Multicenter randomized trial of facilitated percutaneous coronary intervention with low-dose tenecteplase in patients with acute myocardial infarction : the Athens PCI trial
2009 Wiley-Liss, Inc..
OBJECTIVES: To examine the safety and efficacy of low-dose tenecteplase, administered before facilitated percutaneous coronary intervention (PCI) to restore Thrombolysis In Myocardial Infarction (TIMI) grade 2 or 3 blood flow in the infarct related artery (IRA) in patients with ST elevation myocardial infarction (STEMI) scheduled to undergo PCI with a shortest anticipated delay of 30 min.
BACKGROUND: PCI preceded by administration of glycoprotein IIb/IIIa inhibitors, full-dose thrombolytics, or both, is associated with no benefit or a higher incidence of adverse events than PCI alone.
METHODS: Patients with STEMI < 6 hr in duration were randomly assigned to PCI preceded by tenecteplase, 10 mg (facilitated PCI group, n = 143) versus standard PCI (control group, n = 141). All patients received aspirin and unfractionated heparin (70 IU/kg bolus) at time of randomization. Both groups received IIb/IIIa inhibitors in the catheterization laboratory and for at least 20 hr after PCI.
RESULTS: The median door-to-balloon time was 122 min (91-175) in the facilitated PCI versus 120 min (89-175) in the control group. IRA patency on arrival in the catheterization laboratory was 59.5% in the facilitated PCI (24% TIMI-2, 35% TIMI-3), versus 37% in the control (8% TIMI-2, 29% TIMI-3) group (P = 0.0001). During hospitalization, 9 patients (6%) died in the facilitated PCI versus 5 patients (3.5%) in the control group (P = 0.572). A single patient in the facilitated PCI group suffered a non-fatal ischemic stroke.
CONCLUSIONS: Facilitated PCI with low-dose tenecteplase in patients presenting with STEMI was associated with a high IRA patency rate before PCI.
Errataetall: |
CommentIn: Catheter Cardiovasc Interv. 2009 Sep 1;74(3):406-7. - PMID 19681117 |
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Medienart: |
E-Artikel |
Erscheinungsjahr: |
2009 |
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Erschienen: |
2009 |
Enthalten in: |
Zur Gesamtaufnahme - volume:74 |
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Enthalten in: |
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions - 74(2009), 3 vom: 01. Sept., Seite 398-405 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Kanakakis, John [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 29.10.2009 Date Revised 01.12.2018 published: Print CommentIn: Catheter Cardiovasc Interv. 2009 Sep 1;74(3):406-7. - PMID 19681117 Citation Status MEDLINE |
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doi: |
10.1002/ccd.22009 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM187763577 |
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100 | 1 | |a Kanakakis, John |e verfasserin |4 aut | |
245 | 1 | 0 | |a Multicenter randomized trial of facilitated percutaneous coronary intervention with low-dose tenecteplase in patients with acute myocardial infarction |b the Athens PCI trial |
264 | 1 | |c 2009 | |
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500 | |a Date Revised 01.12.2018 | ||
500 | |a published: Print | ||
500 | |a CommentIn: Catheter Cardiovasc Interv. 2009 Sep 1;74(3):406-7. - PMID 19681117 | ||
500 | |a Citation Status MEDLINE | ||
520 | |a 2009 Wiley-Liss, Inc. | ||
520 | |a OBJECTIVES: To examine the safety and efficacy of low-dose tenecteplase, administered before facilitated percutaneous coronary intervention (PCI) to restore Thrombolysis In Myocardial Infarction (TIMI) grade 2 or 3 blood flow in the infarct related artery (IRA) in patients with ST elevation myocardial infarction (STEMI) scheduled to undergo PCI with a shortest anticipated delay of 30 min | ||
520 | |a BACKGROUND: PCI preceded by administration of glycoprotein IIb/IIIa inhibitors, full-dose thrombolytics, or both, is associated with no benefit or a higher incidence of adverse events than PCI alone | ||
520 | |a METHODS: Patients with STEMI < 6 hr in duration were randomly assigned to PCI preceded by tenecteplase, 10 mg (facilitated PCI group, n = 143) versus standard PCI (control group, n = 141). All patients received aspirin and unfractionated heparin (70 IU/kg bolus) at time of randomization. Both groups received IIb/IIIa inhibitors in the catheterization laboratory and for at least 20 hr after PCI | ||
520 | |a RESULTS: The median door-to-balloon time was 122 min (91-175) in the facilitated PCI versus 120 min (89-175) in the control group. IRA patency on arrival in the catheterization laboratory was 59.5% in the facilitated PCI (24% TIMI-2, 35% TIMI-3), versus 37% in the control (8% TIMI-2, 29% TIMI-3) group (P = 0.0001). During hospitalization, 9 patients (6%) died in the facilitated PCI versus 5 patients (3.5%) in the control group (P = 0.572). A single patient in the facilitated PCI group suffered a non-fatal ischemic stroke | ||
520 | |a CONCLUSIONS: Facilitated PCI with low-dose tenecteplase in patients presenting with STEMI was associated with a high IRA patency rate before PCI | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Multicenter Study | |
650 | 4 | |a Randomized Controlled Trial | |
650 | 7 | |a Anticoagulants |2 NLM | |
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650 | 7 | |a Platelet Aggregation Inhibitors |2 NLM | |
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700 | 1 | |a Charbis, Panagiotis |e verfasserin |4 aut | |
700 | 1 | |a Rokas, Stylianos |e verfasserin |4 aut | |
700 | 1 | |a Anastasiou-Nana, Maria |e verfasserin |4 aut | |
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