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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1998-9-8
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pubmed:abstractText |
Intact cardiac compensatory mechanisms are necessary to maintain adequate tissue oxygenation during acute normovolemic hemodilution (ANH). Left ventricular (LV) perfusion, oxygenation and function were analyzed in an experimental whole-body model of profound ANH (Hct 9%) and effectiveness of a perfluorocarbon-based oxygen carrier in maintaining myocardial oxygenation and function was evaluated. A total of 22 anesthetized dogs were hemodiluted to Hct 20% followed by a simulated, controlled blood-loss phase in which dogs were randomized to either: (1) 1:1 exchange of lost blood with autologous red blood cells (RBC-group), (2) 1:1 exchange with a colloid (control-group) and (3) 1:1 exchange with a colloid after a single dose of 1.8 g/kg BW perflubron i.v. (PFC-group). Myocardial oxygen delivery and consumption as well as endocardial perfusion were determined using radioactive microspheres. LV myocardial contractility (LV MC) was assessed from: (1) the relationship between maximum rate of LV pressure increase (LVdp/dtmax) and LV enddiastolic volume (LVEDV) and (2) analysis of the LV endsystolic pressure volume relationship (ESPVR). LV diastolic properties were reflected by (1) minimum rate of LV pressure increase (LVdp/dtmin), (2) slope and intercept of the enddiastolic pressure-volume relationship (EDPVR) and (3) the time-constant of isovolumic LV pressure decline "tau 1/2". Full sets of LV MC data were obtained from 18 dogs (n = 6 per group). LV MC (LVdp/dtmax-LVEDV relation) increased after perflubron administration. At the lowest Hct level, all parameters reflecting LV MC as well as LVdp/dtmin were significantly higher in the PFC-group than in the control-group. After profound normovolemic hemodilution (Hct 9%) superiority of LV MC and LV diastolic properties was found, when myocardial oxygenation was supported by i.v. perflubron emulsion, a temporary O2 carrier.
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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:month |
Apr
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pubmed:issn |
0300-9130
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
197
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
301-18
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9638793-Anemia,
pubmed-meshheading:9638793-Animals,
pubmed-meshheading:9638793-Blood Substitutes,
pubmed-meshheading:9638793-Blood Transfusion, Autologous,
pubmed-meshheading:9638793-Blood Volume,
pubmed-meshheading:9638793-Dogs,
pubmed-meshheading:9638793-Emulsions,
pubmed-meshheading:9638793-Female,
pubmed-meshheading:9638793-Fluorocarbons,
pubmed-meshheading:9638793-Hematocrit,
pubmed-meshheading:9638793-Hemodilution,
pubmed-meshheading:9638793-Hemodynamics,
pubmed-meshheading:9638793-Infusions, Intravenous,
pubmed-meshheading:9638793-Male,
pubmed-meshheading:9638793-Oxygen Consumption,
pubmed-meshheading:9638793-Ventricular Function, Left
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pubmed:year |
1998
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pubmed:articleTitle |
IV perflubron emulsion versus autologous transfusion in severe normovolemic anemia: effects on left ventricular perfusion and function.
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pubmed:affiliation |
Institute for Surgical Research, Ludwig-Maximilians University, Munich, Germany. habler@icf.med.uni-muenchen.de
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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