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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5 Pt 1
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pubmed:dateCreated |
1993-5-27
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pubmed:abstractText |
To determine whether inotropism influences the bradycardic action of tedisamil, hemodynamic assessment was performed in 13 patients with ischemic coronary artery disease including analysis of end-systolic pressure-volume relationships after an infusion of tedisamil, 0.3 mg/kg, at rest, and during paced tachycardia stress. Slope Emax fell by 14% at rest (13 patients) and by 10% during tachycardia (6/13 patients), whereas loops of end-systolic pressure-volume relationships moved rightward; all parameter changes indicated a lack of significant inotropism loss with tedisamil (p > 0.05). Although the mean heart rate decreased from 77.5 to 64.7 beats/min and QTc duration increased by 14% (p < 0.05), filling pressure and dp/dtmin remained unchanged and vascular resistance increased by 30%. Parameters of left ventricular pump function (ejection fraction, stroke volume, left ventricular efficiency) decreased slightly (between 3% and 13%), whereas left ventricular volumes increased (end-diastolic volume by 6%, end-systolic volume by 23%). The respective parameter changes during tachycardia were comparable in tendency, and angina could no longer be induced during postdrug pacing stress. We concluded that the bradycardic effects of tedisamil are selectively generated without impairing either ventricular pump function or contractility in a clinically relevant fashion, whereas the postdrug anginal threshold appears elevated. Thus tedisamil can be used safely in ischemic coronary artery disease.
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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/Bicyclo Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Bicyclo Compounds, Heterocyclic,
http://linkedlifedata.com/resource/pubmed/chemical/Cardiotonic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclopropanes,
http://linkedlifedata.com/resource/pubmed/chemical/tedisamil
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0002-8703
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
125
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1233-46
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8480574-Aged,
pubmed-meshheading:8480574-Bicyclo Compounds,
pubmed-meshheading:8480574-Bicyclo Compounds, Heterocyclic,
pubmed-meshheading:8480574-Cardiotonic Agents,
pubmed-meshheading:8480574-Coronary Disease,
pubmed-meshheading:8480574-Cyclopropanes,
pubmed-meshheading:8480574-Depression, Chemical,
pubmed-meshheading:8480574-Female,
pubmed-meshheading:8480574-Heart Rate,
pubmed-meshheading:8480574-Hemodynamics,
pubmed-meshheading:8480574-Humans,
pubmed-meshheading:8480574-Male,
pubmed-meshheading:8480574-Middle Aged,
pubmed-meshheading:8480574-Myocardial Contraction,
pubmed-meshheading:8480574-Ventricular Function
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pubmed:year |
1993
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pubmed:articleTitle |
Tedisamil (KC 8857) is a new specific bradycardic drug: does it also influence myocardial contractility? Analysis by the conductance (volume) technique in coronary artery disease.
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pubmed:affiliation |
Kerckhoff-Klinik der Max-Planck-Gesellschaft, Bad Nauheim, Germany.
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pubmed:publicationType |
Journal Article,
Clinical Trial
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