructive
    Statistics as Topic
    Vital Capacity
    Life Sciences
    Medicine and Health Sciences
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    Link to Full Text
    http://dx.doi.org/10.1378/chest.06-2308
    Abstract
    BACKGROUND: In contrast to asthma, the indication for bronchodilators prior to bronchoscopy in patients with COPD has not been properly investigated. We therefore performed a randomized, double-blind, placebo-controlled trial to determine whether use of a short-acting bronchodilator provides a protective effect in patients with COPD undergoing bronchoscopy. METHODS: One hundred twenty patients undergoing bronchoscopy were included. Patients with COPD were randomized to receive either 200 mug of salbutamol (n = 40) or placebo (n = 40) before bronchoscopy. Control patients (n = 40) did not receive any inhaled medication. Spirometry was performed before and 2 h after bronchoscopy in all patients. Sedative drug requirements and hemodynamic parameters were recorded. RESULTS: Hemodynamic findings before, during, and after bronchoscopy were similar in patients with COPD randomized to either salbutamol or placebo (p = not significant for all). Compared to prebronchoscopy values, postbronchoscopy percentage of predicted FEV(1) decreased significantly in all three groups: salbutamol (median, - 4.7%; interquartile range [IQR], - 13.3 to 6.6); placebo (median, - 4.8%; IQR, - 19.9 to 8.4); and control subjects (median, - 10.0%; IQR, - 20.2 to - 3.3) [p = 0.023]. The decrease in FEV(1) was similar in all three patient groups (p = 0.432). The relative change in FEV(1) was inversely correlated to the increasing severity of COPD as expressed by Global Initiative for Chronic Obstructive Lung Disease stages (p = 0.01). CONCLUSIONS: Premedication with an inhaled short-acting beta-agonist cannot be recommended in patients with COPD undergoing bronchoscopy.
    Source
    Chest. 2007 Mar;131(3):765-72. Link to article on publisher's site
    DOI
    10.1378/chest.06-2308
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/38382
    PubMed ID
    17356091
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1378/chest.06-2308
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