TY - JOUR
T1 - Thrombolytic therapy vs primary percutaneous coronary intervention for myocardial infarction in patients presenting to hospitals without on-site cardiac surgery
T2 - A randomized controlled trial
AU - Aversano, Thomas
AU - Aversano, Lynnet T.
AU - Passamani, Eugene
AU - Knatterud, Genell L.
AU - Terrin, Michael L.
AU - Williams, David O.
AU - Forman, Sandra A.
N1 - Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 2002/4/17
Y1 - 2002/4/17
N2 - Context: Trials comparing primary percutaneous coronary intervention (PCI) and thrombolytic therapy for treatment of acute myocardial infarction (MI) suggest primary PCI is the superior therapy, although they differ with respect to the durability of benefit. Because PCI is often limited to hospitals that have on-site cardiac surgery programs, most acute MI patients do not have access to this therapy. Objective: To determine whether treatment of acute MI with primary PCI is superior to thrombolytic therapy at hospitals without on-site cardiac surgery and, if so, whether superiority is durable. Design: The Atlantic Cardiovascular Patient Outcomes Research Team (C-PORT) trial, a prospective, randomized trial conducted from July 1996 through December 1999. Setting: Eleven community hospitals in Massachusetts and Maryland without on-site cardiac surgery or extant PCI programs. Patients: Four hundred fifty-one thrombolytic-eligible patients with acute MI of less than 12 hours' duration associated with ST-segment elevation on electrocardiogram. Interventions: After a formal primary PCI development program was completed at all sites, patients were randomly assigned to receive primary PCI (n = 225) or accelerated tissue plasminogen activator (bolus dose of 15 mg and an infusion of 0.75 mg/kg for 30 minutes followed by 0.5 mg/kg for 60 minutes; n=226). After initiation of assigned treatment, all care was determined by treating physicians. Main Outcome Measures: Six-month composite incidence of death, recurrent MI, and stroke; median hospital length of stay. Results: The incidence of the composite end point was reduced in the primary PCI group at 6 weeks (10.7% vs 17.7%; P=.03) and 6 months (12.4% vs 19.9%; P=.03) after index MI. Six-month rates for individual outcomes were 6.2% vs 7.1% for death (P=.72), 5.3% vs 10.6% for recurrent MI (P=.04), and 2.2% vs 4.0% for stroke (P=.28) for primary PCI vs thrombolytic therapy, respectively. Median length of stay was also reduced in the primary PCI group (4.5 vs 6.0 days; P=.02). Conclusions: Compared with thrombolytic therapy, treatment of patients with primary PCI at hospitals without on-site cardiac surgery is associated with better clinical outcomes for 6 months after index MI and a shorter hospital stay.
AB - Context: Trials comparing primary percutaneous coronary intervention (PCI) and thrombolytic therapy for treatment of acute myocardial infarction (MI) suggest primary PCI is the superior therapy, although they differ with respect to the durability of benefit. Because PCI is often limited to hospitals that have on-site cardiac surgery programs, most acute MI patients do not have access to this therapy. Objective: To determine whether treatment of acute MI with primary PCI is superior to thrombolytic therapy at hospitals without on-site cardiac surgery and, if so, whether superiority is durable. Design: The Atlantic Cardiovascular Patient Outcomes Research Team (C-PORT) trial, a prospective, randomized trial conducted from July 1996 through December 1999. Setting: Eleven community hospitals in Massachusetts and Maryland without on-site cardiac surgery or extant PCI programs. Patients: Four hundred fifty-one thrombolytic-eligible patients with acute MI of less than 12 hours' duration associated with ST-segment elevation on electrocardiogram. Interventions: After a formal primary PCI development program was completed at all sites, patients were randomly assigned to receive primary PCI (n = 225) or accelerated tissue plasminogen activator (bolus dose of 15 mg and an infusion of 0.75 mg/kg for 30 minutes followed by 0.5 mg/kg for 60 minutes; n=226). After initiation of assigned treatment, all care was determined by treating physicians. Main Outcome Measures: Six-month composite incidence of death, recurrent MI, and stroke; median hospital length of stay. Results: The incidence of the composite end point was reduced in the primary PCI group at 6 weeks (10.7% vs 17.7%; P=.03) and 6 months (12.4% vs 19.9%; P=.03) after index MI. Six-month rates for individual outcomes were 6.2% vs 7.1% for death (P=.72), 5.3% vs 10.6% for recurrent MI (P=.04), and 2.2% vs 4.0% for stroke (P=.28) for primary PCI vs thrombolytic therapy, respectively. Median length of stay was also reduced in the primary PCI group (4.5 vs 6.0 days; P=.02). Conclusions: Compared with thrombolytic therapy, treatment of patients with primary PCI at hospitals without on-site cardiac surgery is associated with better clinical outcomes for 6 months after index MI and a shorter hospital stay.
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U2 - 10.1001/jama.287.15.1943
DO - 10.1001/jama.287.15.1943
M3 - Article
C2 - 11960536
AN - SCOPUS:0037123206
VL - 287
SP - 1943
EP - 1951
JO - JAMA - Journal of the American Medical Association
JF - JAMA - Journal of the American Medical Association
SN - 0098-7484
IS - 15
ER -