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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3-4
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pubmed:dateCreated |
1990-6-11
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pubmed:abstractText |
In order to assess whether different doses and/or plasma levels of almitrine bismesylate (ABM) could induce preferential effects on ventilation or on lung perfusion, we performed a single-blind placebo-controlled study of ABM treatment with different dosages (0.75, 1.5 and 2.25 mg.kg-1 single oral dose) in 26 patients suffering from chronic obstructive pulmonary disease (COPD). All measurements were performed according to the same time table. At control and at three 1.5-hour intervals, we measured alveolar-arterial (A-a) differences, alveolar dead space, total ventilation and ABM plasma levels. The effect on ventilation was estimated using changes in ventilatory parameters and (A-a)O2 differences. The effect on perfusion was indirectly estimated by analysis of arterial-end-tidal (a-ET)CO2 difference and alveolar dead space. The response to treatment was significant for the 1.5- and the 2.25-mg.kg-1 ABM groups, but not for the 0.75 mg.kg-1 ABM and the placebo group. A ventilatory response was often present in both 1.5- and 2.25-mg.kg-1 ABM groups, but a nonventilatory effect was present only at the highest dose according to the Severinghaus and Stupfel concept. Only the parameters reflecting an effect of the distribution of perfusion (a-ET)CO2 difference and alveolar dead space were significantly correlated with ABM plasma levels. The results suggest that a dose-dependent effect of ABM on lung perfusion may explain the controversial data in the literature about the mode of action of ABM.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0025-7931
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
212-9
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pubmed:dateRevised |
2009-11-11
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pubmed:meshHeading |
pubmed-meshheading:2635350-Administration, Oral,
pubmed-meshheading:2635350-Aged,
pubmed-meshheading:2635350-Almitrine,
pubmed-meshheading:2635350-Dose-Response Relationship, Drug,
pubmed-meshheading:2635350-Humans,
pubmed-meshheading:2635350-Lung Diseases, Obstructive,
pubmed-meshheading:2635350-Male,
pubmed-meshheading:2635350-Pulmonary Gas Exchange,
pubmed-meshheading:2635350-Random Allocation
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pubmed:year |
1989
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pubmed:articleTitle |
Is the mode of action of almitrine bismesylate dose dependent?
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pubmed:affiliation |
Service d'Exploration de la Fonction Respiratoire, Hôpital Aiguelongue, Montpellier, France.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Controlled Clinical Trial
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