Abstract | BACKGROUND: METHODS: From the total number of patients enrolled in the EUROVISION registry, 678 subjects affected by ST-elevation myocardial infarction were selected and included in the analysis. Posology and usage patterns of bivalirudin, as evaluated by dose and time of drug bolus and infusion administered, were evaluated. The 30-day outcome has been assessed by efficacy and safety endpoints. RESULTS: All patients received an initial intravenous bolus of bivalirudin (0.70±0.25 mg/kg) followed by an infusion (1.58±0.47 mg/kg/h; duration: 60 [30, 107] min) in 99.3% of cases. An additional bolus (0.49±0.06 mg/kg) was administered in 9.3% of patients. Bivalirudin infusion was prolonged after procedure in 62.2%. Death occurred in 2.1% of patients, non-fatal myocardial reinfarction in 0.3%, unplanned revascularization in 0.6% and non-fatal stroke in 0.4%. Acute stent thrombosis was not observed. Major bleeding occurred in 1.5% of patients. CONCLUSIONS:
Bivalirudin usage in the setting of primary PCI provided excellent results in terms of 30-day outcome even in a real-world population.
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Authors | U Limbruno, A Picchi, S Galli, K Huber, J Lipiecki, D Bernstein, E Deliargyris, P Anthopoulos, C Nienaber, M Hamon |
Journal | Acute cardiac care
(Acute Card Care)
Vol. 16
Issue 4
Pg. 127-31
(Dec 2014)
ISSN: 1748-295X [Electronic] England |
PMID | 25101656
(Publication Type: Clinical Trial, Phase IV, Journal Article, Multicenter Study)
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Chemical References |
- Antithrombins
- Hirudins
- Peptide Fragments
- Recombinant Proteins
- bivalirudin
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Antithrombins
(adverse effects, therapeutic use)
- Electrocardiography
- Europe
- Female
- Hirudins
(adverse effects)
- Humans
- Male
- Middle Aged
- Myocardial Infarction
(physiopathology, therapy)
- Peptide Fragments
(adverse effects, therapeutic use)
- Percutaneous Coronary Intervention
- Prospective Studies
- Recombinant Proteins
(adverse effects, therapeutic use)
- Registries
- Risk Factors
- Treatment Outcome
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