Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2008-10-30
pubmed:databankReference
pubmed:abstractText
Systemic corticosteroids and additional short-acting beta2-agonists are commonly used in exacerbations of chronic obstructive pulmonary disease (COPD). In this double-blind study, the combination of a high-dose inhaled corticosteroid with a rapid-onset long-acting beta2-agonist was evaluated in the treatment of out-patient COPD exacerbations. The primary aim was to compare 14-day treatment effects of budesonide/formoterol to placebo on sputum eosinophils and, secondarily, on other indices of inflammation, forced expiratory flow in one second (FEV(1)), symptoms, health status, and adverse events. Forty-five patients not using steroids (37 male, 21/24 current/ex smoker, median packyears 38, age 65 years, FEV(1) 61% predicted), experiencing a COPD exacerbation, were treated at home with budesonide/formoterol (320/9 microg 4 times daily), prednisolone (30 mg daily), or placebo for 14 days. Sputum eosinophils were significantly reduced by budesonide/formoterol (-57%) compared to placebo (+24%) (p = 0.01). Budesonide/formoterol reduced total symptom scores significantly (p = 0.01) compared to placebo. The increase in FEV(1) by 2 weeks of treatment with budesonide/formoterol (125 ml) was not significantly different from that of placebo (43 ml) (p = 0.07). Budesonide/ formoterol treatment did not suppress morning serum cortisol compared to placebo (-16%; p = 0.50). In conclusion, budesonide/formoterol reduces sputum eosinophils and improves symptoms in the treatment of out-patient COPD exacerbations.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1541-2563
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
5
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
282-90
pubmed:dateRevised
2009-11-17
pubmed:meshHeading
pubmed-meshheading:18972276-Administration, Inhalation, pubmed-meshheading:18972276-Administration, Oral, pubmed-meshheading:18972276-Aged, pubmed-meshheading:18972276-Anti-Inflammatory Agents, pubmed-meshheading:18972276-Bronchodilator Agents, pubmed-meshheading:18972276-Budesonide, pubmed-meshheading:18972276-Double-Blind Method, pubmed-meshheading:18972276-Drug Combinations, pubmed-meshheading:18972276-Eosinophils, pubmed-meshheading:18972276-Ethanolamines, pubmed-meshheading:18972276-Female, pubmed-meshheading:18972276-Humans, pubmed-meshheading:18972276-Male, pubmed-meshheading:18972276-Middle Aged, pubmed-meshheading:18972276-Prednisolone, pubmed-meshheading:18972276-Pulmonary Disease, Chronic Obstructive, pubmed-meshheading:18972276-Respiratory Function Tests, pubmed-meshheading:18972276-Sputum, pubmed-meshheading:18972276-Treatment Outcome
pubmed:year
2008
pubmed:articleTitle
Anti-inflammatory effects of combined budesonide/formoterol in COPD exacerbations.
pubmed:affiliation
Groningen Research Institute for Asthma and COPD, Department of Pulmonology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands. ebathoorn@gmail.com
pubmed:publicationType
Journal Article, Comparative Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't