Background: Although both beta-adrenergic agonists and anticholinergic agents are widely used in the treatment of patients with COPD, they influence the pulmonary circulation and ventilation differently. We compared the effects of these two agents on gas exchange and distribution of ventilation in COPD.
Methods: Pirbuterol and ipratropium bromide were administered by inhalation via a metered-dose inhaler to 12 and 14 patients with COPD, respectively, in a randomized, double-blind fashion. Pulmonary function tests, arterial blood gas levels, heart rate, resting minute ventilation (VE), physiologic dead space volume to total ventilation ratio (VD/Vt) and oxygen consumption (VO2) were measured prior to and then 5, 15, 30, and 60 min after administration of the respective drugs. The changes in these measurements after administration of the two drugs were analyzed and compared with each other.
Results: The pulmonary function test measurements showed similar improvement after administration of both drugs. Heart rate fell in both groups. After administration of pirbuterol, the alveolar-arterial oxygen pressure difference (P[A-a]O2) and VE rose significantly and the rise in FEV1 showed a negative correlation with the fall in PaO2. In contrast, the use of ipratropium bromide did not produce these effects, but resulted in a fall in VO2 and a rise in VD/Vt.
Conclusion: Pirbuterol and ipratropium are equally effective bronchodilators in COPD. Pirbuterol results in a significant rise in P(A-a)O2 and resting VE. Ipratropium does not affect these measurements and seems to reduce the oxygen cost of breathing. The results suggest significant differences between the effects of the two agents on gas exchange, ventilation, and VO2 which could be of clinical significance.
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http://dx.doi.org/10.1378/chest.107.1.173 | DOI Listing |
The Food and Drug Administration (FDA), after consultation with the Environmental Protection Agency (EPA), is amending FDA's regulation on the use of ozone-depleting substances (ODSs) in self-pressurized containers to remove the essential-use designations for flunisolide, triamcinolone, metaproterenol, pirbuterol, albuterol and ipratropium in combination, cromolyn, and nedocromil used in oral pressurized metered-dose inhalers (MDIs). The Clean Air Act requires FDA, in consultation with the EPA, to determine whether an FDA-regulated product that releases an ODS is an essential use of the ODS. FDA has concluded that there are no substantial technical barriers to formulating flunisolide, triamcinolone, metaproterenol, pirbuterol, albuterol and ipratropium in combination, cromolyn, and nedocromil as products that do not release ODSs, and therefore they will no longer be essential uses of ODSs as of the effective dates of this rule.
View Article and Find Full Text PDFCochrane Database Syst Rev
February 2002
Pulmonary and Critical Care Medicine, Duke University Medical Center, Box 3221, 350 Bell Building, Durham, North Carolina, 27710, USA.
Background: Inhaled short acting beta2 adrenergic agonists and ipratropium bromide are both used in the treatment of acute exacerbations of chronic obstructive pulmonary disease.
Objectives: In patients with acute exacerbations of COPD to: 1. To assess the efficacy of short-acting beta-2 agonists against placebo; 2.
Ann Allergy Asthma Immunol
October 1997
Department of Pediatrics, Wayne State University School of Medicine, Detroit, Michigan, USA.
Background: Oropharyngeal candidiasis is a well-described side effect of inhaled corticosteroids. Nevertheless, few cases of esophageal candidiasis have been reported.
Objective: To present a patient with esophageal candidiasis associated with inhaled corticosteroids.
Chest
January 1995
Department of Medicine, Veterans Affairs Medical Center, Syracuse, NY.
Background: Although both beta-adrenergic agonists and anticholinergic agents are widely used in the treatment of patients with COPD, they influence the pulmonary circulation and ventilation differently. We compared the effects of these two agents on gas exchange and distribution of ventilation in COPD.
Methods: Pirbuterol and ipratropium bromide were administered by inhalation via a metered-dose inhaler to 12 and 14 patients with COPD, respectively, in a randomized, double-blind fashion.
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