Source:http://linkedlifedata.com/resource/pubmed/id/11316640
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2001-4-24
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pubmed:abstractText |
Chronic obstructive pulmonary disease (COPD) is a condition in which continuous bronchodilation may have clinical advantages. This study evaluated salmeterol, a beta-agonist bronchodilator with a duration of action substantially longer than that of short-acting beta-agonists, compared with ipratropium, an anticholinergic bronchodilator, and placebo in patients with COPD. Four hundred and five patients with COPD received either salmeterol 42 microg twice daily, ipratropium bromide 36 microg four times daily, or placebo for 12 wk in this randomized, double-blind, parallel-group study. Patients were stratified on the basis of bronchodilator response to albuterol (> 12% and > 200-ml improvement) and were randomized within each stratum. Bronchodilator response was measured over 12 h four times during the treatment period. Salmeterol provided similar maximal bronchodilatation to ipratropium but had a longer duration of action and a more constant bronchodilatory effect with no evidence of bronchodilator tolerance. Both active treatments were well tolerated. Salmeterol was an effective bronchodilator with a consistent effect over this 12-wk study in patients with COPD, including those "unresponsive" to albuterol. The long duration of action of salmeterol offers the advantage of twice daily dosing compared with the required four times a day dosing with ipratropium.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adrenergic beta-Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Albuterol,
http://linkedlifedata.com/resource/pubmed/chemical/Bronchodilator Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Cholinergic Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Ipratropium,
http://linkedlifedata.com/resource/pubmed/chemical/salmeterol
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1073-449X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
163
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1087-92
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11316640-Adrenergic beta-Agonists,
pubmed-meshheading:11316640-Albuterol,
pubmed-meshheading:11316640-Analysis of Variance,
pubmed-meshheading:11316640-Bronchodilator Agents,
pubmed-meshheading:11316640-Cholinergic Antagonists,
pubmed-meshheading:11316640-Double-Blind Method,
pubmed-meshheading:11316640-Female,
pubmed-meshheading:11316640-Forced Expiratory Volume,
pubmed-meshheading:11316640-Humans,
pubmed-meshheading:11316640-Ipratropium,
pubmed-meshheading:11316640-Lung Diseases, Obstructive,
pubmed-meshheading:11316640-Male,
pubmed-meshheading:11316640-Middle Aged,
pubmed-meshheading:11316640-Quality of Life,
pubmed-meshheading:11316640-Vital Capacity
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pubmed:year |
2001
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pubmed:articleTitle |
Use of a long-acting inhaled beta2-adrenergic agonist, salmeterol xinafoate, in patients with chronic obstructive pulmonary disease.
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pubmed:affiliation |
University of Nebraska Medical Center, Omaha, Nebraska, USA. srennard@mail.unmc.edu
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't,
Multicenter Study
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