A comparison of the VASP index between patients with hemodynamically complicated and uncomplicated acute myocardial infarction
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19902490
DOI
10.1002/ccd.22248
Knihovny.cz E-resources
- MeSH
- Angioplasty, Balloon, Coronary * adverse effects mortality MeSH
- Biomarkers blood MeSH
- Time Factors MeSH
- Down-Regulation MeSH
- Phosphoproteins blood MeSH
- Hemodynamics * MeSH
- Myocardial Infarction blood complications mortality physiopathology therapy MeSH
- Platelet Aggregation Inhibitors therapeutic use MeSH
- International Normalized Ratio MeSH
- Liver Circulation MeSH
- Shock, Cardiogenic blood etiology physiopathology therapy MeSH
- Catecholamines therapeutic use MeSH
- Clopidogrel MeSH
- Middle Aged MeSH
- Humans MeSH
- Microfilament Proteins blood MeSH
- Cell Adhesion Molecules blood MeSH
- Drug Monitoring methods MeSH
- Prospective Studies MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Splanchnic Circulation MeSH
- Case-Control Studies MeSH
- Ticlopidine analogs & derivatives therapeutic use MeSH
- Blood Platelets drug effects metabolism MeSH
- Thrombosis blood etiology mortality prevention & control MeSH
- Respiration, Artificial MeSH
- Platelet Function Tests MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- Phosphoproteins MeSH
- Platelet Aggregation Inhibitors MeSH
- Catecholamines MeSH
- Clopidogrel MeSH
- Microfilament Proteins MeSH
- Cell Adhesion Molecules MeSH
- Ticlopidine MeSH
- Vasodilator-Stimulated Phosphoprotein MeSH
INTRODUCTION: Critically-ill patients with ST-segment elevation myocardial infarction (STEMI) often present with insufficient gastroduodenal motility, liver hypoperfusion, and higher levels of circulating catecholamines. All of these factors can lead to reduced efficacy of clopidogrel, which is only available as a p.o. medication. The aim of the study was to compare clopidogrel effectiveness in unstable STEMI patients on mechanical ventilation with stable STEMI patients. MATERIALS AND METHODS: Two groups of twenty patients with STEMI were enrolled. One group (unstable) consisted of 20 hemodynamically unstable patients on mechanical ventilation and catecholamine support. The other group (stable) consisted of 20 control patients (all patients with STEMI in Killip I class). All patients were treated by primary Percutaneous coronary intervention. Blood samples were drawn before (baseline), at 4h (4h+), 24h (1d+) and 2 days (2d+) after clopidogrel administration. Clopidogrel efficacy was assessed by measurement of vasodilator-stimulated phosphoprotein phosphorylation index. RESULTS: The decrease in the vasodilator-stimulated phosphoprotein (VASP) index was substantially less in unstable patients compared with stable ones (ANOVA, P < 0.001). In stable patients, the VASP index decreased significantly by 20% at 4h+ and by 34% at 1d+, and remained significantly decreased by 31% at 2d+. In unstable patients, the VASP decreased nonsignificantly by 8% at 4h+, and no further decrease of VASP was present (-7% at 1d+, -11% at 2d+). CONCLUSIONS: Laboratory clopidogrel efficacy is lower in patients with MI and severe hemodynamic instability, probably due to splanchnic and liver hypoperfusion and catecholamine use.
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